| geneid | 26958 |
|---|---|
| ensemblid | ENSG00000158623.14 |
| hgncid | 2237 |
| symbol | COPG2 |
| name | COPI coat complex subunit gamma 2 |
| refseq_nuc | NM_012133.6 |
| refseq_prot | NP_036265.3 |
| ensembl_nuc | ENST00000425248.5 |
| ensembl_prot | ENSP00000402346.2 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 130506238 |
| end | 130668748 |
| strand | - |
| ver | v1.2 |
| region | chr7:130506238-130668748 |
| region5000 | chr7:130501238-130673748 |
| regionname0 | COPG2_chr7_130506238_130668748 |
| regionname5000 | COPG2_chr7_130501238_130673748 |
| 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 | 871 | 313 | 87 | 59 | 108 | 13 | 44 | 80 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0002 | 0/0 | 871 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0003 | 0/0 | 871 | 3 | 1 | 0 | 2 | 0 | 0 | 2 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0004 | 0/0 | 871 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0005 | 0/0 | 871 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0006 | 0/0 | 871 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0007 | 0/0 | 871 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0008 | 0/0 | 871 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0009 | 0/0 | 871 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0010 | 0/0 | 871 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2616 | 203 | 63 | 39 | 62 | 11 | 26 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| c0002 | 0/0 | 2616 | 105 | 21 | 20 | 44 | 2 | 18 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| c0003 | 0/0 | 2616 | 3 | 2 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| c0004 | 0/0 | 2616 | 2 | 0 | 0 | 2 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| c0005 | 0/0 | 2616 | 2 | 2 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| c0006 | 0/0 | 2616 | 2 | 0 | 0 | 2 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| c0007 | 0/0 | 2616 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| c0008 | 0/0 | 2616 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| c0009 | 0/0 | 2616 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| c0010 | 0/0 | 2616 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| c0011 | 0/0 | 2616 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| c0012 | 0/0 | 2616 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| c0013 | 0/0 | 2616 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| c0014 | 0/0 | 2616 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| c0015 | 0/0 | 2616 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| 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 | 1/0 | 519 | 179 | 65 | 25 | 59 | 10 | 19 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| t0002 | 0/1 | 518 | 85 | 8 | 18 | 39 | 3 | 16 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| t0003 | 0/0 | 512 | 20 | 0 | 6 | 9 | 1 | 4 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| t0004 | 0/0 | 520 | 12 | 2 | 4 | 2 | 0 | 4 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| t0005 | 0/0 | 519 | 9 | 6 | 3 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| t0006 | 0/0 | 519 | 8 | 2 | 2 | 3 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| t0007 | 0/0 | 519 | 5 | 3 | 2 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| t0008 | 0/0 | 518 | 3 | 3 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| t0009 | 0/0 | 520 | 2 | 2 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| t0010 | 0/0 | 519 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| t0011 | 0/0 | 520 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| t0012 | 0/0 | 518 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0027 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0054 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2616 | 203 | 63 | 39 | 62 | 11 | 26 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0001c0002 | 0/0 | 2616 | 105 | 21 | 20 | 44 | 2 | 18 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0001c0005 | 0/0 | 2616 | 2 | 2 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0001c0006 | 0/0 | 2616 | 2 | 0 | 0 | 2 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0001c0012 | 0/0 | 2616 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0002c0003 | 0/0 | 2616 | 3 | 2 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0003c0004 | 0/0 | 2616 | 2 | 0 | 0 | 2 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0003c0008 | 0/0 | 2616 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0004c0011 | 0/0 | 2616 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0005c0010 | 0/0 | 2616 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0006c0007 | 0/0 | 2616 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0007c0009 | 0/0 | 2616 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0008c0013 | 0/0 | 2616 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0009c0014 | 0/0 | 2616 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0010c0015 | 0/0 | 2616 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3134 | 96 | 43 | 16 | 21 | 8 | 7 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0001c0001t0002 | 0/1 | 3133 | 78 | 5 | 17 | 36 | 3 | 16 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0001c0001t0004 | 0/0 | 3135 | 8 | 2 | 4 | 0 | 0 | 2 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0001c0001t0005 | 0/0 | 3134 | 6 | 6 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0001c0001t0006 | 0/0 | 3134 | 8 | 2 | 2 | 3 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0001c0001t0008 | 0/0 | 3133 | 3 | 3 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0001c0001t0009 | 0/0 | 3135 | 2 | 2 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0001c0001t0010 | 0/0 | 3134 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0001c0001t0012 | 0/0 | 3133 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0001c0002t0001 | 0/0 | 3134 | 71 | 17 | 8 | 33 | 1 | 12 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0001c0002t0002 | 0/0 | 3133 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0001c0002t0003 | 0/0 | 3127 | 20 | 0 | 6 | 9 | 1 | 4 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0001c0002t0004 | 0/0 | 3135 | 4 | 0 | 0 | 2 | 0 | 2 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0001c0002t0005 | 0/0 | 3134 | 3 | 0 | 3 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0001c0002t0007 | 0/0 | 3134 | 5 | 3 | 2 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0001c0002t0011 | 0/0 | 3135 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0001c0005t0002 | 0/0 | 3133 | 2 | 2 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0001c0006t0002 | 0/0 | 3133 | 2 | 0 | 0 | 2 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0001c0012t0002 | 0/0 | 3133 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0002c0003t0001 | 0/0 | 3134 | 3 | 2 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0003c0004t0001 | 0/0 | 3134 | 2 | 0 | 0 | 2 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0003c0008t0001 | 0/0 | 3134 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0004c0011t0001 | 0/0 | 3134 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0005c0010t0001 | 0/0 | 3134 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0006c0007t0001 | 0/0 | 3134 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0007c0009t0002 | 0/0 | 3133 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0008c0013t0001 | 0/0 | 3134 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0009c0014t0001 | 0/0 | 3134 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| a0010c0015t0001 | 0/0 | 3134 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | copy fasta | chr7 | 130501238 | 130673748 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0054 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0027 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0004g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0004g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0004g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0005g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0006g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0006g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0006g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0006g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0006g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0006g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0008g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0008g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0008g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0009g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0009g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0010g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0001t0012g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0004g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0005g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0005g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0005g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0007g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0007g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0007g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0007g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0007g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0002t0011g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0005t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0005t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0006t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0006t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0001c0012t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0002c0003t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0002c0003t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0002c0003t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0003c0004t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0003c0004t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0003c0008t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0004c0011t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0005c0010t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0006c0007t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0007c0009t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0008c0013t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0009c0014t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| a0010c0015t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0036 | EUR | GBR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00099 | hp2 | a0004 | c0011 | t0001 | g0280 | EUR | GBR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0271 | EUR | GBR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0195 | EUR | GBR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00323 | hp1 | a0001 | c0002 | t0003 | g0107 | EUR | FIN | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0325 | EUR | FIN | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | CHS | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | CHS | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00544 | hp1 | a0001 | c0002 | t0003 | g0104 | EAS | CHS | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | CHS | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | CHS | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | CHS | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | CHS | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | CHS | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | CHS | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | CHS | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0180 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0035 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0020 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0248 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0124 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0210 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01192 | hp2 | a0001 | c0002 | t0007 | g0237 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0050 | AMR | PUR | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0088 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01256 | hp1 | a0001 | c0002 | t0005 | g0077 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0324 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01258 | hp1 | a0001 | c0002 | t0005 | g0076 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01261 | hp1 | a0001 | c0001 | t0006 | g0201 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01261 | hp2 | a0001 | c0002 | t0003 | g0087 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0096 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0070 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01433 | hp2 | a0002 | c0003 | t0001 | g0243 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0293 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | CLM | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0221 | EUR | IBS | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | IBS | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0291 | EUR | IBS | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0144 | EUR | IBS | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0314 | EUR | IBS | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0203 | EUR | IBS | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0101 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01891 | hp2 | a0001 | c0001 | t0008 | g0321 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0204 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0208 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01952 | hp2 | a0001 | c0002 | t0003 | g0120 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01975 | hp1 | a0001 | c0002 | t0003 | g0109 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0267 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01981 | hp1 | a0001 | c0002 | t0003 | g0080 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01981 | hp2 | a0001 | c0001 | t0006 | g0178 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01993 | hp1 | a0001 | c0002 | t0007 | g0238 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG01993 | hp2 | a0001 | c0002 | t0005 | g0078 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0040 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02015 | hp1 | a0001 | c0002 | t0003 | g0105 | EAS | KHV | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | KHV | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0256 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | KHV | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02056 | hp2 | a0001 | c0002 | t0003 | g0103 | EAS | KHV | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | KHV | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | KHV | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | KHV | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | KHV | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | KHV | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | KHV | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | KHV | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0063 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0149 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02148 | hp1 | a0001 | c0002 | t0003 | g0108 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | CDX | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | CDX | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | CDX | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | CDX | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0196 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0059 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02300 | hp2 | a0001 | c0002 | t0003 | g0110 | AMR | PEL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02451 | hp2 | a0001 | c0005 | t0002 | g0011 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02523 | hp1 | a0001 | c0002 | t0003 | g0106 | EAS | KHV | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | KHV | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0131 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0046 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02622 | hp1 | a0010 | c0015 | t0001 | g0259 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0247 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0065 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0258 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0315 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0194 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0228 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0254 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0128 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0049 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02738 | hp1 | a0001 | c0001 | t0006 | g0198 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0094 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02809 | hp1 | a0002 | c0003 | t0001 | g0242 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02818 | hp1 | a0001 | c0002 | t0007 | g0239 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0052 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0126 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ESN | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ESN | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0022 | AFR | ESN | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02970 | hp2 | a0001 | c0001 | t0008 | g0318 | AFR | ESN | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02976 | hp1 | a0001 | c0002 | t0007 | g0236 | AFR | ESN | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0250 | AFR | ESN | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0053 | AFR | ESN | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | ESN | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03195 | hp1 | a0001 | c0001 | t0008 | g0322 | AFR | ESN | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03209 | hp1 | a0001 | c0001 | t0009 | g0252 | AFR | MSL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | MSL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0051 | AFR | MSL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0232 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | MSL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0064 | AFR | MSL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | MSL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0033 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03490 | hp2 | a0001 | c0002 | t0003 | g0122 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0229 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0039 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0032 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0218 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0226 | AFR | ESN | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | MSL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0047 | AFR | MSL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0048 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0185 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0062 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | STU | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0234 | SAS | STU | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0019 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0045 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0163 | SAS | PJL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03831 | hp1 | a0001 | c0002 | t0003 | g0068 | SAS | BEB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0157 | SAS | BEB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0177 | SAS | BEB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0125 | SAS | BEB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0249 | SAS | BEB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03927 | hp2 | a0001 | c0002 | t0004 | g0100 | SAS | BEB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0233 | SAS | BEB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03942 | hp2 | a0001 | c0002 | t0003 | g0123 | SAS | BEB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG04115 | hp1 | a0001 | c0002 | t0004 | g0056 | SAS | STU | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0219 | SAS | STU | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG04184 | hp1 | a0001 | c0002 | t0003 | g0121 | SAS | BEB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | BEB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0308 | SAS | STU | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0028 | SAS | STU | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0102 | SAS | STU | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0207 | SAS | STU | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0272 | SAS | STU | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | STU | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0227 | AFR | YRI | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18522 | hp2 | a0001 | c0005 | t0002 | g0010 | AFR | YRI | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | YRI | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0241 | AFR | YRI | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18941 | hp2 | a0001 | c0006 | t0002 | g0153 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18945 | hp1 | a0001 | c0006 | t0002 | g0154 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18947 | hp2 | a0001 | c0001 | t0006 | g0172 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18960 | hp2 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18962 | hp2 | a0006 | c0007 | t0001 | g0095 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18965 | hp1 | a0003 | c0004 | t0001 | g0277 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18966 | hp2 | a0001 | c0002 | t0004 | g0081 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18967 | hp1 | a0001 | c0001 | t0012 | g0206 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19009 | hp1 | a0001 | c0001 | t0006 | g0168 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19010 | hp1 | a0001 | c0002 | t0003 | g0111 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19010 | hp2 | a0003 | c0004 | t0001 | g0297 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19030 | hp1 | a0005 | c0010 | t0001 | g0147 | AFR | LWK | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19030 | hp2 | a0001 | c0002 | t0007 | g0235 | AFR | LWK | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19043 | hp1 | a0001 | c0012 | t0002 | g0166 | AFR | LWK | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | LWK | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19054 | hp1 | a0001 | c0001 | t0006 | g0182 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19054 | hp2 | a0001 | c0002 | t0003 | g0261 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19066 | hp1 | a0001 | c0002 | t0003 | g0113 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19070 | hp1 | a0001 | c0002 | t0003 | g0112 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19078 | hp2 | a0001 | c0002 | t0003 | g0117 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19079 | hp2 | a0008 | c0013 | t0001 | g0067 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19081 | hp1 | a0009 | c0014 | t0001 | g0089 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19082 | hp2 | a0007 | c0009 | t0002 | g0217 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0251 | AFR | ASW | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | ASW | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0136 | EUR | TSI | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0268 | EUR | TSI | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02486 | hp1 | a0001 | c0002 | t0011 | g0240 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0060 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | ACB | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | MSL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | MSL | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG06807 | hp1 | a0003 | c0008 | t0001 | g0114 | AFR | USA | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | USA | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18955 | hp1 | a0001 | c0002 | t0004 | g0083 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | USA | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA20300 | hp2 | a0002 | c0003 | t0001 | g0244 | AFR | USA | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0061 | AFR | LWK | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0027 | REF | REF | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0054 | REF | REF | COPG2_chr7_130501238_130673748 | COPG2 | chr7 | 130501238 | 130673748 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:130506741
|
T | C | 1 | a0005 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.2551A>G | p.Met851Val | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 24/24 | 2631/3134 | 2551/2616 | 851/871 | chr7 | 130506741 | ||
| chr7:130506746
|
A | C | 1 | a0006 | 1 | NA18962.hp2 | missense_variant | MODERATE | c.2546T>G | p.Val849Gly | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 24/24 | 2626/3134 | 2546/2616 | 849/871 | chr7 | 130506746 | ||
| chr7:130506747
|
C | A | 1 | a0006 | 1 | NA18962.hp2 | missense_variant | MODERATE | c.2545G>T | p.Val849Leu | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 24/24 | 2625/3134 | 2545/2616 | 849/871 | chr7 | 130506747 | ||
| chr7:130507288
|
G | A | 1 | a0003 | 3 | HG06807.hp1 NA18965.hp1 NA19010.hp2 |
missense_variant | MODERATE | c.2471C>T | p.Ser824Leu | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 23/24 | 2551/3134 | 2471/2616 | 824/871 | chr7 | 130507288 | ||
| chr7:130547718
|
A | G | 1 | a0007 | 1 | NA19082.hp2 | missense_variant | MODERATE | c.2105T>C | p.Ile702Thr | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/24 | 2185/3134 | 2105/2616 | 702/871 | chr7 | 130547718 | ||
| chr7:130547741
|
G | C | 1 | a0004 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.2082C>G | p.Ser694Arg | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/24 | 2162/3134 | 2082/2616 | 694/871 | chr7 | 130547741 | ||
| chr7:130611083
|
G | C | 1 | a0008 | 1 | NA19079.hp2 | missense_variant | MODERATE | c.607C>G | p.Leu203Val | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/24 | 687/3134 | 607/2616 | 203/871 | chr7 | 130611083 | ||
| chr7:130612195
|
T | C | 1 | a0009 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.536A>G | p.Asn179Ser | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 8/24 | 616/3134 | 536/2616 | 179/871 | chr7 | 130612195 | ||
| chr7:130612222
|
C | T | 1 | a0002 | 3 | HG01433.hp2 HG02809.hp1 NA20300.hp2 |
missense_variant | MODERATE | c.509G>A | p.Ser170Asn | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 8/24 | 589/3134 | 509/2616 | 170/871 | chr7 | 130612222 | ||
| chr7:130667522
|
T | C | 1 | a0010 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.50A>G | p.Asn17Ser | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 2/24 | 130/3134 | 50/2616 | 17/871 | chr7 | 130667522 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:130547783
|
T | C | 1 | a0001c0012 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.2040A>G | p.Pro680Pro | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/24 | 2120/3134 | 2040/2616 | 680/871 | chr7 | 130547783 | ||
| chr7:130549333
|
G | A | 1 | a0001c0005 | 2 | HG02451.hp2 NA18522.hp2 |
synonymous_variant | LOW | c.1818C>T | p.Ser606Ser | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 18/24 | 1898/3134 | 1818/2616 | 606/871 | chr7 | 130549333 | ||
| chr7:130550642
|
C | T | 7 | a0001c0002a0002c0003a0003c0008others(4): Show | 113 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(110): Show |
synonymous_variant | LOW | c.1656G>A | p.Thr552Thr | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/24 | 1736/3134 | 1656/2616 | 552/871 | chr7 | 130550642 | ||
| chr7:130563323
|
G | A | 1 | a0001c0006 | 2 | NA18941.hp2 NA18945.hp1 |
synonymous_variant | LOW | c.885C>T | p.Phe295Phe | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 11/24 | 965/3134 | 885/2616 | 295/871 | chr7 | 130563323 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:130506318
|
T | TC | 5 | a0001c0001t0004a0001c0001t0006a0001c0001t0009others(2): Show | 23 | HG01099.hp2 HG01256.hp2 HG01261.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*357dupG | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 24/24 | 357 | chr7 | 130506318 | |||||
| chr7:130506318
|
TCCCCCCC | T | 1 | a0001c0002t0003 | 20 | HG00323.hp1 HG00544.hp1 HG01261.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*351_*357delGGGGGG others(1): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 24/24 | 351 | chr7 | 130506318 | |||||
| chr7:130506325
|
C | T | 1 | a0001c0001t0008 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*351G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 24/24 | 351 | chr7 | 130506325 | |||||
| chr7:130506473
|
G | A | 2 | a0001c0002t0007a0001c0002t0011 | 6 | HG01192.hp2 HG01993.hp1 HG02486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*203C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 24/24 | 203 | chr7 | 130506473 | |||||
| chr7:130506485
|
GA | G | 9 | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(6): Show | 97 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*190delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 24/24 | 190 | chr7 | 130506485 | |||||
| chr7:130506501
|
C | A | 3 | a0001c0001t0005a0001c0001t0009a0001c0002t0005 | 11 | HG01256.hp1 HG01258.hp1 HG01993.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*175G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 24/24 | 175 | chr7 | 130506501 | |||||
| chr7:130506644
|
T | C | 1 | a0001c0001t0012 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*32A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 24/24 | 32 | chr7 | 130506644 | |||||
| chr7:130668694
|
C | G | 1 | a0001c0001t0010 | 1 | NA18960.hp2 | 5_prime_UTR_variant | MODIFIER | c.-26G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 1/24 | 26 | chr7 | 130668694 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:130506825
|
G | A | 1 | a0006c0007t0001g0095 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2486-19C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 23/23 | chr7 | 130506825 | ||||||
| chr7:130506826
|
A | G | 1 | a0006c0007t0001g0095 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2486-20T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 23/23 | chr7 | 130506826 | ||||||
| chr7:130506866
|
A | C | 1 | a0001c0001t0001g0325 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2486-60T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 23/23 | chr7 | 130506866 | ||||||
| chr7:130507178
|
G | C | 10 | a0001c0002t0001g0079a0001c0002t0001g0090a0001c0002t0001g0091others(7): Show | 10 | NA18939.hp1 NA18941.hp1 NA18944.hp2 others(7): Show |
intron_variant | MODIFIER | c.2485+96C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 23/23 | chr7 | 130507178 | ||||||
| chr7:130507217
|
A | C | 1 | a0006c0007t0001g0095 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2485+57T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 23/23 | chr7 | 130507217 | ||||||
| chr7:130507466
|
T | G | 101 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0200others(98): Show | 101 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.2387-94A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 22/23 | chr7 | 130507466 | ||||||
| chr7:130507868
|
T | C | 1 | a0001c0001t0002g0193 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2248-45A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 21/23 | chr7 | 130507868 | ||||||
| chr7:130507938
|
T | A | 1 | a0006c0007t0001g0095 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2248-115A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 21/23 | chr7 | 130507938 | ||||||
| chr7:130507966
|
A | C | 1 | a0001c0002t0001g0066 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2248-143T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 21/23 | chr7 | 130507966 | ||||||
| chr7:130508135
|
T | G | 3 | a0001c0001t0008g0318a0001c0001t0008g0321a0001c0001t0008g0322 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2248-312A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 21/23 | chr7 | 130508135 | ||||||
| chr7:130508248
|
C | T | 1 | a0001c0001t0001g0281 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2247+314G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 21/23 | chr7 | 130508248 | ||||||
| chr7:130508508
|
G | T | 1 | a0001c0002t0001g0115 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2247+54C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 21/23 | chr7 | 130508508 | ||||||
| chr7:130508666
|
G | A | 93 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(90): Show | 93 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
splice_region_variant&intron_variant | LOW | c.2150-7C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130508666 | ||||||
| chr7:130508718
|
C | A | 1 | a0001c0001t0002g0183 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2150-59G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130508718 | ||||||
| chr7:130508721
|
T | TTCTTAGG others(5): Show |
325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(322): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.2150-63_2150-62ins others(12): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130508721 | ||||||
| chr7:130508731
|
C | A | 3 | a0001c0001t0008g0318a0001c0001t0008g0321a0001c0001t0008g0322 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2150-72G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130508731 | ||||||
| chr7:130508789
|
T | C | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-130A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130508789 | ||||||
| chr7:130508855
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2150-196T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130508855 | ||||||
| chr7:130508976
|
G | A | 89 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(86): Show | 89 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.2150-317C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130508976 | ||||||
| chr7:130509028
|
C | A | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-369G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130509028 | ||||||
| chr7:130509040
|
C | CA | 12 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0278others(9): Show | 12 | HG00099.hp1 HG00639.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.2150-382dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130509040 | ||||||
| chr7:130509062
|
A | G | 106 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0245others(103): Show | 106 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.2150-403T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130509062 | ||||||
| chr7:130509143
|
T | G | 1 | a0001c0001t0001g0290 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2150-484A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130509143 | ||||||
| chr7:130509220
|
G | C | 106 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0245others(103): Show | 106 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.2150-561C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130509220 | ||||||
| chr7:130509406
|
AAAG | A | 4 | a0001c0001t0002g0160a0001c0001t0002g0191a0001c0001t0002g0192others(1): Show | 4 | HG00544.hp2 HG00558.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-750_2150-748d others(5): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130509406 | ||||||
| chr7:130509430
|
G | A | 6 | a0001c0002t0007g0235a0001c0002t0007g0236a0001c0002t0007g0237others(3): Show | 6 | HG01192.hp2 HG01993.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2150-771C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130509430 | ||||||
| chr7:130509435
|
G | A | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-776C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130509435 | ||||||
| chr7:130509485
|
G | A | 100 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(97): Show | 100 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.2150-826C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130509485 | ||||||
| chr7:130509486
|
T | G | 1 | a0001c0001t0002g0156 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2150-827A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130509486 | ||||||
| chr7:130509519
|
A | G | 1 | a0001c0001t0004g0249 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2150-860T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130509519 | ||||||
| chr7:130509733
|
TAAATA | T | 3 | a0001c0001t0008g0318a0001c0001t0008g0321a0001c0001t0008g0322 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2150-1079_2150-107 others(9): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130509733 | ||||||
| chr7:130509833
|
C | T | 7 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(4): Show | 7 | HG01243.hp1 HG02258.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2150-1174G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130509833 | ||||||
| chr7:130509852
|
G | C | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2150-1193C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130509852 | ||||||
| chr7:130510178
|
G | A | 9 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0135others(6): Show | 9 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.2150-1519C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130510178 | ||||||
| chr7:130510271
|
C | G | 6 | a0001c0002t0007g0235a0001c0002t0007g0236a0001c0002t0007g0237others(3): Show | 6 | HG01192.hp2 HG01993.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2150-1612G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130510271 | ||||||
| chr7:130510286
|
A | C | 3 | a0001c0001t0008g0318a0001c0001t0008g0321a0001c0001t0008g0322 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2150-1627T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130510286 | ||||||
| chr7:130510711
|
CTGAAACC others(4): Show |
C | 108 | a0001c0001t0001g0030a0001c0001t0001g0071a0001c0001t0001g0072others(105): Show | 108 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.2150-2063_2150-205 others(15): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130510711 | ||||||
| chr7:130510713
|
G | A | 1 | a0001c0002t0001g0119 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2150-2054C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130510713 | ||||||
| chr7:130510804
|
G | A | 1 | a0001c0001t0002g0176 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2150-2145C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130510804 | ||||||
| chr7:130510824
|
C | T | 1 | a0001c0001t0001g0326 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2150-2165G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130510824 | ||||||
| chr7:130510825
|
G | A | 1 | a0001c0001t0004g0128 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2150-2166C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130510825 | ||||||
| chr7:130510864
|
G | A | 94 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(91): Show | 94 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.2150-2205C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130510864 | ||||||
| chr7:130510884
|
A | C | 2 | a0002c0003t0001g0243a0002c0003t0001g0244 | 2 | HG01433.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2150-2225T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130510884 | ||||||
| chr7:130511091
|
G | C | 3 | a0001c0001t0008g0318a0001c0001t0008g0321a0001c0001t0008g0322 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2150-2432C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130511091 | ||||||
| chr7:130511242
|
A | G | 100 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(97): Show | 100 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.2150-2583T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130511242 | ||||||
| chr7:130511391
|
G | A | 12 | a0001c0001t0001g0127a0001c0001t0001g0132a0001c0001t0001g0133others(9): Show | 12 | HG01891.hp1 HG01943.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.2150-2732C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130511391 | ||||||
| chr7:130511600
|
T | C | 2 | a0001c0002t0005g0076a0001c0002t0005g0077 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2150-2941A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130511600 | ||||||
| chr7:130511642
|
A | G | 2 | a0001c0001t0001g0030a0001c0002t0004g0081 | 2 | HG02818.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.2150-2983T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130511642 | ||||||
| chr7:130511692
|
T | C | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-3033A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130511692 | ||||||
| chr7:130511853
|
T | G | 64 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(61): Show | 64 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.2150-3194A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130511853 | ||||||
| chr7:130512052
|
T | TA | 35 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0016others(32): Show | 35 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.2150-3394dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130512052 | ||||||
| chr7:130512052
|
T | TAA | 20 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0071others(17): Show | 20 | HG00639.hp2 HG01261.hp2 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.2150-3395_2150-339 others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130512052 | ||||||
| chr7:130512052
|
TA | T | 7 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0325others(4): Show | 7 | HG00323.hp2 HG01070.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.2150-3394delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130512052 | ||||||
| chr7:130512052
|
TAAA | T | 86 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(83): Show | 86 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.2150-3396_2150-339 others(7): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130512052 | ||||||
| chr7:130512091
|
G | A | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(2): Show | 5 | HG01934.hp1 HG02165.hp1 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.2150-3432C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130512091 | ||||||
| chr7:130512182
|
C | T | 1 | a0001c0002t0001g0042 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2150-3523G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130512182 | ||||||
| chr7:130512345
|
T | C | 1 | a0001c0001t0002g0156 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2150-3686A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130512345 | ||||||
| chr7:130512473
|
A | G | 1 | a0001c0002t0001g0060 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2150-3814T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130512473 | ||||||
| chr7:130512616
|
C | A | 4 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(1): Show | 4 | HG01099.hp1 HG02257.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-3957G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130512616 | ||||||
| chr7:130512739
|
C | T | 3 | a0001c0001t0002g0179a0001c0001t0002g0180a0001c0001t0006g0201 | 3 | HG00639.hp1 HG01261.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.2150-4080G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130512739 | ||||||
| chr7:130512934
|
G | T | 1 | a0001c0001t0002g0205 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2150-4275C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130512934 | ||||||
| chr7:130513044
|
A | G | 112 | a0001c0001t0001g0030a0001c0001t0001g0071a0001c0001t0001g0072others(109): Show | 112 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.2150-4385T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513044 | ||||||
| chr7:130513210
|
C | G | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-4551G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513210 | ||||||
| chr7:130513290
|
T | TA | 9 | a0001c0001t0002g0156a0001c0001t0002g0167a0001c0001t0002g0170others(6): Show | 9 | HG01433.hp2 HG02004.hp2 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.2150-4632dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513290 | ||||||
| chr7:130513302
|
AAAAAAAA others(13): Show |
A | 1 | a0001c0001t0001g0009 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2150-4663_2150-464 others(24): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513302 | ||||||
| chr7:130513304
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0253 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2150-4646_2150-464 others(14): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513304 | ||||||
| chr7:130513304
|
A | T | 7 | a0001c0002t0001g0020a0001c0002t0001g0046a0001c0002t0001g0047others(4): Show | 7 | HG01099.hp1 HG01358.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2150-4645T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513304 | ||||||
| chr7:130513304
|
AAAAAATA others(3): Show |
A | 1 | a0001c0001t0001g0255 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2150-4655_2150-464 others(14): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513304 | ||||||
| chr7:130513304
|
AAAAAATA others(5): Show |
A | 2 | a0001c0001t0009g0252a0001c0001t0009g0256 | 2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2150-4657_2150-464 others(16): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513304 | ||||||
| chr7:130513304
|
AAAAAATA others(7): Show |
A | 4 | a0001c0001t0005g0247a0001c0001t0005g0251a0001c0001t0005g0254others(1): Show | 4 | HG02630.hp2 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-4659_2150-464 others(18): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513304 | ||||||
| chr7:130513304
|
AAAAAATA others(13): Show |
A | 1 | a0001c0001t0001g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2150-4665_2150-464 others(24): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513304 | ||||||
| chr7:130513304
|
AAAAAATA others(15): Show |
A | 1 | a0001c0001t0001g0016 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2150-4667_2150-464 others(26): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513304 | ||||||
| chr7:130513306
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0004g0293 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2150-4648_2150-464 others(15): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513306 | ||||||
| chr7:130513306
|
A | T | 62 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(59): Show | 62 | HG00099.hp1 HG00597.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.2150-4647T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513306 | ||||||
| chr7:130513308
|
A | AAAAAAAA others(11): Show |
1 | a0001c0001t0001g0135 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2150-4650_2150-464 others(22): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513308 | ||||||
| chr7:130513308
|
A | AAAAAATA others(5): Show |
1 | a0001c0001t0001g0136 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2150-4650_2150-464 others(16): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513308 | ||||||
| chr7:130513308
|
A | AAAAAATA others(7): Show |
1 | a0001c0001t0001g0141 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2150-4650_2150-464 others(18): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513308 | ||||||
| chr7:130513308
|
A | AAT | 6 | a0001c0001t0001g0270a0001c0001t0001g0284a0001c0001t0001g0307others(3): Show | 6 | HG01168.hp2 HG01256.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.2150-4651_2150-465 others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513308 | ||||||
| chr7:130513308
|
A | AATAT | 13 | a0001c0001t0001g0269a0001c0001t0001g0276a0001c0001t0001g0279others(10): Show | 13 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.2150-4653_2150-465 others(8): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513308 | ||||||
| chr7:130513308
|
A | AATATATA others(5): Show |
1 | a0001c0001t0001g0302 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2150-4661_2150-465 others(16): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513308 | ||||||
| chr7:130513308
|
A | AATATATA others(7): Show |
1 | a0001c0001t0001g0299 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2150-4663_2150-465 others(18): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513308 | ||||||
| chr7:130513308
|
A | AT | 4 | a0001c0001t0001g0030a0001c0001t0001g0275a0002c0003t0001g0244others(1): Show | 4 | HG02818.hp2 HG06807.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-4650_2150-464 others(5): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513308 | ||||||
| chr7:130513308
|
A | T | 136 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(133): Show | 136 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.2150-4649T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513308 | ||||||
| chr7:130513308
|
AATATATA others(3): Show |
A | 1 | a0001c0001t0004g0267 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2150-4659_2150-465 others(14): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513308 | ||||||
| chr7:130513310
|
T | A | 89 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(86): Show | 89 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.2150-4651A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513310 | ||||||
| chr7:130513312
|
T | A | 87 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(84): Show | 87 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.2150-4653A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513312 | ||||||
| chr7:130513314
|
T | A | 74 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0027others(71): Show | 74 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.2150-4655A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513314 | ||||||
| chr7:130513315
|
ATATATAT others(37): Show |
A | 3 | a0001c0001t0008g0318a0001c0001t0008g0321a0001c0001t0008g0322 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2150-4700_2150-465 others(48): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513315 | ||||||
| chr7:130513316
|
T | A | 7 | a0001c0001t0002g0173a0001c0001t0002g0190a0001c0001t0002g0207others(4): Show | 7 | HG00597.hp2 HG02083.hp1 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.2150-4657A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513316 | ||||||
| chr7:130513321
|
A | ATATGTGT others(9): Show |
1 | a0006c0007t0001g0095 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2150-4663_2150-466 others(20): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513321 | ||||||
| chr7:130513321
|
A | ATATGTGT others(13): Show |
2 | a0001c0002t0001g0091a0001c0002t0001g0115 | 2 | NA18961.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.2150-4663_2150-466 others(24): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513321 | ||||||
| chr7:130513321
|
A | ATGTGTGT others(5): Show |
1 | a0001c0002t0001g0028 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2150-4663_2150-466 others(16): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513321 | ||||||
| chr7:130513321
|
ATATATAT others(31): Show |
A | 1 | a0001c0002t0007g0238 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2150-4700_2150-466 others(42): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513321 | ||||||
| chr7:130513323
|
A | ATATGTGT others(11): Show |
1 | a0001c0002t0003g0109 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2150-4665_2150-466 others(22): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513323 | ||||||
| chr7:130513323
|
A | ATGTGTGT others(5): Show |
2 | a0001c0002t0001g0037a0001c0002t0001g0046 | 2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2150-4665_2150-466 others(16): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513323 | ||||||
| chr7:130513323
|
A | ATGTGTGT others(7): Show |
33 | a0001c0002t0001g0019a0001c0002t0001g0032a0001c0002t0001g0033others(30): Show | 33 | HG00099.hp1 HG00597.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.2150-4665_2150-466 others(18): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513323 | ||||||
| chr7:130513323
|
A | ATGTGTGT others(9): Show |
53 | a0001c0001t0005g0053a0001c0002t0001g0002a0001c0002t0001g0005others(50): Show | 53 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.2150-4665_2150-466 others(20): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513323 | ||||||
| chr7:130513323
|
A | ATGTGTGT others(11): Show |
11 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0075others(8): Show | 11 | HG03927.hp2 NA18939.hp1 NA18941.hp1 others(8): Show |
intron_variant | MODIFIER | c.2150-4665_2150-466 others(22): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513323 | ||||||
| chr7:130513323
|
A | G | 1 | a0001c0002t0001g0028 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2150-4664T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513323 | ||||||
| chr7:130513325
|
A | ATGTGTGT others(9): Show |
1 | a0001c0002t0001g0062 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2150-4667_2150-466 others(20): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513325 | ||||||
| chr7:130513325
|
A | G | 41 | a0001c0001t0005g0053a0001c0002t0001g0019a0001c0002t0001g0020others(38): Show | 41 | HG00099.hp1 HG00597.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.2150-4666T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513325 | ||||||
| chr7:130513327
|
A | G | 35 | a0001c0002t0001g0019a0001c0002t0001g0028a0001c0002t0001g0032others(32): Show | 35 | HG00099.hp1 HG00597.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.2150-4668T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513327 | ||||||
| chr7:130513329
|
A | G | 4 | a0001c0002t0001g0037a0001c0002t0001g0046a0001c0002t0001g0052others(1): Show | 4 | HG02615.hp2 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-4670T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513329 | ||||||
| chr7:130513331
|
ATATATAT others(21): Show |
A | 1 | a0001c0002t0007g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2150-4700_2150-467 others(32): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513331 | ||||||
| chr7:130513337
|
A | G | 3 | a0001c0001t0001g0262a0001c0001t0001g0264a0001c0001t0001g0265 | 3 | HG02572.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2150-4678T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513337 | ||||||
| chr7:130513339
|
A | G | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-4680T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513339 | ||||||
| chr7:130513341
|
A | ATATATAT others(23): Show |
1 | a0001c0001t0001g0143 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2150-4683_2150-468 others(34): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | ||||||
| chr7:130513341
|
A | ATATATAT others(15): Show |
5 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(2): Show | 5 | HG01346.hp1 HG01891.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.2150-4683_2150-468 others(26): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | ||||||
| chr7:130513341
|
A | ATATATAT others(19): Show |
2 | a0001c0001t0001g0142a0001c0001t0001g0144 | 2 | HG01069.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.2150-4683_2150-468 others(30): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | ||||||
| chr7:130513341
|
A | ATATATAT others(13): Show |
4 | a0001c0001t0001g0273a0001c0001t0001g0315a0001c0001t0001g0325others(1): Show | 4 | HG00323.hp2 HG02683.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-4683_2150-468 others(24): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | ||||||
| chr7:130513341
|
A | ATATATAT others(9): Show |
4 | a0001c0001t0001g0132a0001c0001t0001g0134a0001c0001t0001g0257others(1): Show | 4 | HG02280.hp2 HG02698.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-4683_2150-468 others(20): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | ||||||
| chr7:130513341
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0137 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2150-4683_2150-468 others(22): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | ||||||
| chr7:130513341
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0145 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2150-4683_2150-468 others(18): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | ||||||
| chr7:130513341
|
A | ATATATAT others(9): Show |
3 | a0001c0001t0001g0127a0001c0001t0001g0291a0001c0001t0001g0314 | 3 | HG01516.hp1 HG01517.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2150-4683_2150-468 others(20): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | ||||||
| chr7:130513341
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0290 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2150-4683_2150-468 others(22): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | ||||||
| chr7:130513341
|
A | ATATATAT others(7): Show |
2 | a0001c0001t0004g0131a0001c0001t0004g0249 | 2 | HG02572.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2150-4683_2150-468 others(18): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | ||||||
| chr7:130513341
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0146 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2150-4683_2150-468 others(20): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | ||||||
| chr7:130513341
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0004 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2150-4683_2150-468 others(14): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | ||||||
| chr7:130513341
|
A | ATATATAT others(5): Show |
2 | a0001c0001t0001g0129a0001c0001t0001g0298 | 2 | HG03239.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.2150-4683_2150-468 others(16): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | ||||||
| chr7:130513341
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0133 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2150-4683_2150-468 others(18): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | ||||||
| chr7:130513341
|
A | ATATATAT others(5): Show |
1 | a0005c0010t0001g0147 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2150-4683_2150-468 others(16): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | ||||||
| chr7:130513341
|
A | ATATG | 4 | a0001c0001t0001g0003a0001c0001t0001g0271a0001c0001t0001g0294others(1): Show | 4 | HG00140.hp1 HG02155.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-4683_2150-468 others(8): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | ||||||
| chr7:130513341
|
A | G | 20 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0030others(17): Show | 20 | HG00558.hp2 HG02055.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.2150-4682T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | ||||||
| chr7:130513341
|
ATGTGTGT others(9): Show |
A | 2 | a0001c0001t0002g0024a0001c0001t0012g0206 | 2 | HG01978.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.2150-4698_2150-468 others(20): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | ||||||
| chr7:130513341
|
ATGTGTGT others(11): Show |
A | 1 | a0001c0012t0002g0166 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2150-4700_2150-468 others(22): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513341 | ||||||
| chr7:130513343
|
G | A | 96 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0289others(93): Show | 96 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.2150-4684C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513343 | ||||||
| chr7:130513343
|
GTGTGTGT others(25): Show |
G | 1 | a0001c0002t0007g0237 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2150-4716_2150-468 others(36): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513343 | ||||||
| chr7:130513345
|
G | A | 19 | a0001c0001t0002g0148a0001c0001t0002g0160a0001c0001t0002g0163others(16): Show | 19 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.2150-4686C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513345 | ||||||
| chr7:130513345
|
GTGTGTGT others(23): Show |
G | 6 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0002t0007g0236others(3): Show | 6 | HG02451.hp2 HG02486.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2150-4716_2150-468 others(34): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513345 | ||||||
| chr7:130513347
|
G | A | 4 | a0001c0001t0002g0163a0001c0001t0002g0176a0001c0001t0002g0180others(1): Show | 4 | HG00639.hp1 HG03710.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-4688C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513347 | ||||||
| chr7:130513347
|
GTGTGTGT others(21): Show |
G | 2 | a0001c0001t0002g0193a0001c0002t0007g0239 | 2 | HG00558.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2150-4716_2150-468 others(32): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513347 | ||||||
| chr7:130513349
|
GTGTGTGT others(19): Show |
G | 23 | a0001c0001t0002g0150a0001c0001t0002g0156a0001c0001t0002g0157others(20): Show | 23 | HG00140.hp2 HG01167.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.2150-4716_2150-469 others(30): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513349 | ||||||
| chr7:130513351
|
GTGTGTGT others(17): Show |
G | 47 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0025others(44): Show | 47 | HG00597.hp2 HG01168.hp1 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.2150-4716_2150-469 others(28): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513351 | ||||||
| chr7:130513353
|
GTGTGTGT others(15): Show |
G | 16 | a0001c0001t0002g0027a0001c0001t0002g0148a0001c0001t0002g0160others(13): Show | 16 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.2150-4716_2150-469 others(26): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513353 | ||||||
| chr7:130513355
|
GTGTGTAT others(13): Show |
G | 4 | a0001c0001t0002g0163a0001c0001t0002g0176a0001c0001t0002g0180others(1): Show | 4 | HG00639.hp1 HG03710.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-4716_2150-469 others(24): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513355 | ||||||
| chr7:130513357
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2150-4698C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513357 | ||||||
| chr7:130513359
|
G | A | 68 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0023others(65): Show | 68 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.2150-4700C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513359 | ||||||
| chr7:130513359
|
G | GTA | 5 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0017others(2): Show | 5 | HG01167.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2150-4702_2150-470 others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513359 | ||||||
| chr7:130513359
|
G | GTGTA | 3 | a0001c0001t0001g0029a0001c0001t0001g0130a0001c0001t0001g0136 | 3 | HG03654.hp1 HG06807.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2150-4701_2150-470 others(8): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513359 | ||||||
| chr7:130513361
|
A | G | 6 | a0001c0001t0001g0289a0001c0001t0001g0302a0001c0001t0004g0249others(3): Show | 6 | HG01496.hp1 HG02717.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2150-4702T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513361 | ||||||
| chr7:130513363
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2150-4704T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513363 | ||||||
| chr7:130513369
|
A | G | 2 | a0001c0001t0002g0024a0001c0001t0012g0206 | 2 | HG01978.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.2150-4710T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513369 | ||||||
| chr7:130513371
|
A | G | 3 | a0001c0001t0002g0024a0001c0001t0012g0206a0001c0012t0002g0166 | 3 | HG01978.hp2 NA18967.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2150-4712T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513371 | ||||||
| chr7:130513373
|
A | G | 4 | a0001c0001t0002g0024a0001c0001t0012g0206a0001c0002t0007g0238others(1): Show | 4 | HG01978.hp2 HG01993.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-4714T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513373 | ||||||
| chr7:130513375
|
A | ATG | 5 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0304others(2): Show | 5 | HG01070.hp1 HG01243.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.2150-4718_2150-471 others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513375 | ||||||
| chr7:130513375
|
A | G | 72 | a0001c0001t0001g0023a0001c0001t0001g0270a0001c0001t0002g0024others(69): Show | 72 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.2150-4716T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513375 | ||||||
| chr7:130513377
|
G | A | 3 | a0001c0001t0001g0263a0001c0002t0001g0045a0001c0002t0001g0048 | 3 | HG02922.hp1 HG03654.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.2150-4718C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513377 | ||||||
| chr7:130513387
|
G | GTA | 3 | a0001c0001t0001g0262a0001c0001t0001g0264a0001c0001t0001g0265 | 3 | HG02572.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2150-4729_2150-472 others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513387 | ||||||
| chr7:130513389
|
G | A | 4 | a0001c0001t0001g0262a0001c0001t0001g0264a0001c0001t0001g0265others(1): Show | 4 | HG02572.hp1 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-4730C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513389 | ||||||
| chr7:130513390
|
T | C | 32 | a0001c0001t0001g0029a0001c0001t0001g0127a0001c0001t0001g0130others(29): Show | 32 | HG00099.hp2 HG00323.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.2150-4731A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513390 | ||||||
| chr7:130513391
|
A | G | 4 | a0001c0001t0002g0184a0001c0001t0008g0318a0001c0001t0008g0321others(1): Show | 4 | HG01891.hp2 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-4732T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513391 | ||||||
| chr7:130513393
|
A | G | 1 | a0001c0001t0002g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2150-4734T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513393 | ||||||
| chr7:130513471
|
G | C | 1 | a0001c0001t0002g0152 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2150-4812C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513471 | ||||||
| chr7:130513602
|
T | C | 1 | a0001c0001t0002g0225 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2150-4943A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513602 | ||||||
| chr7:130513656
|
A | C | 1 | a0001c0012t0002g0166 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2150-4997T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513656 | ||||||
| chr7:130513695
|
G | A | 1 | a0001c0002t0001g0069 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2150-5036C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513695 | ||||||
| chr7:130513758
|
C | T | 1 | a0001c0002t0001g0020 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2150-5099G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513758 | ||||||
| chr7:130513856
|
T | C | 3 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007 | 3 | HG00438.hp1 NA18982.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.2150-5197A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513856 | ||||||
| chr7:130513937
|
A | G | 3 | a0001c0002t0001g0041a0001c0002t0001g0043a0001c0002t0001g0057 | 3 | HG00597.hp1 HG00621.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.2150-5278T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130513937 | ||||||
| chr7:130514040
|
T | C | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-5381A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130514040 | ||||||
| chr7:130514132
|
T | C | 13 | a0001c0002t0001g0038a0001c0002t0001g0041a0001c0002t0001g0042others(10): Show | 13 | HG00597.hp1 HG00621.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.2150-5473A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130514132 | ||||||
| chr7:130514356
|
T | G | 93 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0281others(90): Show | 93 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.2150-5697A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130514356 | ||||||
| chr7:130514564
|
T | A | 1 | a0001c0002t0007g0238 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2150-5905A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130514564 | ||||||
| chr7:130514618
|
G | A | 1 | a0001c0001t0002g0189 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2150-5959C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130514618 | ||||||
| chr7:130514644
|
C | T | 10 | a0001c0001t0002g0171a0001c0001t0002g0179a0001c0001t0002g0180others(7): Show | 10 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.2150-5985G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130514644 | ||||||
| chr7:130514662
|
G | A | 98 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(95): Show | 98 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.2150-6003C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130514662 | ||||||
| chr7:130514687
|
A | G | 1 | a0001c0002t0001g0064 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2150-6028T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130514687 | ||||||
| chr7:130514753
|
C | A | 92 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(89): Show | 92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.2150-6094G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130514753 | ||||||
| chr7:130514845
|
T | C | 1 | a0001c0002t0001g0031 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2150-6186A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130514845 | ||||||
| chr7:130515053
|
T | C | 2 | a0001c0001t0001g0266a0001c0001t0004g0267 | 2 | HG01978.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2150-6394A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130515053 | ||||||
| chr7:130515058
|
T | C | 6 | a0001c0002t0007g0235a0001c0002t0007g0236a0001c0002t0007g0237others(3): Show | 6 | HG01192.hp2 HG01993.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2150-6399A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130515058 | ||||||
| chr7:130515226
|
G | A | 1 | a0001c0002t0003g0121 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2150-6567C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130515226 | ||||||
| chr7:130515342
|
A | AGT | 3 | a0001c0001t0008g0318a0001c0001t0008g0321a0001c0001t0008g0322 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2150-6684_2150-668 others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130515342 | ||||||
| chr7:130515346
|
AC | A | 3 | a0001c0001t0008g0318a0001c0001t0008g0321a0001c0001t0008g0322 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2150-6688delG | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130515346 | ||||||
| chr7:130515494
|
G | T | 1 | a0001c0001t0001g0255 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2150-6835C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130515494 | ||||||
| chr7:130515890
|
A | T | 1 | a0001c0012t0002g0166 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2150-7231T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130515890 | ||||||
| chr7:130516079
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2150-7420C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130516079 | ||||||
| chr7:130516200
|
A | G | 3 | a0001c0001t0008g0318a0001c0001t0008g0321a0001c0001t0008g0322 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2150-7541T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130516200 | ||||||
| chr7:130516571
|
T | C | 1 | a0001c0002t0001g0096 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2150-7912A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130516571 | ||||||
| chr7:130516699
|
A | G | 5 | a0001c0001t0002g0179a0001c0001t0002g0180a0001c0001t0002g0181others(2): Show | 5 | HG00140.hp2 HG00639.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.2150-8040T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130516699 | ||||||
| chr7:130516738
|
T | C | 1 | a0001c0002t0001g0048 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2150-8079A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130516738 | ||||||
| chr7:130516842
|
G | A | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-8183C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130516842 | ||||||
| chr7:130516916
|
G | A | 1 | a0001c0002t0001g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2150-8257C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130516916 | ||||||
| chr7:130517065
|
G | C | 1 | a0001c0002t0001g0022 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2150-8406C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130517065 | ||||||
| chr7:130517334
|
G | C | 1 | a0001c0001t0005g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2150-8675C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130517334 | ||||||
| chr7:130517392
|
G | A | 1 | a0001c0001t0002g0222 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2150-8733C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130517392 | ||||||
| chr7:130517753
|
A | G | 1 | a0001c0001t0002g0209 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2150-9094T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130517753 | ||||||
| chr7:130517909
|
A | G | 3 | a0001c0001t0008g0318a0001c0001t0008g0321a0001c0001t0008g0322 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2150-9250T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130517909 | ||||||
| chr7:130517933
|
G | GA | 108 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0200others(105): Show | 108 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.2150-9275dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130517933 | ||||||
| chr7:130518274
|
G | C | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2150-9615C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130518274 | ||||||
| chr7:130518284
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2150-9625T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130518284 | ||||||
| chr7:130518347
|
G | T | 1 | a0001c0001t0001g0257 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2150-9688C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130518347 | ||||||
| chr7:130518496
|
T | C | 1 | a0001c0001t0002g0181 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2150-9837A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130518496 | ||||||
| chr7:130518514
|
G | A | 1 | a0001c0001t0001g0323 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2150-9855C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130518514 | ||||||
| chr7:130518536
|
T | C | 3 | a0001c0001t0008g0318a0001c0001t0008g0321a0001c0001t0008g0322 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2150-9877A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130518536 | ||||||
| chr7:130518660
|
A | G | 1 | a0001c0002t0002g0088 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2150-10001T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130518660 | ||||||
| chr7:130518837
|
C | T | 1 | a0001c0001t0002g0157 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2150-10178G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130518837 | ||||||
| chr7:130518894
|
T | G | 3 | a0001c0002t0001g0241a0002c0003t0001g0243a0002c0003t0001g0244 | 3 | HG01433.hp2 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2150-10235A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130518894 | ||||||
| chr7:130518909
|
G | C | 3 | a0001c0001t0001g0271a0001c0001t0001g0306a0001c0001t0001g0307 | 3 | HG00140.hp1 HG01175.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.2150-10250C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130518909 | ||||||
| chr7:130518931
|
C | T | 1 | a0001c0001t0002g0192 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2150-10272G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130518931 | ||||||
| chr7:130518955
|
G | A | 3 | a0001c0001t0002g0159a0001c0001t0002g0224a0001c0001t0002g0225 | 3 | HG01258.hp2 HG01346.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.2150-10296C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130518955 | ||||||
| chr7:130518988
|
A | G | 1 | a0001c0001t0002g0024 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2150-10329T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130518988 | ||||||
| chr7:130519005
|
C | CA | 208 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.2150-10347dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130519005 | ||||||
| chr7:130519005
|
CA | C | 12 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0002g0169others(9): Show | 12 | HG00140.hp2 HG01346.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.2150-10347delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130519005 | ||||||
| chr7:130519005
|
CAA | C | 93 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(90): Show | 93 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.2150-10348_2150-10 others(8): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130519005 | ||||||
| chr7:130519229
|
T | C | 11 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.2150-10570A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130519229 | ||||||
| chr7:130519240
|
G | C | 2 | a0001c0001t0002g0227a0001c0001t0006g0226 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2150-10581C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130519240 | ||||||
| chr7:130519324
|
G | A | 1 | a0001c0001t0001g0275 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2150-10665C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130519324 | ||||||
| chr7:130519339
|
T | C | 1 | a0001c0002t0011g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2150-10680A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130519339 | ||||||
| chr7:130519364
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2150-10705C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130519364 | ||||||
| chr7:130519807
|
C | G | 2 | a0001c0002t0001g0034a0001c0002t0001g0035 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2150-11148G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130519807 | ||||||
| chr7:130519844
|
T | C | 104 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(101): Show | 104 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.2150-11185A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130519844 | ||||||
| chr7:130519856
|
T | C | 108 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0200others(105): Show | 108 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.2150-11197A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130519856 | ||||||
| chr7:130520011
|
T | C | 3 | a0001c0001t0008g0318a0001c0001t0008g0321a0001c0001t0008g0322 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2150-11352A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130520011 | ||||||
| chr7:130520038
|
T | C | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-11379A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130520038 | ||||||
| chr7:130520062
|
T | C | 2 | a0001c0005t0002g0010a0001c0005t0002g0011 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2150-11403A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130520062 | ||||||
| chr7:130520083
|
T | C | 110 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0200others(107): Show | 110 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.2150-11424A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130520083 | ||||||
| chr7:130520234
|
A | T | 1 | a0001c0001t0002g0152 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2150-11575T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130520234 | ||||||
| chr7:130520375
|
T | C | 1 | a0001c0002t0007g0236 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2150-11716A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130520375 | ||||||
| chr7:130520576
|
A | G | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2150-11917T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130520576 | ||||||
| chr7:130520602
|
A | C | 3 | a0001c0002t0001g0241a0002c0003t0001g0243a0002c0003t0001g0244 | 3 | HG01433.hp2 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2150-11943T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130520602 | ||||||
| chr7:130520611
|
A | G | 215 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(212): Show | 215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.2150-11952T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130520611 | ||||||
| chr7:130520988
|
A | T | 10 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(7): Show | 10 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2150-12329T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130520988 | ||||||
| chr7:130521103
|
C | T | 214 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(211): Show | 214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.2150-12444G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130521103 | ||||||
| chr7:130521106
|
C | T | 92 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(89): Show | 92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.2150-12447G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130521106 | ||||||
| chr7:130521242
|
A | G | 1 | a0001c0002t0001g0125 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2150-12583T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130521242 | ||||||
| chr7:130521296
|
G | C | 1 | a0001c0002t0001g0119 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2150-12637C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130521296 | ||||||
| chr7:130521438
|
A | G | 214 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(211): Show | 214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.2150-12779T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130521438 | ||||||
| chr7:130521441
|
A | G | 214 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(211): Show | 214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.2150-12782T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130521441 | ||||||
| chr7:130521496
|
C | T | 2 | a0001c0001t0002g0169a0001c0001t0006g0178 | 2 | HG01981.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2150-12837G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130521496 | ||||||
| chr7:130521741
|
G | A | 1 | a0001c0002t0001g0007 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2150-13082C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130521741 | ||||||
| chr7:130521845
|
T | C | 214 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(211): Show | 214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.2150-13186A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130521845 | ||||||
| chr7:130521849
|
A | G | 1 | a0001c0001t0001g0298 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2150-13190T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130521849 | ||||||
| chr7:130521939
|
G | A | 1 | a0001c0001t0006g0149 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2150-13280C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130521939 | ||||||
| chr7:130521950
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2150-13291G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130521950 | ||||||
| chr7:130522000
|
G | C | 1 | a0001c0002t0001g0119 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2150-13341C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130522000 | ||||||
| chr7:130522511
|
C | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2150-13852G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130522511 | ||||||
| chr7:130522570
|
A | C | 1 | a0001c0001t0002g0219 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2150-13911T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130522570 | ||||||
| chr7:130522742
|
A | C | 11 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0262others(8): Show | 11 | HG01891.hp2 HG02451.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2150-14083T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130522742 | ||||||
| chr7:130522773
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2150-14114A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130522773 | ||||||
| chr7:130522804
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2150-14145A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130522804 | ||||||
| chr7:130522838
|
T | G | 1 | a0001c0001t0001g0304 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2150-14179A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130522838 | ||||||
| chr7:130523048
|
G | A | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-14389C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523048 | ||||||
| chr7:130523048
|
G | C | 1 | a0001c0001t0006g0178 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2150-14389C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523048 | ||||||
| chr7:130523079
|
C | A | 1 | a0001c0002t0001g0124 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2150-14420G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523079 | ||||||
| chr7:130523106
|
G | T | 10 | a0001c0001t0002g0158a0001c0001t0002g0173a0001c0001t0002g0174others(7): Show | 10 | HG02083.hp1 HG04184.hp2 NA18939.hp2 others(7): Show |
intron_variant | MODIFIER | c.2150-14447C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523106 | ||||||
| chr7:130523119
|
C | CAAAAAAA others(1): Show |
12 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0008g0318others(9): Show | 12 | HG01258.hp1 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.2150-14468_2150-14 others(14): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523119 | ||||||
| chr7:130523119
|
C | CAAAAAAA others(2): Show |
93 | a0001c0001t0001g0270a0001c0001t0001g0289a0001c0001t0001g0303others(90): Show | 93 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.2150-14469_2150-14 others(15): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523119 | ||||||
| chr7:130523119
|
C | CAAAAAAA others(3): Show |
188 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.2150-14470_2150-14 others(16): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523119 | ||||||
| chr7:130523119
|
C | CAAAAAAA others(4): Show |
24 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0127others(21): Show | 24 | HG00639.hp2 HG01361.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.2150-14471_2150-14 others(17): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523119 | ||||||
| chr7:130523119
|
C | CAAAAAAA others(5): Show |
3 | a0001c0001t0002g0231a0001c0002t0001g0075a0001c0002t0011g0240 | 3 | HG02486.hp1 NA19082.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2150-14472_2150-14 others(18): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523119 | ||||||
| chr7:130523119
|
C | CAAAAAAA others(7): Show |
5 | a0001c0001t0001g0030a0001c0001t0001g0262a0001c0001t0001g0263others(2): Show | 5 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2150-14474_2150-14 others(20): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523119 | ||||||
| chr7:130523157
|
G | A | 1 | a0001c0001t0001g0200 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2150-14498C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523157 | ||||||
| chr7:130523161
|
C | G | 1 | a0001c0002t0001g0119 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2150-14502G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523161 | ||||||
| chr7:130523230
|
A | G | 1 | a0005c0010t0001g0147 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2150-14571T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523230 | ||||||
| chr7:130523237
|
G | C | 1 | a0001c0001t0002g0190 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2150-14578C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523237 | ||||||
| chr7:130523458
|
T | C | 106 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(103): Show | 106 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.2150-14799A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523458 | ||||||
| chr7:130523487
|
G | A | 1 | a0001c0001t0002g0169 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2150-14828C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523487 | ||||||
| chr7:130523506
|
C | T | 3 | a0001c0001t0008g0318a0001c0001t0008g0321a0001c0001t0008g0322 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2150-14847G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523506 | ||||||
| chr7:130523570
|
C | G | 1 | a0001c0001t0006g0182 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2150-14911G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523570 | ||||||
| chr7:130523577
|
G | C | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144 | 3 | HG01069.hp1 HG01515.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.2150-14918C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523577 | ||||||
| chr7:130523609
|
T | C | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-14950A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523609 | ||||||
| chr7:130523617
|
A | C | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-14958T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523617 | ||||||
| chr7:130523774
|
CG | C | 92 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(89): Show | 92 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.2150-15116delC | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523774 | ||||||
| chr7:130523965
|
G | A | 7 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0008g0318others(4): Show | 7 | HG01891.hp2 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2150-15306C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523965 | ||||||
| chr7:130523986
|
G | A | 3 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022 | 3 | HG01099.hp1 HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2150-15327C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130523986 | ||||||
| chr7:130524006
|
C | T | 1 | a0001c0002t0001g0058 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2150-15347G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130524006 | ||||||
| chr7:130524007
|
G | A | 1 | a0001c0001t0002g0233 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2150-15348C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130524007 | ||||||
| chr7:130524099
|
GGA | G | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-15442_2150-15 others(8): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130524099 | ||||||
| chr7:130524301
|
T | A | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-15642A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130524301 | ||||||
| chr7:130524308
|
C | A | 22 | a0001c0001t0001g0029a0001c0001t0001g0127a0001c0001t0001g0129others(19): Show | 22 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(19): Show |
intron_variant | MODIFIER | c.2150-15649G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130524308 | ||||||
| chr7:130524348
|
G | T | 106 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(103): Show | 106 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.2150-15689C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130524348 | ||||||
| chr7:130524406
|
A | G | 1 | a0001c0002t0003g0261 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2150-15747T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130524406 | ||||||
| chr7:130524602
|
C | T | 28 | a0001c0002t0001g0019a0001c0002t0001g0028a0001c0002t0001g0034others(25): Show | 28 | HG00597.hp1 HG00621.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.2150-15943G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130524602 | ||||||
| chr7:130524749
|
G | A | 94 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(91): Show | 94 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.2150-16090C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130524749 | ||||||
| chr7:130524830
|
G | T | 3 | a0001c0001t0008g0318a0001c0001t0008g0321a0001c0001t0008g0322 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2150-16171C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130524830 | ||||||
| chr7:130524910
|
C | T | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-16251G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130524910 | ||||||
| chr7:130525052
|
G | T | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-16393C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130525052 | ||||||
| chr7:130525261
|
T | A | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2150-16602A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130525261 | ||||||
| chr7:130525285
|
T | G | 1 | a0001c0001t0001g0008 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2150-16626A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130525285 | ||||||
| chr7:130525437
|
T | C | 1 | a0001c0002t0001g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2150-16778A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130525437 | ||||||
| chr7:130525468
|
C | T | 1 | a0001c0002t0003g0104 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2150-16809G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130525468 | ||||||
| chr7:130525724
|
A | C | 5 | a0001c0001t0001g0030a0001c0001t0001g0262a0001c0001t0001g0263others(2): Show | 5 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2150-17065T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130525724 | ||||||
| chr7:130525914
|
G | C | 1 | a0001c0001t0001g0255 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2150-17255C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130525914 | ||||||
| chr7:130525950
|
G | GAAATGAG others(15): Show |
110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(107): Show | 110 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.2150-17313_2150-17 others(28): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130525950 | ||||||
| chr7:130525960
|
A | ACCTGGAC others(16): Show |
1 | a0003c0004t0001g0277 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2150-17302_2150-17 others(29): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130525960 | ||||||
| chr7:130526087
|
C | A | 3 | a0001c0001t0008g0318a0001c0001t0008g0321a0001c0001t0008g0322 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2150-17428G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130526087 | ||||||
| chr7:130526564
|
G | A | 1 | a0001c0002t0001g0062 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2150-17905C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130526564 | ||||||
| chr7:130526580
|
GGGCAGGA others(8): Show |
G | 1 | a0001c0002t0001g0070 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2150-17936_2150-17 others(21): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130526580 | ||||||
| chr7:130526773
|
A | C | 111 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(108): Show | 111 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.2150-18114T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130526773 | ||||||
| chr7:130526821
|
G | C | 1 | a0001c0002t0001g0096 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2150-18162C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130526821 | ||||||
| chr7:130526845
|
G | A | 2 | a0001c0005t0002g0010a0001c0005t0002g0011 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2150-18186C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130526845 | ||||||
| chr7:130527013
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2150-18354C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130527013 | ||||||
| chr7:130527138
|
TG | T | 96 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(93): Show | 96 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.2150-18480delC | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130527138 | ||||||
| chr7:130527322
|
T | C | 1 | a0001c0002t0011g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2150-18663A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130527322 | ||||||
| chr7:130527331
|
G | C | 5 | a0001c0001t0001g0030a0001c0001t0001g0262a0001c0001t0001g0263others(2): Show | 5 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2150-18672C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130527331 | ||||||
| chr7:130527422
|
C | G | 1 | a0001c0001t0002g0152 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2150-18763G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130527422 | ||||||
| chr7:130527561
|
G | A | 7 | a0001c0001t0001g0130a0001c0001t0001g0135a0001c0001t0001g0136others(4): Show | 7 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.2150-18902C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130527561 | ||||||
| chr7:130527564
|
G | A | 7 | a0001c0001t0001g0130a0001c0001t0001g0135a0001c0001t0001g0136others(4): Show | 7 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.2150-18905C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130527564 | ||||||
| chr7:130527665
|
G | A | 1 | a0001c0002t0011g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2150-19006C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130527665 | ||||||
| chr7:130527680
|
T | TGGACACG others(5): Show |
1 | a0003c0004t0001g0277 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2150-19033_2150-19 others(18): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130527680 | ||||||
| chr7:130527710
|
T | C | 283 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(280): Show | 283 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.2150-19051A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130527710 | ||||||
| chr7:130527712
|
C | T | 283 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(280): Show | 283 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.2150-19053G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130527712 | ||||||
| chr7:130527721
|
C | A | 283 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(280): Show | 283 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.2150-19062G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130527721 | ||||||
| chr7:130527823
|
G | T | 115 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(112): Show | 115 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.2150-19164C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130527823 | ||||||
| chr7:130527957
|
G | C | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2150-19298C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130527957 | ||||||
| chr7:130528013
|
G | A | 14 | a0001c0002t0001g0038a0001c0002t0001g0041a0001c0002t0001g0042others(11): Show | 14 | HG00597.hp1 HG00621.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.2150-19354C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130528013 | ||||||
| chr7:130528046
|
C | A | 1 | a0001c0002t0003g0121 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2150-19387G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130528046 | ||||||
| chr7:130528134
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2150-19475A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130528134 | ||||||
| chr7:130528284
|
C | T | 3 | a0001c0001t0001g0245a0001c0001t0004g0248a0001c0001t0004g0249 | 3 | HG01099.hp2 HG02886.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2149+19390G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130528284 | ||||||
| chr7:130528298
|
A | G | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2149+19376T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130528298 | ||||||
| chr7:130528452
|
G | C | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2149+19222C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130528452 | ||||||
| chr7:130528458
|
T | C | 4 | a0001c0001t0001g0271a0001c0001t0001g0306a0001c0001t0001g0307others(1): Show | 4 | HG00140.hp1 HG01175.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.2149+19216A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130528458 | ||||||
| chr7:130528632
|
G | A | 213 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(210): Show | 213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.2149+19042C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130528632 | ||||||
| chr7:130528786
|
T | C | 2 | a0001c0001t0004g0248a0001c0001t0004g0249 | 2 | HG01099.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2149+18888A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130528786 | ||||||
| chr7:130528807
|
C | T | 3 | a0001c0001t0008g0318a0001c0001t0008g0321a0001c0001t0008g0322 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2149+18867G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130528807 | ||||||
| chr7:130528815
|
T | G | 3 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007 | 3 | HG00438.hp1 NA18982.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.2149+18859A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130528815 | ||||||
| chr7:130528850
|
C | T | 1 | a0001c0001t0002g0152 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2149+18824G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130528850 | ||||||
| chr7:130528851
|
G | A | 22 | a0001c0001t0001g0029a0001c0001t0001g0127a0001c0001t0001g0129others(19): Show | 22 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(19): Show |
intron_variant | MODIFIER | c.2149+18823C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130528851 | ||||||
| chr7:130529019
|
C | T | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144 | 3 | HG01069.hp1 HG01515.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.2149+18655G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130529019 | ||||||
| chr7:130529062
|
G | C | 1 | a0001c0001t0001g0139 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2149+18612C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130529062 | ||||||
| chr7:130529241
|
G | A | 1 | a0001c0001t0002g0260 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2149+18433C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130529241 | ||||||
| chr7:130529328
|
G | A | 106 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(103): Show | 106 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.2149+18346C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130529328 | ||||||
| chr7:130529349
|
C | A | 95 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(92): Show | 95 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.2149+18325G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130529349 | ||||||
| chr7:130529455
|
T | C | 1 | a0001c0002t0007g0239 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2149+18219A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130529455 | ||||||
| chr7:130529459
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2149+18215C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130529459 | ||||||
| chr7:130529473
|
A | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2149+18201T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130529473 | ||||||
| chr7:130530029
|
A | G | 118 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(115): Show | 118 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.2149+17645T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130530029 | ||||||
| chr7:130530051
|
C | T | 115 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(112): Show | 115 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.2149+17623G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130530051 | ||||||
| chr7:130530059
|
G | A | 1 | a0001c0001t0002g0260 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2149+17615C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130530059 | ||||||
| chr7:130530061
|
G | C | 1 | a0001c0001t0005g0258 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2149+17613C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130530061 | ||||||
| chr7:130530313
|
T | G | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2149+17361A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130530313 | ||||||
| chr7:130530336
|
G | A | 60 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(57): Show | 60 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.2149+17338C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130530336 | ||||||
| chr7:130530415
|
G | A | 3 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0265 | 3 | HG02922.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2149+17259C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130530415 | ||||||
| chr7:130530442
|
C | T | 1 | a0001c0002t0001g0069 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2149+17232G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130530442 | ||||||
| chr7:130530810
|
A | C | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(107): Show | 110 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.2149+16864T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130530810 | ||||||
| chr7:130530812
|
T | C | 3 | a0001c0002t0001g0047a0001c0002t0001g0059a0001c0002t0001g0061 | 3 | HG02280.hp1 HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2149+16862A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130530812 | ||||||
| chr7:130530890
|
T | C | 1 | a0001c0002t0001g0037 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2149+16784A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130530890 | ||||||
| chr7:130530950
|
G | C | 3 | a0001c0002t0001g0032a0001c0002t0001g0033a0001c0002t0001g0036 | 3 | HG00099.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2149+16724C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130530950 | ||||||
| chr7:130530978
|
G | A | 3 | a0001c0001t0001g0289a0001c0001t0001g0302a0001c0001t0004g0293 | 3 | HG01496.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2149+16696C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130530978 | ||||||
| chr7:130531038
|
G | A | 1 | a0001c0001t0002g0183 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2149+16636C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130531038 | ||||||
| chr7:130531047
|
G | C | 10 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(7): Show | 10 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2149+16627C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130531047 | ||||||
| chr7:130531198
|
T | G | 1 | a0001c0001t0001g0288 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2149+16476A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130531198 | ||||||
| chr7:130531199
|
G | T | 1 | a0001c0001t0001g0288 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2149+16475C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130531199 | ||||||
| chr7:130531468
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2149+16206A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130531468 | ||||||
| chr7:130531634
|
G | C | 1 | a0001c0001t0001g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2149+16040C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130531634 | ||||||
| chr7:130531716
|
A | G | 3 | a0001c0001t0008g0318a0001c0001t0008g0321a0001c0001t0008g0322 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2149+15958T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130531716 | ||||||
| chr7:130531722
|
T | C | 1 | a0001c0001t0005g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2149+15952A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130531722 | ||||||
| chr7:130531756
|
ACTGGAGA others(4): Show |
A | 1 | a0001c0002t0001g0099 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2149+15907_2149+15 others(17): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130531756 | ||||||
| chr7:130531759
|
G | A | 1 | a0001c0001t0002g0272 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2149+15915C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130531759 | ||||||
| chr7:130531797
|
G | A | 1 | a0001c0001t0004g0308 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2149+15877C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130531797 | ||||||
| chr7:130531810
|
C | T | 2 | a0001c0001t0004g0308a0001c0002t0001g0116 | 2 | HG02155.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2149+15864G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130531810 | ||||||
| chr7:130531831
|
T | A | 1 | a0001c0001t0002g0191 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2149+15843A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130531831 | ||||||
| chr7:130531837
|
A | G | 1 | a0001c0002t0001g0116 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2149+15837T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130531837 | ||||||
| chr7:130531846
|
T | G | 1 | a0001c0002t0001g0099 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2149+15828A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130531846 | ||||||
| chr7:130531968
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2149+15706C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130531968 | ||||||
| chr7:130532110
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2149+15564C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532110 | ||||||
| chr7:130532160
|
G | T | 2 | a0001c0001t0002g0189a0001c0002t0003g0117 | 2 | NA18983.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.2149+15514C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532160 | ||||||
| chr7:130532161
|
G | A | 2 | a0001c0001t0002g0189a0001c0002t0003g0117 | 2 | NA18983.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.2149+15513C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532161 | ||||||
| chr7:130532167
|
T | C | 2 | a0001c0001t0002g0189a0001c0002t0003g0117 | 2 | NA18983.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.2149+15507A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532167 | ||||||
| chr7:130532239
|
T | A | 1 | a0001c0001t0001g0288 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2149+15435A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532239 | ||||||
| chr7:130532281
|
G | A | 1 | a0001c0002t0001g0094 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2149+15393C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532281 | ||||||
| chr7:130532338
|
T | G | 175 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(172): Show | 175 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.2149+15336A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532338 | ||||||
| chr7:130532342
|
C | T | 1 | a0001c0002t0007g0237 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2149+15332G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532342 | ||||||
| chr7:130532344
|
G | T | 1 | a0001c0001t0001g0145 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2149+15330C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532344 | ||||||
| chr7:130532376
|
T | C | 1 | a0001c0002t0003g0110 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2149+15298A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532376 | ||||||
| chr7:130532506
|
C | T | 2 | a0001c0001t0002g0227a0001c0001t0006g0226 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2149+15168G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532506 | ||||||
| chr7:130532551
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2149+15123A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532551 | ||||||
| chr7:130532552
|
T | G | 91 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(88): Show | 91 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.2149+15122A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532552 | ||||||
| chr7:130532667
|
C | T | 323 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(320): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.2149+15007G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532667 | ||||||
| chr7:130532673
|
G | T | 1 | a0001c0001t0001g0288 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2149+15001C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532673 | ||||||
| chr7:130532703
|
G | A | 1 | a0001c0002t0003g0107 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2149+14971C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532703 | ||||||
| chr7:130532800
|
G | A | 2 | a0001c0001t0001g0269a0001c0001t0001g0305 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2149+14874C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532800 | ||||||
| chr7:130532840
|
G | A | 1 | a0001c0001t0002g0176 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2149+14834C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532840 | ||||||
| chr7:130532884
|
A | C | 1 | a0001c0001t0002g0210 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2149+14790T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532884 | ||||||
| chr7:130532888
|
T | C | 1 | a0001c0001t0001g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2149+14786A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532888 | ||||||
| chr7:130532918
|
G | A | 3 | a0001c0002t0003g0121a0001c0002t0003g0122a0001c0002t0003g0123 | 3 | HG03490.hp2 HG03942.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2149+14756C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532918 | ||||||
| chr7:130532959
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2149+14715A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130532959 | ||||||
| chr7:130533048
|
C | G | 4 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287others(1): Show | 4 | NA18945.hp2 NA18963.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.2149+14626G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130533048 | ||||||
| chr7:130533120
|
C | T | 94 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(91): Show | 94 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.2149+14554G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130533120 | ||||||
| chr7:130533121
|
G | A | 1 | a0001c0002t0001g0097 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2149+14553C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130533121 | ||||||
| chr7:130533275
|
C | G | 1 | a0001c0002t0001g0031 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2149+14399G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130533275 | ||||||
| chr7:130533516
|
G | A | 1 | a0001c0002t0001g0060 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2149+14158C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130533516 | ||||||
| chr7:130533639
|
G | C | 1 | a0006c0007t0001g0095 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2149+14035C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130533639 | ||||||
| chr7:130533986
|
T | G | 1 | a0001c0002t0001g0002 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2149+13688A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130533986 | ||||||
| chr7:130533986
|
T | TG | 282 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(279): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.2149+13687dupC | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130533986 | ||||||
| chr7:130533986
|
T | TGG | 36 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0278others(33): Show | 36 | HG01255.hp1 HG01361.hp1 HG01952.hp2 others(33): Show |
intron_variant | MODIFIER | c.2149+13686_2149+13 others(8): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130533986 | ||||||
| chr7:130534037
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2149+13637G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130534037 | ||||||
| chr7:130534058
|
T | C | 2 | a0001c0001t0001g0276a0001c0001t0001g0311 | 2 | HG00639.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2149+13616A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130534058 | ||||||
| chr7:130534085
|
A | T | 1 | a0001c0002t0001g0037 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2149+13589T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130534085 | ||||||
| chr7:130534143
|
C | A | 1 | a0001c0001t0002g0163 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2149+13531G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130534143 | ||||||
| chr7:130534348
|
C | T | 1 | a0001c0002t0001g0049 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2149+13326G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130534348 | ||||||
| chr7:130534350
|
T | A | 1 | a0001c0001t0004g0308 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2149+13324A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130534350 | ||||||
| chr7:130534508
|
G | C | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2149+13166C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130534508 | ||||||
| chr7:130534584
|
A | G | 1 | a0001c0002t0001g0051 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2149+13090T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130534584 | ||||||
| chr7:130534641
|
G | T | 1 | a0001c0001t0001g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2149+13033C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130534641 | ||||||
| chr7:130534670
|
GA | G | 5 | a0001c0001t0001g0245a0001c0001t0001g0253a0001c0001t0001g0257others(2): Show | 5 | HG01099.hp2 HG02886.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2149+13003delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130534670 | ||||||
| chr7:130534902
|
A | G | 217 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0200others(214): Show | 217 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.2149+12772T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130534902 | ||||||
| chr7:130535147
|
G | A | 1 | a0001c0001t0002g0232 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2149+12527C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130535147 | ||||||
| chr7:130535276
|
T | C | 2 | a0003c0004t0001g0277a0003c0004t0001g0297 | 2 | NA18965.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2149+12398A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130535276 | ||||||
| chr7:130535324
|
A | G | 1 | a0001c0002t0001g0124 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2149+12350T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130535324 | ||||||
| chr7:130535374
|
G | A | 93 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(90): Show | 93 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.2149+12300C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130535374 | ||||||
| chr7:130535461
|
A | G | 1 | a0001c0001t0001g0304 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2149+12213T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130535461 | ||||||
| chr7:130535597
|
GGGCCA | G | 4 | a0001c0001t0001g0289a0001c0001t0001g0302a0001c0001t0004g0293others(1): Show | 4 | HG01496.hp1 HG02922.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2149+12072_2149+12 others(11): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130535597 | ||||||
| chr7:130535699
|
G | A | 10 | a0001c0001t0001g0029a0001c0001t0001g0129a0001c0001t0001g0130others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.2149+11975C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130535699 | ||||||
| chr7:130535699
|
G | C | 1 | a0001c0002t0001g0045 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2149+11975C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130535699 | ||||||
| chr7:130535715
|
C | T | 1 | a0001c0001t0006g0198 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2149+11959G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130535715 | ||||||
| chr7:130535782
|
C | T | 209 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0200others(206): Show | 209 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.2149+11892G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130535782 | ||||||
| chr7:130535860
|
G | A | 113 | a0001c0001t0001g0072a0001c0002t0001g0002a0001c0002t0001g0005others(110): Show | 113 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.2149+11814C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130535860 | ||||||
| chr7:130535967
|
T | C | 1 | a0001c0002t0001g0051 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2149+11707A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130535967 | ||||||
| chr7:130536037
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2149+11637G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130536037 | ||||||
| chr7:130536371
|
T | C | 1 | a0001c0001t0002g0177 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2149+11303A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130536371 | ||||||
| chr7:130536387
|
C | T | 1 | a0001c0002t0001g0092 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2149+11287G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130536387 | ||||||
| chr7:130536508
|
C | T | 262 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(259): Show | 262 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.2149+11166G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130536508 | ||||||
| chr7:130536577
|
G | A | 2 | a0001c0005t0002g0010a0001c0005t0002g0011 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2149+11097C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130536577 | ||||||
| chr7:130536613
|
G | C | 2 | a0001c0001t0001g0310a0001c0001t0001g0319 | 2 | HG02055.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2149+11061C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130536613 | ||||||
| chr7:130536685
|
C | T | 263 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(260): Show | 263 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.2149+10989G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130536685 | ||||||
| chr7:130536694
|
G | A | 263 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(260): Show | 263 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.2149+10980C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130536694 | ||||||
| chr7:130536826
|
G | A | 1 | a0001c0002t0001g0006 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2149+10848C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130536826 | ||||||
| chr7:130536830
|
G | A | 1 | a0001c0001t0002g0272 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2149+10844C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130536830 | ||||||
| chr7:130536874
|
C | T | 16 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0245others(13): Show | 16 | HG01099.hp2 HG02055.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.2149+10800G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130536874 | ||||||
| chr7:130536908
|
C | T | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2149+10766G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130536908 | ||||||
| chr7:130536955
|
C | T | 2 | a0001c0002t0001g0063a0001c0002t0001g0064 | 2 | HG02145.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2149+10719G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130536955 | ||||||
| chr7:130536956
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2149+10718C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130536956 | ||||||
| chr7:130536976
|
AAGG | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(54): Show | 57 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.2149+10695_2149+10 others(9): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130536976 | ||||||
| chr7:130537207
|
C | A | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(54): Show | 57 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.2149+10467G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130537207 | ||||||
| chr7:130537348
|
G | T | 53 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(50): Show | 53 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.2149+10326C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130537348 | ||||||
| chr7:130537361
|
G | A | 1 | a0001c0002t0001g0090 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2149+10313C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130537361 | ||||||
| chr7:130537448
|
G | A | 263 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(260): Show | 263 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.2149+10226C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130537448 | ||||||
| chr7:130537556
|
C | T | 1 | a0001c0002t0011g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2149+10118G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130537556 | ||||||
| chr7:130537580
|
C | T | 1 | a0001c0001t0002g0181 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2149+10094G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130537580 | ||||||
| chr7:130537649
|
T | A | 1 | a0001c0001t0002g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2149+10025A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130537649 | ||||||
| chr7:130537685
|
A | T | 1 | a0007c0009t0002g0217 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2149+9989T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130537685 | ||||||
| chr7:130537748
|
G | A | 1 | a0001c0001t0002g0215 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2149+9926C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130537748 | ||||||
| chr7:130537758
|
C | G | 1 | a0001c0002t0003g0107 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2149+9916G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130537758 | ||||||
| chr7:130537771
|
AAAAGGGG others(4419): Show |
A | 1 | a0001c0001t0001g0317 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2149+5477_2149+990 others(4): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130537771 | ||||||
| chr7:130537780
|
G | C | 4 | a0001c0002t0001g0102a0001c0002t0005g0076a0001c0002t0005g0077others(1): Show | 4 | HG01256.hp1 HG01258.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.2149+9894C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130537780 | ||||||
| chr7:130537805
|
G | A | 2 | a0001c0001t0002g0227a0001c0001t0006g0226 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2149+9869C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130537805 | ||||||
| chr7:130537830
|
C | T | 1 | a0001c0002t0007g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2149+9844G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130537830 | ||||||
| chr7:130537941
|
A | G | 1 | a0001c0001t0002g0185 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2149+9733T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130537941 | ||||||
| chr7:130538049
|
C | G | 263 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(260): Show | 263 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.2149+9625G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130538049 | ||||||
| chr7:130538192
|
A | T | 1 | a0001c0001t0001g0271 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2149+9482T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130538192 | ||||||
| chr7:130538283
|
A | T | 1 | a0001c0001t0002g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2149+9391T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130538283 | ||||||
| chr7:130538323
|
G | T | 113 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(110): Show | 113 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.2149+9351C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130538323 | ||||||
| chr7:130538397
|
C | T | 93 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(90): Show | 93 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.2149+9277G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130538397 | ||||||
| chr7:130538398
|
G | A | 1 | a0001c0001t0001g0315 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2149+9276C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130538398 | ||||||
| chr7:130538528
|
A | G | 1 | a0001c0002t0001g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2149+9146T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130538528 | ||||||
| chr7:130538540
|
T | G | 1 | a0001c0001t0001g0133 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2149+9134A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130538540 | ||||||
| chr7:130538688
|
GA | G | 259 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(256): Show | 259 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.2149+8985delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130538688 | ||||||
| chr7:130538814
|
G | T | 1 | a0001c0001t0001g0313 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2149+8860C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130538814 | ||||||
| chr7:130538853
|
A | T | 1 | a0001c0001t0001g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2149+8821T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130538853 | ||||||
| chr7:130539413
|
C | G | 2 | a0001c0001t0002g0227a0001c0001t0006g0226 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2149+8261G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130539413 | ||||||
| chr7:130539531
|
T | C | 1 | a0001c0002t0003g0121 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2149+8143A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130539531 | ||||||
| chr7:130539774
|
A | G | 2 | a0001c0005t0002g0010a0001c0005t0002g0011 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2149+7900T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130539774 | ||||||
| chr7:130539804
|
C | A | 27 | a0001c0002t0001g0019a0001c0002t0001g0028a0001c0002t0001g0034others(24): Show | 27 | HG00597.hp1 HG00621.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.2149+7870G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130539804 | ||||||
| chr7:130539829
|
G | A | 40 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(37): Show | 40 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.2149+7845C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130539829 | ||||||
| chr7:130539832
|
G | T | 4 | a0001c0001t0005g0251a0001c0001t0005g0254a0001c0001t0009g0252others(1): Show | 4 | HG02055.hp2 HG02723.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2149+7842C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130539832 | ||||||
| chr7:130539973
|
T | G | 1 | a0001c0001t0002g0183 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2149+7701A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130539973 | ||||||
| chr7:130540014
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2149+7660A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130540014 | ||||||
| chr7:130540046
|
GGGGATGG others(5): Show |
G | 2 | a0001c0002t0005g0076a0001c0002t0005g0077 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2149+7616_2149+762 others(16): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130540046 | ||||||
| chr7:130540073
|
G | C | 32 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(29): Show | 32 | HG01069.hp1 HG01167.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.2149+7601C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130540073 | ||||||
| chr7:130540076
|
G | A | 116 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.2149+7598C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130540076 | ||||||
| chr7:130540076
|
G | C | 62 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(59): Show | 62 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.2149+7598C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130540076 | ||||||
| chr7:130540218
|
A | C | 1 | a0001c0002t0001g0002 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2149+7456T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130540218 | ||||||
| chr7:130540305
|
C | T | 51 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(48): Show | 51 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.2149+7369G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130540305 | ||||||
| chr7:130540356
|
A | C | 1 | a0001c0001t0006g0182 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2149+7318T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130540356 | ||||||
| chr7:130540506
|
A | T | 1 | a0001c0002t0003g0120 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2149+7168T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130540506 | ||||||
| chr7:130540521
|
G | A | 1 | a0001c0001t0005g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2149+7153C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130540521 | ||||||
| chr7:130540753
|
A | G | 1 | a0001c0002t0005g0078 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2149+6921T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130540753 | ||||||
| chr7:130540908
|
A | G | 1 | a0001c0002t0001g0094 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2149+6766T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130540908 | ||||||
| chr7:130540937
|
T | G | 1 | a0001c0012t0002g0166 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2149+6737A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130540937 | ||||||
| chr7:130540987
|
C | T | 60 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(57): Show | 60 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.2149+6687G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130540987 | ||||||
| chr7:130541008
|
C | T | 5 | a0001c0001t0001g0030a0001c0001t0002g0024a0001c0001t0002g0025others(2): Show | 5 | HG01168.hp1 HG01978.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.2149+6666G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130541008 | ||||||
| chr7:130541027
|
G | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2149+6647C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130541027 | ||||||
| chr7:130541082
|
G | A | 1 | a0001c0001t0002g0204 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2149+6592C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130541082 | ||||||
| chr7:130541140
|
C | A | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2149+6534G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130541140 | ||||||
| chr7:130541173
|
G | A | 324 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.2149+6501C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130541173 | ||||||
| chr7:130541304
|
C | T | 1 | a0001c0005t0002g0011 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2149+6370G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130541304 | ||||||
| chr7:130541338
|
C | T | 1 | a0001c0002t0001g0060 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2149+6336G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130541338 | ||||||
| chr7:130541398
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2149+6276G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130541398 | ||||||
| chr7:130541406
|
A | AAGGAGGG others(3): Show |
1 | a0001c0002t0001g0241 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2149+6258_2149+626 others(14): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130541406 | ||||||
| chr7:130541695
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2149+5979C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130541695 | ||||||
| chr7:130541813
|
C | A | 1 | a0001c0001t0001g0288 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2149+5861G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130541813 | ||||||
| chr7:130541867
|
C | G | 2 | a0001c0001t0001g0127a0010c0015t0001g0259 | 2 | HG02622.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2149+5807G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130541867 | ||||||
| chr7:130541874
|
G | A | 1 | a0001c0001t0002g0187 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2149+5800C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130541874 | ||||||
| chr7:130541914
|
C | T | 21 | a0001c0001t0001g0029a0001c0001t0001g0129a0001c0001t0001g0130others(18): Show | 21 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.2149+5760G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130541914 | ||||||
| chr7:130542058
|
A | G | 8 | a0001c0002t0001g0019a0001c0002t0001g0028a0001c0002t0001g0034others(5): Show | 8 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.2149+5616T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130542058 | ||||||
| chr7:130542095
|
G | A | 116 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.2149+5579C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130542095 | ||||||
| chr7:130542197
|
C | A | 116 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.2149+5477G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130542197 | ||||||
| chr7:130542205
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2149+5469A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130542205 | ||||||
| chr7:130542242
|
G | A | 1 | a0001c0001t0002g0189 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2149+5432C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130542242 | ||||||
| chr7:130542362
|
C | T | 1 | a0001c0001t0002g0188 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2149+5312G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130542362 | ||||||
| chr7:130542435
|
G | A | 65 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0266others(62): Show | 65 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.2149+5239C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130542435 | ||||||
| chr7:130542520
|
C | T | 1 | a0008c0013t0001g0067 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2149+5154G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130542520 | ||||||
| chr7:130542548
|
C | A | 210 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(207): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.2149+5126G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130542548 | ||||||
| chr7:130542557
|
G | C | 1 | a0001c0001t0001g0298 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2149+5117C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130542557 | ||||||
| chr7:130542810
|
G | T | 4 | a0001c0002t0007g0236a0001c0002t0007g0237a0001c0002t0007g0238others(1): Show | 4 | HG01192.hp2 HG01993.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2149+4864C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130542810 | ||||||
| chr7:130543133
|
A | G | 1 | a0001c0001t0002g0173 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2149+4541T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130543133 | ||||||
| chr7:130543202
|
G | A | 61 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.2149+4472C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130543202 | ||||||
| chr7:130543256
|
C | A | 1 | a0001c0002t0007g0239 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2149+4418G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130543256 | ||||||
| chr7:130543438
|
G | T | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2149+4236C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130543438 | ||||||
| chr7:130543610
|
T | C | 65 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0266others(62): Show | 65 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.2149+4064A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130543610 | ||||||
| chr7:130543789
|
T | C | 3 | a0001c0001t0001g0289a0001c0001t0001g0302a0001c0001t0004g0293 | 3 | HG01496.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2149+3885A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130543789 | ||||||
| chr7:130543858
|
T | C | 1 | a0001c0001t0001g0307 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2149+3816A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130543858 | ||||||
| chr7:130543876
|
T | C | 1 | a0001c0002t0001g0050 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2149+3798A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130543876 | ||||||
| chr7:130543878
|
G | A | 1 | a0001c0002t0001g0062 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2149+3796C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130543878 | ||||||
| chr7:130543955
|
A | T | 1 | a0001c0002t0007g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2149+3719T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130543955 | ||||||
| chr7:130543969
|
C | T | 93 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(90): Show | 93 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.2149+3705G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130543969 | ||||||
| chr7:130544169
|
A | C | 1 | a0001c0002t0001g0042 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2149+3505T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130544169 | ||||||
| chr7:130544379
|
A | G | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2149+3295T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130544379 | ||||||
| chr7:130544407
|
A | G | 93 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(90): Show | 93 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.2149+3267T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130544407 | ||||||
| chr7:130544749
|
G | A | 5 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0246others(2): Show | 5 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2149+2925C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130544749 | ||||||
| chr7:130545170
|
T | TATTTC | 62 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(59): Show | 62 | HG00438.hp1 HG00544.hp1 HG01106.hp1 others(59): Show |
intron_variant | MODIFIER | c.2149+2499_2149+250 others(9): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130545170 | ||||||
| chr7:130545170
|
T | TATTTCAT others(3): Show |
29 | a0001c0002t0001g0019a0001c0002t0001g0028a0001c0002t0001g0034others(26): Show | 29 | HG00597.hp1 HG00621.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.2149+2494_2149+250 others(14): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130545170 | ||||||
| chr7:130545170
|
T | TATTTCAT others(8): Show |
3 | a0001c0002t0001g0036a0001c0002t0001g0060a0001c0002t0002g0088 | 3 | HG00099.hp1 HG01255.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2149+2489_2149+250 others(19): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130545170 | ||||||
| chr7:130545170
|
T | TATTTCAT others(18): Show |
2 | a0001c0002t0001g0032a0001c0002t0001g0033 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2149+2479_2149+250 others(29): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130545170 | ||||||
| chr7:130545170
|
TATTTC | T | 155 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0246others(152): Show | 155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.2149+2499_2149+250 others(9): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130545170 | ||||||
| chr7:130545170
|
TATTTCAT others(3): Show |
T | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2149+2494_2149+250 others(14): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130545170 | ||||||
| chr7:130545170
|
TATTTCAT others(8): Show |
T | 52 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(49): Show | 52 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(49): Show |
intron_variant | MODIFIER | c.2149+2489_2149+250 others(19): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130545170 | ||||||
| chr7:130545479
|
A | G | 6 | a0001c0002t0001g0079a0001c0002t0001g0090a0001c0002t0001g0091others(3): Show | 6 | NA18941.hp1 NA18944.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.2149+2195T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130545479 | ||||||
| chr7:130545485
|
G | T | 1 | a0001c0002t0003g0104 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2149+2189C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130545485 | ||||||
| chr7:130545497
|
G | A | 118 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(115): Show | 118 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.2149+2177C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130545497 | ||||||
| chr7:130545700
|
T | A | 53 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(50): Show | 53 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.2149+1974A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130545700 | ||||||
| chr7:130545829
|
C | A | 3 | a0001c0002t0001g0047a0001c0002t0001g0059a0001c0002t0001g0061 | 3 | HG02280.hp1 HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2149+1845G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130545829 | ||||||
| chr7:130546019
|
G | A | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2149+1655C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130546019 | ||||||
| chr7:130546079
|
T | A | 65 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0266others(62): Show | 65 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.2149+1595A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130546079 | ||||||
| chr7:130546183
|
T | A | 1 | a0001c0002t0001g0241 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2149+1491A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130546183 | ||||||
| chr7:130546326
|
T | C | 61 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.2149+1348A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130546326 | ||||||
| chr7:130546550
|
G | T | 113 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(110): Show | 113 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.2149+1124C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130546550 | ||||||
| chr7:130546579
|
G | A | 1 | a0010c0015t0001g0259 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2149+1095C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130546579 | ||||||
| chr7:130546645
|
G | A | 1 | a0001c0001t0004g0249 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2149+1029C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130546645 | ||||||
| chr7:130546704
|
C | T | 49 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(46): Show | 49 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.2149+970G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130546704 | ||||||
| chr7:130547430
|
C | T | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2149+244G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130547430 | ||||||
| chr7:130547496
|
A | G | 1 | a0001c0001t0002g0220 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2149+178T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130547496 | ||||||
| chr7:130547562
|
CATT | C | 3 | a0001c0002t0005g0076a0001c0002t0005g0077a0001c0002t0005g0078 | 3 | HG01256.hp1 HG01258.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.2149+109_2149+111d others(5): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 20/23 | chr7 | 130547562 | ||||||
| chr7:130548355
|
A | G | 53 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(50): Show | 53 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.1977+48T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 19/23 | chr7 | 130548355 | ||||||
| chr7:130548782
|
G | GT | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1838-241dupA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 18/23 | chr7 | 130548782 | ||||||
| chr7:130548811
|
G | A | 1 | a0001c0001t0005g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1838-269C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 18/23 | chr7 | 130548811 | ||||||
| chr7:130548871
|
T | C | 1 | a0006c0007t0001g0095 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1838-329A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 18/23 | chr7 | 130548871 | ||||||
| chr7:130549043
|
C | CA | 102 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(99): Show | 102 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1837+270dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 18/23 | chr7 | 130549043 | ||||||
| chr7:130549043
|
CAA | C | 48 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0023others(45): Show | 48 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.1837+269_1837+270d others(4): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 18/23 | chr7 | 130549043 | ||||||
| chr7:130549043
|
CAAA | C | 9 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1837+268_1837+270d others(5): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 18/23 | chr7 | 130549043 | ||||||
| chr7:130549290
|
C | T | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.1837+24G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 18/23 | chr7 | 130549290 | ||||||
| chr7:130549291
|
G | A | 1 | a0001c0002t0001g0051 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1837+23C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 18/23 | chr7 | 130549291 | ||||||
| chr7:130549432
|
C | G | 17 | a0001c0002t0003g0068a0001c0002t0003g0080a0001c0002t0003g0087others(14): Show | 17 | HG00323.hp1 HG00544.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.1775-56G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130549432 | ||||||
| chr7:130549436
|
G | A | 10 | a0001c0001t0001g0029a0001c0001t0001g0129a0001c0001t0001g0130others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.1775-60C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130549436 | ||||||
| chr7:130549597
|
A | G | 1 | a0001c0001t0002g0186 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1775-221T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130549597 | ||||||
| chr7:130549815
|
AG | A | 113 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(110): Show | 113 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.1775-440delC | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130549815 | ||||||
| chr7:130549816
|
G | A | 212 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(209): Show | 212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.1775-440C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130549816 | ||||||
| chr7:130549817
|
A | G | 212 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(209): Show | 212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.1775-441T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130549817 | ||||||
| chr7:130549838
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1775-462A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130549838 | ||||||
| chr7:130549852
|
C | T | 3 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007 | 3 | HG00438.hp1 NA18982.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1775-476G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130549852 | ||||||
| chr7:130549853
|
G | T | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(54): Show | 57 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.1775-477C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130549853 | ||||||
| chr7:130549938
|
C | T | 1 | a0001c0001t0004g0324 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1775-562G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130549938 | ||||||
| chr7:130549989
|
C | T | 3 | a0001c0001t0008g0318a0001c0001t0008g0321a0001c0001t0008g0322 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1774+535G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130549989 | ||||||
| chr7:130550074
|
T | A | 53 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(50): Show | 53 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.1774+450A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130550074 | ||||||
| chr7:130550105
|
A | T | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1774+419T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130550105 | ||||||
| chr7:130550204
|
A | G | 1 | a0001c0001t0002g0027 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1774+320T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130550204 | ||||||
| chr7:130550411
|
C | CA | 232 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0266others(229): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1774+112dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130550411 | ||||||
| chr7:130550411
|
C | CAA | 21 | a0001c0001t0001g0299a0001c0001t0001g0306a0001c0001t0002g0159others(18): Show | 21 | HG01175.hp1 HG01192.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.1774+111_1774+112d others(4): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130550411 | ||||||
| chr7:130550411
|
C | CAAAAAA | 30 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(27): Show | 30 | HG01099.hp2 HG01167.hp1 HG01515.hp2 others(27): Show |
intron_variant | MODIFIER | c.1774+107_1774+112d others(8): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130550411 | ||||||
| chr7:130550411
|
C | CAAAAAAA | 17 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0012others(14): Show | 17 | HG01243.hp1 HG02055.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.1774+106_1774+112d others(9): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130550411 | ||||||
| chr7:130550510
|
T | C | 263 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(260): Show | 263 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.1774+14A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 17/23 | chr7 | 130550510 | ||||||
| chr7:130550665
|
A | C | 1 | a0001c0001t0001g0014 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1649-16T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 16/23 | chr7 | 130550665 | ||||||
| chr7:130550871
|
C | A | 32 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(29): Show | 32 | HG01069.hp1 HG01167.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.1649-222G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 16/23 | chr7 | 130550871 | ||||||
| chr7:130550949
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1648+292C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 16/23 | chr7 | 130550949 | ||||||
| chr7:130551037
|
A | G | 1 | a0001c0001t0002g0148 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1648+204T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 16/23 | chr7 | 130551037 | ||||||
| chr7:130551091
|
TATAAACA others(1): Show |
T | 9 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026others(6): Show | 9 | HG01167.hp2 HG01168.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1648+142_1648+149d others(10): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 16/23 | chr7 | 130551091 | ||||||
| chr7:130551101
|
G | A | 9 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026others(6): Show | 9 | HG01167.hp2 HG01168.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1648+140C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 16/23 | chr7 | 130551101 | ||||||
| chr7:130551102
|
G | T | 9 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026others(6): Show | 9 | HG01167.hp2 HG01168.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1648+139C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 16/23 | chr7 | 130551102 | ||||||
| chr7:130551361
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1545-17C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 15/23 | chr7 | 130551361 | ||||||
| chr7:130551396
|
T | C | 1 | a0004c0011t0001g0280 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1545-52A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 15/23 | chr7 | 130551396 | ||||||
| chr7:130551446
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1545-102A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 15/23 | chr7 | 130551446 | ||||||
| chr7:130551726
|
T | C | 1 | a0001c0001t0002g0192 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1545-382A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 15/23 | chr7 | 130551726 | ||||||
| chr7:130551972
|
T | C | 1 | a0001c0002t0001g0063 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1544+383A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 15/23 | chr7 | 130551972 | ||||||
| chr7:130552179
|
T | C | 20 | a0001c0002t0003g0068a0001c0002t0003g0080a0001c0002t0003g0087others(17): Show | 20 | HG00323.hp1 HG00544.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.1544+176A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 15/23 | chr7 | 130552179 | ||||||
| chr7:130552247
|
T | A | 1 | a0001c0002t0001g0006 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1544+108A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 15/23 | chr7 | 130552247 | ||||||
| chr7:130552274
|
G | A | 1 | a0001c0001t0001g0299 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1544+81C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 15/23 | chr7 | 130552274 | ||||||
| chr7:130552614
|
A | C | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1469-184T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130552614 | ||||||
| chr7:130552962
|
T | C | 1 | a0001c0001t0001g0304 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1469-532A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130552962 | ||||||
| chr7:130553002
|
C | T | 4 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287others(1): Show | 4 | NA18945.hp2 NA18963.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.1469-572G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130553002 | ||||||
| chr7:130553004
|
G | A | 1 | a0001c0001t0002g0193 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1469-574C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130553004 | ||||||
| chr7:130553133
|
C | T | 53 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(50): Show | 53 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.1469-703G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130553133 | ||||||
| chr7:130553330
|
C | T | 1 | a0001c0001t0002g0181 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1469-900G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130553330 | ||||||
| chr7:130553333
|
C | T | 32 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(29): Show | 32 | HG01069.hp1 HG01167.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.1469-903G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130553333 | ||||||
| chr7:130553461
|
T | C | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468+1020A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130553461 | ||||||
| chr7:130553671
|
A | G | 1 | a0010c0015t0001g0259 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1468+810T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130553671 | ||||||
| chr7:130553772
|
G | A | 266 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(263): Show | 266 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.1468+709C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130553772 | ||||||
| chr7:130553905
|
T | G | 2 | a0001c0001t0001g0269a0001c0001t0001g0305 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1468+576A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130553905 | ||||||
| chr7:130553951
|
C | G | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1468+530G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130553951 | ||||||
| chr7:130553959
|
T | C | 1 | a0001c0001t0012g0206 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1468+522A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130553959 | ||||||
| chr7:130553966
|
G | A | 32 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(29): Show | 32 | HG01069.hp1 HG01167.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.1468+515C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130553966 | ||||||
| chr7:130554032
|
C | A | 1 | a0001c0001t0001g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1468+449G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130554032 | ||||||
| chr7:130554176
|
G | A | 2 | a0001c0005t0002g0010a0001c0005t0002g0011 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1468+305C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130554176 | ||||||
| chr7:130554183
|
A | AATAT | 40 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(37): Show | 40 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.1468+294_1468+297d others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 14/23 | chr7 | 130554183 | ||||||
| chr7:130554935
|
C | T | 1 | a0001c0002t0001g0070 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1224+102G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 13/23 | chr7 | 130554935 | ||||||
| chr7:130555624
|
C | T | 5 | a0001c0002t0007g0235a0001c0002t0007g0236a0001c0002t0007g0237others(2): Show | 5 | HG01192.hp2 HG01993.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1129-492G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130555624 | ||||||
| chr7:130555664
|
TA | T | 61 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1129-533delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130555664 | ||||||
| chr7:130555717
|
T | C | 14 | a0001c0002t0001g0038a0001c0002t0001g0041a0001c0002t0001g0042others(11): Show | 14 | HG00597.hp1 HG00621.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.1129-585A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130555717 | ||||||
| chr7:130555977
|
C | T | 53 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(50): Show | 53 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.1129-845G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130555977 | ||||||
| chr7:130556435
|
G | C | 1 | a0001c0001t0001g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1129-1303C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130556435 | ||||||
| chr7:130556574
|
T | C | 2 | a0001c0006t0002g0153a0001c0006t0002g0154 | 2 | NA18941.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.1129-1442A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130556574 | ||||||
| chr7:130556656
|
T | C | 12 | a0001c0001t0001g0127a0001c0001t0001g0132a0001c0001t0001g0133others(9): Show | 12 | HG01891.hp1 HG01943.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1129-1524A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130556656 | ||||||
| chr7:130556704
|
T | G | 118 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(115): Show | 118 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.1129-1572A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130556704 | ||||||
| chr7:130557241
|
A | G | 1 | a0001c0002t0001g0069 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1129-2109T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130557241 | ||||||
| chr7:130557310
|
T | C | 1 | a0001c0001t0002g0156 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1129-2178A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130557310 | ||||||
| chr7:130557408
|
G | A | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1129-2276C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130557408 | ||||||
| chr7:130557459
|
T | C | 1 | a0001c0001t0002g0170 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1129-2327A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130557459 | ||||||
| chr7:130557578
|
G | A | 1 | a0001c0002t0001g0031 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1129-2446C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130557578 | ||||||
| chr7:130557723
|
G | A | 93 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(90): Show | 93 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.1129-2591C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130557723 | ||||||
| chr7:130557817
|
C | CAAAAA | 54 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(51): Show | 54 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.1129-2690_1129-268 others(9): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130557817 | ||||||
| chr7:130557817
|
C | CAAAAAA | 102 | a0001c0001t0001g0266a0001c0001t0001g0273a0001c0001t0001g0278others(99): Show | 102 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1129-2691_1129-268 others(10): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130557817 | ||||||
| chr7:130557817
|
C | CAAAAAAA | 91 | a0001c0001t0001g0030a0001c0001t0001g0071a0001c0001t0001g0072others(88): Show | 91 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1129-2692_1129-268 others(11): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130557817 | ||||||
| chr7:130557817
|
C | CAAAAAAA others(1): Show |
48 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(45): Show | 48 | HG01069.hp1 HG01106.hp2 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.1129-2693_1129-268 others(12): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130557817 | ||||||
| chr7:130557817
|
C | CAAAAAAA others(2): Show |
19 | a0001c0001t0001g0013a0001c0001t0001g0029a0001c0001t0001g0129others(16): Show | 19 | HG01099.hp2 HG02055.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.1129-2694_1129-268 others(13): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130557817 | ||||||
| chr7:130557817
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0001g0253a0001c0001t0005g0250 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1129-2695_1129-268 others(14): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130557817 | ||||||
| chr7:130557817
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1129-2696_1129-268 others(15): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130557817 | ||||||
| chr7:130557817
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0004 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1129-2697_1129-268 others(16): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130557817 | ||||||
| chr7:130557817
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0003 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1129-2698_1129-268 others(17): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130557817 | ||||||
| chr7:130557839
|
T | A | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(322): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.1129-2707A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130557839 | ||||||
| chr7:130558003
|
C | T | 1 | a0001c0001t0002g0177 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1129-2871G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130558003 | ||||||
| chr7:130558004
|
G | A | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1129-2872C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130558004 | ||||||
| chr7:130558157
|
T | C | 6 | a0001c0001t0002g0150a0001c0001t0002g0196a0001c0001t0002g0203others(3): Show | 6 | HG01175.hp2 HG01515.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1128+2876A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130558157 | ||||||
| chr7:130558202
|
A | G | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1128+2831T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130558202 | ||||||
| chr7:130558580
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1128+2453T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130558580 | ||||||
| chr7:130558608
|
C | A | 1 | a0001c0002t0001g0050 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1128+2425G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130558608 | ||||||
| chr7:130558706
|
G | C | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.1128+2327C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130558706 | ||||||
| chr7:130558926
|
C | A | 61 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1128+2107G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130558926 | ||||||
| chr7:130559069
|
T | C | 3 | a0001c0001t0002g0148a0001c0001t0002g0167a0001c0001t0002g0176 | 3 | HG00621.hp1 NA18954.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.1128+1964A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130559069 | ||||||
| chr7:130559079
|
G | A | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128+1954C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130559079 | ||||||
| chr7:130559197
|
A | C | 10 | a0001c0001t0001g0029a0001c0001t0001g0129a0001c0001t0001g0130others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.1128+1836T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130559197 | ||||||
| chr7:130559203
|
A | G | 6 | a0001c0001t0002g0150a0001c0001t0002g0196a0001c0001t0002g0203others(3): Show | 6 | HG01175.hp2 HG01515.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1128+1830T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130559203 | ||||||
| chr7:130559647
|
A | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(3): Show | 6 | HG01243.hp1 HG02258.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1128+1386T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130559647 | ||||||
| chr7:130559796
|
A | G | 2 | a0001c0002t0001g0098a0001c0002t0001g0099 | 2 | NA18980.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1128+1237T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130559796 | ||||||
| chr7:130559877
|
G | A | 1 | a0001c0001t0002g0232 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1128+1156C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130559877 | ||||||
| chr7:130560196
|
T | C | 1 | a0001c0001t0002g0190 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1128+837A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130560196 | ||||||
| chr7:130560308
|
G | A | 1 | a0001c0001t0002g0223 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1128+725C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130560308 | ||||||
| chr7:130560549
|
G | A | 118 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(115): Show | 118 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.1128+484C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130560549 | ||||||
| chr7:130560586
|
A | G | 1 | a0001c0002t0001g0069 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1128+447T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130560586 | ||||||
| chr7:130560810
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1128+223A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130560810 | ||||||
| chr7:130560905
|
G | A | 61 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.1128+128C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 12/23 | chr7 | 130560905 | ||||||
| chr7:130561839
|
C | A | 6 | a0001c0002t0001g0079a0001c0002t0001g0090a0001c0002t0001g0091others(3): Show | 6 | NA18941.hp1 NA18944.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.940-618G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 11/23 | chr7 | 130561839 | ||||||
| chr7:130561865
|
C | T | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.940-644G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 11/23 | chr7 | 130561865 | ||||||
| chr7:130562215
|
C | T | 5 | a0001c0002t0007g0235a0001c0002t0007g0236a0001c0002t0007g0237others(2): Show | 5 | HG01192.hp2 HG01993.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.940-994G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 11/23 | chr7 | 130562215 | ||||||
| chr7:130562314
|
G | A | 1 | a0001c0012t0002g0166 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.939+955C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 11/23 | chr7 | 130562314 | ||||||
| chr7:130562454
|
C | T | 2 | a0001c0001t0002g0227a0001c0001t0006g0226 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.939+815G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 11/23 | chr7 | 130562454 | ||||||
| chr7:130562758
|
T | C | 1 | a0001c0001t0009g0256 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.939+511A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 11/23 | chr7 | 130562758 | ||||||
| chr7:130563067
|
A | C | 53 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(50): Show | 53 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.939+202T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 11/23 | chr7 | 130563067 | ||||||
| chr7:130563345
|
A | AAAT | 6 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(3): Show | 6 | HG02129.hp1 HG02155.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.872-12_872-10dupAT others(1): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 10/23 | chr7 | 130563345 | ||||||
| chr7:130563345
|
A | T | 61 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(58): Show | 61 | HG01069.hp1 HG01099.hp2 HG01106.hp1 others(58): Show |
intron_variant | MODIFIER | c.872-9T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 10/23 | chr7 | 130563345 | ||||||
| chr7:130563362
|
T | C | 2 | a0001c0001t0005g0247a0001c0001t0005g0258 | 2 | HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.872-26A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 10/23 | chr7 | 130563362 | ||||||
| chr7:130563394
|
G | A | 10 | a0001c0001t0001g0029a0001c0001t0001g0129a0001c0001t0001g0130others(7): Show | 10 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.872-58C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 10/23 | chr7 | 130563394 | ||||||
| chr7:130563537
|
A | C | 1 | a0001c0002t0001g0070 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.872-201T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 10/23 | chr7 | 130563537 | ||||||
| chr7:130563666
|
A | G | 1 | a0001c0002t0001g0093 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.872-330T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 10/23 | chr7 | 130563666 | ||||||
| chr7:130563772
|
A | G | 1 | a0001c0001t0002g0186 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.872-436T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 10/23 | chr7 | 130563772 | ||||||
| chr7:130563773
|
A | G | 149 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0266others(146): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.872-437T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 10/23 | chr7 | 130563773 | ||||||
| chr7:130563774
|
G | A | 150 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0266others(147): Show | 150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.872-438C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 10/23 | chr7 | 130563774 | ||||||
| chr7:130563774
|
G | GA | 151 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0029others(148): Show | 151 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.872-439dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 10/23 | chr7 | 130563774 | ||||||
| chr7:130563895
|
T | C | 1 | a0001c0001t0002g0186 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.871+365A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 10/23 | chr7 | 130563895 | ||||||
| chr7:130563919
|
C | T | 1 | a0001c0012t0002g0166 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.871+341G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 10/23 | chr7 | 130563919 | ||||||
| chr7:130563957
|
A | C | 1 | a0001c0001t0002g0179 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.871+303T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 10/23 | chr7 | 130563957 | ||||||
| chr7:130564021
|
T | C | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.871+239A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 10/23 | chr7 | 130564021 | ||||||
| chr7:130564122
|
T | A | 1 | a0001c0002t0001g0065 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.871+138A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 10/23 | chr7 | 130564122 | ||||||
| chr7:130564194
|
T | C | 118 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(115): Show | 118 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.871+66A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 10/23 | chr7 | 130564194 | ||||||
| chr7:130564438
|
G | C | 58 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(55): Show | 58 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.738-45C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130564438 | ||||||
| chr7:130564519
|
C | A | 1 | a0001c0001t0001g0299 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.738-126G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130564519 | ||||||
| chr7:130564866
|
G | A | 93 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(90): Show | 93 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.738-473C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130564866 | ||||||
| chr7:130565135
|
A | G | 1 | a0001c0002t0003g0121 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.738-742T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130565135 | ||||||
| chr7:130565145
|
C | T | 1 | a0001c0002t0003g0121 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.738-752G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130565145 | ||||||
| chr7:130565230
|
G | A | 61 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.738-837C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130565230 | ||||||
| chr7:130565765
|
T | C | 1 | a0010c0015t0001g0259 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.738-1372A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130565765 | ||||||
| chr7:130565827
|
T | A | 1 | a0001c0002t0001g0028 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.738-1434A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130565827 | ||||||
| chr7:130565859
|
G | C | 1 | a0001c0002t0001g0073 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.738-1466C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130565859 | ||||||
| chr7:130566058
|
T | G | 1 | a0001c0001t0002g0165 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.738-1665A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130566058 | ||||||
| chr7:130566160
|
T | C | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.738-1767A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130566160 | ||||||
| chr7:130566278
|
T | C | 48 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(45): Show | 48 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.738-1885A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130566278 | ||||||
| chr7:130566597
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.738-2204G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130566597 | ||||||
| chr7:130566599
|
G | A | 1 | a0001c0002t0003g0122 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.738-2206C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130566599 | ||||||
| chr7:130566873
|
A | G | 53 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(50): Show | 53 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.738-2480T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130566873 | ||||||
| chr7:130566879
|
T | C | 1 | a0001c0002t0007g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.738-2486A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130566879 | ||||||
| chr7:130567221
|
A | G | 1 | a0001c0002t0001g0116 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.738-2828T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130567221 | ||||||
| chr7:130568068
|
G | A | 3 | a0001c0001t0008g0318a0001c0001t0008g0321a0001c0001t0008g0322 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.738-3675C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130568068 | ||||||
| chr7:130568135
|
C | A | 1 | a0001c0002t0001g0099 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.738-3742G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130568135 | ||||||
| chr7:130568211
|
G | A | 1 | a0001c0002t0003g0104 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.738-3818C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130568211 | ||||||
| chr7:130568314
|
G | A | 5 | a0001c0001t0001g0030a0001c0001t0001g0262a0001c0001t0001g0263others(2): Show | 5 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.738-3921C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130568314 | ||||||
| chr7:130568324
|
T | C | 5 | a0001c0001t0001g0030a0001c0001t0001g0262a0001c0001t0001g0263others(2): Show | 5 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.738-3931A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130568324 | ||||||
| chr7:130568413
|
A | G | 1 | a0001c0001t0002g0186 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.738-4020T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130568413 | ||||||
| chr7:130568745
|
A | T | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.738-4352T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130568745 | ||||||
| chr7:130568783
|
A | G | 1 | a0001c0002t0001g0098 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.738-4390T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130568783 | ||||||
| chr7:130568960
|
T | C | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.738-4567A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130568960 | ||||||
| chr7:130569014
|
C | T | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.738-4621G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130569014 | ||||||
| chr7:130569096
|
A | G | 3 | a0001c0002t0001g0032a0001c0002t0001g0033a0001c0002t0001g0036 | 3 | HG00099.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.738-4703T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130569096 | ||||||
| chr7:130569190
|
G | C | 1 | a0001c0001t0001g0257 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.738-4797C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130569190 | ||||||
| chr7:130569302
|
C | T | 118 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(115): Show | 118 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.738-4909G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130569302 | ||||||
| chr7:130569366
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.738-4973C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130569366 | ||||||
| chr7:130570182
|
T | C | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-5789A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130570182 | ||||||
| chr7:130570248
|
A | G | 5 | a0001c0001t0001g0030a0001c0001t0001g0262a0001c0001t0001g0263others(2): Show | 5 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.738-5855T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130570248 | ||||||
| chr7:130570408
|
G | A | 48 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(45): Show | 48 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.738-6015C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130570408 | ||||||
| chr7:130570586
|
G | T | 1 | a0001c0002t0001g0051 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.738-6193C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130570586 | ||||||
| chr7:130570587
|
A | T | 1 | a0001c0002t0001g0051 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.738-6194T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130570587 | ||||||
| chr7:130570654
|
C | T | 5 | a0001c0001t0002g0179a0001c0001t0002g0180a0001c0001t0002g0181others(2): Show | 5 | HG00140.hp2 HG00639.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.738-6261G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130570654 | ||||||
| chr7:130570941
|
A | G | 1 | a0001c0002t0001g0098 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.738-6548T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130570941 | ||||||
| chr7:130570992
|
G | C | 1 | a0001c0001t0002g0177 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.738-6599C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130570992 | ||||||
| chr7:130571020
|
C | A | 1 | a0001c0001t0012g0206 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.738-6627G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130571020 | ||||||
| chr7:130571228
|
C | T | 1 | a0001c0001t0001g0299 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.738-6835G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130571228 | ||||||
| chr7:130571229
|
G | A | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.738-6836C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130571229 | ||||||
| chr7:130571338
|
C | T | 2 | a0001c0002t0001g0037a0001c0002t0001g0060 | 2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.738-6945G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130571338 | ||||||
| chr7:130571667
|
A | G | 92 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(89): Show | 92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.738-7274T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130571667 | ||||||
| chr7:130571834
|
C | CCT | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(98): Show | 101 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.738-7443_738-7442d others(4): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130571834 | ||||||
| chr7:130571845
|
C | A | 5 | a0001c0001t0001g0030a0001c0001t0001g0071a0001c0001t0001g0072others(2): Show | 5 | HG02486.hp2 HG02717.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.738-7452G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130571845 | ||||||
| chr7:130571845
|
C | CTA | 12 | a0001c0001t0001g0029a0001c0001t0001g0129a0001c0001t0001g0130others(9): Show | 12 | HG01099.hp2 HG01167.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.738-7454_738-7453d others(4): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130571845 | ||||||
| chr7:130571847
|
A | C | 273 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.738-7454T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130571847 | ||||||
| chr7:130571849
|
A | C | 140 | a0001c0001t0001g0127a0001c0001t0001g0134a0001c0001t0001g0137others(137): Show | 140 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.738-7456T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130571849 | ||||||
| chr7:130571873
|
G | A | 61 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.738-7480C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130571873 | ||||||
| chr7:130572005
|
C | A | 4 | a0001c0002t0007g0236a0001c0002t0007g0237a0001c0002t0007g0238others(1): Show | 4 | HG01192.hp2 HG01993.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.738-7612G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130572005 | ||||||
| chr7:130572072
|
T | C | 1 | a0001c0002t0003g0105 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.738-7679A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130572072 | ||||||
| chr7:130572683
|
A | G | 1 | a0001c0001t0002g0151 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.738-8290T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130572683 | ||||||
| chr7:130572831
|
A | T | 1 | a0001c0001t0001g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.738-8438T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130572831 | ||||||
| chr7:130572991
|
C | T | 3 | a0001c0001t0008g0318a0001c0001t0008g0321a0001c0001t0008g0322 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.738-8598G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130572991 | ||||||
| chr7:130573213
|
C | CA | 97 | a0001c0001t0001g0129a0001c0001t0001g0200a0001c0001t0001g0213others(94): Show | 97 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.738-8821dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130573213 | ||||||
| chr7:130573213
|
CA | C | 101 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(98): Show | 101 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.738-8821delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130573213 | ||||||
| chr7:130573285
|
C | T | 1 | a0001c0002t0003g0261 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.738-8892G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130573285 | ||||||
| chr7:130573382
|
A | G | 4 | a0001c0001t0005g0251a0001c0001t0005g0254a0001c0001t0009g0252others(1): Show | 4 | HG02055.hp2 HG02723.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.738-8989T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130573382 | ||||||
| chr7:130573501
|
T | C | 3 | a0001c0001t0001g0289a0001c0001t0001g0302a0001c0001t0004g0293 | 3 | HG01496.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.738-9108A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130573501 | ||||||
| chr7:130573610
|
A | G | 4 | a0001c0002t0001g0052a0001c0002t0001g0063a0001c0002t0001g0064others(1): Show | 4 | HG02145.hp1 HG02647.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-9217T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130573610 | ||||||
| chr7:130573900
|
G | A | 2 | a0001c0001t0002g0024a0001c0001t0002g0026 | 2 | HG01978.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.738-9507C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130573900 | ||||||
| chr7:130573956
|
A | G | 4 | a0001c0002t0001g0241a0002c0003t0001g0242a0002c0003t0001g0243others(1): Show | 4 | HG01433.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-9563T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130573956 | ||||||
| chr7:130574125
|
G | A | 4 | a0001c0002t0001g0241a0002c0003t0001g0242a0002c0003t0001g0243others(1): Show | 4 | HG01433.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-9732C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130574125 | ||||||
| chr7:130574177
|
A | C | 3 | a0001c0001t0008g0318a0001c0001t0008g0321a0001c0001t0008g0322 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.738-9784T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130574177 | ||||||
| chr7:130574274
|
G | T | 1 | a0001c0001t0002g0205 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.738-9881C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130574274 | ||||||
| chr7:130574425
|
C | T | 1 | a0001c0002t0001g0047 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.738-10032G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130574425 | ||||||
| chr7:130574519
|
C | T | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-10126G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130574519 | ||||||
| chr7:130574529
|
A | T | 1 | a0001c0001t0001g0312 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.738-10136T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130574529 | ||||||
| chr7:130574654
|
C | A | 282 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(279): Show | 282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.738-10261G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130574654 | ||||||
| chr7:130574823
|
A | G | 1 | a0001c0001t0004g0128 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.738-10430T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130574823 | ||||||
| chr7:130574935
|
G | C | 1 | a0001c0002t0001g0028 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.738-10542C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130574935 | ||||||
| chr7:130575092
|
A | G | 118 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(115): Show | 118 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.738-10699T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130575092 | ||||||
| chr7:130575174
|
T | G | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.738-10781A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130575174 | ||||||
| chr7:130575197
|
C | T | 53 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(50): Show | 53 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.738-10804G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130575197 | ||||||
| chr7:130575277
|
G | A | 1 | a0001c0002t0003g0104 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.738-10884C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130575277 | ||||||
| chr7:130575285
|
T | C | 10 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(7): Show | 10 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.738-10892A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130575285 | ||||||
| chr7:130575454
|
A | G | 1 | a0001c0001t0001g0275 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.738-11061T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130575454 | ||||||
| chr7:130575455
|
G | C | 1 | a0001c0002t0001g0090 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.738-11062C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130575455 | ||||||
| chr7:130575522
|
C | T | 1 | a0001c0001t0002g0194 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.738-11129G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130575522 | ||||||
| chr7:130576401
|
C | G | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.738-12008G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130576401 | ||||||
| chr7:130576527
|
G | A | 1 | a0001c0001t0002g0214 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.738-12134C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130576527 | ||||||
| chr7:130576611
|
T | C | 1 | a0001c0001t0001g0307 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.738-12218A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130576611 | ||||||
| chr7:130576695
|
T | C | 2 | a0001c0001t0001g0273a0004c0011t0001g0280 | 2 | HG00099.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.738-12302A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130576695 | ||||||
| chr7:130576761
|
G | C | 1 | a0001c0002t0001g0102 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.738-12368C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130576761 | ||||||
| chr7:130576781
|
GAAAC | G | 6 | a0001c0002t0007g0235a0001c0002t0007g0236a0001c0002t0007g0237others(3): Show | 6 | HG01192.hp2 HG01993.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.738-12392_738-1238 others(8): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130576781 | ||||||
| chr7:130576796
|
A | T | 2 | a0001c0001t0002g0227a0001c0001t0006g0226 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.738-12403T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130576796 | ||||||
| chr7:130576797
|
C | A | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-12404G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130576797 | ||||||
| chr7:130577273
|
T | C | 32 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(29): Show | 32 | HG01069.hp1 HG01167.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.738-12880A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577273 | ||||||
| chr7:130577304
|
T | C | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.738-12911A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577304 | ||||||
| chr7:130577329
|
G | A | 93 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(90): Show | 93 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.738-12936C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577329 | ||||||
| chr7:130577345
|
T | C | 1 | a0001c0002t0001g0022 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.738-12952A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577345 | ||||||
| chr7:130577363
|
G | T | 61 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.738-12970C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577363 | ||||||
| chr7:130577446
|
T | C | 4 | a0001c0002t0001g0241a0002c0003t0001g0242a0002c0003t0001g0243others(1): Show | 4 | HG01433.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-13053A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577446 | ||||||
| chr7:130577551
|
G | C | 1 | a0001c0001t0001g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.738-13158C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577551 | ||||||
| chr7:130577683
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.738-13290G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577683 | ||||||
| chr7:130577755
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.738-13362C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577755 | ||||||
| chr7:130577767
|
C | CA | 40 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(37): Show | 40 | HG00621.hp2 HG01167.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.738-13375dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577767 | ||||||
| chr7:130577767
|
C | CAA | 6 | a0001c0002t0001g0085a0001c0002t0001g0125a0001c0002t0001g0241others(3): Show | 6 | HG03834.hp2 HG04115.hp1 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.738-13376_738-1337 others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577767 | ||||||
| chr7:130577767
|
CA | C | 52 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(49): Show | 52 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.738-13375delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577767 | ||||||
| chr7:130577775
|
A | C | 93 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(90): Show | 93 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.738-13382T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577775 | ||||||
| chr7:130577777
|
A | C | 3 | a0001c0001t0001g0133a0001c0001t0001g0253a0001c0001t0001g0257 | 3 | HG02630.hp1 HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.738-13384T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577777 | ||||||
| chr7:130577781
|
A | C | 8 | a0001c0001t0002g0162a0001c0001t0002g0181a0001c0001t0002g0219others(5): Show | 8 | HG02451.hp1 HG02717.hp2 HG04115.hp2 others(5): Show |
intron_variant | MODIFIER | c.738-13388T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577781 | ||||||
| chr7:130577784
|
A | AC | 4 | a0001c0001t0001g0030a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG02818.hp2 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-13392_738-1339 others(5): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577784 | ||||||
| chr7:130577785
|
A | C | 92 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(89): Show | 92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.738-13392T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577785 | ||||||
| chr7:130577788
|
A | C | 1 | a0001c0001t0004g0324 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.738-13395T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577788 | ||||||
| chr7:130577789
|
C | A | 9 | a0001c0001t0001g0307a0001c0001t0004g0324a0001c0002t0001g0241others(6): Show | 9 | HG01256.hp2 HG01361.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.738-13396G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577789 | ||||||
| chr7:130577793
|
A | C | 8 | a0001c0001t0002g0151a0001c0001t0002g0159a0001c0001t0002g0160others(5): Show | 8 | HG00544.hp2 HG01258.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.738-13400T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577793 | ||||||
| chr7:130577841
|
G | T | 2 | a0001c0002t0001g0032a0001c0002t0001g0033 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.738-13448C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577841 | ||||||
| chr7:130577858
|
A | G | 5 | a0001c0002t0007g0235a0001c0002t0007g0236a0001c0002t0007g0237others(2): Show | 5 | HG01192.hp2 HG01993.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.738-13465T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577858 | ||||||
| chr7:130577896
|
T | C | 1 | a0003c0008t0001g0114 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.738-13503A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577896 | ||||||
| chr7:130577904
|
G | A | 1 | a0010c0015t0001g0259 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.738-13511C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130577904 | ||||||
| chr7:130578015
|
C | A | 1 | a0001c0001t0001g0274 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.738-13622G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130578015 | ||||||
| chr7:130578226
|
C | A | 53 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(50): Show | 53 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.738-13833G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130578226 | ||||||
| chr7:130578322
|
G | A | 93 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(90): Show | 93 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.738-13929C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130578322 | ||||||
| chr7:130578482
|
A | G | 1 | a0001c0001t0002g0161 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.738-14089T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130578482 | ||||||
| chr7:130578510
|
C | T | 2 | a0001c0001t0001g0271a0001c0001t0002g0209 | 2 | HG00140.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.738-14117G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130578510 | ||||||
| chr7:130578715
|
A | G | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.738-14322T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130578715 | ||||||
| chr7:130578750
|
A | G | 5 | a0001c0001t0001g0030a0001c0001t0001g0262a0001c0001t0001g0263others(2): Show | 5 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.738-14357T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130578750 | ||||||
| chr7:130578779
|
G | A | 1 | a0001c0002t0001g0091 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.738-14386C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130578779 | ||||||
| chr7:130578866
|
A | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.738-14473T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130578866 | ||||||
| chr7:130578938
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.738-14545T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130578938 | ||||||
| chr7:130579043
|
T | C | 20 | a0001c0002t0003g0068a0001c0002t0003g0080a0001c0002t0003g0087others(17): Show | 20 | HG00323.hp1 HG00544.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.738-14650A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130579043 | ||||||
| chr7:130579114
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.738-14721G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130579114 | ||||||
| chr7:130579152
|
G | A | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144 | 3 | HG01069.hp1 HG01515.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.738-14759C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130579152 | ||||||
| chr7:130579370
|
A | G | 93 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(90): Show | 93 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.738-14977T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130579370 | ||||||
| chr7:130579415
|
C | T | 1 | a0001c0002t0001g0097 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.738-15022G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130579415 | ||||||
| chr7:130579477
|
G | A | 1 | a0001c0002t0007g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.738-15084C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130579477 | ||||||
| chr7:130579550
|
T | C | 61 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.738-15157A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130579550 | ||||||
| chr7:130579572
|
C | T | 1 | a0001c0001t0002g0185 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.738-15179G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130579572 | ||||||
| chr7:130579737
|
C | A | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.738-15344G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130579737 | ||||||
| chr7:130580077
|
T | C | 1 | a0001c0002t0011g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.738-15684A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130580077 | ||||||
| chr7:130580269
|
C | A | 48 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(45): Show | 48 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.738-15876G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130580269 | ||||||
| chr7:130580334
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.738-15941C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130580334 | ||||||
| chr7:130580444
|
G | C | 1 | a0001c0001t0002g0151 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.738-16051C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130580444 | ||||||
| chr7:130580448
|
G | C | 1 | a0001c0001t0002g0155 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.738-16055C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130580448 | ||||||
| chr7:130580461
|
CA | C | 93 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(90): Show | 93 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.738-16069delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130580461 | ||||||
| chr7:130580467
|
C | G | 93 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(90): Show | 93 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.738-16074G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130580467 | ||||||
| chr7:130580472
|
A | G | 1 | a0001c0001t0002g0189 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.738-16079T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130580472 | ||||||
| chr7:130580590
|
G | A | 1 | a0010c0015t0001g0259 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.738-16197C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130580590 | ||||||
| chr7:130580594
|
G | A | 1 | a0003c0008t0001g0114 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.738-16201C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130580594 | ||||||
| chr7:130580634
|
A | G | 7 | a0001c0001t0005g0247a0001c0001t0005g0250a0001c0001t0005g0251others(4): Show | 7 | HG02055.hp2 HG02630.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.738-16241T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130580634 | ||||||
| chr7:130580673
|
A | G | 53 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(50): Show | 53 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.738-16280T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130580673 | ||||||
| chr7:130580723
|
C | T | 1 | a0001c0002t0002g0088 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.738-16330G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130580723 | ||||||
| chr7:130580794
|
AG | A | 48 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(45): Show | 48 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.738-16402delC | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130580794 | ||||||
| chr7:130580903
|
A | T | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.738-16510T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130580903 | ||||||
| chr7:130581092
|
T | C | 211 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(208): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.738-16699A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130581092 | ||||||
| chr7:130581188
|
C | T | 1 | a0001c0001t0002g0272 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.738-16795G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130581188 | ||||||
| chr7:130581195
|
C | G | 2 | a0001c0002t0001g0020a0001c0002t0001g0021 | 2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.738-16802G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130581195 | ||||||
| chr7:130581195
|
C | T | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.738-16802G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130581195 | ||||||
| chr7:130581465
|
C | T | 2 | a0001c0002t0001g0047a0001c0002t0001g0059 | 2 | HG02280.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.738-17072G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130581465 | ||||||
| chr7:130581723
|
A | G | 93 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(90): Show | 93 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.738-17330T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130581723 | ||||||
| chr7:130581745
|
C | T | 2 | a0001c0001t0002g0218a0001c0001t0002g0229 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.738-17352G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130581745 | ||||||
| chr7:130581857
|
C | G | 1 | a0001c0001t0001g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.738-17464G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130581857 | ||||||
| chr7:130581956
|
A | C | 1 | a0001c0001t0001g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.738-17563T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130581956 | ||||||
| chr7:130581999
|
T | A | 61 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.738-17606A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130581999 | ||||||
| chr7:130582188
|
C | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0140 | 2 | HG01891.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.738-17795G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130582188 | ||||||
| chr7:130582248
|
AGGATTCC others(5289): Show |
A | 1 | a0001c0002t0001g0062 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.738-23151_738-1785 others(4): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130582248 | ||||||
| chr7:130582249
|
G | A | 2 | a0001c0001t0002g0218a0001c0001t0002g0229 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.738-17856C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130582249 | ||||||
| chr7:130582333
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.738-17940A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130582333 | ||||||
| chr7:130582344
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.738-17951T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130582344 | ||||||
| chr7:130582370
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.738-17977C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130582370 | ||||||
| chr7:130582432
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.738-18039G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130582432 | ||||||
| chr7:130582488
|
T | C | 1 | a0001c0001t0002g0233 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.738-18095A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130582488 | ||||||
| chr7:130582580
|
A | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.738-18187T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130582580 | ||||||
| chr7:130582666
|
C | A | 1 | a0001c0002t0004g0083 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.738-18273G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130582666 | ||||||
| chr7:130582684
|
G | A | 1 | a0001c0002t0007g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.738-18291C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130582684 | ||||||
| chr7:130582700
|
C | T | 61 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.738-18307G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130582700 | ||||||
| chr7:130582760
|
C | G | 1 | a0001c0001t0002g0183 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.738-18367G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130582760 | ||||||
| chr7:130582814
|
G | A | 1 | a0010c0015t0001g0259 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.738-18421C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130582814 | ||||||
| chr7:130582870
|
A | G | 6 | a0001c0001t0001g0269a0001c0001t0001g0271a0001c0001t0001g0305others(3): Show | 6 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.738-18477T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130582870 | ||||||
| chr7:130583047
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.738-18654G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583047 | ||||||
| chr7:130583061
|
A | C | 48 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(45): Show | 48 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.738-18668T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583061 | ||||||
| chr7:130583061
|
A | G | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-18668T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583061 | ||||||
| chr7:130583120
|
G | A | 9 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0278others(6): Show | 9 | HG00639.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.738-18727C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583120 | ||||||
| chr7:130583241
|
G | A | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.738-18848C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583241 | ||||||
| chr7:130583348
|
G | A | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.738-18955C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583348 | ||||||
| chr7:130583357
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.738-18964C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583357 | ||||||
| chr7:130583366
|
G | A | 3 | a0001c0001t0001g0289a0001c0001t0001g0302a0001c0001t0004g0293 | 3 | HG01496.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.738-18973C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583366 | ||||||
| chr7:130583493
|
T | TA | 38 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0137others(35): Show | 38 | HG01099.hp2 HG01106.hp1 HG01175.hp1 others(35): Show |
intron_variant | MODIFIER | c.738-19101dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583493 | ||||||
| chr7:130583493
|
T | TAA | 10 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(7): Show | 10 | HG02258.hp1 HG02451.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.738-19102_738-1910 others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583493 | ||||||
| chr7:130583493
|
T | TAAA | 7 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.738-19103_738-1910 others(7): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583493 | ||||||
| chr7:130583493
|
TA | T | 92 | a0001c0001t0001g0030a0001c0001t0001g0071a0001c0001t0001g0200others(89): Show | 92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.738-19101delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583493 | ||||||
| chr7:130583493
|
TAA | T | 6 | a0001c0001t0001g0072a0001c0001t0002g0155a0001c0001t0002g0167others(3): Show | 6 | HG02523.hp2 HG02717.hp1 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.738-19102_738-1910 others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583493 | ||||||
| chr7:130583533
|
G | A | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.738-19140C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583533 | ||||||
| chr7:130583544
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0129 | 2 | HG03239.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.738-19151G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583544 | ||||||
| chr7:130583794
|
A | G | 93 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(90): Show | 93 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.738-19401T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583794 | ||||||
| chr7:130583805
|
C | CA | 75 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0001g0200others(72): Show | 75 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.738-19413dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583805 | ||||||
| chr7:130583805
|
C | CAA | 11 | a0001c0001t0002g0190a0001c0001t0002g0218a0001c0001t0006g0168others(8): Show | 11 | HG00597.hp2 HG02080.hp1 HG03492.hp2 others(8): Show |
intron_variant | MODIFIER | c.738-19414_738-1941 others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583805 | ||||||
| chr7:130583805
|
CA | C | 50 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(47): Show | 50 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.738-19413delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583805 | ||||||
| chr7:130583805
|
CAA | C | 44 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0029others(41): Show | 44 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.738-19414_738-1941 others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583805 | ||||||
| chr7:130583928
|
C | G | 1 | a0001c0001t0001g0257 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.738-19535G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583928 | ||||||
| chr7:130583950
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.738-19557C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130583950 | ||||||
| chr7:130584240
|
G | C | 5 | a0001c0002t0003g0080a0001c0002t0003g0087a0001c0002t0003g0108others(2): Show | 5 | HG01261.hp2 HG01975.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.738-19847C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130584240 | ||||||
| chr7:130584244
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.738-19851A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130584244 | ||||||
| chr7:130584469
|
G | T | 1 | a0001c0002t0003g0120 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.738-20076C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130584469 | ||||||
| chr7:130584676
|
G | C | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.738-20283C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130584676 | ||||||
| chr7:130585010
|
A | G | 211 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(208): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.738-20617T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130585010 | ||||||
| chr7:130585046
|
A | G | 1 | a0001c0001t0002g0186 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.738-20653T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130585046 | ||||||
| chr7:130585281
|
T | C | 1 | a0001c0001t0001g0270 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.738-20888A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130585281 | ||||||
| chr7:130585301
|
T | C | 1 | a0001c0002t0001g0102 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.738-20908A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130585301 | ||||||
| chr7:130585392
|
T | C | 1 | a0006c0007t0001g0095 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.738-20999A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130585392 | ||||||
| chr7:130585588
|
T | C | 1 | a0001c0002t0001g0094 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.738-21195A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130585588 | ||||||
| chr7:130585701
|
G | A | 61 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.738-21308C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130585701 | ||||||
| chr7:130585738
|
G | A | 1 | a0001c0002t0001g0070 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.738-21345C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130585738 | ||||||
| chr7:130585761
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.738-21368T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130585761 | ||||||
| chr7:130585783
|
C | T | 1 | a0001c0001t0002g0232 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.738-21390G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130585783 | ||||||
| chr7:130586170
|
A | T | 9 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0278others(6): Show | 9 | HG00639.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.738-21777T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130586170 | ||||||
| chr7:130586285
|
A | G | 211 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(208): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.738-21892T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130586285 | ||||||
| chr7:130586361
|
A | AGT | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-21970_738-2196 others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130586361 | ||||||
| chr7:130586367
|
T | C | 1 | a0001c0001t0002g0232 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.738-21974A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130586367 | ||||||
| chr7:130586500
|
T | G | 4 | a0001c0002t0001g0241a0002c0003t0001g0242a0002c0003t0001g0243others(1): Show | 4 | HG01433.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-22107A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130586500 | ||||||
| chr7:130586611
|
C | T | 5 | a0001c0001t0001g0030a0001c0001t0001g0262a0001c0001t0001g0263others(2): Show | 5 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.738-22218G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130586611 | ||||||
| chr7:130586623
|
G | A | 6 | a0001c0002t0007g0235a0001c0002t0007g0236a0001c0002t0007g0237others(3): Show | 6 | HG01192.hp2 HG01993.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.738-22230C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130586623 | ||||||
| chr7:130586656
|
A | G | 210 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(207): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.738-22263T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130586656 | ||||||
| chr7:130586819
|
T | C | 3 | a0001c0002t0001g0032a0001c0002t0001g0033a0001c0002t0001g0036 | 3 | HG00099.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.738-22426A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130586819 | ||||||
| chr7:130586844
|
C | G | 1 | a0001c0001t0001g0129 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.738-22451G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130586844 | ||||||
| chr7:130587033
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.738-22640C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130587033 | ||||||
| chr7:130587060
|
A | C | 1 | a0001c0002t0001g0040 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.738-22667T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130587060 | ||||||
| chr7:130587081
|
C | A | 48 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(45): Show | 48 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.738-22688G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130587081 | ||||||
| chr7:130587233
|
G | A | 4 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287others(1): Show | 4 | NA18945.hp2 NA18963.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.738-22840C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130587233 | ||||||
| chr7:130587246
|
A | G | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(111): Show | 114 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.738-22853T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130587246 | ||||||
| chr7:130587256
|
G | A | 1 | a0001c0002t0001g0002 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.738-22863C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130587256 | ||||||
| chr7:130587773
|
A | G | 1 | a0001c0001t0001g0302 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.737+23180T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130587773 | ||||||
| chr7:130587778
|
C | A | 48 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(45): Show | 48 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.737+23175G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130587778 | ||||||
| chr7:130587988
|
T | C | 3 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007 | 3 | HG00438.hp1 NA18982.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.737+22965A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130587988 | ||||||
| chr7:130588025
|
A | G | 2 | a0001c0002t0001g0096a0008c0013t0001g0067 | 2 | HG01358.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.737+22928T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588025 | ||||||
| chr7:130588038
|
T | C | 1 | a0001c0002t0011g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.737+22915A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588038 | ||||||
| chr7:130588102
|
T | A | 1 | a0001c0001t0004g0308 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.737+22851A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588102 | ||||||
| chr7:130588108
|
A | G | 211 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(208): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.737+22845T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588108 | ||||||
| chr7:130588109
|
A | C | 211 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(208): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.737+22844T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588109 | ||||||
| chr7:130588167
|
GAGAAATA others(11): Show |
G | 1 | a0001c0001t0005g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.737+22768_737+2278 others(22): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588167 | ||||||
| chr7:130588186
|
A | G | 1 | a0001c0001t0005g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.737+22767T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588186 | ||||||
| chr7:130588187
|
C | T | 1 | a0001c0001t0005g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.737+22766G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588187 | ||||||
| chr7:130588188
|
A | G | 1 | a0001c0001t0005g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.737+22765T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588188 | ||||||
| chr7:130588417
|
C | G | 62 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(59): Show | 62 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.737+22536G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588417 | ||||||
| chr7:130588418
|
C | T | 1 | a0001c0001t0002g0231 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.737+22535G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588418 | ||||||
| chr7:130588452
|
A | G | 1 | a0001c0002t0002g0088 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.737+22501T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588452 | ||||||
| chr7:130588651
|
C | A | 1 | a0001c0012t0002g0166 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.737+22302G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588651 | ||||||
| chr7:130588720
|
A | G | 1 | a0001c0002t0001g0062 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.737+22233T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588720 | ||||||
| chr7:130588726
|
G | A | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(111): Show | 114 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.737+22227C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588726 | ||||||
| chr7:130588762
|
G | A | 93 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(90): Show | 93 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.737+22191C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588762 | ||||||
| chr7:130588768
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.737+22185G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588768 | ||||||
| chr7:130588799
|
TA | T | 16 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0245others(13): Show | 16 | HG01099.hp2 HG02055.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.737+22153delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588799 | ||||||
| chr7:130588840
|
A | G | 1 | a0001c0001t0001g0295 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.737+22113T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588840 | ||||||
| chr7:130588896
|
T | G | 210 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(207): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.737+22057A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588896 | ||||||
| chr7:130588902
|
G | T | 1 | a0001c0001t0001g0135 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.737+22051C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130588902 | ||||||
| chr7:130589018
|
A | G | 1 | a0001c0001t0002g0272 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.737+21935T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130589018 | ||||||
| chr7:130589084
|
C | T | 3 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0075 | 3 | NA19062.hp2 NA19064.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.737+21869G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130589084 | ||||||
| chr7:130589281
|
CT | C | 15 | a0001c0001t0001g0018a0001c0001t0001g0315a0001c0001t0002g0158others(12): Show | 15 | HG01975.hp2 HG02083.hp1 HG02683.hp1 others(12): Show |
intron_variant | MODIFIER | c.737+21671delA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130589281 | ||||||
| chr7:130589361
|
T | G | 1 | a0001c0001t0010g0001 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.737+21592A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130589361 | ||||||
| chr7:130589705
|
C | T | 211 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(208): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.737+21248G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130589705 | ||||||
| chr7:130589911
|
C | T | 94 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(91): Show | 94 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.737+21042G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130589911 | ||||||
| chr7:130589929
|
G | A | 118 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(115): Show | 118 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.737+21024C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130589929 | ||||||
| chr7:130590222
|
T | TCTCTCCC others(16): Show |
4 | a0001c0001t0002g0159a0001c0001t0002g0187a0001c0001t0002g0224others(1): Show | 4 | HG01167.hp2 HG01258.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.737+20708_737+2073 others(27): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590222 | ||||||
| chr7:130590336
|
G | C | 62 | a0001c0001t0001g0135a0001c0001t0001g0266a0001c0001t0001g0268others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.737+20617C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590336 | ||||||
| chr7:130590347
|
A | T | 7 | a0001c0002t0001g0082a0001c0002t0001g0084a0001c0002t0001g0085others(4): Show | 7 | NA18947.hp1 NA18955.hp1 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.737+20606T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590347 | ||||||
| chr7:130590391
|
G | T | 5 | a0001c0001t0001g0245a0001c0001t0001g0253a0001c0001t0001g0257others(2): Show | 5 | HG01099.hp2 HG02886.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.737+20562C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590391 | ||||||
| chr7:130590404
|
C | T | 2 | a0001c0001t0002g0227a0001c0001t0006g0226 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.737+20549G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590404 | ||||||
| chr7:130590501
|
G | A | 1 | a0001c0001t0005g0251 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.737+20452C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590501 | ||||||
| chr7:130590545
|
C | T | 323 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(320): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.737+20408G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590545 | ||||||
| chr7:130590549
|
C | T | 1 | a0001c0002t0004g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.737+20404G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590549 | ||||||
| chr7:130590589
|
A | G | 118 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(115): Show | 118 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.737+20364T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590589 | ||||||
| chr7:130590596
|
C | T | 1 | a0001c0001t0002g0195 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.737+20357G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590596 | ||||||
| chr7:130590668
|
C | T | 5 | a0001c0001t0001g0030a0001c0001t0001g0262a0001c0001t0001g0263others(2): Show | 5 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.737+20285G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590668 | ||||||
| chr7:130590687
|
G | C | 4 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022others(1): Show | 4 | HG01099.hp1 HG02257.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+20266C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590687 | ||||||
| chr7:130590776
|
T | C | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+20177A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590776 | ||||||
| chr7:130590784
|
T | C | 211 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(208): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.737+20169A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590784 | ||||||
| chr7:130590869
|
C | T | 1 | a0001c0001t0002g0158 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.737+20084G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590869 | ||||||
| chr7:130590910
|
GTCTGAGA others(33): Show |
G | 1 | a0003c0008t0001g0114 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.737+20003_737+2004 others(44): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590910 | ||||||
| chr7:130590950
|
A | G | 211 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(208): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.737+20003T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590950 | ||||||
| chr7:130590974
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.737+19979C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590974 | ||||||
| chr7:130590977
|
C | T | 1 | a0001c0001t0002g0211 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.737+19976G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130590977 | ||||||
| chr7:130591017
|
C | T | 1 | a0001c0001t0002g0157 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.737+19936G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591017 | ||||||
| chr7:130591071
|
C | T | 2 | a0001c0002t0001g0034a0001c0002t0001g0035 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.737+19882G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591071 | ||||||
| chr7:130591091
|
T | TG | 41 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(38): Show | 41 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.737+19861dupC | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591091 | ||||||
| chr7:130591092
|
G | C | 1 | a0001c0002t0011g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.737+19861C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591092 | ||||||
| chr7:130591109
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.737+19844C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591109 | ||||||
| chr7:130591120
|
T | C | 40 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(37): Show | 40 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.737+19833A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591120 | ||||||
| chr7:130591123
|
C | CCCGTCCG others(70): Show |
39 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(36): Show | 39 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.737+19829_737+1983 others(81): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591123 | ||||||
| chr7:130591132
|
A | G | 40 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(37): Show | 40 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.737+19821T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591132 | ||||||
| chr7:130591134
|
G | GGTGAGGG others(197): Show |
1 | a0001c0002t0001g0094 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.737+19818_737+1981 others(208): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591134 | ||||||
| chr7:130591140
|
TG | T | 39 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(36): Show | 39 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.737+19812delC | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591140 | ||||||
| chr7:130591143
|
G | T | 1 | a0001c0001t0002g0202 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.737+19810C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591143 | ||||||
| chr7:130591147
|
G | C | 39 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(36): Show | 39 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.737+19806C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591147 | ||||||
| chr7:130591159
|
G | A | 1 | a0001c0002t0001g0094 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.737+19794C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591159 | ||||||
| chr7:130591163
|
G | A | 5 | a0001c0001t0001g0030a0001c0001t0001g0262a0001c0001t0001g0263others(2): Show | 5 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.737+19790C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591163 | ||||||
| chr7:130591171
|
G | A | 1 | a0001c0002t0001g0094 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.737+19782C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591171 | ||||||
| chr7:130591176
|
G | A | 61 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.737+19777C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591176 | ||||||
| chr7:130591194
|
G | A | 5 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(2): Show | 5 | HG00099.hp1 HG02572.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.737+19759C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591194 | ||||||
| chr7:130591211
|
C | T | 1 | a0001c0002t0001g0094 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.737+19742G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591211 | ||||||
| chr7:130591223
|
T | A | 1 | a0001c0002t0001g0094 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.737+19730A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591223 | ||||||
| chr7:130591228
|
A | AG | 40 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(37): Show | 40 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.737+19724_737+1972 others(5): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591228 | ||||||
| chr7:130591233
|
T | TCTGCCCA others(498): Show |
1 | a0001c0002t0001g0099 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.737+19719_737+1972 others(509): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591233 | ||||||
| chr7:130591233
|
T | TCTGCCCA others(498): Show |
1 | a0001c0002t0004g0100 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.737+19719_737+1972 others(509): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591233 | ||||||
| chr7:130591233
|
T | TCTGCCCA others(496): Show |
3 | a0001c0002t0001g0091a0001c0002t0001g0101a0001c0002t0001g0102 | 3 | HG01884.hp1 HG04204.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.737+19719_737+1972 others(507): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591233 | ||||||
| chr7:130591233
|
T | TCTGCCCA others(495): Show |
33 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(30): Show | 33 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.737+19719_737+1972 others(506): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591233 | ||||||
| chr7:130591235
|
T | TGCCCAGC others(495): Show |
1 | a0001c0002t0001g0097 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.737+19717_737+1971 others(506): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591235 | ||||||
| chr7:130591239
|
T | C | 40 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(37): Show | 40 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.737+19714A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591239 | ||||||
| chr7:130591247
|
C | T | 1 | a0001c0002t0001g0051 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.737+19706G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591247 | ||||||
| chr7:130591250
|
T | C | 40 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(37): Show | 40 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.737+19703A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591250 | ||||||
| chr7:130591253
|
G | A | 4 | a0001c0002t0001g0241a0002c0003t0001g0242a0002c0003t0001g0243others(1): Show | 4 | HG01433.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.737+19700C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591253 | ||||||
| chr7:130591257
|
G | A | 1 | a0001c0002t0001g0094 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.737+19696C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591257 | ||||||
| chr7:130591273
|
C | G | 40 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(37): Show | 40 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.737+19680G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591273 | ||||||
| chr7:130591274
|
G | A | 39 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(36): Show | 39 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.737+19679C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591274 | ||||||
| chr7:130591285
|
G | A | 1 | a0001c0002t0001g0094 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.737+19668C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591285 | ||||||
| chr7:130591296
|
C | T | 39 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(36): Show | 39 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.737+19657G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591296 | ||||||
| chr7:130591301
|
C | CGTCCGGG others(371): Show |
1 | a0001c0002t0001g0094 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.737+19651_737+1965 others(382): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591301 | ||||||
| chr7:130591301
|
C | T | 39 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(36): Show | 39 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.737+19652G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591301 | ||||||
| chr7:130591306
|
G | A | 11 | a0001c0001t0001g0274a0001c0001t0001g0279a0001c0001t0001g0292others(8): Show | 11 | HG02129.hp1 HG02155.hp1 NA18952.hp1 others(8): Show |
intron_variant | MODIFIER | c.737+19647C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591306 | ||||||
| chr7:130591319
|
C | T | 40 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(37): Show | 40 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.737+19634G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591319 | ||||||
| chr7:130591344
|
C | G | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(322): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.737+19609G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591344 | ||||||
| chr7:130591367
|
A | G | 251 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(248): Show | 251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.737+19586T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591367 | ||||||
| chr7:130591369
|
C | A | 40 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(37): Show | 40 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.737+19584G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591369 | ||||||
| chr7:130591383
|
T | C | 40 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(37): Show | 40 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.737+19570A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591383 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(629): Show |
1 | a0001c0002t0003g0103 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.737+19565_737+1956 others(640): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(628): Show |
1 | a0001c0002t0003g0087 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.737+19565_737+1956 others(639): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(625): Show |
2 | a0001c0001t0004g0324a0001c0002t0007g0237 | 2 | HG01192.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.737+19565_737+1956 others(636): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(624): Show |
1 | a0001c0002t0001g0042 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(635): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(626): Show |
1 | a0001c0001t0002g0199 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.737+19565_737+1956 others(637): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(623): Show |
1 | a0001c0001t0002g0207 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.737+19565_737+1956 others(634): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(625): Show |
1 | a0001c0001t0001g0313 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(636): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(624): Show |
2 | a0001c0001t0001g0129a0001c0001t0001g0135 | 2 | HG02129.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.737+19565_737+1956 others(635): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(526): Show |
1 | a0001c0001t0001g0130 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(537): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(623): Show |
18 | a0001c0001t0001g0029a0001c0001t0001g0127a0001c0001t0001g0132others(15): Show | 18 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.737+19565_737+1956 others(634): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(623): Show |
1 | a0001c0001t0004g0131 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.737+19565_737+1956 others(634): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(626): Show |
1 | a0001c0002t0001g0057 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(637): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(625): Show |
1 | a0001c0001t0002g0190 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.737+19565_737+1956 others(636): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(624): Show |
1 | a0001c0001t0004g0267 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(635): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(625): Show |
1 | a0001c0001t0006g0198 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(636): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(623): Show |
1 | a0001c0001t0002g0148 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(634): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(624): Show |
1 | a0001c0001t0002g0150 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.737+19565_737+1956 others(635): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(623): Show |
10 | a0001c0001t0002g0152a0001c0001t0002g0158a0001c0001t0002g0160others(7): Show | 10 | HG00544.hp2 HG01192.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.737+19565_737+1956 others(634): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(397): Show |
1 | a0001c0001t0002g0272 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(408): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(622): Show |
1 | a0001c0001t0002g0025 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(633): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(622): Show |
70 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(67): Show | 70 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.737+19565_737+1956 others(633): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(622): Show |
1 | a0001c0001t0002g0170 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.737+19565_737+1956 others(633): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(621): Show |
1 | a0001c0001t0002g0209 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.737+19565_737+1956 others(632): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(625): Show |
1 | a0001c0002t0003g0110 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.737+19565_737+1956 others(636): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(626): Show |
1 | a0001c0002t0001g0043 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(637): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(625): Show |
1 | a0001c0001t0004g0248 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.737+19565_737+1956 others(636): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(625): Show |
1 | a0001c0001t0004g0249 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(636): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(624): Show |
1 | a0001c0002t0007g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.737+19565_737+1956 others(635): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(625): Show |
1 | a0001c0002t0003g0121 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(636): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(624): Show |
1 | a0001c0002t0004g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(635): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(624): Show |
2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.737+19565_737+1956 others(635): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(625): Show |
3 | a0001c0002t0003g0108a0001c0002t0003g0113a0001c0002t0003g0117 | 3 | HG02148.hp1 NA19066.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.737+19565_737+1956 others(636): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(625): Show |
1 | a0001c0002t0001g0022 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(636): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(624): Show |
10 | a0001c0002t0003g0068a0001c0002t0003g0080a0001c0002t0003g0104others(7): Show | 10 | HG00544.hp1 HG01952.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.737+19565_737+1956 others(635): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(624): Show |
21 | a0001c0001t0001g0015a0001c0001t0001g0257a0001c0001t0001g0271others(18): Show | 21 | HG00140.hp1 HG01243.hp1 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.737+19565_737+1956 others(635): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(623): Show |
4 | a0001c0001t0001g0023a0001c0002t0001g0126a0001c0002t0003g0107others(1): Show | 4 | HG00323.hp1 HG02809.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+19565_737+1956 others(634): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(623): Show |
1 | a0001c0001t0001g0312 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(634): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(624): Show |
1 | a0001c0001t0001g0278 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.737+19565_737+1956 others(635): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(623): Show |
101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.737+19565_737+1956 others(634): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(622): Show |
2 | a0001c0001t0001g0304a0001c0002t0001g0041 | 2 | HG00621.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.737+19565_737+1956 others(633): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(621): Show |
1 | a0001c0002t0011g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(632): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(571): Show |
4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.737+19565_737+1956 others(582): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(624): Show |
2 | a0001c0002t0003g0122a0001c0002t0003g0123 | 2 | HG03490.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.737+19565_737+1956 others(635): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(624): Show |
2 | a0001c0005t0002g0010a0001c0005t0002g0011 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.737+19565_737+1956 others(635): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(625): Show |
1 | a0001c0001t0006g0201 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(636): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(397): Show |
1 | a0001c0001t0002g0260 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(408): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AAGGAGGT others(624): Show |
1 | a0001c0001t0002g0223 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.737+19565_737+1956 others(635): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591387
|
A | AG | 40 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(37): Show | 40 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.737+19565dupC | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591387 | ||||||
| chr7:130591397
|
G | A | 2 | a0001c0001t0001g0276a0001c0001t0001g0311 | 2 | HG00639.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.737+19556C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591397 | ||||||
| chr7:130591411
|
G | A | 1 | a0001c0002t0001g0036 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.737+19542C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591411 | ||||||
| chr7:130591414
|
C | T | 1 | a0002c0003t0001g0242 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.737+19539G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591414 | ||||||
| chr7:130591416
|
G | C | 20 | a0001c0002t0003g0068a0001c0002t0003g0080a0001c0002t0003g0087others(17): Show | 20 | HG00323.hp1 HG00544.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.737+19537C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591416 | ||||||
| chr7:130591423
|
G | GC | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(322): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.737+19529dupG | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591423 | ||||||
| chr7:130591430
|
C | CA | 6 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(3): Show | 6 | HG01243.hp1 HG02258.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.737+19522_737+1952 others(5): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591430 | ||||||
| chr7:130591430
|
C | CG | 319 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(316): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.737+19522dupC | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591430 | ||||||
| chr7:130591453
|
C | CCCCTGCC others(10): Show |
1 | a0001c0001t0002g0272 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.737+19499_737+1950 others(21): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591453 | ||||||
| chr7:130591454
|
G | C | 1 | a0001c0001t0002g0272 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.737+19499C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591454 | ||||||
| chr7:130591462
|
G | A | 16 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0245others(13): Show | 16 | HG01099.hp2 HG02055.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.737+19491C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591462 | ||||||
| chr7:130591476
|
G | A | 1 | a0001c0002t0001g0021 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.737+19477C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591476 | ||||||
| chr7:130591479
|
G | A | 1 | a0001c0001t0002g0272 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.737+19474C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591479 | ||||||
| chr7:130591485
|
C | A | 1 | a0001c0012t0002g0166 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.737+19468G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591485 | ||||||
| chr7:130591490
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.737+19463G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591490 | ||||||
| chr7:130591502
|
C | T | 1 | a0001c0001t0002g0272 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.737+19451G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591502 | ||||||
| chr7:130591503
|
G | A | 2 | a0001c0002t0001g0079a0001c0002t0001g0118 | 2 | NA18941.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.737+19450C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591503 | ||||||
| chr7:130591507
|
C | T | 1 | a0001c0001t0002g0272 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.737+19446G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591507 | ||||||
| chr7:130591508
|
A | G | 1 | a0001c0001t0002g0272 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.737+19445T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591508 | ||||||
| chr7:130591511
|
C | T | 1 | a0001c0001t0002g0272 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.737+19442G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591511 | ||||||
| chr7:130591512
|
G | A | 2 | a0001c0001t0001g0302a0001c0001t0004g0293 | 2 | HG01496.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.737+19441C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591512 | ||||||
| chr7:130591573
|
G | A | 1 | a0001c0002t0001g0045 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.737+19380C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591573 | ||||||
| chr7:130591575
|
C | A | 1 | a0001c0001t0002g0272 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.737+19378G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591575 | ||||||
| chr7:130591579
|
C | A | 10 | a0001c0002t0003g0080a0001c0002t0003g0087a0001c0002t0003g0108others(7): Show | 10 | HG01261.hp2 HG01975.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.737+19374G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591579 | ||||||
| chr7:130591582
|
C | T | 1 | a0001c0002t0001g0062 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.737+19371G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591582 | ||||||
| chr7:130591585
|
C | T | 1 | a0001c0001t0002g0272 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.737+19368G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591585 | ||||||
| chr7:130591663
|
G | A | 6 | a0001c0002t0003g0068a0001c0002t0003g0103a0001c0002t0003g0104others(3): Show | 6 | HG00544.hp1 HG01952.hp2 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.737+19290C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591663 | ||||||
| chr7:130591711
|
C | T | 53 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(50): Show | 53 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.737+19242G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591711 | ||||||
| chr7:130591730
|
GGGGGTCA others(42): Show |
G | 1 | a0001c0001t0001g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.737+19174_737+1922 others(53): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591730 | ||||||
| chr7:130591731
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.737+19222C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591731 | ||||||
| chr7:130591813
|
C | G | 10 | a0001c0002t0003g0080a0001c0002t0003g0087a0001c0002t0003g0108others(7): Show | 10 | HG01261.hp2 HG01975.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.737+19140G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591813 | ||||||
| chr7:130591836
|
T | C | 211 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(208): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.737+19117A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130591836 | ||||||
| chr7:130592002
|
G | A | 5 | a0001c0001t0002g0171a0001c0001t0002g0207a0001c0001t0002g0210others(2): Show | 5 | HG01106.hp2 HG01192.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.737+18951C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130592002 | ||||||
| chr7:130592195
|
T | C | 9 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.737+18758A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130592195 | ||||||
| chr7:130592395
|
C | CA | 50 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(47): Show | 50 | HG00544.hp2 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.737+18557dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130592395 | ||||||
| chr7:130592454
|
T | C | 2 | a0001c0002t0001g0052a0001c0002t0001g0065 | 2 | HG02647.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.737+18499A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130592454 | ||||||
| chr7:130592643
|
C | T | 4 | a0001c0001t0001g0030a0001c0002t0001g0041a0001c0002t0001g0043others(1): Show | 4 | HG00597.hp1 HG00621.hp2 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+18310G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130592643 | ||||||
| chr7:130592677
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.737+18276A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130592677 | ||||||
| chr7:130592763
|
G | A | 1 | a0001c0001t0002g0170 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.737+18190C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130592763 | ||||||
| chr7:130592869
|
C | T | 1 | a0001c0002t0001g0045 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.737+18084G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130592869 | ||||||
| chr7:130593157
|
T | C | 1 | a0001c0002t0003g0122 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.737+17796A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130593157 | ||||||
| chr7:130593424
|
T | C | 1 | a0001c0001t0002g0161 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.737+17529A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130593424 | ||||||
| chr7:130593728
|
G | T | 1 | a0001c0001t0001g0268 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.737+17225C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130593728 | ||||||
| chr7:130593764
|
G | GA | 12 | a0001c0001t0001g0127a0001c0001t0001g0132a0001c0001t0001g0133others(9): Show | 12 | HG01891.hp1 HG01943.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.737+17188dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130593764 | ||||||
| chr7:130593764
|
GA | G | 92 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(89): Show | 92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.737+17188delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130593764 | ||||||
| chr7:130593775
|
T | A | 1 | a0001c0001t0001g0298 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.737+17178A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130593775 | ||||||
| chr7:130593870
|
G | C | 1 | a0001c0001t0002g0160 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.737+17083C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130593870 | ||||||
| chr7:130594025
|
CACATACA others(4): Show |
C | 1 | a0001c0002t0001g0124 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.737+16917_737+1692 others(15): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130594025 | ||||||
| chr7:130595733
|
G | A | 5 | a0001c0001t0001g0030a0001c0001t0001g0262a0001c0001t0001g0263others(2): Show | 5 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.737+15220C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130595733 | ||||||
| chr7:130595803
|
A | AC | 57 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0141others(54): Show | 57 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.737+15149dupG | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130595803 | ||||||
| chr7:130595803
|
AC | A | 58 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(55): Show | 58 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.737+15149delG | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130595803 | ||||||
| chr7:130595810
|
C | G | 1 | a0001c0002t0001g0055 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.737+15143G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130595810 | ||||||
| chr7:130595811
|
C | A | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.737+15142G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130595811 | ||||||
| chr7:130595811
|
C | G | 1 | a0001c0001t0002g0196 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.737+15142G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130595811 | ||||||
| chr7:130595870
|
C | T | 209 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(206): Show | 209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.737+15083G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130595870 | ||||||
| chr7:130596090
|
T | TG | 4 | a0001c0002t0001g0041a0001c0002t0001g0042a0001c0002t0001g0043others(1): Show | 4 | HG00597.hp1 HG00621.hp2 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+14862dupC | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130596090 | ||||||
| chr7:130596105
|
T | C | 53 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(50): Show | 53 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.737+14848A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130596105 | ||||||
| chr7:130596210
|
C | T | 2 | a0001c0005t0002g0010a0001c0005t0002g0011 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.737+14743G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130596210 | ||||||
| chr7:130596411
|
T | C | 1 | a0001c0002t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.737+14542A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130596411 | ||||||
| chr7:130596522
|
C | T | 1 | a0001c0001t0002g0024 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.737+14431G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130596522 | ||||||
| chr7:130596607
|
G | C | 1 | a0010c0015t0001g0259 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.737+14346C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130596607 | ||||||
| chr7:130596619
|
A | G | 1 | a0001c0001t0001g0289 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.737+14334T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130596619 | ||||||
| chr7:130597032
|
C | T | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+13921G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130597032 | ||||||
| chr7:130597111
|
C | A | 1 | a0001c0001t0001g0268 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.737+13842G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130597111 | ||||||
| chr7:130597114
|
T | A | 1 | a0001c0001t0001g0271 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.737+13839A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130597114 | ||||||
| chr7:130597126
|
C | G | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+13827G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130597126 | ||||||
| chr7:130597409
|
C | G | 1 | a0001c0001t0001g0009 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.737+13544G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130597409 | ||||||
| chr7:130597513
|
C | A | 53 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(50): Show | 53 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.737+13440G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130597513 | ||||||
| chr7:130597947
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.737+13006C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130597947 | ||||||
| chr7:130598033
|
G | A | 1 | a0001c0002t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.737+12920C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130598033 | ||||||
| chr7:130598106
|
A | C | 1 | a0001c0001t0002g0164 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.737+12847T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130598106 | ||||||
| chr7:130598160
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.737+12793A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130598160 | ||||||
| chr7:130598241
|
C | G | 1 | a0001c0002t0001g0060 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.737+12712G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130598241 | ||||||
| chr7:130598606
|
C | T | 1 | a0001c0001t0002g0170 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.737+12347G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130598606 | ||||||
| chr7:130598865
|
A | G | 1 | a0002c0003t0001g0244 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.737+12088T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130598865 | ||||||
| chr7:130599047
|
C | T | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144 | 3 | HG01069.hp1 HG01515.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.737+11906G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130599047 | ||||||
| chr7:130599320
|
C | T | 3 | a0001c0002t0001g0047a0001c0002t0001g0059a0001c0002t0001g0061 | 3 | HG02280.hp1 HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.737+11633G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130599320 | ||||||
| chr7:130599434
|
G | C | 61 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.737+11519C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130599434 | ||||||
| chr7:130599564
|
C | T | 1 | a0001c0002t0007g0237 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.737+11389G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130599564 | ||||||
| chr7:130599631
|
T | A | 3 | a0001c0001t0002g0148a0001c0001t0002g0167a0001c0001t0002g0176 | 3 | HG00621.hp1 NA18954.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.737+11322A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130599631 | ||||||
| chr7:130599684
|
C | T | 13 | a0001c0001t0001g0245a0001c0001t0001g0253a0001c0001t0001g0255others(10): Show | 13 | HG01099.hp2 HG02055.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.737+11269G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130599684 | ||||||
| chr7:130599797
|
C | T | 5 | a0001c0001t0001g0030a0001c0001t0001g0262a0001c0001t0001g0263others(2): Show | 5 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.737+11156G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130599797 | ||||||
| chr7:130599839
|
G | A | 1 | a0001c0001t0002g0156 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.737+11114C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130599839 | ||||||
| chr7:130599953
|
AT | A | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.737+10999delA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130599953 | ||||||
| chr7:130599960
|
A | G | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.737+10993T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130599960 | ||||||
| chr7:130600038
|
A | C | 53 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(50): Show | 53 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.737+10915T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130600038 | ||||||
| chr7:130600078
|
T | G | 1 | a0001c0001t0001g0304 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.737+10875A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130600078 | ||||||
| chr7:130600217
|
T | A | 1 | a0001c0001t0001g0130 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.737+10736A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130600217 | ||||||
| chr7:130600284
|
A | T | 4 | a0001c0001t0002g0148a0001c0001t0002g0164a0001c0001t0002g0167others(1): Show | 4 | HG00438.hp2 HG00621.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+10669T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130600284 | ||||||
| chr7:130600297
|
G | A | 61 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.737+10656C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130600297 | ||||||
| chr7:130600625
|
C | T | 1 | a0001c0002t0001g0119 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.737+10328G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130600625 | ||||||
| chr7:130600628
|
G | T | 61 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.737+10325C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130600628 | ||||||
| chr7:130600776
|
T | G | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.737+10177A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130600776 | ||||||
| chr7:130600960
|
C | T | 1 | a0001c0001t0001g0306 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.737+9993G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130600960 | ||||||
| chr7:130601129
|
G | A | 1 | a0001c0002t0003g0106 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.737+9824C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130601129 | ||||||
| chr7:130601283
|
T | C | 1 | a0001c0002t0001g0037 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.737+9670A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130601283 | ||||||
| chr7:130601886
|
AGAAG | A | 42 | a0001c0001t0001g0030a0001c0002t0001g0002a0001c0002t0001g0005others(39): Show | 42 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.737+9063_737+9066d others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130601886 | ||||||
| chr7:130601891
|
GA | G | 61 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.737+9061delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130601891 | ||||||
| chr7:130602037
|
C | T | 1 | a0001c0002t0001g0102 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.737+8916G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130602037 | ||||||
| chr7:130602038
|
G | A | 1 | a0001c0002t0004g0081 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.737+8915C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130602038 | ||||||
| chr7:130602228
|
T | C | 1 | a0001c0002t0001g0066 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.737+8725A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130602228 | ||||||
| chr7:130602330
|
T | G | 42 | a0001c0001t0001g0273a0001c0002t0001g0002a0001c0002t0001g0005others(39): Show | 42 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.737+8623A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130602330 | ||||||
| chr7:130602357
|
T | C | 1 | a0001c0002t0007g0238 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.737+8596A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130602357 | ||||||
| chr7:130602417
|
T | C | 6 | a0001c0002t0007g0235a0001c0002t0007g0236a0001c0002t0007g0237others(3): Show | 6 | HG01192.hp2 HG01993.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.737+8536A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130602417 | ||||||
| chr7:130602450
|
T | C | 6 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(3): Show | 6 | HG00558.hp1 HG01934.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.737+8503A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130602450 | ||||||
| chr7:130602693
|
G | A | 22 | a0001c0001t0001g0029a0001c0001t0001g0127a0001c0001t0001g0129others(19): Show | 22 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(19): Show |
intron_variant | MODIFIER | c.737+8260C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130602693 | ||||||
| chr7:130602769
|
G | A | 1 | a0001c0002t0003g0107 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.737+8184C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130602769 | ||||||
| chr7:130602809
|
G | C | 10 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(7): Show | 10 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.737+8144C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130602809 | ||||||
| chr7:130602979
|
A | T | 27 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(24): Show | 27 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.737+7974T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130602979 | ||||||
| chr7:130603005
|
T | C | 1 | a0001c0002t0001g0096 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.737+7948A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130603005 | ||||||
| chr7:130603021
|
T | C | 3 | a0001c0001t0001g0289a0001c0001t0001g0302a0001c0001t0004g0293 | 3 | HG01496.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.737+7932A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130603021 | ||||||
| chr7:130603044
|
C | T | 5 | a0001c0002t0007g0235a0001c0002t0007g0236a0001c0002t0007g0237others(2): Show | 5 | HG01192.hp2 HG01993.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.737+7909G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130603044 | ||||||
| chr7:130603105
|
T | C | 3 | a0001c0001t0002g0151a0001c0001t0002g0222a0001c0002t0001g0044 | 3 | NA18964.hp2 NA19084.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.737+7848A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130603105 | ||||||
| chr7:130603216
|
C | T | 1 | a0001c0002t0001g0119 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.737+7737G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130603216 | ||||||
| chr7:130603259
|
G | T | 1 | a0001c0002t0001g0119 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.737+7694C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130603259 | ||||||
| chr7:130603339
|
A | G | 1 | a0001c0002t0011g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.737+7614T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130603339 | ||||||
| chr7:130603375
|
T | C | 1 | a0001c0001t0001g0255 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.737+7578A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130603375 | ||||||
| chr7:130603589
|
T | C | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+7364A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130603589 | ||||||
| chr7:130603721
|
C | CA | 99 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0279others(96): Show | 99 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.737+7231dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130603721 | ||||||
| chr7:130603721
|
CA | C | 12 | a0001c0001t0001g0018a0001c0001t0001g0071a0001c0001t0001g0072others(9): Show | 12 | HG01167.hp2 HG01168.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.737+7231delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130603721 | ||||||
| chr7:130603721
|
CAAAA | C | 9 | a0001c0001t0001g0274a0001c0001t0001g0292a0001c0001t0001g0294others(6): Show | 9 | HG02129.hp1 HG02155.hp1 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.737+7228_737+7231d others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130603721 | ||||||
| chr7:130603746
|
A | T | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0005t0002g0010others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+7207T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130603746 | ||||||
| chr7:130603885
|
C | T | 1 | a0001c0001t0001g0313 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.737+7068G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130603885 | ||||||
| chr7:130604504
|
G | A | 2 | a0001c0002t0001g0032a0001c0002t0001g0033 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.737+6449C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130604504 | ||||||
| chr7:130604632
|
G | A | 62 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(59): Show | 62 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.737+6321C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130604632 | ||||||
| chr7:130604897
|
C | T | 1 | a0001c0001t0002g0179 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.737+6056G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130604897 | ||||||
| chr7:130605175
|
C | G | 1 | a0001c0001t0001g0294 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.737+5778G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130605175 | ||||||
| chr7:130605201
|
T | A | 1 | a0001c0001t0001g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.737+5752A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130605201 | ||||||
| chr7:130605346
|
A | G | 3 | a0001c0001t0001g0245a0001c0001t0004g0248a0001c0001t0004g0249 | 3 | HG01099.hp2 HG02886.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.737+5607T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130605346 | ||||||
| chr7:130605355
|
G | A | 1 | a0001c0002t0001g0092 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.737+5598C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130605355 | ||||||
| chr7:130605605
|
G | A | 2 | a0001c0001t0002g0191a0001c0001t0002g0192 | 2 | NA18944.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.737+5348C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130605605 | ||||||
| chr7:130605937
|
G | A | 1 | a0001c0002t0001g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.737+5016C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130605937 | ||||||
| chr7:130606081
|
T | C | 219 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(216): Show | 219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.737+4872A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130606081 | ||||||
| chr7:130606240
|
A | AAG | 69 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(66): Show | 69 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.737+4711_737+4712d others(4): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130606240 | ||||||
| chr7:130606240
|
A | AAGAG | 3 | a0001c0001t0008g0318a0001c0001t0008g0321a0001c0001t0008g0322 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.737+4709_737+4712d others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130606240 | ||||||
| chr7:130606331
|
A | T | 1 | a0001c0002t0001g0093 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.737+4622T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130606331 | ||||||
| chr7:130606429
|
T | C | 221 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(218): Show | 221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.737+4524A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130606429 | ||||||
| chr7:130606493
|
G | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.737+4460C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130606493 | ||||||
| chr7:130606521
|
T | C | 1 | a0001c0001t0002g0223 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.737+4432A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130606521 | ||||||
| chr7:130607129
|
T | C | 4 | a0001c0002t0007g0236a0001c0002t0007g0237a0001c0002t0007g0238others(1): Show | 4 | HG01192.hp2 HG01993.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+3824A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130607129 | ||||||
| chr7:130607240
|
C | CATAA | 24 | a0001c0001t0001g0023a0001c0001t0001g0130a0001c0001t0001g0200others(21): Show | 24 | HG00621.hp1 HG01167.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.737+3709_737+3712d others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130607240 | ||||||
| chr7:130607240
|
CATAA | C | 99 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0015others(96): Show | 99 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.737+3709_737+3712d others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130607240 | ||||||
| chr7:130607240
|
CATAAATA others(1): Show |
C | 64 | a0001c0001t0001g0008a0001c0001t0001g0030a0001c0001t0001g0262others(61): Show | 64 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.737+3705_737+3712d others(10): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130607240 | ||||||
| chr7:130607240
|
CATAAATA others(5): Show |
C | 6 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(3): Show | 6 | HG00558.hp1 HG01934.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.737+3701_737+3712d others(14): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130607240 | ||||||
| chr7:130607339
|
T | C | 219 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(216): Show | 219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.737+3614A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130607339 | ||||||
| chr7:130607372
|
T | C | 1 | a0001c0001t0002g0027 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.737+3581A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130607372 | ||||||
| chr7:130607380
|
T | C | 3 | a0001c0001t0001g0289a0001c0001t0001g0302a0001c0001t0004g0293 | 3 | HG01496.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.737+3573A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130607380 | ||||||
| chr7:130607660
|
T | C | 92 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(89): Show | 92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.737+3293A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130607660 | ||||||
| chr7:130607838
|
G | C | 20 | a0001c0002t0003g0068a0001c0002t0003g0080a0001c0002t0003g0087others(17): Show | 20 | HG00323.hp1 HG00544.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.737+3115C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130607838 | ||||||
| chr7:130607931
|
C | T | 3 | a0001c0001t0002g0179a0001c0001t0002g0180a0001c0001t0006g0201 | 3 | HG00639.hp1 HG01261.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.737+3022G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130607931 | ||||||
| chr7:130607991
|
G | A | 1 | a0001c0012t0002g0166 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.737+2962C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130607991 | ||||||
| chr7:130608005
|
G | T | 7 | a0001c0002t0001g0079a0001c0002t0001g0090a0001c0002t0001g0091others(4): Show | 7 | NA18941.hp1 NA18944.hp2 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.737+2948C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130608005 | ||||||
| chr7:130608100
|
T | G | 2 | a0001c0001t0002g0227a0001c0001t0006g0226 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.737+2853A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130608100 | ||||||
| chr7:130608121
|
A | G | 1 | a0001c0001t0012g0206 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.737+2832T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130608121 | ||||||
| chr7:130608151
|
C | T | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.737+2802G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130608151 | ||||||
| chr7:130608426
|
C | T | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.737+2527G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130608426 | ||||||
| chr7:130608605
|
G | C | 1 | a0001c0002t0001g0044 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.737+2348C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130608605 | ||||||
| chr7:130608718
|
T | A | 3 | a0001c0002t0003g0121a0001c0002t0003g0122a0001c0002t0003g0123 | 3 | HG03490.hp2 HG03942.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.737+2235A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130608718 | ||||||
| chr7:130608920
|
G | A | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0141 | 3 | HG01167.hp1 HG02129.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.737+2033C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130608920 | ||||||
| chr7:130609333
|
C | A | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.737+1620G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130609333 | ||||||
| chr7:130609477
|
T | C | 1 | a0001c0001t0002g0155 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.737+1476A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130609477 | ||||||
| chr7:130609815
|
G | T | 4 | a0001c0002t0001g0041a0001c0002t0001g0042a0001c0002t0001g0043others(1): Show | 4 | HG00597.hp1 HG00621.hp2 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+1138C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130609815 | ||||||
| chr7:130610070
|
C | G | 1 | a0001c0002t0001g0062 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.737+883G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130610070 | ||||||
| chr7:130610119
|
T | C | 1 | a0001c0002t0001g0028 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.737+834A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130610119 | ||||||
| chr7:130610451
|
T | C | 10 | a0001c0002t0001g0241a0001c0002t0007g0235a0001c0002t0007g0236others(7): Show | 10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.737+502A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130610451 | ||||||
| chr7:130610654
|
T | C | 59 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(56): Show | 59 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.737+299A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130610654 | ||||||
| chr7:130610820
|
T | A | 2 | a0001c0001t0001g0266a0001c0001t0004g0267 | 2 | HG01978.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.737+133A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130610820 | ||||||
| chr7:130610829
|
G | A | 62 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(59): Show | 62 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.737+124C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130610829 | ||||||
| chr7:130610900
|
G | T | 6 | a0001c0002t0007g0235a0001c0002t0007g0236a0001c0002t0007g0237others(3): Show | 6 | HG01192.hp2 HG01993.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.737+53C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 9/23 | chr7 | 130610900 | ||||||
| chr7:130611175
|
T | C | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.580-65A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 8/23 | chr7 | 130611175 | ||||||
| chr7:130611385
|
C | T | 55 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(52): Show | 55 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(52): Show |
intron_variant | MODIFIER | c.580-275G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 8/23 | chr7 | 130611385 | ||||||
| chr7:130611432
|
A | G | 12 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.580-322T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 8/23 | chr7 | 130611432 | ||||||
| chr7:130611612
|
T | C | 1 | a0001c0001t0002g0211 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.580-502A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 8/23 | chr7 | 130611612 | ||||||
| chr7:130611657
|
G | A | 164 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0266others(161): Show | 164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.579+495C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 8/23 | chr7 | 130611657 | ||||||
| chr7:130611709
|
A | C | 50 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(47): Show | 50 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.579+443T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 8/23 | chr7 | 130611709 | ||||||
| chr7:130612078
|
G | A | 315 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(312): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.579+74C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 8/23 | chr7 | 130612078 | ||||||
| chr7:130612147
|
A | C | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.579+5T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 8/23 | chr7 | 130612147 | ||||||
| chr7:130612248
|
GA | G | 219 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(216): Show | 219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.493-11delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 7/23 | chr7 | 130612248 | ||||||
| chr7:130612360
|
T | G | 5 | a0001c0002t0007g0235a0001c0002t0007g0236a0001c0002t0007g0237others(2): Show | 5 | HG01192.hp2 HG01993.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.493-122A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 7/23 | chr7 | 130612360 | ||||||
| chr7:130612683
|
C | T | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.493-445G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 7/23 | chr7 | 130612683 | ||||||
| chr7:130612725
|
T | C | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.493-487A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 7/23 | chr7 | 130612725 | ||||||
| chr7:130612752
|
T | C | 7 | a0001c0001t0005g0247a0001c0001t0005g0250a0001c0001t0005g0251others(4): Show | 7 | HG02055.hp2 HG02630.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.493-514A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 7/23 | chr7 | 130612752 | ||||||
| chr7:130613091
|
A | T | 72 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(69): Show | 72 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.492+453T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 7/23 | chr7 | 130613091 | ||||||
| chr7:130613285
|
G | A | 1 | a0001c0002t0011g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.492+259C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 7/23 | chr7 | 130613285 | ||||||
| chr7:130613390
|
ACCCCTGC others(14): Show |
A | 10 | a0001c0002t0001g0241a0001c0002t0007g0235a0001c0002t0007g0236others(7): Show | 10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.492+133_492+153del others(21): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 7/23 | chr7 | 130613390 | ||||||
| chr7:130613484
|
T | C | 3 | a0001c0002t0001g0047a0001c0002t0001g0059a0001c0002t0001g0061 | 3 | HG02280.hp1 HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.492+60A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 7/23 | chr7 | 130613484 | ||||||
| chr7:130613538
|
A | G | 1 | a0003c0008t0001g0114 | 1 | HG06807.hp1 | splice_region_variant&intron_variant | LOW | c.492+6T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 7/23 | chr7 | 130613538 | ||||||
| chr7:130613679
|
C | T | 219 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(216): Show | 219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.400-43G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130613679 | ||||||
| chr7:130613811
|
C | A | 6 | a0001c0001t0005g0247a0001c0001t0005g0251a0001c0001t0005g0254others(3): Show | 6 | HG02055.hp2 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.400-175G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130613811 | ||||||
| chr7:130614738
|
A | G | 1 | a0001c0001t0001g0288 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.400-1102T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130614738 | ||||||
| chr7:130614879
|
G | T | 55 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(52): Show | 55 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(52): Show |
intron_variant | MODIFIER | c.400-1243C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130614879 | ||||||
| chr7:130615007
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.400-1371T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130615007 | ||||||
| chr7:130615129
|
T | C | 1 | a0001c0005t0002g0011 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.400-1493A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130615129 | ||||||
| chr7:130615321
|
G | C | 50 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(47): Show | 50 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.399+1669C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130615321 | ||||||
| chr7:130615325
|
T | C | 219 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(216): Show | 219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.399+1665A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130615325 | ||||||
| chr7:130615371
|
G | T | 1 | a0001c0001t0004g0249 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.399+1619C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130615371 | ||||||
| chr7:130615399
|
T | C | 92 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(89): Show | 92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.399+1591A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130615399 | ||||||
| chr7:130615436
|
T | C | 1 | a0001c0002t0001g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.399+1554A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130615436 | ||||||
| chr7:130615495
|
A | T | 219 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(216): Show | 219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.399+1495T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130615495 | ||||||
| chr7:130615628
|
A | G | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0141 | 3 | HG01167.hp1 HG02129.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.399+1362T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130615628 | ||||||
| chr7:130615651
|
C | T | 1 | a0001c0001t0012g0206 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.399+1339G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130615651 | ||||||
| chr7:130615933
|
G | T | 12 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.399+1057C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130615933 | ||||||
| chr7:130615950
|
T | A | 1 | a0001c0001t0002g0164 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.399+1040A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130615950 | ||||||
| chr7:130615957
|
T | A | 1 | a0001c0001t0002g0164 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.399+1033A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130615957 | ||||||
| chr7:130616072
|
T | C | 1 | a0001c0002t0001g0116 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.399+918A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130616072 | ||||||
| chr7:130616194
|
G | T | 34 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(31): Show | 34 | HG01069.hp1 HG01167.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.399+796C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130616194 | ||||||
| chr7:130616221
|
T | C | 2 | a0001c0001t0002g0158a0010c0015t0001g0259 | 2 | HG02622.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.399+769A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130616221 | ||||||
| chr7:130616278
|
A | G | 6 | a0001c0001t0001g0030a0001c0001t0001g0262a0001c0001t0001g0263others(3): Show | 6 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.399+712T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130616278 | ||||||
| chr7:130616385
|
A | G | 22 | a0001c0001t0001g0029a0001c0001t0001g0127a0001c0001t0001g0129others(19): Show | 22 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(19): Show |
intron_variant | MODIFIER | c.399+605T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130616385 | ||||||
| chr7:130616423
|
C | T | 1 | a0001c0001t0001g0279 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.399+567G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130616423 | ||||||
| chr7:130616584
|
C | T | 3 | a0001c0002t0001g0019a0001c0002t0001g0039a0001c0002t0001g0040 | 3 | HG02004.hp1 HG03491.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.399+406G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130616584 | ||||||
| chr7:130616635
|
C | A | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.399+355G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130616635 | ||||||
| chr7:130616778
|
G | A | 22 | a0001c0001t0001g0029a0001c0001t0001g0127a0001c0001t0001g0129others(19): Show | 22 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(19): Show |
intron_variant | MODIFIER | c.399+212C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130616778 | ||||||
| chr7:130616805
|
A | T | 1 | a0001c0002t0001g0097 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.399+185T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 6/23 | chr7 | 130616805 | ||||||
| chr7:130617205
|
T | C | 3 | a0001c0001t0008g0318a0001c0001t0008g0321a0001c0001t0008g0322 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.324-140A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130617205 | ||||||
| chr7:130617216
|
A | C | 14 | a0001c0002t0001g0038a0001c0002t0001g0041a0001c0002t0001g0042others(11): Show | 14 | HG00597.hp1 HG00621.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.324-151T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130617216 | ||||||
| chr7:130617335
|
C | T | 1 | a0001c0002t0001g0028 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.324-270G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130617335 | ||||||
| chr7:130617805
|
T | C | 50 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(47): Show | 50 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.324-740A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130617805 | ||||||
| chr7:130617994
|
G | C | 3 | a0001c0001t0001g0291a0001c0001t0001g0314a0001c0001t0001g0325 | 3 | HG00323.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.324-929C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130617994 | ||||||
| chr7:130618100
|
C | CA | 12 | a0001c0002t0001g0048a0001c0002t0001g0058a0001c0002t0003g0080others(9): Show | 12 | HG01975.hp1 HG01981.hp1 HG02148.hp1 others(9): Show |
intron_variant | MODIFIER | c.324-1036dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130618100 | ||||||
| chr7:130618100
|
C | CAAAAA | 52 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(49): Show | 52 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(49): Show |
intron_variant | MODIFIER | c.324-1040_324-1036d others(7): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130618100 | ||||||
| chr7:130618100
|
C | CAAAAAA | 70 | a0001c0001t0001g0130a0001c0001t0001g0138a0001c0001t0001g0146others(67): Show | 70 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.324-1041_324-1036d others(8): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130618100 | ||||||
| chr7:130618100
|
C | CAAAAAAA | 73 | a0001c0001t0001g0003a0001c0001t0001g0213a0001c0001t0001g0287others(70): Show | 73 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.324-1042_324-1036d others(9): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130618100 | ||||||
| chr7:130618100
|
C | CAAAAAAA others(1): Show |
23 | a0001c0001t0001g0030a0001c0001t0001g0200a0001c0001t0002g0025others(20): Show | 23 | HG00140.hp2 HG00621.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.324-1043_324-1036d others(10): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130618100 | ||||||
| chr7:130618100
|
CA | C | 6 | a0001c0002t0001g0052a0001c0002t0001g0063a0001c0002t0001g0064others(3): Show | 6 | HG02145.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.324-1036delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130618100 | ||||||
| chr7:130618144
|
CT | C | 92 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(89): Show | 92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.324-1080delA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130618144 | ||||||
| chr7:130618146
|
T | C | 92 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(89): Show | 92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.324-1081A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130618146 | ||||||
| chr7:130618221
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.324-1156C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130618221 | ||||||
| chr7:130618343
|
T | G | 1 | a0001c0001t0001g0294 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.324-1278A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130618343 | ||||||
| chr7:130618503
|
A | T | 1 | a0001c0001t0001g0294 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.324-1438T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130618503 | ||||||
| chr7:130618522
|
A | G | 1 | a0001c0002t0001g0063 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.324-1457T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130618522 | ||||||
| chr7:130619148
|
G | C | 1 | a0001c0001t0006g0201 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.324-2083C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130619148 | ||||||
| chr7:130619228
|
T | G | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.324-2163A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130619228 | ||||||
| chr7:130619230
|
T | C | 1 | a0001c0001t0001g0281 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.324-2165A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130619230 | ||||||
| chr7:130619472
|
C | T | 92 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(89): Show | 92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.324-2407G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130619472 | ||||||
| chr7:130619624
|
A | G | 3 | a0001c0001t0001g0289a0001c0001t0001g0302a0001c0001t0004g0293 | 3 | HG01496.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.324-2559T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130619624 | ||||||
| chr7:130619660
|
C | A | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.324-2595G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130619660 | ||||||
| chr7:130619874
|
T | C | 1 | a0001c0001t0005g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.324-2809A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130619874 | ||||||
| chr7:130619916
|
T | C | 6 | a0001c0001t0001g0030a0001c0001t0001g0262a0001c0001t0001g0263others(3): Show | 6 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.324-2851A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130619916 | ||||||
| chr7:130620234
|
A | C | 10 | a0001c0002t0001g0241a0001c0002t0007g0235a0001c0002t0007g0236others(7): Show | 10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.324-3169T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130620234 | ||||||
| chr7:130620363
|
G | T | 3 | a0001c0002t0001g0032a0001c0002t0001g0033a0001c0002t0001g0036 | 3 | HG00099.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.324-3298C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130620363 | ||||||
| chr7:130620580
|
A | G | 1 | a0001c0001t0005g0254 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.324-3515T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130620580 | ||||||
| chr7:130620608
|
A | G | 92 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(89): Show | 92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.324-3543T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130620608 | ||||||
| chr7:130620765
|
G | A | 1 | a0001c0002t0001g0048 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.324-3700C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130620765 | ||||||
| chr7:130621051
|
C | T | 20 | a0001c0002t0003g0068a0001c0002t0003g0080a0001c0002t0003g0087others(17): Show | 20 | HG00323.hp1 HG00544.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.324-3986G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130621051 | ||||||
| chr7:130621147
|
G | A | 1 | a0001c0001t0002g0197 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.324-4082C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130621147 | ||||||
| chr7:130621612
|
C | T | 62 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(59): Show | 62 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.324-4547G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130621612 | ||||||
| chr7:130621745
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.324-4680G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130621745 | ||||||
| chr7:130621845
|
G | A | 1 | a0001c0002t0002g0088 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.324-4780C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130621845 | ||||||
| chr7:130621942
|
TC | T | 5 | a0001c0001t0002g0171a0001c0001t0002g0207a0001c0001t0002g0210others(2): Show | 5 | HG01106.hp2 HG01192.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.324-4878delG | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130621942 | ||||||
| chr7:130621943
|
CA | C | 63 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(60): Show | 63 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.324-4879delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130621943 | ||||||
| chr7:130621943
|
CAA | C | 59 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(56): Show | 59 | HG01069.hp1 HG01070.hp1 HG01099.hp2 others(56): Show |
intron_variant | MODIFIER | c.324-4880_324-4879d others(4): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130621943 | ||||||
| chr7:130621943
|
CAAAAAAA others(4): Show |
C | 4 | a0001c0002t0001g0241a0002c0003t0001g0242a0002c0003t0001g0243others(1): Show | 4 | HG01433.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.324-4889_324-4879d others(13): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130621943 | ||||||
| chr7:130621944
|
A | G | 5 | a0001c0001t0002g0171a0001c0001t0002g0207a0001c0001t0002g0210others(2): Show | 5 | HG01106.hp2 HG01192.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.324-4879T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130621944 | ||||||
| chr7:130622564
|
C | T | 92 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(89): Show | 92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.324-5499G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130622564 | ||||||
| chr7:130622605
|
G | A | 1 | a0001c0002t0011g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.324-5540C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130622605 | ||||||
| chr7:130623131
|
A | G | 56 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(53): Show | 56 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.324-6066T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130623131 | ||||||
| chr7:130623504
|
C | G | 22 | a0001c0002t0001g0126a0001c0002t0003g0068a0001c0002t0003g0080others(19): Show | 22 | HG00323.hp1 HG00544.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.324-6439G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130623504 | ||||||
| chr7:130623729
|
C | T | 1 | a0001c0001t0002g0191 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.324-6664G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130623729 | ||||||
| chr7:130624165
|
C | CCTT | 4 | a0001c0002t0001g0241a0002c0003t0001g0242a0002c0003t0001g0243others(1): Show | 4 | HG01433.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.324-7101_324-7100i others(5): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130624165 | ||||||
| chr7:130624168
|
C | T | 4 | a0001c0002t0001g0241a0002c0003t0001g0242a0002c0003t0001g0243others(1): Show | 4 | HG01433.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.324-7103G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130624168 | ||||||
| chr7:130624171
|
A | T | 1 | a0001c0002t0003g0122 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.324-7106T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130624171 | ||||||
| chr7:130624177
|
A | T | 6 | a0001c0002t0001g0079a0001c0002t0001g0090a0001c0002t0001g0091others(3): Show | 6 | NA18941.hp1 NA18944.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.324-7112T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130624177 | ||||||
| chr7:130624346
|
T | G | 10 | a0001c0002t0001g0241a0001c0002t0007g0235a0001c0002t0007g0236others(7): Show | 10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.324-7281A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130624346 | ||||||
| chr7:130625365
|
A | C | 4 | a0001c0002t0001g0241a0002c0003t0001g0242a0002c0003t0001g0243others(1): Show | 4 | HG01433.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.324-8300T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130625365 | ||||||
| chr7:130625672
|
G | GT | 22 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(19): Show | 22 | HG01192.hp2 HG01243.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.324-8608dupA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130625672 | ||||||
| chr7:130625698
|
C | T | 50 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(47): Show | 50 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.324-8633G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130625698 | ||||||
| chr7:130625755
|
T | C | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.324-8690A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130625755 | ||||||
| chr7:130625953
|
C | T | 1 | a0001c0001t0006g0172 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.324-8888G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130625953 | ||||||
| chr7:130625974
|
T | C | 62 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(59): Show | 62 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.324-8909A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130625974 | ||||||
| chr7:130626187
|
T | C | 1 | a0001c0001t0001g0320 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.324-9122A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130626187 | ||||||
| chr7:130626203
|
A | G | 92 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(89): Show | 92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.324-9138T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130626203 | ||||||
| chr7:130626252
|
C | A | 3 | a0001c0001t0008g0318a0001c0001t0008g0321a0001c0001t0008g0322 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.324-9187G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130626252 | ||||||
| chr7:130626312
|
C | G | 50 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(47): Show | 50 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.324-9247G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130626312 | ||||||
| chr7:130626354
|
C | A | 3 | a0001c0002t0001g0019a0001c0002t0001g0039a0001c0002t0001g0040 | 3 | HG02004.hp1 HG03491.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.324-9289G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130626354 | ||||||
| chr7:130626388
|
C | T | 1 | a0001c0002t0003g0123 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.324-9323G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130626388 | ||||||
| chr7:130626400
|
AT | A | 140 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0023others(137): Show | 140 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.324-9336delA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130626400 | ||||||
| chr7:130626400
|
ATT | A | 97 | a0001c0001t0001g0029a0001c0001t0001g0132a0001c0001t0001g0200others(94): Show | 97 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.324-9337_324-9336d others(4): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130626400 | ||||||
| chr7:130626400
|
ATTT | A | 6 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(3): Show | 6 | HG02572.hp1 HG02735.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.324-9338_324-9336d others(5): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130626400 | ||||||
| chr7:130626421
|
TC | T | 11 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.324-9357delG | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130626421 | ||||||
| chr7:130626515
|
C | T | 1 | a0001c0001t0002g0159 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.324-9450G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130626515 | ||||||
| chr7:130626580
|
C | T | 3 | a0001c0001t0008g0318a0001c0001t0008g0321a0001c0001t0008g0322 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.324-9515G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130626580 | ||||||
| chr7:130626642
|
G | C | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.324-9577C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130626642 | ||||||
| chr7:130626946
|
C | T | 3 | a0001c0002t0003g0121a0001c0002t0003g0122a0001c0002t0003g0123 | 3 | HG03490.hp2 HG03942.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.324-9881G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130626946 | ||||||
| chr7:130627063
|
C | T | 50 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(47): Show | 50 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.324-9998G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130627063 | ||||||
| chr7:130627083
|
G | A | 1 | a0001c0001t0002g0189 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.324-10018C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130627083 | ||||||
| chr7:130627473
|
A | T | 5 | a0001c0002t0001g0079a0001c0002t0001g0090a0001c0002t0001g0091others(2): Show | 5 | NA18941.hp1 NA18944.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.324-10408T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130627473 | ||||||
| chr7:130627665
|
C | T | 1 | a0001c0002t0001g0066 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.324-10600G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130627665 | ||||||
| chr7:130627941
|
G | T | 1 | a0002c0003t0001g0242 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.324-10876C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130627941 | ||||||
| chr7:130628442
|
T | C | 6 | a0001c0001t0001g0030a0001c0001t0001g0262a0001c0001t0001g0263others(3): Show | 6 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.324-11377A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130628442 | ||||||
| chr7:130628687
|
A | G | 1 | a0001c0001t0002g0196 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.324-11622T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130628687 | ||||||
| chr7:130628875
|
T | C | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(281): Show | 284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.324-11810A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130628875 | ||||||
| chr7:130628935
|
C | G | 2 | a0001c0001t0002g0211a0001c0001t0002g0216 | 2 | HG01255.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.324-11870G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130628935 | ||||||
| chr7:130629184
|
T | G | 1 | a0001c0002t0001g0241 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.324-12119A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130629184 | ||||||
| chr7:130629213
|
T | A | 2 | a0001c0001t0002g0227a0001c0001t0006g0226 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.324-12148A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130629213 | ||||||
| chr7:130629229
|
C | T | 1 | a0001c0001t0001g0282 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.324-12164G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130629229 | ||||||
| chr7:130629231
|
G | A | 50 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(47): Show | 50 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.324-12166C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130629231 | ||||||
| chr7:130629283
|
G | A | 4 | a0001c0001t0005g0251a0001c0001t0005g0254a0001c0001t0009g0252others(1): Show | 4 | HG02055.hp2 HG02723.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.324-12218C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130629283 | ||||||
| chr7:130629325
|
G | C | 50 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(47): Show | 50 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.324-12260C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130629325 | ||||||
| chr7:130629399
|
A | AT | 11 | a0001c0001t0001g0306a0001c0001t0002g0194a0001c0002t0001g0241others(8): Show | 11 | HG01175.hp1 HG01192.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.324-12335dupA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130629399 | ||||||
| chr7:130629399
|
A | ATT | 92 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(89): Show | 92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.324-12336_324-1233 others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130629399 | ||||||
| chr7:130629459
|
A | G | 4 | a0001c0001t0002g0160a0001c0001t0002g0191a0001c0001t0002g0192others(1): Show | 4 | HG00544.hp2 HG00558.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.324-12394T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130629459 | ||||||
| chr7:130629464
|
G | A | 27 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(24): Show | 27 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.324-12399C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130629464 | ||||||
| chr7:130629483
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.324-12418G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130629483 | ||||||
| chr7:130630019
|
G | A | 1 | a0010c0015t0001g0259 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.324-12954C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130630019 | ||||||
| chr7:130630052
|
G | A | 2 | a0001c0002t0005g0076a0001c0002t0005g0077 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.324-12987C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130630052 | ||||||
| chr7:130630063
|
C | T | 1 | a0001c0001t0001g0317 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.324-12998G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130630063 | ||||||
| chr7:130630102
|
G | A | 1 | a0001c0002t0001g0007 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.324-13037C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130630102 | ||||||
| chr7:130630200
|
C | T | 1 | a0001c0002t0001g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.324-13135G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130630200 | ||||||
| chr7:130630207
|
G | A | 10 | a0001c0002t0001g0241a0001c0002t0007g0235a0001c0002t0007g0236others(7): Show | 10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.324-13142C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130630207 | ||||||
| chr7:130630420
|
A | G | 92 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(89): Show | 92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.324-13355T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130630420 | ||||||
| chr7:130630531
|
A | C | 3 | a0001c0002t0001g0047a0001c0002t0001g0059a0001c0002t0001g0061 | 3 | HG02280.hp1 HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.324-13466T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130630531 | ||||||
| chr7:130630729
|
T | A | 92 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(89): Show | 92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.324-13664A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130630729 | ||||||
| chr7:130630820
|
T | C | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.324-13755A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130630820 | ||||||
| chr7:130631070
|
G | A | 3 | a0001c0001t0008g0318a0001c0001t0008g0321a0001c0001t0008g0322 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.324-14005C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130631070 | ||||||
| chr7:130631078
|
T | A | 1 | a0001c0002t0001g0102 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.324-14013A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130631078 | ||||||
| chr7:130631081
|
A | T | 1 | a0001c0002t0001g0042 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.324-14016T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130631081 | ||||||
| chr7:130631089
|
A | G | 4 | a0001c0002t0001g0052a0001c0002t0001g0063a0001c0002t0001g0064others(1): Show | 4 | HG02145.hp1 HG02647.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.324-14024T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130631089 | ||||||
| chr7:130631172
|
C | CT | 61 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(58): Show | 61 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.324-14108dupA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130631172 | ||||||
| chr7:130631172
|
CT | C | 212 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(209): Show | 212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.324-14108delA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130631172 | ||||||
| chr7:130631193
|
ATGGAGAC others(18): Show |
A | 2 | a0001c0001t0002g0191a0001c0001t0002g0192 | 2 | NA18944.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.324-14153_324-1412 others(29): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130631193 | ||||||
| chr7:130631282
|
C | T | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.324-14217G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130631282 | ||||||
| chr7:130631484
|
C | A | 8 | a0001c0002t0001g0019a0001c0002t0001g0028a0001c0002t0001g0034others(5): Show | 8 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.324-14419G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130631484 | ||||||
| chr7:130631513
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.324-14448A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130631513 | ||||||
| chr7:130631573
|
GT | G | 21 | a0001c0001t0001g0029a0001c0001t0001g0127a0001c0001t0001g0129others(18): Show | 21 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.324-14509delA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130631573 | ||||||
| chr7:130631744
|
T | TAAGA | 220 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(217): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.324-14680_324-1467 others(8): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130631744 | ||||||
| chr7:130632557
|
T | C | 1 | a0001c0001t0002g0205 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.324-15492A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130632557 | ||||||
| chr7:130632633
|
T | G | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.324-15568A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130632633 | ||||||
| chr7:130632788
|
G | A | 1 | a0010c0015t0001g0259 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.324-15723C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130632788 | ||||||
| chr7:130632826
|
C | T | 316 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(313): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.324-15761G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130632826 | ||||||
| chr7:130632901
|
C | A | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.324-15836G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130632901 | ||||||
| chr7:130633048
|
T | G | 2 | a0001c0002t0001g0032a0001c0002t0001g0033 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.324-15983A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130633048 | ||||||
| chr7:130633149
|
G | C | 10 | a0001c0002t0001g0241a0001c0002t0007g0235a0001c0002t0007g0236others(7): Show | 10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.324-16084C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130633149 | ||||||
| chr7:130633266
|
G | A | 20 | a0001c0002t0003g0068a0001c0002t0003g0080a0001c0002t0003g0087others(17): Show | 20 | HG00323.hp1 HG00544.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.324-16201C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130633266 | ||||||
| chr7:130633431
|
G | A | 3 | a0001c0002t0001g0047a0001c0002t0001g0059a0001c0002t0001g0061 | 3 | HG02280.hp1 HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.324-16366C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130633431 | ||||||
| chr7:130633516
|
T | C | 6 | a0001c0001t0001g0030a0001c0001t0001g0262a0001c0001t0001g0263others(3): Show | 6 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.324-16451A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130633516 | ||||||
| chr7:130633571
|
G | A | 3 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022 | 3 | HG01099.hp1 HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.324-16506C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130633571 | ||||||
| chr7:130633624
|
T | C | 1 | a0001c0001t0002g0232 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.324-16559A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130633624 | ||||||
| chr7:130633727
|
G | C | 1 | a0001c0001t0002g0196 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.324-16662C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130633727 | ||||||
| chr7:130633821
|
G | A | 6 | a0001c0001t0001g0030a0001c0001t0001g0262a0001c0001t0001g0263others(3): Show | 6 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.324-16756C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130633821 | ||||||
| chr7:130633967
|
T | G | 3 | a0001c0001t0001g0245a0001c0001t0004g0248a0001c0001t0004g0249 | 3 | HG01099.hp2 HG02886.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.324-16902A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130633967 | ||||||
| chr7:130634069
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.324-17004C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130634069 | ||||||
| chr7:130634103
|
C | T | 92 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(89): Show | 92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.324-17038G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130634103 | ||||||
| chr7:130634104
|
G | A | 1 | a0001c0002t0001g0070 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.324-17039C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130634104 | ||||||
| chr7:130634105
|
C | T | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.324-17040G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130634105 | ||||||
| chr7:130634107
|
G | A | 1 | a0001c0002t0001g0055 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.324-17042C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130634107 | ||||||
| chr7:130634214
|
G | A | 1 | a0001c0001t0002g0207 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.324-17149C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130634214 | ||||||
| chr7:130634316
|
T | C | 1 | a0001c0012t0002g0166 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.324-17251A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130634316 | ||||||
| chr7:130634613
|
G | A | 50 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(47): Show | 50 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.324-17548C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130634613 | ||||||
| chr7:130634664
|
G | C | 1 | a0001c0002t0001g0085 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.324-17599C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130634664 | ||||||
| chr7:130634780
|
C | G | 5 | a0001c0001t0002g0171a0001c0001t0002g0207a0001c0001t0002g0210others(2): Show | 5 | HG01106.hp2 HG01192.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.324-17715G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130634780 | ||||||
| chr7:130635267
|
G | A | 220 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(217): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.323+17602C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130635267 | ||||||
| chr7:130635298
|
T | C | 1 | a0001c0002t0001g0002 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.323+17571A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130635298 | ||||||
| chr7:130635464
|
T | C | 9 | a0001c0001t0002g0152a0001c0001t0002g0155a0001c0001t0002g0165others(6): Show | 9 | HG02015.hp2 HG02523.hp2 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+17405A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130635464 | ||||||
| chr7:130635539
|
G | GT | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.323+17329dupA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130635539 | ||||||
| chr7:130635653
|
A | C | 10 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026others(7): Show | 10 | HG01167.hp2 HG01168.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.323+17216T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130635653 | ||||||
| chr7:130636043
|
T | C | 164 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0266others(161): Show | 164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.323+16826A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130636043 | ||||||
| chr7:130636103
|
G | A | 1 | a0001c0002t0004g0083 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.323+16766C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130636103 | ||||||
| chr7:130636131
|
A | T | 222 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(219): Show | 222 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.323+16738T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130636131 | ||||||
| chr7:130636152
|
T | C | 220 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(217): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.323+16717A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130636152 | ||||||
| chr7:130636325
|
T | C | 1 | a0001c0002t0001g0052 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.323+16544A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130636325 | ||||||
| chr7:130636508
|
C | G | 6 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(3): Show | 6 | HG00558.hp1 HG01934.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.323+16361G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130636508 | ||||||
| chr7:130636538
|
G | GT | 7 | a0001c0002t0001g0021a0001c0002t0001g0037a0001c0002t0001g0046others(4): Show | 7 | HG00597.hp1 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.323+16330dupA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130636538 | ||||||
| chr7:130636538
|
G | T | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.323+16331C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130636538 | ||||||
| chr7:130636538
|
GT | G | 71 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0030others(68): Show | 71 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.323+16330delA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130636538 | ||||||
| chr7:130636538
|
GTT | G | 40 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(37): Show | 40 | HG01069.hp1 HG01167.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.323+16329_323+1633 others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130636538 | ||||||
| chr7:130636538
|
GTTT | G | 141 | a0001c0001t0001g0213a0001c0001t0001g0266a0001c0001t0001g0268others(138): Show | 141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.323+16328_323+1633 others(7): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130636538 | ||||||
| chr7:130636626
|
G | A | 1 | a0001c0001t0002g0185 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.323+16243C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130636626 | ||||||
| chr7:130636705
|
G | T | 1 | a0001c0001t0001g0281 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.323+16164C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130636705 | ||||||
| chr7:130636890
|
T | C | 56 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(53): Show | 56 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.323+15979A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130636890 | ||||||
| chr7:130637023
|
TTTTC | T | 6 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287others(3): Show | 6 | NA18945.hp2 NA18963.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.323+15842_323+1584 others(8): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130637023 | ||||||
| chr7:130637129
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.323+15740C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130637129 | ||||||
| chr7:130637217
|
C | T | 64 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(61): Show | 64 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.323+15652G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130637217 | ||||||
| chr7:130637310
|
A | C | 1 | a0001c0002t0001g0066 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.323+15559T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130637310 | ||||||
| chr7:130637405
|
G | A | 164 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0266others(161): Show | 164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.323+15464C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130637405 | ||||||
| chr7:130637577
|
G | T | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.323+15292C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130637577 | ||||||
| chr7:130637628
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.323+15241G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130637628 | ||||||
| chr7:130637691
|
T | A | 1 | a0001c0002t0001g0119 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.323+15178A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130637691 | ||||||
| chr7:130637985
|
G | C | 1 | a0001c0001t0001g0255 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.323+14884C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130637985 | ||||||
| chr7:130637994
|
C | T | 1 | a0003c0008t0001g0114 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.323+14875G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130637994 | ||||||
| chr7:130638072
|
T | C | 12 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.323+14797A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130638072 | ||||||
| chr7:130638081
|
G | C | 1 | a0001c0001t0002g0185 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.323+14788C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130638081 | ||||||
| chr7:130638273
|
CT | C | 10 | a0001c0002t0001g0241a0001c0002t0007g0235a0001c0002t0007g0236others(7): Show | 10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.323+14595delA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130638273 | ||||||
| chr7:130638295
|
A | C | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.323+14574T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130638295 | ||||||
| chr7:130638329
|
G | A | 1 | a0001c0001t0002g0214 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.323+14540C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130638329 | ||||||
| chr7:130638488
|
G | A | 1 | a0001c0001t0001g0268 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.323+14381C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130638488 | ||||||
| chr7:130638711
|
TCAGCCCC others(5): Show |
T | 59 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(56): Show | 59 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.323+14146_323+1415 others(16): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130638711 | ||||||
| chr7:130638747
|
C | T | 1 | a0001c0002t0007g0239 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.323+14122G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130638747 | ||||||
| chr7:130638803
|
G | A | 1 | a0001c0002t0001g0058 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.323+14066C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130638803 | ||||||
| chr7:130638862
|
G | A | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.323+14007C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130638862 | ||||||
| chr7:130639042
|
A | C | 222 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(219): Show | 222 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.323+13827T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130639042 | ||||||
| chr7:130639102
|
T | C | 92 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(89): Show | 92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.323+13767A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130639102 | ||||||
| chr7:130639428
|
C | G | 1 | a0001c0002t0007g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.323+13441G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130639428 | ||||||
| chr7:130639984
|
C | G | 7 | a0001c0002t0001g0079a0001c0002t0001g0090a0001c0002t0001g0091others(4): Show | 7 | NA18941.hp1 NA18944.hp2 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.323+12885G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130639984 | ||||||
| chr7:130640131
|
G | A | 164 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0266others(161): Show | 164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.323+12738C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130640131 | ||||||
| chr7:130640158
|
C | CT | 118 | a0001c0001t0001g0132a0001c0001t0001g0142a0001c0001t0001g0143others(115): Show | 118 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.323+12710dupA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130640158 | ||||||
| chr7:130640158
|
C | CTT | 8 | a0001c0001t0002g0157a0001c0001t0002g0188a0001c0001t0002g0202others(5): Show | 8 | HG00621.hp2 HG01952.hp1 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.323+12709_323+1271 others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130640158 | ||||||
| chr7:130640158
|
CTT | C | 58 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(55): Show | 58 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.323+12709_323+1271 others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130640158 | ||||||
| chr7:130640335
|
T | C | 1 | a0001c0002t0001g0031 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.323+12534A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130640335 | ||||||
| chr7:130640464
|
T | C | 59 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(56): Show | 59 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.323+12405A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130640464 | ||||||
| chr7:130640580
|
T | C | 15 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0245others(12): Show | 15 | HG01099.hp2 HG02055.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.323+12289A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130640580 | ||||||
| chr7:130640726
|
G | T | 1 | a0001c0002t0001g0031 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.323+12143C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130640726 | ||||||
| chr7:130640900
|
A | G | 4 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287others(1): Show | 4 | NA18945.hp2 NA18963.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.323+11969T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130640900 | ||||||
| chr7:130640979
|
T | C | 1 | a0001c0002t0001g0045 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.323+11890A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130640979 | ||||||
| chr7:130640983
|
C | G | 72 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(69): Show | 72 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.323+11886G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130640983 | ||||||
| chr7:130641067
|
T | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.323+11802A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130641067 | ||||||
| chr7:130641175
|
C | CA | 89 | a0001c0001t0001g0030a0001c0001t0001g0200a0001c0001t0001g0213others(86): Show | 89 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.323+11693dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130641175 | ||||||
| chr7:130641175
|
CA | C | 65 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0127others(62): Show | 65 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.323+11693delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130641175 | ||||||
| chr7:130641402
|
C | T | 40 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(37): Show | 40 | HG00438.hp1 HG01106.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.323+11467G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130641402 | ||||||
| chr7:130641574
|
T | C | 1 | a0001c0001t0001g0298 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.323+11295A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130641574 | ||||||
| chr7:130641620
|
T | C | 1 | a0001c0002t0007g0237 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.323+11249A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130641620 | ||||||
| chr7:130641736
|
G | A | 1 | a0001c0002t0007g0238 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.323+11133C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130641736 | ||||||
| chr7:130641907
|
C | T | 1 | a0001c0012t0002g0166 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.323+10962G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130641907 | ||||||
| chr7:130641968
|
G | A | 221 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(218): Show | 221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.323+10901C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130641968 | ||||||
| chr7:130642138
|
T | G | 4 | a0001c0002t0003g0111a0001c0002t0003g0112a0001c0002t0003g0113others(1): Show | 4 | NA19010.hp1 NA19066.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.323+10731A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130642138 | ||||||
| chr7:130642245
|
C | CT | 324 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.323+10623dupA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130642245 | ||||||
| chr7:130642571
|
T | C | 3 | a0001c0001t0008g0318a0001c0001t0008g0321a0001c0001t0008g0322 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.323+10298A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130642571 | ||||||
| chr7:130642676
|
C | T | 91 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(88): Show | 91 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.323+10193G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130642676 | ||||||
| chr7:130642689
|
G | A | 56 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(53): Show | 56 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.323+10180C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130642689 | ||||||
| chr7:130642699
|
C | A | 1 | a0001c0002t0003g0117 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.323+10170G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130642699 | ||||||
| chr7:130642794
|
G | A | 2 | a0001c0001t0001g0310a0001c0001t0001g0319 | 2 | HG02055.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.323+10075C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130642794 | ||||||
| chr7:130642967
|
T | G | 56 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(53): Show | 56 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.323+9902A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130642967 | ||||||
| chr7:130643067
|
C | T | 2 | a0001c0002t0001g0124a0001c0002t0001g0125 | 2 | HG01106.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.323+9802G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130643067 | ||||||
| chr7:130643251
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.323+9618G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130643251 | ||||||
| chr7:130643259
|
C | T | 1 | a0001c0002t0003g0087 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.323+9610G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130643259 | ||||||
| chr7:130643274
|
G | C | 10 | a0001c0002t0001g0241a0001c0002t0007g0235a0001c0002t0007g0236others(7): Show | 10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.323+9595C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130643274 | ||||||
| chr7:130643281
|
C | T | 2 | a0001c0002t0005g0076a0001c0002t0005g0077 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.323+9588G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130643281 | ||||||
| chr7:130643294
|
C | CA | 21 | a0001c0001t0001g0129a0001c0001t0001g0139a0001c0001t0001g0273others(18): Show | 21 | HG00558.hp2 HG00639.hp2 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.323+9574dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130643294 | ||||||
| chr7:130643425
|
T | C | 1 | a0001c0001t0005g0250 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.323+9444A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130643425 | ||||||
| chr7:130643554
|
C | T | 1 | a0001c0002t0001g0049 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.323+9315G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130643554 | ||||||
| chr7:130643623
|
G | T | 1 | a0001c0001t0004g0308 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.323+9246C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130643623 | ||||||
| chr7:130643816
|
C | G | 10 | a0001c0002t0001g0241a0001c0002t0007g0235a0001c0002t0007g0236others(7): Show | 10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.323+9053G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130643816 | ||||||
| chr7:130644044
|
G | A | 1 | a0001c0001t0002g0186 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.323+8825C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130644044 | ||||||
| chr7:130644141
|
TAAAACAA | T | 92 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(89): Show | 92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.323+8721_323+8727d others(9): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130644141 | ||||||
| chr7:130644180
|
G | A | 1 | a0001c0001t0002g0216 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.323+8689C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130644180 | ||||||
| chr7:130644446
|
C | T | 6 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283others(3): Show | 6 | HG00558.hp1 HG01934.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.323+8423G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130644446 | ||||||
| chr7:130644452
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.323+8417T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130644452 | ||||||
| chr7:130644455
|
T | C | 92 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(89): Show | 92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.323+8414A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130644455 | ||||||
| chr7:130644524
|
T | A | 1 | a0001c0001t0001g0323 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.323+8345A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130644524 | ||||||
| chr7:130644621
|
T | C | 1 | a0001c0002t0001g0115 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.323+8248A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130644621 | ||||||
| chr7:130644659
|
T | C | 1 | a0001c0002t0001g0116 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.323+8210A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130644659 | ||||||
| chr7:130644828
|
G | A | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.323+8041C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130644828 | ||||||
| chr7:130644835
|
G | A | 1 | a0001c0001t0002g0024 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.323+8034C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130644835 | ||||||
| chr7:130644860
|
G | A | 1 | a0001c0002t0011g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.323+8009C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130644860 | ||||||
| chr7:130645037
|
G | C | 10 | a0001c0002t0001g0241a0001c0002t0007g0235a0001c0002t0007g0236others(7): Show | 10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.323+7832C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130645037 | ||||||
| chr7:130645062
|
C | G | 1 | a0001c0001t0002g0158 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.323+7807G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130645062 | ||||||
| chr7:130645068
|
CA | C | 189 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.323+7800delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130645068 | ||||||
| chr7:130645298
|
A | G | 1 | a0001c0005t0002g0010 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.323+7571T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130645298 | ||||||
| chr7:130645300
|
G | A | 1 | a0001c0002t0001g0125 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.323+7569C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130645300 | ||||||
| chr7:130645445
|
T | C | 56 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(53): Show | 56 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.323+7424A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130645445 | ||||||
| chr7:130645454
|
C | T | 32 | a0001c0002t0001g0019a0001c0002t0001g0028a0001c0002t0001g0032others(29): Show | 32 | HG00099.hp1 HG00597.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.323+7415G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130645454 | ||||||
| chr7:130645472
|
C | T | 1 | a0001c0012t0002g0166 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.323+7397G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130645472 | ||||||
| chr7:130645534
|
C | T | 3 | a0001c0002t0007g0236a0001c0002t0007g0238a0001c0002t0007g0239 | 3 | HG01993.hp1 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.323+7335G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130645534 | ||||||
| chr7:130645586
|
C | A | 1 | a0001c0002t0001g0031 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.323+7283G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130645586 | ||||||
| chr7:130645623
|
G | A | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.323+7246C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130645623 | ||||||
| chr7:130645679
|
A | C | 5 | a0001c0002t0001g0082a0001c0002t0001g0084a0001c0002t0001g0085others(2): Show | 5 | NA18947.hp1 NA18955.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.323+7190T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130645679 | ||||||
| chr7:130645747
|
G | GAC | 220 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(217): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.323+7120_323+7121d others(4): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130645747 | ||||||
| chr7:130645888
|
C | A | 62 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(59): Show | 62 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.323+6981G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130645888 | ||||||
| chr7:130646056
|
T | C | 1 | a0001c0001t0001g0246 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.323+6813A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646056 | ||||||
| chr7:130646117
|
A | T | 2 | a0001c0001t0001g0273a0004c0011t0001g0280 | 2 | HG00099.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.323+6752T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646117 | ||||||
| chr7:130646197
|
C | T | 1 | a0001c0002t0004g0081 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.323+6672G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646197 | ||||||
| chr7:130646218
|
T | A | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.323+6651A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646218 | ||||||
| chr7:130646263
|
G | A | 1 | a0001c0001t0002g0148 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.323+6606C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646263 | ||||||
| chr7:130646466
|
AT | A | 10 | a0001c0002t0001g0241a0001c0002t0007g0235a0001c0002t0007g0236others(7): Show | 10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.323+6402delA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646466 | ||||||
| chr7:130646467
|
T | C | 1 | a0001c0001t0002g0223 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.323+6402A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646467 | ||||||
| chr7:130646471
|
T | A | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.323+6398A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646471 | ||||||
| chr7:130646532
|
C | T | 22 | a0001c0002t0001g0019a0001c0002t0001g0028a0001c0002t0001g0034others(19): Show | 22 | HG00597.hp1 HG00621.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.323+6337G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646532 | ||||||
| chr7:130646623
|
G | A | 1 | a0007c0009t0002g0217 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.323+6246C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646623 | ||||||
| chr7:130646749
|
G | A | 50 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(47): Show | 50 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.323+6120C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646749 | ||||||
| chr7:130646813
|
C | T | 50 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(47): Show | 50 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.323+6056G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646813 | ||||||
| chr7:130646828
|
G | C | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144 | 3 | HG01069.hp1 HG01515.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.323+6041C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646828 | ||||||
| chr7:130646859
|
G | A | 2 | a0001c0001t0002g0218a0001c0001t0002g0229 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.323+6010C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646859 | ||||||
| chr7:130646865
|
G | A | 91 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(88): Show | 91 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.323+6004C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646865 | ||||||
| chr7:130646921
|
TTG | T | 92 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(89): Show | 92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.323+5946_323+5947d others(4): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646921 | ||||||
| chr7:130646943
|
G | A | 3 | a0001c0001t0005g0247a0001c0001t0005g0258a0001c0002t0001g0048 | 3 | HG02630.hp2 HG02647.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.323+5926C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646943 | ||||||
| chr7:130646943
|
GTA | G | 54 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(51): Show | 54 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(51): Show |
intron_variant | MODIFIER | c.323+5924_323+5925d others(4): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646943 | ||||||
| chr7:130646944
|
T | C | 2 | a0001c0001t0005g0247a0001c0001t0005g0258 | 2 | HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.323+5925A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646944 | ||||||
| chr7:130646958
|
CAT | C | 89 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(86): Show | 89 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.323+5909_323+5910d others(4): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646958 | ||||||
| chr7:130646958
|
CATATATA others(21): Show |
C | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(149): Show | 152 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.323+5883_323+5910d others(30): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646958 | ||||||
| chr7:130646958
|
CATATATA others(23): Show |
C | 72 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(69): Show | 72 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.323+5881_323+5910d others(32): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646958 | ||||||
| chr7:130646967
|
A | G | 3 | a0001c0001t0002g0151a0001c0001t0002g0165a0001c0001t0002g0222 | 3 | HG02015.hp2 NA18964.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.323+5902T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646967 | ||||||
| chr7:130646971
|
G | A | 3 | a0001c0001t0002g0151a0001c0001t0002g0165a0001c0001t0002g0222 | 3 | HG02015.hp2 NA18964.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.323+5898C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646971 | ||||||
| chr7:130646973
|
A | G | 2 | a0001c0001t0001g0253a0001c0001t0001g0257 | 2 | HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.323+5896T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646973 | ||||||
| chr7:130646973
|
ATATATAT others(19): Show |
A | 89 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(86): Show | 89 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.323+5870_323+5895d others(28): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646973 | ||||||
| chr7:130646983
|
GTATATAT others(5): Show |
G | 1 | a0001c0001t0002g0222 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.323+5874_323+5885d others(14): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646983 | ||||||
| chr7:130646983
|
GTATATAT others(23): Show |
G | 4 | a0001c0002t0001g0052a0001c0002t0001g0063a0001c0002t0001g0064others(1): Show | 4 | HG02145.hp1 HG02647.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.323+5856_323+5885d others(32): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646983 | ||||||
| chr7:130646984
|
T | C | 2 | a0001c0001t0001g0253a0001c0001t0001g0257 | 2 | HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.323+5885A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646984 | ||||||
| chr7:130646986
|
T | TATATATA others(5): Show |
1 | a0010c0015t0001g0259 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.323+5882_323+5883i others(14): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646986 | ||||||
| chr7:130646998
|
T | C | 1 | a0010c0015t0001g0259 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.323+5871A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646998 | ||||||
| chr7:130646999
|
G | A | 1 | a0001c0001t0002g0222 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.323+5870C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130646999 | ||||||
| chr7:130647001
|
A | ATATATAT others(19): Show |
2 | a0001c0001t0001g0253a0001c0001t0001g0257 | 2 | HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.323+5867_323+5868i others(28): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647001 | ||||||
| chr7:130647001
|
A | G | 14 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0245others(11): Show | 14 | HG01099.hp2 HG02055.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.323+5868T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647001 | ||||||
| chr7:130647003
|
ATATATAT others(17): Show |
A | 1 | a0001c0001t0002g0165 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.323+5842_323+5865d others(26): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647003 | ||||||
| chr7:130647012
|
T | C | 50 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(47): Show | 50 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.323+5857A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647012 | ||||||
| chr7:130647013
|
A | G | 3 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0002g0197 | 3 | HG02486.hp2 HG02717.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.323+5856T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647013 | ||||||
| chr7:130647023
|
A | G | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.323+5846T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647023 | ||||||
| chr7:130647029
|
A | G | 1 | a0001c0002t0001g0021 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.323+5840T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647029 | ||||||
| chr7:130647035
|
A | T | 1 | a0001c0001t0002g0165 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.323+5834T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647035 | ||||||
| chr7:130647039
|
T | A | 1 | a0001c0002t0001g0049 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.323+5830A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647039 | ||||||
| chr7:130647226
|
G | C | 6 | a0001c0001t0005g0247a0001c0001t0005g0251a0001c0001t0005g0254others(3): Show | 6 | HG02055.hp2 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.323+5643C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647226 | ||||||
| chr7:130647278
|
C | T | 1 | a0001c0002t0007g0238 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.323+5591G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647278 | ||||||
| chr7:130647436
|
C | G | 10 | a0001c0002t0001g0241a0001c0002t0007g0235a0001c0002t0007g0236others(7): Show | 10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.323+5433G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647436 | ||||||
| chr7:130647712
|
A | G | 2 | a0001c0002t0001g0063a0001c0002t0001g0064 | 2 | HG02145.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.323+5157T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647712 | ||||||
| chr7:130647730
|
A | AT | 12 | a0001c0001t0001g0015a0001c0001t0001g0030a0001c0001t0001g0071others(9): Show | 12 | HG00438.hp2 HG01243.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.323+5138dupA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647730 | ||||||
| chr7:130647730
|
AT | A | 63 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(60): Show | 63 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.323+5138delA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647730 | ||||||
| chr7:130647747
|
T | C | 2 | a0001c0002t0001g0031a0001c0002t0001g0062 | 2 | HG03486.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.323+5122A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647747 | ||||||
| chr7:130647749
|
G | C | 1 | a0001c0001t0001g0306 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.323+5120C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647749 | ||||||
| chr7:130647844
|
C | T | 1 | a0001c0001t0001g0279 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.323+5025G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647844 | ||||||
| chr7:130647888
|
G | A | 1 | a0001c0001t0002g0231 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.323+4981C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647888 | ||||||
| chr7:130647892
|
A | G | 1 | a0001c0002t0001g0051 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.323+4977T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647892 | ||||||
| chr7:130647951
|
C | T | 1 | a0001c0001t0001g0268 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.323+4918G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647951 | ||||||
| chr7:130647966
|
A | G | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.323+4903T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647966 | ||||||
| chr7:130647980
|
T | C | 50 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(47): Show | 50 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.323+4889A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647980 | ||||||
| chr7:130647990
|
A | C | 1 | a0001c0002t0001g0050 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.323+4879T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130647990 | ||||||
| chr7:130648015
|
C | A | 1 | a0001c0001t0002g0202 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.323+4854G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130648015 | ||||||
| chr7:130648396
|
C | T | 50 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(47): Show | 50 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.323+4473G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130648396 | ||||||
| chr7:130649267
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.323+3602A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130649267 | ||||||
| chr7:130649368
|
C | T | 1 | a0001c0002t0011g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.323+3501G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130649368 | ||||||
| chr7:130649376
|
C | T | 220 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(217): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.323+3493G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130649376 | ||||||
| chr7:130649525
|
T | C | 1 | a0001c0001t0001g0326 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.323+3344A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130649525 | ||||||
| chr7:130649535
|
A | C | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(281): Show | 284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.323+3334T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130649535 | ||||||
| chr7:130649727
|
T | C | 1 | a0001c0001t0004g0308 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.323+3142A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130649727 | ||||||
| chr7:130649799
|
C | A | 16 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0245others(13): Show | 16 | HG01099.hp2 HG02055.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.323+3070G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130649799 | ||||||
| chr7:130649951
|
A | C | 3 | a0001c0001t0008g0318a0001c0001t0008g0321a0001c0001t0008g0322 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.323+2918T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130649951 | ||||||
| chr7:130649969
|
T | G | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(281): Show | 284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.323+2900A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130649969 | ||||||
| chr7:130650593
|
C | T | 6 | a0001c0001t0002g0150a0001c0001t0002g0196a0001c0001t0002g0203others(3): Show | 6 | HG01175.hp2 HG01515.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.323+2276G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130650593 | ||||||
| chr7:130650695
|
C | G | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.323+2174G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130650695 | ||||||
| chr7:130650718
|
A | T | 62 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(59): Show | 62 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.323+2151T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130650718 | ||||||
| chr7:130650730
|
G | A | 10 | a0001c0002t0001g0241a0001c0002t0007g0235a0001c0002t0007g0236others(7): Show | 10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.323+2139C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130650730 | ||||||
| chr7:130651059
|
G | T | 1 | a0001c0001t0002g0219 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.323+1810C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651059 | ||||||
| chr7:130651184
|
T | C | 92 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(89): Show | 92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.323+1685A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651184 | ||||||
| chr7:130651201
|
T | C | 1 | a0001c0001t0002g0190 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.323+1668A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651201 | ||||||
| chr7:130651322
|
G | GT | 69 | a0001c0001t0001g0030a0001c0001t0001g0262a0001c0001t0001g0263others(66): Show | 69 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.323+1546dupA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651322 | ||||||
| chr7:130651379
|
C | T | 1 | a0001c0002t0001g0022 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.323+1490G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651379 | ||||||
| chr7:130651393
|
C | T | 2 | a0001c0001t0002g0157a0001c0001t0002g0232 | 2 | HG03239.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.323+1476G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651393 | ||||||
| chr7:130651413
|
C | T | 3 | a0001c0002t0001g0028a0001c0002t0001g0034a0001c0002t0001g0035 | 3 | HG01070.hp2 HG01071.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.323+1456G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651413 | ||||||
| chr7:130651428
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.323+1441G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651428 | ||||||
| chr7:130651494
|
A | AT | 13 | a0001c0002t0001g0032a0001c0002t0001g0034a0001c0002t0001g0035others(10): Show | 13 | HG00099.hp1 HG00621.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.323+1374dupA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651494 | ||||||
| chr7:130651494
|
ATT | A | 25 | a0001c0001t0001g0200a0001c0001t0002g0027a0001c0001t0002g0150others(22): Show | 25 | HG00544.hp2 HG01175.hp2 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.323+1373_323+1374d others(4): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651494 | ||||||
| chr7:130651494
|
ATTT | A | 71 | a0001c0001t0001g0213a0001c0001t0002g0024a0001c0001t0002g0026others(68): Show | 71 | HG00140.hp2 HG00438.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.323+1372_323+1374d others(5): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651494 | ||||||
| chr7:130651494
|
ATTTT | A | 12 | a0001c0001t0001g0009a0001c0001t0001g0127a0001c0001t0001g0262others(9): Show | 12 | HG00558.hp2 HG01168.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.323+1371_323+1374d others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651494 | ||||||
| chr7:130651494
|
ATTTTT | A | 41 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(38): Show | 41 | HG01175.hp1 HG01243.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.323+1370_323+1374d others(7): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651494 | ||||||
| chr7:130651494
|
ATTTTTT | A | 60 | a0001c0001t0001g0030a0001c0001t0001g0140a0001c0001t0001g0141others(57): Show | 60 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.323+1369_323+1374d others(8): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651494 | ||||||
| chr7:130651494
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0255 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.323+1365_323+1374d others(12): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651494 | ||||||
| chr7:130651494
|
ATTTTTTT others(4): Show |
A | 2 | a0001c0001t0002g0233a0001c0001t0002g0234 | 2 | HG03688.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.323+1364_323+1374d others(13): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651494 | ||||||
| chr7:130651494
|
ATTTTTTT others(5): Show |
A | 6 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(3): Show | 6 | HG01069.hp1 HG01515.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.323+1363_323+1374d others(14): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651494 | ||||||
| chr7:130651494
|
ATTTTTTT others(6): Show |
A | 60 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(57): Show | 60 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.323+1362_323+1374d others(15): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651494 | ||||||
| chr7:130651494
|
ATTTTTTT others(7): Show |
A | 3 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0002t0001g0118 | 3 | HG02486.hp2 HG02717.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.323+1361_323+1374d others(16): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651494 | ||||||
| chr7:130651533
|
G | A | 92 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(89): Show | 92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.323+1336C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651533 | ||||||
| chr7:130651586
|
G | A | 2 | a0001c0001t0009g0252a0001c0001t0009g0256 | 2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.323+1283C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651586 | ||||||
| chr7:130651605
|
T | C | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.323+1264A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651605 | ||||||
| chr7:130651678
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.323+1191C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651678 | ||||||
| chr7:130651706
|
C | T | 3 | a0001c0002t0001g0019a0001c0002t0001g0039a0001c0002t0001g0040 | 3 | HG02004.hp1 HG03491.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.323+1163G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651706 | ||||||
| chr7:130651716
|
C | T | 56 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(53): Show | 56 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.323+1153G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651716 | ||||||
| chr7:130651754
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.323+1115C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651754 | ||||||
| chr7:130651795
|
T | C | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.323+1074A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651795 | ||||||
| chr7:130651806
|
G | A | 1 | a0001c0002t0001g0119 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.323+1063C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651806 | ||||||
| chr7:130651885
|
G | A | 1 | a0001c0002t0001g0066 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.323+984C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651885 | ||||||
| chr7:130651902
|
G | A | 2 | a0001c0006t0002g0153a0001c0006t0002g0154 | 2 | NA18941.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.323+967C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130651902 | ||||||
| chr7:130652123
|
C | T | 1 | a0001c0001t0002g0156 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.323+746G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130652123 | ||||||
| chr7:130652288
|
A | C | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.323+581T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130652288 | ||||||
| chr7:130652306
|
A | G | 2 | a0001c0001t0001g0274a0001c0001t0001g0309 | 2 | NA18967.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.323+563T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130652306 | ||||||
| chr7:130652419
|
C | A | 1 | a0001c0002t0007g0236 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.323+450G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130652419 | ||||||
| chr7:130652645
|
G | C | 1 | a0001c0002t0003g0123 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.323+224C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130652645 | ||||||
| chr7:130652650
|
A | G | 1 | a0001c0001t0002g0260 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.323+219T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130652650 | ||||||
| chr7:130652816
|
A | T | 1 | a0001c0002t0001g0031 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.323+53T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 5/23 | chr7 | 130652816 | ||||||
| chr7:130653074
|
CA | C | 50 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(47): Show | 50 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.244-127delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130653074 | ||||||
| chr7:130653408
|
C | G | 1 | a0001c0002t0001g0038 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.244-460G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130653408 | ||||||
| chr7:130653609
|
G | A | 6 | a0001c0001t0001g0030a0001c0001t0001g0262a0001c0001t0001g0263others(3): Show | 6 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.244-661C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130653609 | ||||||
| chr7:130653729
|
T | C | 22 | a0001c0001t0001g0029a0001c0001t0001g0127a0001c0001t0001g0129others(19): Show | 22 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(19): Show |
intron_variant | MODIFIER | c.244-781A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130653729 | ||||||
| chr7:130653958
|
C | T | 1 | a0001c0002t0001g0126 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.244-1010G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130653958 | ||||||
| chr7:130653968
|
GA | G | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.244-1021delT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130653968 | ||||||
| chr7:130654010
|
C | T | 1 | a0001c0002t0001g0037 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.244-1062G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130654010 | ||||||
| chr7:130654011
|
G | GA | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.244-1064dupT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130654011 | ||||||
| chr7:130654086
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.244-1138G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130654086 | ||||||
| chr7:130654106
|
G | A | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.244-1158C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130654106 | ||||||
| chr7:130654309
|
G | C | 3 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007 | 3 | HG00438.hp1 NA18982.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.244-1361C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130654309 | ||||||
| chr7:130654362
|
T | A | 3 | a0001c0001t0008g0318a0001c0001t0008g0321a0001c0001t0008g0322 | 3 | HG01891.hp2 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.244-1414A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130654362 | ||||||
| chr7:130654603
|
G | A | 4 | a0001c0002t0001g0241a0002c0003t0001g0242a0002c0003t0001g0243others(1): Show | 4 | HG01433.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.244-1655C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130654603 | ||||||
| chr7:130654644
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.244-1696C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130654644 | ||||||
| chr7:130654666
|
T | C | 220 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(217): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.244-1718A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130654666 | ||||||
| chr7:130654675
|
T | C | 1 | a0001c0001t0002g0194 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.244-1727A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130654675 | ||||||
| chr7:130654692
|
G | C | 10 | a0001c0002t0001g0241a0001c0002t0007g0235a0001c0002t0007g0236others(7): Show | 10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.244-1744C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130654692 | ||||||
| chr7:130654699
|
T | C | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.244-1751A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130654699 | ||||||
| chr7:130654726
|
A | T | 1 | a0001c0001t0002g0228 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.244-1778T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130654726 | ||||||
| chr7:130654782
|
C | T | 2 | a0001c0006t0002g0153a0001c0006t0002g0154 | 2 | NA18941.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.244-1834G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130654782 | ||||||
| chr7:130654833
|
TTTTG | T | 92 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(89): Show | 92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.244-1889_244-1886d others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130654833 | ||||||
| chr7:130655148
|
C | A | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(281): Show | 284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.244-2200G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130655148 | ||||||
| chr7:130655184
|
G | A | 6 | a0001c0002t0007g0235a0001c0002t0007g0236a0001c0002t0007g0237others(3): Show | 6 | HG01192.hp2 HG01993.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.244-2236C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130655184 | ||||||
| chr7:130655364
|
A | G | 1 | a0001c0001t0001g0268 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.244-2416T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130655364 | ||||||
| chr7:130655475
|
T | G | 6 | a0001c0001t0001g0030a0001c0001t0001g0262a0001c0001t0001g0263others(3): Show | 6 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.244-2527A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130655475 | ||||||
| chr7:130655586
|
C | G | 1 | a0001c0001t0004g0131 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.244-2638G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130655586 | ||||||
| chr7:130655628
|
T | C | 220 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(217): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.244-2680A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130655628 | ||||||
| chr7:130655768
|
G | GTGTCTCT others(8): Show |
1 | a0001c0002t0001g0022 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.244-2821_244-2820i others(17): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130655768 | ||||||
| chr7:130655921
|
A | T | 160 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0266others(157): Show | 160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.244-2973T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130655921 | ||||||
| chr7:130656011
|
G | A | 1 | a0001c0002t0001g0069 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.244-3063C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130656011 | ||||||
| chr7:130656121
|
C | T | 1 | a0001c0001t0002g0155 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.244-3173G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130656121 | ||||||
| chr7:130656160
|
T | C | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.244-3212A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130656160 | ||||||
| chr7:130656207
|
CT | C | 7 | a0001c0001t0002g0223a0001c0002t0007g0235a0001c0002t0007g0236others(4): Show | 7 | HG01192.hp2 HG01993.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.244-3260delA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130656207 | ||||||
| chr7:130656388
|
C | T | 92 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(89): Show | 92 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.244-3440G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130656388 | ||||||
| chr7:130657193
|
C | T | 220 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(217): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.244-4245G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130657193 | ||||||
| chr7:130657376
|
T | C | 1 | a0001c0001t0002g0220 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.244-4428A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130657376 | ||||||
| chr7:130657550
|
AAT | A | 6 | a0001c0002t0007g0235a0001c0002t0007g0236a0001c0002t0007g0237others(3): Show | 6 | HG01192.hp2 HG01993.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.244-4604_244-4603d others(4): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130657550 | ||||||
| chr7:130657603
|
T | C | 60 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(57): Show | 60 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(57): Show |
intron_variant | MODIFIER | c.244-4655A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130657603 | ||||||
| chr7:130657686
|
T | G | 3 | a0001c0002t0001g0032a0001c0002t0001g0033a0001c0002t0001g0036 | 3 | HG00099.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.244-4738A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130657686 | ||||||
| chr7:130657701
|
T | C | 1 | a0001c0001t0004g0308 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.244-4753A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130657701 | ||||||
| chr7:130657758
|
C | T | 1 | a0001c0001t0002g0233 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.244-4810G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130657758 | ||||||
| chr7:130657963
|
T | C | 6 | a0001c0002t0007g0235a0001c0002t0007g0236a0001c0002t0007g0237others(3): Show | 6 | HG01192.hp2 HG01993.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.243+5004A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130657963 | ||||||
| chr7:130658138
|
A | G | 10 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(7): Show | 10 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.243+4829T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130658138 | ||||||
| chr7:130658201
|
C | T | 3 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022 | 3 | HG01099.hp1 HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.243+4766G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130658201 | ||||||
| chr7:130658389
|
G | A | 2 | a0001c0001t0001g0253a0001c0001t0001g0257 | 2 | HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.243+4578C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130658389 | ||||||
| chr7:130658463
|
G | A | 1 | a0001c0001t0002g0195 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.243+4504C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130658463 | ||||||
| chr7:130658670
|
T | C | 1 | a0001c0001t0005g0258 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.243+4297A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130658670 | ||||||
| chr7:130658880
|
C | T | 3 | a0001c0002t0005g0076a0001c0002t0005g0077a0001c0002t0005g0078 | 3 | HG01256.hp1 HG01258.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.243+4087G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130658880 | ||||||
| chr7:130659127
|
G | A | 6 | a0001c0002t0007g0235a0001c0002t0007g0236a0001c0002t0007g0237others(3): Show | 6 | HG01192.hp2 HG01993.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.243+3840C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659127 | ||||||
| chr7:130659152
|
G | A | 1 | a0001c0002t0003g0120 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.243+3815C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659152 | ||||||
| chr7:130659171
|
C | G | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.243+3796G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659171 | ||||||
| chr7:130659197
|
T | C | 1 | a0001c0001t0010g0001 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.243+3770A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659197 | ||||||
| chr7:130659208
|
A | G | 3 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0075 | 3 | NA19062.hp2 NA19064.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.243+3759T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659208 | ||||||
| chr7:130659224
|
G | T | 1 | a0001c0001t0001g0304 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.243+3743C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659224 | ||||||
| chr7:130659354
|
C | CAAAAAAA others(6): Show |
32 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0029others(29): Show | 32 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.243+3600_243+3612d others(15): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659354 | ||||||
| chr7:130659354
|
C | CAAAAAAA others(7): Show |
115 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(112): Show | 115 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.243+3599_243+3612d others(16): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659354 | ||||||
| chr7:130659354
|
C | CAAAAAAA others(8): Show |
52 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(49): Show | 52 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.243+3612_243+3613i others(17): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659354 | ||||||
| chr7:130659354
|
C | CAAAAAAA others(9): Show |
13 | a0001c0001t0001g0030a0001c0001t0001g0319a0001c0001t0001g0320others(10): Show | 13 | HG01175.hp2 HG01515.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.243+3612_243+3613i others(18): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659354 | ||||||
| chr7:130659354
|
C | CAAAAAAA others(10): Show |
4 | a0001c0002t0007g0237a0001c0002t0007g0238a0001c0002t0007g0239others(1): Show | 4 | HG01192.hp2 HG01993.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.243+3612_243+3613i others(19): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659354 | ||||||
| chr7:130659356
|
A | AAAAAAAA others(7): Show |
4 | a0001c0002t0001g0241a0002c0003t0001g0242a0002c0003t0001g0243others(1): Show | 4 | HG01433.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.243+3610_243+3611i others(16): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659356 | ||||||
| chr7:130659525
|
C | T | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.243+3442G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659525 | ||||||
| chr7:130659638
|
G | T | 1 | a0001c0002t0001g0036 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.243+3329C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659638 | ||||||
| chr7:130659724
|
C | T | 2 | a0001c0002t0001g0034a0001c0002t0001g0035 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.243+3243G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659724 | ||||||
| chr7:130659887
|
G | A | 1 | a0001c0002t0001g0070 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.243+3080C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659887 | ||||||
| chr7:130659926
|
G | T | 55 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(52): Show | 55 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(52): Show |
intron_variant | MODIFIER | c.243+3041C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130659926 | ||||||
| chr7:130660005
|
T | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | HG02486.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.243+2962A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130660005 | ||||||
| chr7:130660023
|
G | A | 1 | a0001c0001t0001g0018 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.243+2944C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130660023 | ||||||
| chr7:130660096
|
G | A | 218 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(215): Show | 218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.243+2871C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130660096 | ||||||
| chr7:130660370
|
T | C | 3 | a0001c0002t0003g0121a0001c0002t0003g0122a0001c0002t0003g0123 | 3 | HG03490.hp2 HG03942.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.243+2597A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130660370 | ||||||
| chr7:130660925
|
G | A | 2 | a0001c0001t0002g0224a0001c0001t0002g0225 | 2 | HG01258.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.243+2042C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130660925 | ||||||
| chr7:130660965
|
C | G | 1 | a0001c0001t0001g0130 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.243+2002G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130660965 | ||||||
| chr7:130661027
|
C | G | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.243+1940G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130661027 | ||||||
| chr7:130661070
|
G | A | 1 | a0001c0002t0001g0031 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.243+1897C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130661070 | ||||||
| chr7:130661205
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.243+1762C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130661205 | ||||||
| chr7:130661389
|
A | C | 4 | a0001c0002t0001g0241a0002c0003t0001g0242a0002c0003t0001g0243others(1): Show | 4 | HG01433.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.243+1578T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130661389 | ||||||
| chr7:130661632
|
A | G | 221 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(218): Show | 221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.243+1335T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130661632 | ||||||
| chr7:130661638
|
C | T | 51 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(48): Show | 51 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.243+1329G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130661638 | ||||||
| chr7:130661698
|
G | A | 1 | a0001c0002t0007g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.243+1269C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130661698 | ||||||
| chr7:130661713
|
G | T | 221 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(218): Show | 221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.243+1254C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130661713 | ||||||
| chr7:130661784
|
T | G | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.243+1183A>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130661784 | ||||||
| chr7:130661898
|
G | T | 4 | a0001c0002t0001g0241a0002c0003t0001g0242a0002c0003t0001g0243others(1): Show | 4 | HG01433.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.243+1069C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130661898 | ||||||
| chr7:130661977
|
C | G | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.243+990G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130661977 | ||||||
| chr7:130662022
|
G | T | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.243+945C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130662022 | ||||||
| chr7:130662031
|
A | G | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.243+936T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130662031 | ||||||
| chr7:130662119
|
A | G | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.243+848T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130662119 | ||||||
| chr7:130662187
|
C | T | 6 | a0001c0002t0007g0235a0001c0002t0007g0236a0001c0002t0007g0237others(3): Show | 6 | HG01192.hp2 HG01993.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.243+780G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130662187 | ||||||
| chr7:130662371
|
G | A | 10 | a0001c0002t0001g0241a0001c0002t0007g0235a0001c0002t0007g0236others(7): Show | 10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.243+596C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130662371 | ||||||
| chr7:130662537
|
T | C | 1 | a0001c0002t0001g0125 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.243+430A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130662537 | ||||||
| chr7:130662785
|
T | C | 1 | a0001c0001t0001g0323 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.243+182A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130662785 | ||||||
| chr7:130662795
|
A | G | 23 | a0001c0001t0001g0029a0001c0001t0001g0127a0001c0001t0001g0129others(20): Show | 23 | HG01069.hp1 HG01167.hp1 HG01515.hp2 others(20): Show |
intron_variant | MODIFIER | c.243+172T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130662795 | ||||||
| chr7:130662847
|
A | G | 10 | a0001c0002t0001g0241a0001c0002t0007g0235a0001c0002t0007g0236others(7): Show | 10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.243+120T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130662847 | ||||||
| chr7:130662934
|
TTTTCATC others(8): Show |
T | 12 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.243+18_243+32delTT others(13): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130662934 | ||||||
| chr7:130662961
|
A | T | 1 | a0001c0001t0002g0152 | 1 | NA18955.hp2 | splice_region_variant&intron_variant | LOW | c.243+6T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 4/23 | chr7 | 130662961 | ||||||
| chr7:130663097
|
C | A | 1 | a0001c0001t0004g0324 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.172-59G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130663097 | ||||||
| chr7:130663204
|
C | T | 223 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(220): Show | 223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.172-166G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130663204 | ||||||
| chr7:130663283
|
G | A | 2 | a0001c0002t0001g0124a0001c0002t0001g0125 | 2 | HG01106.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.172-245C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130663283 | ||||||
| chr7:130663324
|
TG | T | 10 | a0001c0002t0001g0241a0001c0002t0007g0235a0001c0002t0007g0236others(7): Show | 10 | HG01192.hp2 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.172-287delC | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130663324 | ||||||
| chr7:130663464
|
A | C | 1 | a0001c0001t0002g0151 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.172-426T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130663464 | ||||||
| chr7:130663576
|
T | C | 2 | a0001c0001t0002g0227a0001c0001t0006g0226 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.172-538A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130663576 | ||||||
| chr7:130663714
|
A | T | 2 | a0001c0001t0001g0266a0001c0001t0004g0267 | 2 | HG01978.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.172-676T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130663714 | ||||||
| chr7:130663730
|
CT | C | 158 | a0001c0001t0001g0004a0001c0001t0001g0071a0001c0001t0001g0072others(155): Show | 158 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.172-693delA | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130663730 | ||||||
| chr7:130663730
|
CTT | C | 55 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(52): Show | 55 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(52): Show |
intron_variant | MODIFIER | c.172-694_172-693del others(2): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130663730 | ||||||
| chr7:130663769
|
C | T | 1 | a0001c0002t0007g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.172-731G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130663769 | ||||||
| chr7:130663786
|
T | C | 51 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(48): Show | 51 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.172-748A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130663786 | ||||||
| chr7:130663887
|
C | T | 2 | a0001c0002t0001g0032a0001c0002t0001g0033 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.172-849G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130663887 | ||||||
| chr7:130663898
|
C | T | 2 | a0001c0001t0001g0127a0001c0001t0004g0128 | 2 | HG02723.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.172-860G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130663898 | ||||||
| chr7:130664103
|
G | A | 6 | a0001c0001t0001g0030a0001c0001t0001g0262a0001c0001t0001g0263others(3): Show | 6 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.172-1065C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130664103 | ||||||
| chr7:130664160
|
T | C | 4 | a0001c0002t0001g0241a0002c0003t0001g0242a0002c0003t0001g0243others(1): Show | 4 | HG01433.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.172-1122A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130664160 | ||||||
| chr7:130664199
|
T | C | 221 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(218): Show | 221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.172-1161A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130664199 | ||||||
| chr7:130664326
|
A | G | 221 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(218): Show | 221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.172-1288T>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130664326 | ||||||
| chr7:130664637
|
T | A | 1 | a0001c0001t0002g0232 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.172-1599A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130664637 | ||||||
| chr7:130665010
|
G | A | 51 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(48): Show | 51 | HG01069.hp1 HG01099.hp2 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.171+1839C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130665010 | ||||||
| chr7:130665084
|
AG | A | 102 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0002g0024others(99): Show | 102 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.171+1764delC | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130665084 | ||||||
| chr7:130665167
|
G | A | 16 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0245others(13): Show | 16 | HG01099.hp2 HG02055.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.171+1682C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130665167 | ||||||
| chr7:130665276
|
A | C | 2 | a0001c0001t0001g0029a0001c0002t0001g0028 | 2 | HG04199.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.171+1573T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130665276 | ||||||
| chr7:130665436
|
T | A | 1 | a0001c0002t0011g0240 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.171+1413A>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130665436 | ||||||
| chr7:130665441
|
C | G | 4 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026others(1): Show | 4 | HG01168.hp1 HG01978.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+1408G>C | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130665441 | ||||||
| chr7:130665473
|
T | C | 2 | a0001c0001t0002g0233a0001c0001t0002g0234 | 2 | HG03688.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.171+1376A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130665473 | ||||||
| chr7:130665610
|
CTAAG | C | 6 | a0001c0002t0007g0235a0001c0002t0007g0236a0001c0002t0007g0237others(3): Show | 6 | HG01192.hp2 HG01993.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.171+1235_171+1238d others(6): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130665610 | ||||||
| chr7:130665668
|
C | T | 12 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.171+1181G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130665668 | ||||||
| chr7:130666000
|
C | T | 3 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0022 | 3 | HG01099.hp1 HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.171+849G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130666000 | ||||||
| chr7:130666436
|
T | C | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.171+413A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130666436 | ||||||
| chr7:130666642
|
G | A | 20 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0245others(17): Show | 20 | HG01099.hp2 HG01433.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.171+207C>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 3/23 | chr7 | 130666642 | ||||||
| chr7:130667044
|
T | C | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.91-115A>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 2/23 | chr7 | 130667044 | ||||||
| chr7:130667226
|
A | T | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.90+256T>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 2/23 | chr7 | 130667226 | ||||||
| chr7:130667725
|
C | T | 1 | a0001c0002t0001g0019 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.38-191G>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 1/23 | chr7 | 130667725 | ||||||
| chr7:130667816
|
CACA | C | 11 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.38-285_38-283delTG others(1): Show |
COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 1/23 | chr7 | 130667816 | ||||||
| chr7:130667930
|
A | C | 3 | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0007 | 3 | HG00438.hp1 NA18982.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.38-396T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 1/23 | chr7 | 130667930 | ||||||
| chr7:130668084
|
G | C | 1 | a0001c0001t0002g0260 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.37+548C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 1/23 | chr7 | 130668084 | ||||||
| chr7:130668239
|
C | A | 1 | a0001c0002t0003g0261 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.37+393G>T | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 1/23 | chr7 | 130668239 | ||||||
| chr7:130668351
|
A | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.37+281T>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 1/23 | chr7 | 130668351 | ||||||
| chr7:130668376
|
AAG | A | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(1): Show | 4 | HG02572.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.37+254_37+255delCT | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 1/23 | chr7 | 130668376 | ||||||
| chr7:130668380
|
G | T | 1 | a0001c0002t0001g0002 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.37+252C>A | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 1/23 | chr7 | 130668380 | ||||||
| chr7:130668391
|
G | C | 62 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.37+241C>G | COPG2 | ENSG00000158623.14 | transcript | ENST00000425248.5 | protein_coding | 1/23 | chr7 | 130668391 |