Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 256356 |
|---|---|
| ensemblid | ENSG00000175066.16 |
| hgncid | 28635 |
| symbol | GK5 |
| name | glycerol kinase 5 |
| refseq_nuc | NM_001039547.3 |
| refseq_prot | NP_001034636.1 |
| ensembl_nuc | ENST00000392993.7 |
| ensembl_prot | ENSP00000418001.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 142157527 |
| end | 142225585 |
| strand | - |
| ver | v1.2 |
| region | chr3:142157527-142225585 |
| region5000 | chr3:142152527-142230585 |
| regionname0 | GK5_chr3_142157527_142225585 |
| regionname5000 | GK5_chr3_142152527_142230585 |
| 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 | 529 | 270 | 87 | 60 | 73 | 14 | 34 | 45 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0002 | 0/0 | 529 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0003 | 0/0 | 529 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| 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 | 1590 | 257 | 80 | 60 | 70 | 14 | 31 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| c0002 | 0/0 | 1590 | 12 | 6 | 0 | 3 | 0 | 3 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| c0003 | 0/0 | 1590 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| c0004 | 0/0 | 1590 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| c0005 | 0/0 | 1590 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| 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 | 8226 | 81 | 13 | 20 | 37 | 1 | 9 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0002 | 0/1 | 8222 | 20 | 3 | 4 | 5 | 1 | 6 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0003 | 0/0 | 8227 | 16 | 9 | 5 | 0 | 1 | 1 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0004 | 0/0 | 8213 | 12 | 0 | 4 | 3 | 4 | 1 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0005 | 0/0 | 8237 | 12 | 0 | 2 | 7 | 1 | 2 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0006 | 0/0 | 8243 | 6 | 6 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0007 | 0/0 | 8227 | 6 | 0 | 5 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0008 | 0/0 | 8240 | 6 | 5 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0009 | 0/0 | 8226 | 5 | 5 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0010 | 0/0 | 8222 | 4 | 0 | 4 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0011 | 0/0 | 8219 | 4 | 4 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0012 | 0/0 | 8227 | 4 | 1 | 0 | 1 | 0 | 2 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0013 | 0/0 | 8227 | 4 | 4 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0014 | 0/0 | 8238 | 3 | 0 | 0 | 0 | 1 | 2 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0015 | 0/0 | 8221 | 3 | 3 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0016 | 0/0 | 8227 | 3 | 0 | 0 | 0 | 2 | 1 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0017 | 0/0 | 8227 | 3 | 0 | 0 | 2 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0018 | 0/0 | 8238 | 3 | 0 | 1 | 1 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0019 | 0/0 | 8236 | 2 | 2 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0020 | 0/0 | 8242 | 2 | 2 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0021 | 0/0 | 8248 | 2 | 1 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0022 | 0/0 | 8247 | 2 | 2 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0023 | 0/0 | 8247 | 2 | 1 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0024 | 0/0 | 8227 | 2 | 2 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0025 | 0/0 | 8235 | 2 | 2 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0026 | 0/0 | 8222 | 2 | 0 | 0 | 0 | 2 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0027 | 0/0 | 8226 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0028 | 0/0 | 8227 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0029 | 0/0 | 8221 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0030 | 0/0 | 8223 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0031 | 0/0 | 8239 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0032 | 0/0 | 8238 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0033 | 0/0 | 8250 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0034 | 0/0 | 8248 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0035 | 0/0 | 8258 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0036 | 0/0 | 8252 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0037 | 0/0 | 8237 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0038 | 0/0 | 8244 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0039 | 0/0 | 8245 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0040 | 0/0 | 8244 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0041 | 0/0 | 8244 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0042 | 0/0 | 8241 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0043 | 0/0 | 8241 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0044 | 0/0 | 8247 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0045 | 0/0 | 8246 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0046 | 0/0 | 8237 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0047 | 0/0 | 8226 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0048 | 0/0 | 8227 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0049 | 0/0 | 8227 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0050 | 0/0 | 8218 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0051 | 0/0 | 8227 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0052 | 0/0 | 8228 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0053 | 0/0 | 8228 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0054 | 0/0 | 8226 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0055 | 0/0 | 8227 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0056 | 0/0 | 8222 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0057 | 0/0 | 8226 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0058 | 0/0 | 8224 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0059 | 0/0 | 8226 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0060 | 0/0 | 8222 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0061 | 0/0 | 8223 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0062 | 0/0 | 8222 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0063 | 0/0 | 8224 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0064 | 0/0 | 8225 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0065 | 0/0 | 8226 | 1 | 0 | 0 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0066 | 0/0 | 8226 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0067 | 0/0 | 8226 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0068 | 0/0 | 8227 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0069 | 0/0 | 8222 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0070 | 0/0 | 8223 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0071 | 0/0 | 8226 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0072 | 0/0 | 8226 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0073 | 0/0 | 8214 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0074 | 0/0 | 8226 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0075 | 0/0 | 8238 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0076 | 0/0 | 8222 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0077 | 0/0 | 8223 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0078 | 0/0 | 8244 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0079 | 0/0 | 8240 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0080 | 0/0 | 8239 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0081 | 0/0 | 8239 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0082 | 0/0 | 8236 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0083 | 0/0 | 8238 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0084 | 0/0 | 8243 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0085 | 0/0 | 8235 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0086 | 0/0 | 8226 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| t0087 | 0/0 | 8238 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0002 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0003 | 1/0 | 3 | 0 | 2 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0009 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| 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 | 1590 | 257 | 80 | 60 | 70 | 14 | 31 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0002 | 0/0 | 1590 | 12 | 6 | 0 | 3 | 0 | 3 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0003 | 0/0 | 1590 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0002c0004 | 0/0 | 1590 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0003c0005 | 0/0 | 1590 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 9815 | 80 | 13 | 20 | 36 | 1 | 9 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0002 | 0/1 | 9811 | 20 | 3 | 4 | 5 | 1 | 6 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0003 | 0/0 | 9816 | 15 | 9 | 5 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0004 | 0/0 | 9802 | 12 | 0 | 4 | 3 | 4 | 1 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0005 | 0/0 | 9826 | 12 | 0 | 2 | 7 | 1 | 2 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0006 | 0/0 | 9832 | 6 | 6 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0007 | 0/0 | 9816 | 6 | 0 | 5 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0008 | 0/0 | 9829 | 6 | 5 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0009 | 0/0 | 9815 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0010 | 0/0 | 9811 | 4 | 0 | 4 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0011 | 0/0 | 9808 | 4 | 4 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0012 | 0/0 | 9816 | 4 | 1 | 0 | 1 | 0 | 2 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0013 | 0/0 | 9816 | 4 | 4 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0014 | 0/0 | 9827 | 3 | 0 | 0 | 0 | 1 | 2 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0015 | 0/0 | 9810 | 2 | 2 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0016 | 0/0 | 9816 | 3 | 0 | 0 | 0 | 2 | 1 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0018 | 0/0 | 9827 | 3 | 0 | 1 | 1 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0019 | 0/0 | 9825 | 2 | 2 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0020 | 0/0 | 9831 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0021 | 0/0 | 9837 | 2 | 1 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0022 | 0/0 | 9836 | 2 | 2 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0023 | 0/0 | 9836 | 2 | 1 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0024 | 0/0 | 9816 | 2 | 2 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0025 | 0/0 | 9824 | 2 | 2 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0026 | 0/0 | 9811 | 2 | 0 | 0 | 0 | 2 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0027 | 0/0 | 9815 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0028 | 0/0 | 9816 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0029 | 0/0 | 9810 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0030 | 0/0 | 9812 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0031 | 0/0 | 9828 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0032 | 0/0 | 9827 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0033 | 0/0 | 9839 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0035 | 0/0 | 9847 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0036 | 0/0 | 9841 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0037 | 0/0 | 9826 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0038 | 0/0 | 9833 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0039 | 0/0 | 9834 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0040 | 0/0 | 9833 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0041 | 0/0 | 9833 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0042 | 0/0 | 9830 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0043 | 0/0 | 9830 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0044 | 0/0 | 9836 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0045 | 0/0 | 9835 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0046 | 0/0 | 9826 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0047 | 0/0 | 9815 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0048 | 0/0 | 9816 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0049 | 0/0 | 9816 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0050 | 0/0 | 9807 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0054 | 0/0 | 9815 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0055 | 0/0 | 9816 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0056 | 0/0 | 9811 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0057 | 0/0 | 9815 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0058 | 0/0 | 9813 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0059 | 0/0 | 9815 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0060 | 0/0 | 9811 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0061 | 0/0 | 9812 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0062 | 0/0 | 9811 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0063 | 0/0 | 9813 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0064 | 0/0 | 9814 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0065 | 0/0 | 9815 | 1 | 0 | 0 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0066 | 0/0 | 9815 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0067 | 0/0 | 9815 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0068 | 0/0 | 9816 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0069 | 0/0 | 9811 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0070 | 0/0 | 9812 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0071 | 0/0 | 9815 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0072 | 0/0 | 9815 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0073 | 0/0 | 9803 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0074 | 0/0 | 9815 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0075 | 0/0 | 9827 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0076 | 0/0 | 9811 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0077 | 0/0 | 9812 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0078 | 0/0 | 9833 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0079 | 0/0 | 9829 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0080 | 0/0 | 9828 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0081 | 0/0 | 9828 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0082 | 0/0 | 9825 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0083 | 0/0 | 9827 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0084 | 0/0 | 9832 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0085 | 0/0 | 9824 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0086 | 0/0 | 9815 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0001t0087 | 0/0 | 9827 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0002t0003 | 0/0 | 9816 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0002t0009 | 0/0 | 9815 | 3 | 3 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0002t0015 | 0/0 | 9810 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0002t0017 | 0/0 | 9816 | 3 | 0 | 0 | 2 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0002t0034 | 0/0 | 9837 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0002t0051 | 0/0 | 9816 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0002t0052 | 0/0 | 9817 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0002t0053 | 0/0 | 9817 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0001c0003t0009 | 0/0 | 9815 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0002c0004t0001 | 0/0 | 9815 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| a0003c0005t0020 | 0/0 | 9831 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | copy fasta | chr3 | 142152527 | 142230585 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0003 | 1/0 | 3 | 0 | 2 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0002g0009 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0004g0002 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0004g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0005g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0005g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0005g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0005g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0005g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0005g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0005g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0005g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0005g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0005g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0006g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0007g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0007g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0007g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0007g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0007g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0007g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0008g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0008g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0008g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0008g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0008g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0008g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0009g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0010g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0010g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0010g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0010g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0011g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0011g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0011g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0011g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0012g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0012g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0012g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0012g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0013g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0013g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0013g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0013g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0014g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0014g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0014g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0015g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0015g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0016g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0016g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0016g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0018g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0018g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0018g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0019g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0019g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0020g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0021g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0021g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0022g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0022g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0023g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0023g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0024g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0024g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0025g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0025g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0026g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0027g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0028g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0029g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0030g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0031g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0032g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0033g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0035g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0036g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0037g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0038g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0039g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0040g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0041g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0042g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0043g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0044g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0045g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0046g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0047g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0048g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0049g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0050g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0054g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0055g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0056g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0057g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0058g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0059g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0060g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0061g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0062g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0063g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0064g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0065g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0066g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0067g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0068g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0069g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0070g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0071g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0072g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0073g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0074g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0075g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0076g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0077g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0078g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0079g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0080g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0081g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0082g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0083g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0084g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0085g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0086g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0001t0087g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0002t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0002t0009g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0002t0009g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0002t0009g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0002t0015g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0002t0017g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0002t0017g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0002t0017g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0002t0034g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0002t0051g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0002t0052g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0002t0053g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0001c0003t0009g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0002c0004t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| a0003c0005t0020g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0014 | g0208 | EUR | GBR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0249 | EUR | GBR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG00140 | hp1 | a0001 | c0001 | t0005 | g0091 | EUR | GBR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0002 | EUR | GBR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | CHS | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG00408 | hp2 | a0001 | c0001 | t0005 | g0194 | EAS | CHS | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | CHS | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG00597 | hp2 | a0001 | c0001 | t0079 | g0067 | EAS | CHS | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG00639 | hp1 | a0001 | c0001 | t0029 | g0107 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG00642 | hp2 | a0001 | c0001 | t0031 | g0207 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG00738 | hp1 | a0001 | c0001 | t0048 | g0095 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0055 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG00741 | hp2 | a0001 | c0001 | t0087 | g0257 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01069 | hp2 | a0001 | c0001 | t0018 | g0086 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0098 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01074 | hp2 | a0001 | c0001 | t0049 | g0155 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0079 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01099 | hp1 | a0001 | c0001 | t0007 | g0105 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01106 | hp2 | a0001 | c0001 | t0007 | g0209 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01109 | hp1 | a0001 | c0001 | t0086 | g0256 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0058 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01168 | hp2 | a0001 | c0001 | t0062 | g0083 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01175 | hp1 | a0001 | c0001 | t0070 | g0175 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0084 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01243 | hp2 | a0001 | c0001 | t0021 | g0034 | AMR | PUR | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0211 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01256 | hp1 | a0001 | c0001 | t0007 | g0111 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01358 | hp1 | a0001 | c0001 | t0007 | g0113 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01358 | hp2 | a0001 | c0001 | t0010 | g0033 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01361 | hp2 | a0001 | c0001 | t0047 | g0039 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01433 | hp1 | a0001 | c0001 | t0008 | g0233 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01433 | hp2 | a0001 | c0001 | t0010 | g0171 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0040 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01496 | hp2 | a0001 | c0001 | t0023 | g0137 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01515 | hp1 | a0001 | c0001 | t0065 | g0243 | EUR | IBS | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0008 | EUR | IBS | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01516 | hp1 | a0001 | c0001 | t0026 | g0012 | EUR | IBS | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0043 | EUR | IBS | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0008 | EUR | IBS | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01517 | hp2 | a0001 | c0001 | t0026 | g0012 | EUR | IBS | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01884 | hp1 | a0001 | c0001 | t0009 | g0119 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01891 | hp1 | a0001 | c0001 | t0013 | g0234 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01891 | hp2 | a0001 | c0001 | t0020 | g0149 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01934 | hp1 | a0001 | c0001 | t0030 | g0109 | AMR | PEL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01934 | hp2 | a0001 | c0001 | t0007 | g0123 | AMR | PEL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01993 | hp1 | a0001 | c0001 | t0010 | g0110 | AMR | PEL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02004 | hp1 | a0001 | c0001 | t0010 | g0108 | AMR | PEL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02040 | hp1 | a0001 | c0001 | t0083 | g0222 | EAS | KHV | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0127 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02055 | hp2 | a0001 | c0001 | t0021 | g0163 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02056 | hp1 | a0001 | c0001 | t0012 | g0120 | EAS | KHV | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02056 | hp2 | a0001 | c0001 | t0067 | g0182 | EAS | KHV | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02071 | hp2 | a0001 | c0001 | t0018 | g0022 | EAS | KHV | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02083 | hp2 | a0001 | c0001 | t0081 | g0065 | EAS | KHV | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02135 | hp2 | a0001 | c0001 | t0080 | g0073 | EAS | KHV | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02145 | hp1 | a0001 | c0001 | t0035 | g0154 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02145 | hp2 | a0001 | c0001 | t0077 | g0129 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CDX | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CDX | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02257 | hp1 | a0001 | c0001 | t0012 | g0045 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02257 | hp2 | a0001 | c0001 | t0011 | g0148 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02280 | hp1 | a0001 | c0001 | t0078 | g0141 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02300 | hp1 | a0001 | c0001 | t0076 | g0082 | AMR | PEL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02523 | hp1 | a0001 | c0001 | t0055 | g0081 | EAS | KHV | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02523 | hp2 | a0001 | c0001 | t0056 | g0027 | EAS | KHV | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02572 | hp2 | a0001 | c0001 | t0039 | g0115 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02602 | hp1 | a0001 | c0002 | t0003 | g0242 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0072 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02615 | hp1 | a0001 | c0001 | t0008 | g0215 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02615 | hp2 | a0001 | c0001 | t0028 | g0035 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02622 | hp1 | a0001 | c0001 | t0040 | g0037 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02622 | hp2 | a0001 | c0001 | t0011 | g0117 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0145 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02630 | hp2 | a0001 | c0001 | t0085 | g0160 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02647 | hp2 | a0001 | c0001 | t0015 | g0238 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02683 | hp1 | a0001 | c0001 | t0018 | g0069 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0146 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0231 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02723 | hp2 | a0001 | c0001 | t0019 | g0224 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0053 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02738 | hp1 | a0001 | c0001 | t0012 | g0250 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02738 | hp2 | a0001 | c0001 | t0012 | g0177 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02809 | hp1 | a0001 | c0001 | t0008 | g0089 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02809 | hp2 | a0001 | c0002 | t0034 | g0044 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0212 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0059 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02886 | hp1 | a0001 | c0001 | t0019 | g0151 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02895 | hp1 | a0001 | c0001 | t0022 | g0158 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02895 | hp2 | a0001 | c0001 | t0013 | g0235 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02896 | hp1 | a0001 | c0002 | t0009 | g0219 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02896 | hp2 | a0001 | c0001 | t0024 | g0049 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02897 | hp1 | a0001 | c0001 | t0013 | g0237 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02897 | hp2 | a0001 | c0001 | t0024 | g0050 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02965 | hp1 | a0001 | c0001 | t0045 | g0139 | AFR | ESN | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02965 | hp2 | a0001 | c0001 | t0037 | g0147 | AFR | ESN | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0210 | AFR | ESN | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02970 | hp2 | a0003 | c0005 | t0020 | g0203 | AFR | ESN | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02976 | hp1 | a0001 | c0001 | t0011 | g0094 | AFR | ESN | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02976 | hp2 | a0001 | c0003 | t0009 | g0161 | AFR | ESN | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03017 | hp1 | a0001 | c0001 | t0059 | g0052 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0246 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03041 | hp1 | a0001 | c0001 | t0043 | g0150 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03098 | hp1 | a0001 | c0001 | t0025 | g0116 | AFR | MSL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0061 | AFR | MSL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0142 | AFR | ESN | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | ESN | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0030 | AFR | MSL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03225 | hp1 | a0001 | c0001 | t0022 | g0114 | AFR | MSL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03225 | hp2 | a0001 | c0001 | t0058 | g0157 | AFR | MSL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03453 | hp1 | a0001 | c0001 | t0075 | g0159 | AFR | MSL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0029 | AFR | MSL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03486 | hp2 | a0001 | c0002 | t0009 | g0218 | AFR | MSL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03490 | hp1 | a0001 | c0001 | t0068 | g0112 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ESN | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03516 | hp2 | a0001 | c0001 | t0025 | g0097 | AFR | ESN | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03540 | hp1 | a0001 | c0002 | t0015 | g0252 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0047 | AFR | GWD | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03579 | hp1 | a0001 | c0001 | t0013 | g0236 | AFR | MSL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03579 | hp2 | a0001 | c0001 | t0064 | g0214 | AFR | MSL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0191 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03704 | hp2 | a0001 | c0002 | t0052 | g0176 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03710 | hp2 | a0001 | c0001 | t0016 | g0133 | SAS | PJL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | BEB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03831 | hp2 | a0001 | c0001 | t0014 | g0041 | SAS | BEB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03834 | hp1 | a0001 | c0001 | t0074 | g0190 | SAS | BEB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0046 | SAS | BEB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03927 | hp2 | a0001 | c0001 | t0061 | g0032 | SAS | BEB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03942 | hp1 | a0001 | c0001 | t0014 | g0125 | SAS | BEB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | STU | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG04115 | hp2 | a0001 | c0001 | t0063 | g0204 | SAS | STU | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG04228 | hp1 | a0001 | c0002 | t0017 | g0216 | SAS | STU | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | STU | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0028 | EAS | CHB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA18906 | hp1 | a0001 | c0001 | t0044 | g0140 | AFR | YRI | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA18906 | hp2 | a0001 | c0001 | t0038 | g0144 | AFR | YRI | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA18947 | hp2 | a0001 | c0002 | t0017 | g0187 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA18948 | hp2 | a0001 | c0002 | t0051 | g0188 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA18950 | hp1 | a0001 | c0001 | t0007 | g0169 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0229 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0166 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA18956 | hp1 | a0001 | c0001 | t0071 | g0087 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA18970 | hp2 | a0001 | c0001 | t0005 | g0165 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA18971 | hp2 | a0001 | c0001 | t0005 | g0023 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA18973 | hp2 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA18982 | hp2 | a0001 | c0001 | t0027 | g0013 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA18986 | hp1 | a0001 | c0001 | t0072 | g0017 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA18986 | hp2 | a0001 | c0001 | t0005 | g0016 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA18992 | hp2 | a0001 | c0001 | t0073 | g0026 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA19009 | hp1 | a0001 | c0001 | t0005 | g0019 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA19009 | hp2 | a0001 | c0001 | t0082 | g0221 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA19010 | hp1 | a0001 | c0001 | t0057 | g0103 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA19030 | hp1 | a0001 | c0001 | t0033 | g0153 | AFR | LWK | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA19030 | hp2 | a0001 | c0001 | t0008 | g0213 | AFR | LWK | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA19043 | hp1 | a0001 | c0001 | t0036 | g0232 | AFR | LWK | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA19043 | hp2 | a0001 | c0001 | t0008 | g0162 | AFR | LWK | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA19060 | hp2 | a0001 | c0001 | t0005 | g0223 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA19064 | hp2 | a0001 | c0002 | t0017 | g0189 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA19079 | hp2 | a0001 | c0001 | t0069 | g0196 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA19083 | hp1 | a0001 | c0001 | t0066 | g0078 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA19086 | hp1 | a0001 | c0001 | t0054 | g0227 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA19091 | hp1 | a0002 | c0004 | t0001 | g0217 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | YRI | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | YRI | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA20129 | hp1 | a0001 | c0001 | t0015 | g0255 | AFR | ASW | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ASW | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0174 | EUR | TSI | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA20752 | hp2 | a0001 | c0001 | t0016 | g0131 | EUR | TSI | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0185 | EUR | TSI | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA20805 | hp2 | a0001 | c0001 | t0016 | g0132 | EUR | TSI | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA20905 | hp1 | a0001 | c0001 | t0060 | g0186 | SAS | GIH | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA20905 | hp2 | a0001 | c0001 | t0032 | g0042 | SAS | GIH | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01123 | hp1 | a0001 | c0001 | t0050 | g0096 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02109 | hp1 | a0001 | c0001 | t0023 | g0138 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02109 | hp2 | a0001 | c0001 | t0011 | g0092 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02486 | hp1 | a0001 | c0001 | t0041 | g0038 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0152 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02559 | hp1 | a0001 | c0002 | t0009 | g0251 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03471 | hp1 | a0001 | c0001 | t0046 | g0239 | AFR | MSL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG03471 | hp2 | a0001 | c0002 | t0053 | g0220 | AFR | MSL | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG06807 | hp1 | a0001 | c0001 | t0084 | g0093 | AFR | USA | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | USA | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0062 | AFR | USA | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | USA | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA21309 | hp1 | a0001 | c0001 | t0042 | g0143 | AFR | LWK | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | LWK | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0009 | REF | REF | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0003 | REF | REF | GK5_chr3_142152527_142230585 | GK5 | chr3 | 142152527 | 142230585 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:142172440
|
G | A | 1 | a0002 | 1 | NA19091.hp1 | missense_variant | MODERATE | c.1160C>T | p.Pro387Leu | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 13/16 | 1290/9815 | 1160/1590 | 387/529 | chr3 | 142172440 | ||
| chr3:142182959
|
T | C | 1 | a0003 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.907A>G | p.Ile303Val | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 10/16 | 1037/9815 | 907/1590 | 303/529 | chr3 | 142182959 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:142181525
|
G | A | 1 | a0001c0002 | 12 | HG02559.hp1 HG02602.hp1 HG02809.hp2 others(9): Show |
synonymous_variant | LOW | c.984C>T | p.Val328Val | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/16 | 1114/9815 | 984/1590 | 328/529 | chr3 | 142181525 | ||
| chr3:142186503
|
A | G | 1 | a0001c0003 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.630T>C | p.Tyr210Tyr | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 7/16 | 760/9815 | 630/1590 | 210/529 | chr3 | 142186503 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:142157957
|
G | GT | 29 | a0001c0001t0003a0001c0001t0006a0001c0001t0011others(26): Show | 58 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*7664dupA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 7664 | chr3 | 142157957 | |||||
| chr3:142158086
|
G | A | 2 | a0001c0001t0033a0001c0001t0035 | 2 | HG02145.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7536C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 7536 | chr3 | 142158086 | |||||
| chr3:142158145
|
G | A | 5 | a0001c0001t0014a0001c0001t0019a0001c0001t0031others(2): Show | 8 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7477C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 7477 | chr3 | 142158145 | |||||
| chr3:142158242
|
T | C | 53 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(50): Show | 118 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*7380A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 7380 | chr3 | 142158242 | |||||
| chr3:142158315
|
T | G | 1 | a0001c0001t0066 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7307A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 7307 | chr3 | 142158315 | |||||
| chr3:142158419
|
T | C | 1 | a0001c0001t0084 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7203A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 7203 | chr3 | 142158419 | |||||
| chr3:142158565
|
T | G | 40 | a0001c0001t0005a0001c0001t0006a0001c0001t0008others(37): Show | 71 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*7057A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 7057 | chr3 | 142158565 | |||||
| chr3:142158710
|
G | C | 1 | a0001c0001t0043 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6912C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 6912 | chr3 | 142158710 | |||||
| chr3:142158740
|
A | G | 1 | a0001c0001t0069 | 1 | NA19079.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6882T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 6882 | chr3 | 142158740 | |||||
| chr3:142158755
|
C | T | 1 | a0001c0001t0060 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6867G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 6867 | chr3 | 142158755 | |||||
| chr3:142158768
|
G | A | 10 | a0001c0001t0003a0001c0001t0011a0001c0001t0016others(7): Show | 30 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*6854C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 6854 | chr3 | 142158768 | |||||
| chr3:142158865
|
C | A | 18 | a0001c0001t0006a0001c0001t0015a0001c0001t0020others(15): Show | 27 | HG01243.hp2 HG01496.hp2 HG01891.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*6757G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 6757 | chr3 | 142158865 | |||||
| chr3:142158984
|
A | T | 1 | a0001c0001t0065 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6638T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 6638 | chr3 | 142158984 | |||||
| chr3:142159179
|
G | T | 1 | a0001c0001t0057 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6443C>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 6443 | chr3 | 142159179 | |||||
| chr3:142159254
|
C | CA | 8 | a0001c0001t0005a0001c0001t0018a0001c0001t0079others(5): Show | 21 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*6367dupT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 6367 | chr3 | 142159254 | |||||
| chr3:142159311
|
G | A | 1 | a0001c0001t0062 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6311C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 6311 | chr3 | 142159311 | |||||
| chr3:142159351
|
A | G | 4 | a0001c0001t0014a0001c0001t0031a0001c0001t0032others(1): Show | 6 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6271T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 6271 | chr3 | 142159351 | |||||
| chr3:142159377
|
G | A | 10 | a0001c0001t0003a0001c0001t0011a0001c0001t0016others(7): Show | 30 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*6245C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 6245 | chr3 | 142159377 | |||||
| chr3:142159619
|
G | C | 1 | a0001c0001t0032 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6003C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 6003 | chr3 | 142159619 | |||||
| chr3:142159630
|
TA | T | 38 | a0001c0001t0004a0001c0001t0006a0001c0001t0008others(35): Show | 67 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*5991delT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5991 | chr3 | 142159630 | |||||
| chr3:142159694
|
G | A | 2 | a0001c0001t0044a0001c0001t0045 | 2 | HG02965.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5928C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5928 | chr3 | 142159694 | |||||
| chr3:142159780
|
C | T | 1 | a0001c0001t0049 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5842G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5842 | chr3 | 142159780 | |||||
| chr3:142159789
|
G | A | 1 | a0001c0001t0025 | 2 | HG03098.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5833C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5833 | chr3 | 142159789 | |||||
| chr3:142159795
|
G | A | 1 | a0001c0001t0081 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5827C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5827 | chr3 | 142159795 | |||||
| chr3:142159826
|
G | A | 28 | a0001c0001t0006a0001c0001t0014a0001c0001t0015others(25): Show | 40 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*5796C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5796 | chr3 | 142159826 | |||||
| chr3:142159826
|
GCTTTCTC others(1): Show |
G | 2 | a0001c0001t0011a0001c0001t0050 | 5 | HG01123.hp1 HG02109.hp2 HG02257.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5788_*5795delAGAG others(4): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5788 | chr3 | 142159826 | |||||
| chr3:142159829
|
T | C | 7 | a0001c0001t0003a0001c0001t0016a0001c0001t0024others(4): Show | 24 | HG00738.hp2 HG01074.hp1 HG01074.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*5793A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5793 | chr3 | 142159829 | |||||
| chr3:142159829
|
T | TTC | 2 | a0001c0001t0013a0001c0002t0053 | 5 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5791_*5792dupGA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5792 | chr3 | 142159829 | |||||
| chr3:142159829
|
TTC | T | 3 | a0001c0001t0015a0001c0001t0063a0001c0002t0015 | 4 | HG02647.hp2 HG03540.hp1 HG04115.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5791_*5792delGA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5791 | chr3 | 142159829 | |||||
| chr3:142159829
|
TTCTC | T | 13 | a0001c0001t0002a0001c0001t0010a0001c0001t0026others(10): Show | 36 | HG00408.hp1 HG00438.hp1 HG00639.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*5789_*5792delGAGA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5789 | chr3 | 142159829 | |||||
| chr3:142159831
|
C | T | 6 | a0001c0001t0014a0001c0001t0019a0001c0001t0031others(3): Show | 9 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5791G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5791 | chr3 | 142159831 | |||||
| chr3:142159841
|
C | T | 7 | a0001c0001t0003a0001c0001t0016a0001c0001t0024others(4): Show | 24 | HG00738.hp2 HG01074.hp1 HG01074.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*5781G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5781 | chr3 | 142159841 | |||||
| chr3:142159847
|
C | CTTTTTTT others(11): Show |
2 | a0001c0001t0042a0001c0001t0043 | 2 | HG03041.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5774_*5775insAAAA others(14): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5774 | chr3 | 142159847 | |||||
| chr3:142159847
|
C | CTTTTTTT others(12): Show |
3 | a0001c0001t0020a0001c0001t0045a0003c0005t0020 | 3 | HG01891.hp2 HG02965.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5774_*5775insAAAA others(15): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5774 | chr3 | 142159847 | |||||
| chr3:142159847
|
C | CTTTTTTT others(13): Show |
4 | a0001c0001t0006a0001c0001t0022a0001c0001t0023others(1): Show | 11 | HG01496.hp2 HG02109.hp1 HG02630.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5774_*5775insAAAA others(16): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5774 | chr3 | 142159847 | |||||
| chr3:142159847
|
C | CTTTTTTT others(14): Show |
3 | a0001c0001t0021a0001c0001t0040a0001c0001t0078 | 4 | HG01243.hp2 HG02055.hp2 HG02280.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5774_*5775insAAAA others(17): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5774 | chr3 | 142159847 | |||||
| chr3:142159847
|
C | CTTTTTTT others(15): Show |
2 | a0001c0001t0039a0001c0002t0034 | 2 | HG02572.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5774_*5775insAAAA others(18): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5774 | chr3 | 142159847 | |||||
| chr3:142159849
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0037 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5772_*5773insAAAA others(10): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5772 | chr3 | 142159849 | |||||
| chr3:142159849
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0038 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5772_*5773insAAAA others(16): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5772 | chr3 | 142159849 | |||||
| chr3:142159849
|
C | CTTTTTTT others(14): Show |
1 | a0001c0001t0041 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5772_*5773insAAAA others(17): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5772 | chr3 | 142159849 | |||||
| chr3:142159849
|
C | T | 16 | a0001c0001t0006a0001c0001t0011a0001c0001t0020others(13): Show | 27 | HG01123.hp1 HG01243.hp2 HG01496.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*5773G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5773 | chr3 | 142159849 | |||||
| chr3:142159851
|
C | CTTTTTTT others(19): Show |
1 | a0001c0001t0036 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5770_*5771insAAAA others(22): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5770 | chr3 | 142159851 | |||||
| chr3:142159851
|
C | CTTTTTTT others(21): Show |
1 | a0001c0001t0033 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5770_*5771insAAAA others(24): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5770 | chr3 | 142159851 | |||||
| chr3:142159851
|
C | CTTTTTTT others(25): Show |
1 | a0001c0001t0035 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5770_*5771insAAAA others(28): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5770 | chr3 | 142159851 | |||||
| chr3:142159851
|
C | T | 19 | a0001c0001t0006a0001c0001t0015a0001c0001t0020others(16): Show | 28 | HG01243.hp2 HG01496.hp2 HG01891.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*5771G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5771 | chr3 | 142159851 | |||||
| chr3:142159853
|
C | CT | 4 | a0001c0001t0007a0001c0001t0057a0001c0001t0059others(1): Show | 9 | HG01099.hp1 HG01106.hp2 HG01256.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5768dupA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | |||||
| chr3:142159853
|
C | CTCTCTCT others(7): Show |
1 | a0001c0001t0075 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5768_*5769insAAAA others(10): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | |||||
| chr3:142159853
|
C | CTCTCTCT others(9): Show |
3 | a0001c0001t0014a0001c0001t0032a0001c0001t0087 | 5 | HG00099.hp1 HG00741.hp2 HG03831.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5768_*5769insAAAA others(12): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | |||||
| chr3:142159853
|
C | CTCTCTCT others(10): Show |
1 | a0001c0001t0031 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5768_*5769insAAAA others(13): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | |||||
| chr3:142159853
|
C | CTCTCTTT others(7): Show |
1 | a0001c0001t0019 | 2 | HG02723.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5768_*5769insAAAA others(10): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | |||||
| chr3:142159853
|
C | CTCTTTTT others(6): Show |
1 | a0001c0001t0046 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5768_*5769insAAAA others(9): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | |||||
| chr3:142159853
|
C | CTCTTTTT others(12): Show |
1 | a0001c0001t0008 | 6 | HG01433.hp1 HG02615.hp1 HG02717.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5768_*5769insAAAA others(15): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | |||||
| chr3:142159853
|
C | CTCTTTTT others(13): Show |
1 | a0001c0001t0083 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5768_*5769insAAAA others(16): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | |||||
| chr3:142159853
|
C | CTCTTTTT others(15): Show |
2 | a0001c0001t0081a0001c0001t0084 | 2 | HG02083.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5768_*5769insAAAA others(18): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | |||||
| chr3:142159853
|
C | CTTTTT | 2 | a0001c0001t0004a0001c0001t0073 | 13 | HG00140.hp2 HG00639.hp2 HG01081.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*5764_*5768dupAAAA others(1): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | |||||
| chr3:142159853
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0025 | 2 | HG03098.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5768_*5769insAAAA others(9): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | |||||
| chr3:142159853
|
C | CTTTTTTT others(11): Show |
1 | a0001c0001t0085 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5768_*5769insAAAA others(14): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | |||||
| chr3:142159853
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0082 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5768_*5769insAAAA others(15): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | |||||
| chr3:142159853
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0005 | 12 | HG00140.hp1 HG00408.hp2 HG01256.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5768_*5769insAAAA others(16): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | |||||
| chr3:142159853
|
C | CTTTTTTT others(14): Show |
1 | a0001c0001t0018 | 3 | HG01069.hp2 HG02071.hp2 HG02683.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5768_*5769insAAAA others(17): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | |||||
| chr3:142159853
|
C | CTTTTTTT others(15): Show |
1 | a0001c0001t0080 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5768_*5769insAAAA others(18): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | |||||
| chr3:142159853
|
C | CTTTTTTT others(16): Show |
1 | a0001c0001t0079 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5768_*5769insAAAA others(19): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5768 | chr3 | 142159853 | |||||
| chr3:142159853
|
C | T | 22 | a0001c0001t0006a0001c0001t0015a0001c0001t0020others(19): Show | 31 | HG01243.hp2 HG01496.hp2 HG01891.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*5769G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5769 | chr3 | 142159853 | |||||
| chr3:142159855
|
T | C | 1 | a0001c0001t0067 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5767A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5767 | chr3 | 142159855 | |||||
| chr3:142159871
|
A | G | 8 | a0001c0001t0005a0001c0001t0018a0001c0001t0079others(5): Show | 21 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*5751T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5751 | chr3 | 142159871 | |||||
| chr3:142159908
|
C | A | 10 | a0001c0001t0003a0001c0001t0011a0001c0001t0016others(7): Show | 30 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*5714G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5714 | chr3 | 142159908 | |||||
| chr3:142159932
|
C | T | 1 | a0001c0001t0085 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5690G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5690 | chr3 | 142159932 | |||||
| chr3:142159936
|
G | A | 1 | a0001c0001t0068 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5686C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5686 | chr3 | 142159936 | |||||
| chr3:142159983
|
G | A | 1 | a0001c0001t0023 | 2 | HG01496.hp2 HG02109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5639C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5639 | chr3 | 142159983 | |||||
| chr3:142160128
|
G | A | 24 | a0001c0001t0004a0001c0001t0006a0001c0001t0015others(21): Show | 44 | HG00140.hp2 HG00639.hp2 HG01081.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*5494C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5494 | chr3 | 142160128 | |||||
| chr3:142160132
|
G | A | 1 | a0001c0001t0046 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5490C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5490 | chr3 | 142160132 | |||||
| chr3:142160393
|
C | G | 1 | a0001c0001t0046 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5229G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5229 | chr3 | 142160393 | |||||
| chr3:142160398
|
A | G | 1 | a0001c0001t0084 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5224T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5224 | chr3 | 142160398 | |||||
| chr3:142160536
|
T | C | 1 | a0001c0001t0025 | 2 | HG03098.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5086A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5086 | chr3 | 142160536 | |||||
| chr3:142160618
|
G | C | 22 | a0001c0001t0006a0001c0001t0015a0001c0001t0020others(19): Show | 31 | HG01243.hp2 HG01496.hp2 HG01891.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*5004C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 5004 | chr3 | 142160618 | |||||
| chr3:142160809
|
C | A | 27 | a0001c0001t0006a0001c0001t0014a0001c0001t0015others(24): Show | 39 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*4813G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 4813 | chr3 | 142160809 | |||||
| chr3:142160896
|
A | T | 1 | a0001c0001t0085 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4726T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 4726 | chr3 | 142160896 | |||||
| chr3:142160915
|
G | T | 1 | a0001c0001t0008 | 6 | HG01433.hp1 HG02615.hp1 HG02717.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4707C>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 4707 | chr3 | 142160915 | |||||
| chr3:142161078
|
CTTTTGTT others(7): Show |
C | 2 | a0001c0001t0004a0001c0001t0073 | 13 | HG00140.hp2 HG00639.hp2 HG01081.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*4530_*4543delACAA others(10): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 4530 | chr3 | 142161078 | |||||
| chr3:142161079
|
T | G | 3 | a0001c0001t0033a0001c0001t0035a0001c0001t0036 | 3 | HG02145.hp1 NA19030.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4543A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 4543 | chr3 | 142161079 | |||||
| chr3:142161084
|
TTTTTTTG | T | 8 | a0001c0001t0005a0001c0001t0018a0001c0001t0079others(5): Show | 21 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*4531_*4537delCAAA others(3): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 4531 | chr3 | 142161084 | |||||
| chr3:142161090
|
TG | T | 29 | a0001c0001t0006a0001c0001t0008a0001c0001t0014others(26): Show | 47 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*4531delC | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 4531 | chr3 | 142161090 | |||||
| chr3:142161091
|
G | T | 13 | a0001c0001t0003a0001c0001t0011a0001c0001t0013others(10): Show | 36 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*4531C>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 4531 | chr3 | 142161091 | |||||
| chr3:142161097
|
G | T | 1 | a0001c0001t0024 | 2 | HG02896.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4525C>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 4525 | chr3 | 142161097 | |||||
| chr3:142161163
|
G | A | 8 | a0001c0001t0005a0001c0001t0018a0001c0001t0079others(5): Show | 21 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*4459C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 4459 | chr3 | 142161163 | |||||
| chr3:142161479
|
C | T | 1 | a0001c0001t0037 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4143G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 4143 | chr3 | 142161479 | |||||
| chr3:142161491
|
A | G | 2 | a0001c0001t0004a0001c0001t0073 | 13 | HG00140.hp2 HG00639.hp2 HG01081.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*4131T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 4131 | chr3 | 142161491 | |||||
| chr3:142161582
|
G | C | 2 | a0001c0001t0016a0001c0001t0049 | 4 | HG01074.hp2 HG03710.hp2 NA20752.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4040C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 4040 | chr3 | 142161582 | |||||
| chr3:142161617
|
T | G | 1 | a0001c0001t0082 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4005A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 4005 | chr3 | 142161617 | |||||
| chr3:142161624
|
C | T | 1 | a0001c0001t0084 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3998G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 3998 | chr3 | 142161624 | |||||
| chr3:142161789
|
T | TATTG | 8 | a0001c0001t0021a0001c0001t0022a0001c0001t0023others(5): Show | 11 | HG01243.hp2 HG01496.hp2 HG02055.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3829_*3832dupCAAT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 3832 | chr3 | 142161789 | |||||
| chr3:142161811
|
T | C | 1 | a0001c0001t0050 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3811A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 3811 | chr3 | 142161811 | |||||
| chr3:142161997
|
G | A | 8 | a0001c0001t0009a0001c0001t0086a0001c0002t0009others(5): Show | 12 | HG01109.hp1 HG01884.hp1 HG02559.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3625C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 3625 | chr3 | 142161997 | |||||
| chr3:142162366
|
G | C | 18 | a0001c0001t0006a0001c0001t0015a0001c0001t0020others(15): Show | 27 | HG01243.hp2 HG01496.hp2 HG01891.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*3256C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 3256 | chr3 | 142162366 | |||||
| chr3:142162509
|
T | C | 53 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(50): Show | 118 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*3113A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 3113 | chr3 | 142162509 | |||||
| chr3:142162517
|
G | A | 1 | a0001c0001t0069 | 1 | NA19079.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3105C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 3105 | chr3 | 142162517 | |||||
| chr3:142162749
|
G | A | 3 | a0001c0002t0017a0001c0002t0051a0001c0002t0052 | 5 | HG03704.hp2 HG04228.hp1 NA18947.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2873C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2873 | chr3 | 142162749 | |||||
| chr3:142162763
|
C | T | 1 | a0001c0002t0051 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2859G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2859 | chr3 | 142162763 | |||||
| chr3:142162926
|
A | G | 53 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(50): Show | 118 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*2696T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2696 | chr3 | 142162926 | |||||
| chr3:142162945
|
G | A | 1 | a0001c0001t0082 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2677C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2677 | chr3 | 142162945 | |||||
| chr3:142162995
|
C | CA | 14 | a0001c0001t0003a0001c0001t0011a0001c0001t0012others(11): Show | 37 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2626dupT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2626 | chr3 | 142162995 | |||||
| chr3:142162995
|
CA | C | 40 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(37): Show | 81 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*2626delT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2626 | chr3 | 142162995 | |||||
| chr3:142163032
|
C | T | 1 | a0001c0001t0056 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2590G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2590 | chr3 | 142163032 | |||||
| chr3:142163037
|
T | C | 1 | a0001c0001t0071 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2585A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2585 | chr3 | 142163037 | |||||
| chr3:142163085
|
T | C | 1 | a0001c0001t0072 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2537A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2537 | chr3 | 142163085 | |||||
| chr3:142163114
|
T | C | 2 | a0001c0001t0004a0001c0001t0073 | 13 | HG00140.hp2 HG00639.hp2 HG01081.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2508A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2508 | chr3 | 142163114 | |||||
| chr3:142163265
|
A | G | 8 | a0001c0001t0005a0001c0001t0018a0001c0001t0079others(5): Show | 21 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2357T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2357 | chr3 | 142163265 | |||||
| chr3:142163277
|
C | CT | 4 | a0001c0001t0055a0001c0002t0017a0001c0002t0051others(1): Show | 6 | HG02523.hp1 HG03704.hp2 HG04228.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2344dupA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2344 | chr3 | 142163277 | |||||
| chr3:142163277
|
CT | C | 53 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(50): Show | 118 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*2344delA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2344 | chr3 | 142163277 | |||||
| chr3:142163297
|
C | T | 11 | a0001c0001t0005a0001c0001t0008a0001c0001t0018others(8): Show | 30 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2325G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2325 | chr3 | 142163297 | |||||
| chr3:142163303
|
G | A | 2 | a0001c0001t0008a0001c0001t0084 | 7 | HG01433.hp1 HG02615.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2319C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2319 | chr3 | 142163303 | |||||
| chr3:142163305
|
C | T | 1 | a0001c0001t0054 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2317G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2317 | chr3 | 142163305 | |||||
| chr3:142163403
|
TA | T | 2 | a0001c0001t0004a0001c0001t0073 | 13 | HG00140.hp2 HG00639.hp2 HG01081.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2218delT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2218 | chr3 | 142163403 | |||||
| chr3:142163617
|
C | T | 39 | a0001c0001t0005a0001c0001t0006a0001c0001t0008others(36): Show | 70 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*2005G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 2005 | chr3 | 142163617 | |||||
| chr3:142163801
|
C | T | 8 | a0001c0001t0009a0001c0001t0086a0001c0002t0009others(5): Show | 12 | HG01109.hp1 HG01884.hp1 HG02559.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1821G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 1821 | chr3 | 142163801 | |||||
| chr3:142163813
|
C | T | 52 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(49): Show | 114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*1809G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 1809 | chr3 | 142163813 | |||||
| chr3:142164189
|
T | C | 2 | a0001c0001t0004a0001c0001t0073 | 13 | HG00140.hp2 HG00639.hp2 HG01081.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1433A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 1433 | chr3 | 142164189 | |||||
| chr3:142164213
|
A | C | 3 | a0001c0001t0010a0001c0001t0029a0001c0001t0030 | 6 | HG00639.hp1 HG01358.hp2 HG01433.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1409T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 1409 | chr3 | 142164213 | |||||
| chr3:142164496
|
G | A | 1 | a0001c0001t0074 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1126C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 1126 | chr3 | 142164496 | |||||
| chr3:142164570
|
T | C | 1 | a0001c0001t0075 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1052A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 1052 | chr3 | 142164570 | |||||
| chr3:142164651
|
C | T | 1 | a0001c0001t0028 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*971G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 971 | chr3 | 142164651 | |||||
| chr3:142164792
|
G | C | 1 | a0001c0001t0085 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*830C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 830 | chr3 | 142164792 | |||||
| chr3:142165043
|
T | C | 3 | a0001c0001t0026a0001c0001t0076a0001c0001t0077 | 4 | HG01516.hp1 HG01517.hp2 HG02145.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*579A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 579 | chr3 | 142165043 | |||||
| chr3:142165166
|
T | A | 1 | a0001c0001t0078 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*456A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 456 | chr3 | 142165166 | |||||
| chr3:142165457
|
GT | G | 11 | a0001c0001t0005a0001c0001t0008a0001c0001t0018others(8): Show | 30 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*164delA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 164 | chr3 | 142165457 | |||||
| chr3:142165504
|
T | C | 1 | a0001c0001t0013 | 4 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*118A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 16/16 | 118 | chr3 | 142165504 | |||||
| chr3:142225502
|
C | A | 1 | a0001c0001t0086 | 1 | HG01109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-47G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/16 | 47 | chr3 | 142225502 | |||||
| chr3:142225524
|
G | C | 1 | a0001c0001t0026 | 2 | HG01516.hp1 HG01517.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-69C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/16 | chr3 | 142225524 | ||||||
| chr3:142225529
|
C | T | 1 | a0001c0001t0027 | 1 | NA18982.hp2 | 5_prime_UTR_variant | MODIFIER | c.-74G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/16 | 74 | chr3 | 142225529 | |||||
| chr3:142225549
|
C | A | 1 | a0001c0001t0087 | 1 | HG00741.hp2 | 5_prime_UTR_variant | MODIFIER | c.-94G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/16 | 94 | chr3 | 142225549 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:142165966
|
T | C | 4 | a0001c0001t0013g0234a0001c0001t0013g0235a0001c0001t0013g0236others(1): Show | 4 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1442-196A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142165966 | ||||||
| chr3:142166005
|
C | T | 10 | a0001c0001t0004g0002a0001c0001t0004g0008a0001c0001t0004g0028others(7): Show | 13 | HG00140.hp2 HG00639.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1442-235G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142166005 | ||||||
| chr3:142166270
|
A | G | 10 | a0001c0001t0004g0002a0001c0001t0004g0008a0001c0001t0004g0028others(7): Show | 13 | HG00140.hp2 HG00639.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1442-500T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142166270 | ||||||
| chr3:142166288
|
G | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0195a0001c0001t0001g0197others(1): Show | 4 | HG01192.hp2 HG01361.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.1442-518C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142166288 | ||||||
| chr3:142166303
|
T | C | 1 | a0003c0005t0020g0203 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1442-533A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142166303 | ||||||
| chr3:142166646
|
G | GC | 41 | a0001c0001t0005g0005a0001c0001t0005g0016a0001c0001t0005g0019others(38): Show | 42 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.1442-877dupG | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142166646 | ||||||
| chr3:142166659
|
G | A | 1 | a0001c0001t0046g0239 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1442-889C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142166659 | ||||||
| chr3:142166694
|
C | T | 1 | a0001c0001t0013g0236 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1442-924G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142166694 | ||||||
| chr3:142166814
|
T | C | 126 | a0001c0001t0003g0036a0001c0001t0003g0040a0001c0001t0003g0043others(123): Show | 130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1442-1044A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142166814 | ||||||
| chr3:142166824
|
A | G | 1 | a0001c0001t0075g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1442-1054T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142166824 | ||||||
| chr3:142167278
|
G | A | 30 | a0001c0001t0003g0036a0001c0001t0003g0040a0001c0001t0003g0043others(27): Show | 30 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.1442-1508C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142167278 | ||||||
| chr3:142167305
|
C | T | 1 | a0002c0004t0001g0217 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1442-1535G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142167305 | ||||||
| chr3:142167384
|
A | T | 1 | a0001c0001t0003g0211 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1442-1614T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142167384 | ||||||
| chr3:142167385
|
A | T | 126 | a0001c0001t0003g0036a0001c0001t0003g0040a0001c0001t0003g0043others(123): Show | 130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1442-1615T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142167385 | ||||||
| chr3:142167390
|
T | A | 126 | a0001c0001t0003g0036a0001c0001t0003g0040a0001c0001t0003g0043others(123): Show | 130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1442-1620A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142167390 | ||||||
| chr3:142167659
|
C | A | 3 | a0001c0001t0002g0004a0001c0001t0002g0054a0001c0001t0002g0060 | 4 | HG01257.hp2 HG01258.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1442-1889G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142167659 | ||||||
| chr3:142167756
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1442-1986C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142167756 | ||||||
| chr3:142167926
|
C | T | 10 | a0001c0001t0004g0002a0001c0001t0004g0008a0001c0001t0004g0028others(7): Show | 13 | HG00140.hp2 HG00639.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1442-2156G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142167926 | ||||||
| chr3:142167973
|
T | C | 1 | a0001c0001t0010g0171 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1442-2203A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142167973 | ||||||
| chr3:142167979
|
T | C | 1 | a0001c0001t0023g0138 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1442-2209A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142167979 | ||||||
| chr3:142168011
|
C | CAAACA | 31 | a0001c0001t0006g0029a0001c0001t0006g0030a0001c0001t0006g0142others(28): Show | 31 | HG01243.hp2 HG01496.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.1442-2246_1442-224 others(9): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142168011 | ||||||
| chr3:142168011
|
C | CAAACAAA others(3): Show |
1 | a0001c0001t0036g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1442-2251_1442-224 others(14): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142168011 | ||||||
| chr3:142168081
|
G | A | 12 | a0001c0001t0009g0119a0001c0001t0086g0256a0001c0002t0009g0218others(9): Show | 12 | HG01109.hp1 HG01884.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1441+2244C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142168081 | ||||||
| chr3:142168101
|
T | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0134 | 2 | HG02074.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1441+2224A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142168101 | ||||||
| chr3:142168109
|
T | C | 1 | a0001c0002t0052g0176 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1441+2216A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142168109 | ||||||
| chr3:142168143
|
A | C | 4 | a0001c0001t0021g0034a0001c0001t0021g0163a0001c0001t0022g0114others(1): Show | 4 | HG01243.hp2 HG02055.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1441+2182T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142168143 | ||||||
| chr3:142168469
|
A | G | 2 | a0001c0001t0025g0097a0001c0001t0025g0116 | 2 | HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1441+1856T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142168469 | ||||||
| chr3:142168644
|
C | T | 31 | a0001c0001t0006g0029a0001c0001t0006g0030a0001c0001t0006g0142others(28): Show | 31 | HG01243.hp2 HG01496.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.1441+1681G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142168644 | ||||||
| chr3:142168679
|
T | C | 1 | a0001c0001t0075g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1441+1646A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142168679 | ||||||
| chr3:142168682
|
T | C | 3 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0080 | 3 | HG00642.hp1 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1441+1643A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142168682 | ||||||
| chr3:142168733
|
C | A | 1 | a0001c0001t0085g0160 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1441+1592G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142168733 | ||||||
| chr3:142168739
|
C | T | 1 | a0001c0001t0012g0250 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1441+1586G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142168739 | ||||||
| chr3:142168900
|
T | A | 3 | a0001c0001t0033g0153a0001c0001t0035g0154a0001c0001t0036g0232 | 3 | HG02145.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1441+1425A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142168900 | ||||||
| chr3:142168904
|
A | G | 27 | a0001c0001t0003g0036a0001c0001t0003g0040a0001c0001t0003g0043others(24): Show | 27 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1441+1421T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142168904 | ||||||
| chr3:142168986
|
C | A | 1 | a0001c0001t0001g0226 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1441+1339G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142168986 | ||||||
| chr3:142169067
|
G | T | 3 | a0001c0001t0033g0153a0001c0001t0035g0154a0001c0001t0036g0232 | 3 | HG02145.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1441+1258C>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142169067 | ||||||
| chr3:142169161
|
C | T | 41 | a0001c0001t0003g0036a0001c0001t0003g0040a0001c0001t0003g0043others(38): Show | 44 | HG00140.hp2 HG00639.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.1441+1164G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142169161 | ||||||
| chr3:142169236
|
C | T | 1 | a0001c0001t0048g0095 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1441+1089G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142169236 | ||||||
| chr3:142169306
|
T | C | 32 | a0001c0001t0003g0036a0001c0001t0003g0040a0001c0001t0003g0043others(29): Show | 32 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.1441+1019A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142169306 | ||||||
| chr3:142169555
|
T | C | 1 | a0001c0001t0084g0093 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1441+770A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142169555 | ||||||
| chr3:142169669
|
C | CT | 60 | a0001c0001t0004g0002a0001c0001t0004g0008a0001c0001t0004g0028others(57): Show | 64 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.1441+655dupA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142169669 | ||||||
| chr3:142169669
|
C | CTTT | 7 | a0001c0001t0008g0089a0001c0001t0008g0162a0001c0001t0008g0213others(4): Show | 7 | HG01109.hp1 HG01433.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1441+653_1441+655d others(5): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142169669 | ||||||
| chr3:142169669
|
CT | C | 9 | a0001c0001t0001g0020a0001c0001t0001g0056a0001c0001t0021g0034others(6): Show | 9 | HG01169.hp1 HG01243.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.1441+655delA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142169669 | ||||||
| chr3:142169748
|
T | A | 1 | a0001c0001t0021g0034 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1441+577A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142169748 | ||||||
| chr3:142169756
|
T | C | 42 | a0001c0001t0003g0036a0001c0001t0003g0040a0001c0001t0003g0043others(39): Show | 45 | HG00140.hp2 HG00639.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1441+569A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142169756 | ||||||
| chr3:142170055
|
C | T | 4 | a0001c0001t0013g0234a0001c0001t0013g0235a0001c0001t0013g0236others(1): Show | 4 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1441+270G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142170055 | ||||||
| chr3:142170167
|
T | G | 22 | a0001c0001t0005g0005a0001c0001t0005g0016a0001c0001t0005g0019others(19): Show | 23 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.1441+158A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142170167 | ||||||
| chr3:142170181
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1441+144C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142170181 | ||||||
| chr3:142170217
|
C | T | 1 | a0001c0001t0082g0221 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1441+108G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142170217 | ||||||
| chr3:142170241
|
G | T | 2 | a0001c0001t0023g0137a0001c0001t0023g0138 | 2 | HG01496.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1441+84C>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 15/15 | chr3 | 142170241 | ||||||
| chr3:142170540
|
A | G | 12 | a0001c0001t0009g0119a0001c0001t0086g0256a0001c0002t0009g0218others(9): Show | 12 | HG01109.hp1 HG01884.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1308-82T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 14/15 | chr3 | 142170540 | ||||||
| chr3:142170633
|
T | G | 30 | a0001c0001t0006g0029a0001c0001t0006g0030a0001c0001t0006g0142others(27): Show | 30 | HG01243.hp2 HG01496.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.1308-175A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 14/15 | chr3 | 142170633 | ||||||
| chr3:142170641
|
T | A | 1 | a0001c0001t0083g0222 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1308-183A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 14/15 | chr3 | 142170641 | ||||||
| chr3:142170756
|
A | T | 1 | a0002c0004t0001g0217 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1308-298T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 14/15 | chr3 | 142170756 | ||||||
| chr3:142170796
|
A | ATAGC | 115 | a0001c0001t0001g0063a0001c0001t0003g0036a0001c0001t0003g0040others(112): Show | 119 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.1308-339_1308-338i others(6): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 14/15 | chr3 | 142170796 | ||||||
| chr3:142170973
|
A | G | 4 | a0001c0001t0015g0238a0001c0001t0015g0255a0001c0001t0037g0147others(1): Show | 4 | HG02647.hp2 HG02965.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1307+446T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 14/15 | chr3 | 142170973 | ||||||
| chr3:142171156
|
A | C | 1 | a0001c0001t0070g0175 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1307+263T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 14/15 | chr3 | 142171156 | ||||||
| chr3:142171246
|
T | TA | 59 | a0001c0001t0003g0036a0001c0001t0003g0040a0001c0001t0003g0043others(56): Show | 59 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(56): Show |
intron_variant | MODIFIER | c.1307+172dupT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 14/15 | chr3 | 142171246 | ||||||
| chr3:142171247
|
A | T | 11 | a0001c0001t0004g0002a0001c0001t0004g0008a0001c0001t0004g0028others(8): Show | 14 | HG00140.hp2 HG00639.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.1307+172T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 14/15 | chr3 | 142171247 | ||||||
| chr3:142171265
|
T | C | 1 | a0001c0001t0062g0083 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1307+154A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 14/15 | chr3 | 142171265 | ||||||
| chr3:142171670
|
G | A | 4 | a0001c0001t0013g0234a0001c0001t0013g0235a0001c0001t0013g0236others(1): Show | 4 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1248-192C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 13/15 | chr3 | 142171670 | ||||||
| chr3:142171749
|
C | G | 1 | a0001c0001t0004g0084 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1248-271G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 13/15 | chr3 | 142171749 | ||||||
| chr3:142172110
|
A | T | 1 | a0001c0001t0001g0164 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1247+243T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 13/15 | chr3 | 142172110 | ||||||
| chr3:142172123
|
A | G | 10 | a0001c0001t0004g0002a0001c0001t0004g0008a0001c0001t0004g0028others(7): Show | 13 | HG00140.hp2 HG00639.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1247+230T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 13/15 | chr3 | 142172123 | ||||||
| chr3:142172543
|
C | A | 10 | a0001c0001t0004g0002a0001c0001t0004g0008a0001c0001t0004g0028others(7): Show | 13 | HG00140.hp2 HG00639.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1144-87G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142172543 | ||||||
| chr3:142172669
|
T | C | 1 | a0001c0001t0001g0156 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1144-213A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142172669 | ||||||
| chr3:142172703
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1144-247A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142172703 | ||||||
| chr3:142172769
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1144-313G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142172769 | ||||||
| chr3:142172852
|
C | G | 2 | a0001c0001t0001g0121a0001c0001t0012g0120 | 2 | HG02056.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1144-396G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142172852 | ||||||
| chr3:142173031
|
C | T | 1 | a0001c0001t0014g0125 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1144-575G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173031 | ||||||
| chr3:142173130
|
G | A | 1 | a0001c0001t0075g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1144-674C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173130 | ||||||
| chr3:142173199
|
T | TA | 15 | a0001c0001t0001g0063a0001c0001t0001g0077a0001c0001t0001g0080others(12): Show | 15 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.1144-744dupT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173199 | ||||||
| chr3:142173199
|
TA | T | 33 | a0001c0001t0002g0031a0001c0001t0003g0036a0001c0001t0003g0040others(30): Show | 33 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.1144-744delT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173199 | ||||||
| chr3:142173224
|
C | CA | 27 | a0001c0001t0006g0029a0001c0001t0006g0030a0001c0001t0006g0142others(24): Show | 27 | HG01243.hp2 HG01496.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1144-769dupT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173224 | ||||||
| chr3:142173459
|
G | A | 1 | a0001c0001t0075g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1144-1003C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173459 | ||||||
| chr3:142173485
|
C | T | 2 | a0001c0001t0003g0040a0001c0001t0047g0039 | 2 | HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1144-1029G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173485 | ||||||
| chr3:142173530
|
A | G | 1 | a0001c0001t0008g0233 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1144-1074T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173530 | ||||||
| chr3:142173550
|
G | A | 6 | a0001c0001t0008g0089a0001c0001t0008g0162a0001c0001t0008g0213others(3): Show | 6 | HG01433.hp1 HG02615.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1144-1094C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173550 | ||||||
| chr3:142173578
|
G | T | 10 | a0001c0001t0004g0002a0001c0001t0004g0008a0001c0001t0004g0028others(7): Show | 13 | HG00140.hp2 HG00639.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1144-1122C>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173578 | ||||||
| chr3:142173609
|
G | A | 7 | a0001c0001t0008g0089a0001c0001t0008g0162a0001c0001t0008g0213others(4): Show | 7 | HG01433.hp1 HG02615.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-1153C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173609 | ||||||
| chr3:142173615
|
C | T | 3 | a0001c0001t0003g0152a0001c0001t0003g0211a0001c0001t0003g0212 | 3 | HG01255.hp1 HG02486.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1144-1159G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173615 | ||||||
| chr3:142173632
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1144-1176C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173632 | ||||||
| chr3:142173683
|
C | CAAAACA | 37 | a0001c0001t0001g0063a0001c0001t0001g0244a0001c0001t0005g0005others(34): Show | 38 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.1144-1233_1144-122 others(10): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173683 | ||||||
| chr3:142173683
|
C | CAAAACAA others(5): Show |
1 | a0001c0001t0005g0072 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1144-1239_1144-122 others(16): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173683 | ||||||
| chr3:142173683
|
C | CAAAACAA others(11): Show |
1 | a0001c0001t0075g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1144-1245_1144-122 others(22): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173683 | ||||||
| chr3:142173683
|
CAAAACA | C | 54 | a0001c0001t0003g0036a0001c0001t0003g0040a0001c0001t0003g0043others(51): Show | 57 | HG00140.hp2 HG00639.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.1144-1233_1144-122 others(10): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173683 | ||||||
| chr3:142173743
|
G | T | 2 | a0001c0001t0001g0121a0001c0001t0012g0120 | 2 | HG02056.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1144-1287C>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173743 | ||||||
| chr3:142173805
|
T | C | 42 | a0001c0001t0003g0036a0001c0001t0003g0040a0001c0001t0003g0043others(39): Show | 45 | HG00140.hp2 HG00639.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1144-1349A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173805 | ||||||
| chr3:142173834
|
G | A | 27 | a0001c0001t0006g0029a0001c0001t0006g0030a0001c0001t0006g0142others(24): Show | 27 | HG01243.hp2 HG01496.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1144-1378C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173834 | ||||||
| chr3:142173911
|
C | T | 2 | a0001c0001t0027g0013a0001c0001t0054g0227 | 2 | NA18982.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1144-1455G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173911 | ||||||
| chr3:142173968
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1144-1512C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142173968 | ||||||
| chr3:142174126
|
C | G | 28 | a0001c0001t0006g0029a0001c0001t0006g0030a0001c0001t0006g0142others(25): Show | 28 | HG01243.hp2 HG01496.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1144-1670G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142174126 | ||||||
| chr3:142174214
|
T | C | 1 | a0001c0001t0001g0001 | 3 | HG02559.hp2 HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1144-1758A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142174214 | ||||||
| chr3:142174386
|
G | A | 5 | a0001c0001t0003g0152a0001c0001t0003g0211a0001c0001t0003g0212others(2): Show | 5 | HG01255.hp1 HG02486.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1144-1930C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142174386 | ||||||
| chr3:142174665
|
A | G | 1 | a0001c0001t0084g0093 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1144-2209T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142174665 | ||||||
| chr3:142174725
|
TC | T | 4 | a0001c0001t0003g0061a0001c0001t0009g0119a0001c0002t0009g0251others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1144-2270delG | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142174725 | ||||||
| chr3:142174922
|
T | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0022g0158others(1): Show | 6 | HG02559.hp2 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1144-2466A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142174922 | ||||||
| chr3:142175059
|
G | A | 108 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0056others(105): Show | 109 | HG00099.hp1 HG00642.hp2 HG00738.hp1 others(106): Show |
intron_variant | MODIFIER | c.1143+2423C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142175059 | ||||||
| chr3:142175191
|
T | A | 89 | a0001c0001t0001g0006a0001c0001t0001g0056a0001c0001t0001g0057others(86): Show | 90 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(87): Show |
intron_variant | MODIFIER | c.1143+2291A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142175191 | ||||||
| chr3:142175414
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1143+2068G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142175414 | ||||||
| chr3:142175588
|
C | T | 130 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(127): Show | 132 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(129): Show |
intron_variant | MODIFIER | c.1143+1894G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142175588 | ||||||
| chr3:142175837
|
TATTATTA others(13): Show |
T | 2 | a0001c0001t0014g0208a0001c0001t0031g0207 | 2 | HG00099.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.1143+1625_1143+164 others(24): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142175837 | ||||||
| chr3:142175854
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1143+1628A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142175854 | ||||||
| chr3:142176047
|
T | C | 2 | a0001c0001t0001g0071a0001c0001t0007g0169 | 2 | NA18950.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1143+1435A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176047 | ||||||
| chr3:142176074
|
A | G | 1 | a0001c0001t0001g0102 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1143+1408T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176074 | ||||||
| chr3:142176131
|
T | G | 1 | a0001c0001t0001g0134 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1143+1351A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176131 | ||||||
| chr3:142176208
|
A | G | 2 | a0001c0001t0001g0122a0001c0001t0002g0025 | 2 | HG02886.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1143+1274T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176208 | ||||||
| chr3:142176333
|
G | C | 43 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0024others(40): Show | 43 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.1143+1149C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176333 | ||||||
| chr3:142176337
|
A | C | 3 | a0001c0001t0001g0240a0001c0001t0003g0152a0001c0001t0025g0116 | 3 | HG02486.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1143+1145T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176337 | ||||||
| chr3:142176345
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1143+1137C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176345 | ||||||
| chr3:142176352
|
A | G | 2 | a0001c0001t0014g0041a0001c0001t0032g0042 | 2 | HG03831.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1143+1130T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176352 | ||||||
| chr3:142176361
|
T | C | 1 | a0001c0001t0001g0240 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1143+1121A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176361 | ||||||
| chr3:142176402
|
G | T | 2 | a0001c0001t0033g0153a0001c0001t0035g0154 | 2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1143+1080C>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176402 | ||||||
| chr3:142176497
|
A | T | 1 | a0001c0001t0001g0122 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1143+985T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176497 | ||||||
| chr3:142176607
|
T | G | 1 | a0001c0002t0034g0044 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1143+875A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176607 | ||||||
| chr3:142176658
|
A | AT | 28 | a0001c0001t0001g0134a0001c0001t0001g0181a0001c0001t0001g0197others(25): Show | 28 | HG00621.hp2 HG00741.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.1143+823dupA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176658 | ||||||
| chr3:142176658
|
AT | A | 22 | a0001c0001t0001g0057a0001c0001t0001g0170a0001c0001t0003g0043others(19): Show | 22 | HG01168.hp1 HG01433.hp2 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.1143+823delA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176658 | ||||||
| chr3:142176725
|
C | CATG | 145 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(142): Show | 147 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(144): Show |
intron_variant | MODIFIER | c.1143+756_1143+757i others(5): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176725 | ||||||
| chr3:142176731
|
G | A | 11 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0127others(8): Show | 11 | HG01496.hp2 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1143+751C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176731 | ||||||
| chr3:142176736
|
A | C | 3 | a0001c0001t0001g0240a0001c0001t0003g0152a0001c0001t0025g0116 | 3 | HG02486.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1143+746T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176736 | ||||||
| chr3:142176766
|
A | G | 2 | a0001c0001t0033g0153a0001c0001t0035g0154 | 2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1143+716T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176766 | ||||||
| chr3:142176770
|
T | C | 2 | a0001c0001t0001g0071a0001c0001t0007g0169 | 2 | NA18950.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1143+712A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176770 | ||||||
| chr3:142176879
|
T | G | 1 | a0001c0001t0001g0099 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1143+603A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176879 | ||||||
| chr3:142176953
|
G | A | 2 | a0001c0001t0033g0153a0001c0001t0035g0154 | 2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1143+529C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142176953 | ||||||
| chr3:142177088
|
A | G | 1 | a0001c0002t0003g0242 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1143+394T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142177088 | ||||||
| chr3:142177268
|
A | G | 2 | a0001c0001t0024g0049a0001c0001t0024g0050 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1143+214T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142177268 | ||||||
| chr3:142177476
|
A | G | 1 | a0001c0001t0007g0209 | 1 | HG01106.hp2 | splice_region_variant&intron_variant | LOW | c.1143+6T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 12/15 | chr3 | 142177476 | ||||||
| chr3:142177680
|
T | A | 43 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0024others(40): Show | 43 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.1049-104A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142177680 | ||||||
| chr3:142177690
|
T | C | 43 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0024others(40): Show | 43 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.1049-114A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142177690 | ||||||
| chr3:142177711
|
C | T | 16 | a0001c0001t0006g0029a0001c0001t0006g0030a0001c0001t0006g0142others(13): Show | 16 | HG01891.hp2 HG02280.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.1049-135G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142177711 | ||||||
| chr3:142177787
|
T | C | 2 | a0001c0001t0046g0239a0001c0001t0082g0221 | 2 | HG03471.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1049-211A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142177787 | ||||||
| chr3:142177791
|
A | T | 16 | a0001c0001t0006g0029a0001c0001t0006g0030a0001c0001t0006g0142others(13): Show | 16 | HG01891.hp2 HG02280.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.1049-215T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142177791 | ||||||
| chr3:142177831
|
T | C | 10 | a0001c0001t0001g0063a0001c0001t0001g0253a0001c0001t0001g0254others(7): Show | 10 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.1049-255A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142177831 | ||||||
| chr3:142177842
|
A | C | 145 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(142): Show | 147 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(144): Show |
intron_variant | MODIFIER | c.1049-266T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142177842 | ||||||
| chr3:142177855
|
T | G | 1 | a0001c0002t0017g0216 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1049-279A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142177855 | ||||||
| chr3:142177857
|
C | CT | 6 | a0001c0001t0004g0028a0001c0001t0009g0119a0001c0001t0011g0092others(3): Show | 6 | HG01175.hp1 HG01884.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1049-282dupA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142177857 | ||||||
| chr3:142177857
|
CT | C | 59 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0024others(56): Show | 60 | HG00639.hp1 HG01081.hp2 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.1049-282delA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142177857 | ||||||
| chr3:142177867
|
T | C | 3 | a0001c0001t0001g0240a0001c0001t0003g0152a0001c0001t0025g0116 | 3 | HG02486.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1049-291A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142177867 | ||||||
| chr3:142178016
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1049-440C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142178016 | ||||||
| chr3:142178044
|
G | A | 1 | a0001c0001t0062g0083 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1049-468C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142178044 | ||||||
| chr3:142178137
|
C | T | 104 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(101): Show | 105 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(102): Show |
intron_variant | MODIFIER | c.1049-561G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142178137 | ||||||
| chr3:142178140
|
G | T | 43 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0024others(40): Show | 43 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.1049-564C>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142178140 | ||||||
| chr3:142178144
|
C | T | 2 | a0001c0001t0014g0208a0001c0001t0031g0207 | 2 | HG00099.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.1049-568G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142178144 | ||||||
| chr3:142178160
|
T | C | 3 | a0001c0001t0001g0240a0001c0001t0003g0152a0001c0001t0025g0116 | 3 | HG02486.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1049-584A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142178160 | ||||||
| chr3:142178242
|
A | G | 1 | a0001c0001t0001g0199 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1049-666T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142178242 | ||||||
| chr3:142178410
|
T | A | 2 | a0001c0001t0033g0153a0001c0001t0035g0154 | 2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1049-834A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142178410 | ||||||
| chr3:142178553
|
C | T | 1 | a0001c0001t0057g0103 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1049-977G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142178553 | ||||||
| chr3:142178686
|
G | C | 1 | a0001c0001t0074g0190 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1049-1110C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142178686 | ||||||
| chr3:142178755
|
T | C | 4 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0003g0040others(1): Show | 4 | HG01168.hp1 HG01169.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1049-1179A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142178755 | ||||||
| chr3:142178889
|
C | A | 1 | a0001c0001t0075g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1049-1313G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142178889 | ||||||
| chr3:142179056
|
TAAAGTGA others(7): Show |
T | 3 | a0001c0001t0001g0240a0001c0001t0003g0152a0001c0001t0025g0116 | 3 | HG02486.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1049-1494_1049-148 others(18): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142179056 | ||||||
| chr3:142179502
|
C | T | 1 | a0001c0001t0023g0138 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1049-1926G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142179502 | ||||||
| chr3:142179816
|
T | C | 145 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(142): Show | 147 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(144): Show |
intron_variant | MODIFIER | c.1048+1645A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142179816 | ||||||
| chr3:142179860
|
C | T | 1 | a0001c0001t0018g0069 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1048+1601G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142179860 | ||||||
| chr3:142180135
|
G | A | 39 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0099others(36): Show | 40 | HG00639.hp1 HG01081.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.1048+1326C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142180135 | ||||||
| chr3:142180138
|
T | C | 103 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(100): Show | 105 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(102): Show |
intron_variant | MODIFIER | c.1048+1323A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142180138 | ||||||
| chr3:142180269
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1048+1192C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142180269 | ||||||
| chr3:142180306
|
TC | T | 5 | a0001c0002t0017g0187a0001c0002t0017g0189a0001c0002t0017g0216others(2): Show | 5 | HG03704.hp2 HG04228.hp1 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.1048+1154delG | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142180306 | ||||||
| chr3:142180307
|
C | CT | 6 | a0001c0001t0003g0152a0001c0001t0005g0072a0001c0001t0025g0116others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.1048+1153dupA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142180307 | ||||||
| chr3:142180372
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0090 | 3 | HG02280.hp2 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1048+1089C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142180372 | ||||||
| chr3:142180451
|
C | T | 1 | a0001c0001t0002g0004 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1048+1010G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142180451 | ||||||
| chr3:142180464
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1048+997C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142180464 | ||||||
| chr3:142180494
|
G | C | 8 | a0001c0001t0001g0020a0001c0001t0005g0016a0001c0001t0005g0019others(5): Show | 8 | HG02040.hp1 HG02071.hp2 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.1048+967C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142180494 | ||||||
| chr3:142180521
|
C | T | 3 | a0001c0001t0001g0240a0001c0001t0003g0152a0001c0001t0025g0116 | 3 | HG02486.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1048+940G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142180521 | ||||||
| chr3:142180764
|
A | G | 1 | a0001c0001t0005g0091 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1048+697T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142180764 | ||||||
| chr3:142180819
|
G | A | 6 | a0001c0001t0002g0106a0001c0001t0010g0033a0001c0001t0010g0108others(3): Show | 6 | HG00639.hp1 HG01081.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.1048+642C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142180819 | ||||||
| chr3:142180917
|
G | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0068a0001c0001t0001g0075others(1): Show | 6 | HG02559.hp2 HG02572.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1048+544C>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142180917 | ||||||
| chr3:142181190
|
C | G | 1 | a0001c0001t0011g0148 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1048+271G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142181190 | ||||||
| chr3:142181207
|
G | A | 1 | a0001c0001t0083g0222 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1048+254C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142181207 | ||||||
| chr3:142181211
|
A | G | 2 | a0001c0001t0003g0212a0001c0001t0008g0089 | 2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1048+250T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142181211 | ||||||
| chr3:142181328
|
T | C | 1 | a0001c0001t0046g0239 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1048+133A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142181328 | ||||||
| chr3:142181412
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1048+49A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 11/15 | chr3 | 142181412 | ||||||
| chr3:142181585
|
A | C | 2 | a0001c0001t0033g0153a0001c0001t0035g0154 | 2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.944-20T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 10/15 | chr3 | 142181585 | ||||||
| chr3:142181782
|
T | C | 1 | a0001c0001t0025g0097 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.944-217A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 10/15 | chr3 | 142181782 | ||||||
| chr3:142181886
|
G | A | 13 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0127others(10): Show | 13 | HG01496.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.944-321C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 10/15 | chr3 | 142181886 | ||||||
| chr3:142181925
|
T | C | 17 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0003g0040others(14): Show | 17 | HG00738.hp2 HG01074.hp1 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.944-360A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 10/15 | chr3 | 142181925 | ||||||
| chr3:142182128
|
C | T | 7 | a0001c0001t0001g0118a0001c0001t0007g0105a0001c0001t0007g0111others(4): Show | 7 | HG01099.hp1 HG01106.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.944-563G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 10/15 | chr3 | 142182128 | ||||||
| chr3:142182350
|
A | ATTTTTTT others(4): Show |
2 | a0001c0001t0003g0152a0001c0001t0025g0116 | 2 | HG02486.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.943+562_943+572dup others(11): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 10/15 | chr3 | 142182350 | ||||||
| chr3:142182406
|
G | A | 1 | a0001c0001t0036g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.943+517C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 10/15 | chr3 | 142182406 | ||||||
| chr3:142182569
|
G | C | 1 | a0001c0001t0083g0222 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.943+354C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 10/15 | chr3 | 142182569 | ||||||
| chr3:142183106
|
T | C | 2 | a0001c0001t0001g0121a0001c0001t0012g0120 | 2 | HG02056.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.817-57A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142183106 | ||||||
| chr3:142183232
|
C | T | 31 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0099others(28): Show | 32 | HG00639.hp1 HG01081.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.817-183G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142183232 | ||||||
| chr3:142183420
|
A | G | 2 | a0001c0001t0004g0166a0001c0001t0005g0165 | 2 | NA18952.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.817-371T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142183420 | ||||||
| chr3:142183422
|
T | C | 1 | a0001c0001t0006g0029 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.817-373A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142183422 | ||||||
| chr3:142183435
|
A | G | 1 | a0001c0002t0052g0176 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.817-386T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142183435 | ||||||
| chr3:142183658
|
A | G | 12 | a0001c0002t0003g0242a0001c0002t0009g0218a0001c0002t0009g0219others(9): Show | 12 | HG02559.hp1 HG02602.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.817-609T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142183658 | ||||||
| chr3:142183778
|
T | G | 31 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0099others(28): Show | 32 | HG00639.hp1 HG01081.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.817-729A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142183778 | ||||||
| chr3:142183819
|
A | C | 1 | a0001c0001t0035g0154 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.817-770T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142183819 | ||||||
| chr3:142183996
|
C | T | 2 | a0001c0001t0033g0153a0001c0001t0035g0154 | 2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.817-947G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142183996 | ||||||
| chr3:142183997
|
G | A | 1 | a0001c0001t0074g0190 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.817-948C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142183997 | ||||||
| chr3:142184046
|
C | T | 2 | a0001c0001t0015g0238a0001c0001t0015g0255 | 2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.817-997G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184046 | ||||||
| chr3:142184086
|
A | G | 5 | a0001c0002t0009g0218a0001c0002t0009g0219a0001c0002t0009g0251others(2): Show | 5 | HG02559.hp1 HG02896.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.817-1037T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184086 | ||||||
| chr3:142184131
|
G | A | 14 | a0001c0001t0001g0006a0001c0001t0001g0090a0001c0002t0003g0242others(11): Show | 15 | HG02280.hp2 HG02559.hp1 HG02602.hp1 others(12): Show |
intron_variant | MODIFIER | c.817-1082C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184131 | ||||||
| chr3:142184198
|
T | G | 1 | a0001c0001t0001g0074 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.817-1149A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184198 | ||||||
| chr3:142184260
|
C | CA | 26 | a0001c0001t0001g0063a0001c0001t0001g0240a0001c0001t0001g0241others(23): Show | 27 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.817-1212dupT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184260 | ||||||
| chr3:142184260
|
C | CAA | 6 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0127others(3): Show | 6 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.817-1213_817-1212d others(4): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184260 | ||||||
| chr3:142184260
|
C | CAAA | 13 | a0001c0001t0001g0102a0001c0001t0005g0019a0001c0001t0033g0153others(10): Show | 13 | HG02559.hp1 HG02809.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.817-1214_817-1212d others(5): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184260 | ||||||
| chr3:142184260
|
C | CAAAA | 53 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(50): Show | 55 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.817-1215_817-1212d others(6): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184260 | ||||||
| chr3:142184260
|
C | CAAAAA | 30 | a0001c0001t0001g0015a0001c0001t0001g0090a0001c0001t0001g0100others(27): Show | 30 | HG00639.hp1 HG01099.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.817-1216_817-1212d others(7): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184260 | ||||||
| chr3:142184260
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0019g0151 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.817-1222_817-1212d others(13): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184260 | ||||||
| chr3:142184260
|
C | CAAAAAAA others(5): Show |
3 | a0001c0001t0006g0145a0001c0001t0037g0147a0001c0001t0038g0144 | 3 | HG02630.hp1 HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.817-1223_817-1212d others(14): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184260 | ||||||
| chr3:142184260
|
C | CAAAAAAA others(6): Show |
5 | a0001c0001t0006g0029a0001c0001t0006g0030a0001c0001t0006g0146others(2): Show | 5 | HG01891.hp2 HG02717.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-1224_817-1212d others(15): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184260 | ||||||
| chr3:142184260
|
C | CAAAAAAA others(7): Show |
5 | a0001c0001t0006g0142a0001c0001t0039g0115a0001c0001t0040g0037others(2): Show | 5 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.817-1225_817-1212d others(16): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184260 | ||||||
| chr3:142184260
|
C | CAAAAAAA others(8): Show |
2 | a0001c0001t0042g0143a0001c0001t0043g0150 | 2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.817-1226_817-1212d others(17): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184260 | ||||||
| chr3:142184275
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.817-1226T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184275 | ||||||
| chr3:142184578
|
C | T | 1 | a0001c0001t0002g0085 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.816+1351G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184578 | ||||||
| chr3:142184663
|
C | T | 2 | a0001c0001t0033g0153a0001c0001t0035g0154 | 2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.816+1266G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184663 | ||||||
| chr3:142184956
|
G | A | 3 | a0001c0001t0001g0240a0001c0001t0003g0152a0001c0001t0025g0116 | 3 | HG02486.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.816+973C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142184956 | ||||||
| chr3:142185063
|
C | A | 146 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(143): Show | 148 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(145): Show |
intron_variant | MODIFIER | c.816+866G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142185063 | ||||||
| chr3:142185145
|
A | G | 146 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(143): Show | 148 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(145): Show |
intron_variant | MODIFIER | c.816+784T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142185145 | ||||||
| chr3:142185150
|
T | A | 11 | a0001c0001t0001g0230a0001c0001t0003g0211a0001c0001t0003g0212others(8): Show | 11 | HG01175.hp2 HG01255.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.816+779A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142185150 | ||||||
| chr3:142185345
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.816+584G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142185345 | ||||||
| chr3:142185412
|
CA | C | 123 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(120): Show | 125 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(122): Show |
intron_variant | MODIFIER | c.816+516delT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142185412 | ||||||
| chr3:142185412
|
CAA | C | 22 | a0001c0001t0001g0063a0001c0001t0001g0100a0001c0001t0001g0122others(19): Show | 22 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.816+515_816+516del others(2): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142185412 | ||||||
| chr3:142185413
|
A | G | 1 | a0001c0001t0064g0214 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.816+516T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142185413 | ||||||
| chr3:142185632
|
C | T | 146 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(143): Show | 148 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(145): Show |
intron_variant | MODIFIER | c.816+297G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142185632 | ||||||
| chr3:142185689
|
G | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0090 | 3 | HG02280.hp2 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.816+240C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 9/15 | chr3 | 142185689 | ||||||
| chr3:142186080
|
G | C | 10 | a0001c0001t0009g0119a0001c0001t0011g0092a0001c0001t0011g0094others(7): Show | 10 | HG00738.hp1 HG01123.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.756-91C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 8/15 | chr3 | 142186080 | ||||||
| chr3:142186130
|
C | T | 1 | a0001c0002t0017g0216 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.755+64G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 8/15 | chr3 | 142186130 | ||||||
| chr3:142186135
|
G | A | 147 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(144): Show | 149 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(146): Show |
intron_variant | MODIFIER | c.755+59C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 8/15 | chr3 | 142186135 | ||||||
| chr3:142186339
|
T | C | 1 | a0001c0001t0002g0085 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.682-72A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 7/15 | chr3 | 142186339 | ||||||
| chr3:142186411
|
C | A | 47 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0099others(44): Show | 48 | HG00639.hp1 HG01081.hp2 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.681+41G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 7/15 | chr3 | 142186411 | ||||||
| chr3:142186417
|
T | G | 47 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0099others(44): Show | 48 | HG00639.hp1 HG01081.hp2 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.681+35A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 7/15 | chr3 | 142186417 | ||||||
| chr3:142186419
|
T | G | 47 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0099others(44): Show | 48 | HG00639.hp1 HG01081.hp2 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.681+33A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 7/15 | chr3 | 142186419 | ||||||
| chr3:142186435
|
GA | G | 13 | a0001c0001t0001g0156a0001c0002t0003g0242a0001c0002t0009g0218others(10): Show | 13 | HG02559.hp1 HG02602.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.681+16delT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 7/15 | chr3 | 142186435 | ||||||
| chr3:142186444
|
A | T | 1 | a0001c0001t0046g0239 | 1 | HG03471.hp1 | splice_region_variant&intron_variant | LOW | c.681+8T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 7/15 | chr3 | 142186444 | ||||||
| chr3:142186572
|
G | A | 3 | a0001c0001t0006g0030a0001c0001t0040g0037a0001c0001t0041g0038 | 3 | HG02486.hp1 HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.620-59C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 6/15 | chr3 | 142186572 | ||||||
| chr3:142186630
|
C | CT | 19 | a0001c0001t0001g0063a0001c0001t0001g0075a0001c0001t0001g0197others(16): Show | 19 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.620-118dupA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 6/15 | chr3 | 142186630 | ||||||
| chr3:142186630
|
CT | C | 8 | a0001c0001t0001g0122a0001c0001t0001g0130a0001c0001t0001g0240others(5): Show | 8 | HG01257.hp1 HG02486.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.620-118delA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 6/15 | chr3 | 142186630 | ||||||
| chr3:142186632
|
T | C | 1 | a0001c0001t0004g0008 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.620-119A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 6/15 | chr3 | 142186632 | ||||||
| chr3:142186769
|
T | G | 80 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0099others(77): Show | 81 | HG00639.hp1 HG01081.hp2 HG01099.hp1 others(78): Show |
intron_variant | MODIFIER | c.620-256A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 6/15 | chr3 | 142186769 | ||||||
| chr3:142186778
|
G | A | 6 | a0001c0001t0002g0106a0001c0001t0010g0033a0001c0001t0010g0108others(3): Show | 6 | HG00639.hp1 HG01081.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.620-265C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 6/15 | chr3 | 142186778 | ||||||
| chr3:142186788
|
A | G | 146 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(143): Show | 148 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(145): Show |
intron_variant | MODIFIER | c.620-275T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 6/15 | chr3 | 142186788 | ||||||
| chr3:142186863
|
T | C | 3 | a0001c0001t0001g0240a0001c0001t0003g0152a0001c0001t0025g0116 | 3 | HG02486.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.620-350A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 6/15 | chr3 | 142186863 | ||||||
| chr3:142187042
|
C | T | 1 | a0001c0001t0043g0150 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.620-529G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 6/15 | chr3 | 142187042 | ||||||
| chr3:142187341
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.619+363G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 6/15 | chr3 | 142187341 | ||||||
| chr3:142187555
|
T | C | 2 | a0001c0001t0001g0121a0001c0001t0012g0120 | 2 | HG02056.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.619+149A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 6/15 | chr3 | 142187555 | ||||||
| chr3:142187575
|
C | A | 3 | a0001c0001t0001g0240a0001c0001t0003g0152a0001c0001t0025g0116 | 3 | HG02486.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.619+129G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 6/15 | chr3 | 142187575 | ||||||
| chr3:142187604
|
C | CA | 15 | a0001c0001t0001g0128a0001c0001t0001g0172a0001c0001t0001g0197others(12): Show | 15 | HG01175.hp1 HG01358.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.619+99dupT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 6/15 | chr3 | 142187604 | ||||||
| chr3:142187604
|
CA | C | 15 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0063others(12): Show | 16 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.619+99delT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 6/15 | chr3 | 142187604 | ||||||
| chr3:142187996
|
A | G | 1 | a0003c0005t0020g0203 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.544-217T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142187996 | ||||||
| chr3:142188032
|
C | T | 3 | a0001c0001t0001g0240a0001c0001t0003g0152a0001c0001t0025g0116 | 3 | HG02486.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.544-253G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142188032 | ||||||
| chr3:142188125
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.544-346C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142188125 | ||||||
| chr3:142188163
|
G | A | 42 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0024others(39): Show | 42 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.544-384C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142188163 | ||||||
| chr3:142188300
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.544-521C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142188300 | ||||||
| chr3:142188322
|
G | C | 1 | a0001c0001t0003g0040 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.544-543C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142188322 | ||||||
| chr3:142188342
|
T | C | 1 | a0001c0001t0035g0154 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.544-563A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142188342 | ||||||
| chr3:142188357
|
C | T | 4 | a0001c0001t0013g0234a0001c0001t0013g0235a0001c0001t0013g0236others(1): Show | 4 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-578G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142188357 | ||||||
| chr3:142188464
|
G | A | 18 | a0001c0001t0006g0029a0001c0001t0006g0030a0001c0001t0006g0142others(15): Show | 18 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.544-685C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142188464 | ||||||
| chr3:142188541
|
C | CA | 6 | a0001c0001t0001g0007a0001c0001t0001g0102a0001c0001t0001g0104others(3): Show | 7 | HG04115.hp2 NA18941.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.544-763dupT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142188541 | ||||||
| chr3:142188561
|
G | C | 18 | a0001c0001t0006g0029a0001c0001t0006g0030a0001c0001t0006g0142others(15): Show | 18 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.544-782C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142188561 | ||||||
| chr3:142188627
|
A | G | 3 | a0001c0001t0001g0240a0001c0001t0003g0152a0001c0001t0025g0116 | 3 | HG02486.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.544-848T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142188627 | ||||||
| chr3:142188734
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.544-955C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142188734 | ||||||
| chr3:142188835
|
C | T | 2 | a0001c0001t0044g0140a0001c0001t0045g0139 | 2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.544-1056G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142188835 | ||||||
| chr3:142188837
|
A | G | 13 | a0001c0001t0001g0156a0001c0002t0003g0242a0001c0002t0009g0218others(10): Show | 13 | HG02559.hp1 HG02602.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.544-1058T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142188837 | ||||||
| chr3:142189724
|
C | T | 6 | a0001c0001t0003g0211a0001c0001t0003g0212a0001c0001t0006g0210others(3): Show | 6 | HG01255.hp1 HG02809.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.544-1945G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142189724 | ||||||
| chr3:142190161
|
G | A | 3 | a0001c0001t0006g0030a0001c0001t0040g0037a0001c0001t0041g0038 | 3 | HG02486.hp1 HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.544-2382C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142190161 | ||||||
| chr3:142190319
|
C | T | 5 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0127others(2): Show | 5 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.544-2540G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142190319 | ||||||
| chr3:142190331
|
A | G | 20 | a0001c0001t0001g0063a0001c0001t0001g0122a0001c0001t0003g0061others(17): Show | 20 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.544-2552T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142190331 | ||||||
| chr3:142190351
|
C | T | 42 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0024others(39): Show | 42 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.544-2572G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142190351 | ||||||
| chr3:142190455
|
C | A | 1 | a0001c0001t0060g0186 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.544-2676G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142190455 | ||||||
| chr3:142190639
|
A | C | 145 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(142): Show | 146 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(143): Show |
intron_variant | MODIFIER | c.544-2860T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142190639 | ||||||
| chr3:142190713
|
T | C | 1 | a0001c0001t0036g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.544-2934A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142190713 | ||||||
| chr3:142191002
|
A | G | 3 | a0001c0001t0001g0240a0001c0001t0003g0152a0001c0001t0025g0116 | 3 | HG02486.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.544-3223T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142191002 | ||||||
| chr3:142191048
|
AT | A | 50 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0099others(47): Show | 51 | HG00639.hp1 HG01081.hp2 HG01099.hp1 others(48): Show |
intron_variant | MODIFIER | c.544-3270delA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142191048 | ||||||
| chr3:142191189
|
C | T | 1 | a0001c0001t0001g0179 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.544-3410G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142191189 | ||||||
| chr3:142191319
|
C | T | 42 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0024others(39): Show | 42 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.544-3540G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142191319 | ||||||
| chr3:142191870
|
G | A | 2 | a0001c0001t0044g0140a0001c0001t0045g0139 | 2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.544-4091C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142191870 | ||||||
| chr3:142191899
|
G | A | 4 | a0001c0001t0013g0234a0001c0001t0013g0235a0001c0001t0013g0236others(1): Show | 4 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-4120C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142191899 | ||||||
| chr3:142192095
|
T | C | 31 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0099others(28): Show | 32 | HG00639.hp1 HG01081.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.544-4316A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142192095 | ||||||
| chr3:142192564
|
G | C | 13 | a0001c0001t0001g0156a0001c0002t0003g0242a0001c0002t0009g0218others(10): Show | 13 | HG02559.hp1 HG02602.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.544-4785C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142192564 | ||||||
| chr3:142192570
|
C | G | 3 | a0001c0001t0006g0030a0001c0001t0040g0037a0001c0001t0041g0038 | 3 | HG02486.hp1 HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.544-4791G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142192570 | ||||||
| chr3:142192589
|
T | C | 144 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(141): Show | 145 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(142): Show |
intron_variant | MODIFIER | c.544-4810A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142192589 | ||||||
| chr3:142192590
|
C | T | 1 | a0001c0001t0025g0116 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.544-4811G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142192590 | ||||||
| chr3:142192664
|
T | C | 3 | a0001c0001t0001g0240a0001c0001t0003g0152a0001c0001t0025g0116 | 3 | HG02486.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.544-4885A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142192664 | ||||||
| chr3:142192758
|
T | C | 147 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(144): Show | 149 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(146): Show |
intron_variant | MODIFIER | c.544-4979A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142192758 | ||||||
| chr3:142192763
|
C | CA | 14 | a0001c0001t0001g0118a0001c0001t0001g0173a0001c0001t0001g0193others(11): Show | 14 | HG01099.hp1 HG01106.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.544-4985dupT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142192763 | ||||||
| chr3:142192763
|
C | CAA | 18 | a0001c0001t0006g0029a0001c0001t0006g0030a0001c0001t0006g0142others(15): Show | 18 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.544-4986_544-4985d others(4): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142192763 | ||||||
| chr3:142192763
|
CA | C | 6 | a0001c0001t0003g0059a0001c0001t0044g0140a0001c0001t0045g0139others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.544-4985delT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142192763 | ||||||
| chr3:142193086
|
T | G | 1 | a0003c0005t0020g0203 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.544-5307A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142193086 | ||||||
| chr3:142193261
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.544-5482T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142193261 | ||||||
| chr3:142193483
|
C | CA | 33 | a0001c0001t0001g0071a0001c0001t0001g0240a0001c0001t0003g0061others(30): Show | 33 | HG01496.hp2 HG01891.hp2 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.543+5318dupT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142193483 | ||||||
| chr3:142193489
|
A | C | 4 | a0001c0001t0013g0234a0001c0001t0013g0235a0001c0001t0013g0236others(1): Show | 4 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+5313T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142193489 | ||||||
| chr3:142193708
|
T | C | 2 | a0001c0001t0003g0036a0001c0001t0028g0035 | 2 | HG02615.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.543+5094A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142193708 | ||||||
| chr3:142193793
|
T | G | 1 | a0001c0001t0001g0183 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.543+5009A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142193793 | ||||||
| chr3:142193929
|
C | T | 11 | a0001c0001t0001g0230a0001c0001t0003g0211a0001c0001t0003g0212others(8): Show | 11 | HG01175.hp2 HG01255.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.543+4873G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142193929 | ||||||
| chr3:142193983
|
C | T | 1 | a0001c0002t0034g0044 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.543+4819G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142193983 | ||||||
| chr3:142194127
|
G | C | 1 | a0001c0001t0003g0152 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.543+4675C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142194127 | ||||||
| chr3:142194394
|
C | T | 12 | a0001c0001t0001g0122a0001c0001t0003g0061a0001c0001t0003g0062others(9): Show | 12 | HG01496.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.543+4408G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142194394 | ||||||
| chr3:142194489
|
GC | G | 11 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0024others(8): Show | 11 | HG00642.hp1 HG02040.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.543+4312delG | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142194489 | ||||||
| chr3:142194525
|
C | T | 1 | a0001c0001t0058g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.543+4277G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142194525 | ||||||
| chr3:142194527
|
A | G | 1 | a0001c0002t0003g0242 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.543+4275T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142194527 | ||||||
| chr3:142194634
|
T | A | 1 | a0001c0001t0020g0149 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.543+4168A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142194634 | ||||||
| chr3:142194694
|
A | C | 1 | a0001c0001t0001g0099 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.543+4108T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142194694 | ||||||
| chr3:142194724
|
T | C | 147 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(144): Show | 149 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(146): Show |
intron_variant | MODIFIER | c.543+4078A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142194724 | ||||||
| chr3:142194729
|
C | G | 147 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(144): Show | 149 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(146): Show |
intron_variant | MODIFIER | c.543+4073G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142194729 | ||||||
| chr3:142194974
|
C | T | 1 | a0001c0001t0063g0204 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.543+3828G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142194974 | ||||||
| chr3:142195151
|
T | C | 63 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0099others(60): Show | 64 | HG00639.hp1 HG01081.hp2 HG01099.hp1 others(61): Show |
intron_variant | MODIFIER | c.543+3651A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142195151 | ||||||
| chr3:142195314
|
C | T | 1 | a0001c0001t0078g0141 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.543+3488G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142195314 | ||||||
| chr3:142195325
|
T | G | 11 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0127others(8): Show | 11 | HG01496.hp2 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.543+3477A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142195325 | ||||||
| chr3:142195612
|
A | G | 1 | a0003c0005t0020g0203 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.543+3190T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142195612 | ||||||
| chr3:142195654
|
G | C | 1 | a0001c0001t0001g0240 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.543+3148C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142195654 | ||||||
| chr3:142195744
|
T | C | 12 | a0001c0001t0001g0184a0001c0001t0002g0004a0001c0001t0002g0009others(9): Show | 15 | HG01175.hp1 HG01192.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.543+3058A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142195744 | ||||||
| chr3:142196172
|
A | G | 12 | a0001c0001t0001g0122a0001c0001t0003g0061a0001c0001t0003g0062others(9): Show | 12 | HG01496.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.543+2630T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142196172 | ||||||
| chr3:142196514
|
T | A | 1 | a0001c0001t0001g0248 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.543+2288A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142196514 | ||||||
| chr3:142196573
|
C | G | 1 | a0001c0001t0001g0225 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.543+2229G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142196573 | ||||||
| chr3:142196678
|
C | A | 1 | a0001c0001t0001g0080 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.543+2124G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142196678 | ||||||
| chr3:142196723
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0090 | 3 | HG02280.hp2 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.543+2079A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142196723 | ||||||
| chr3:142197079
|
C | T | 1 | a0001c0001t0003g0047 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.543+1723G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142197079 | ||||||
| chr3:142197236
|
T | C | 1 | a0001c0001t0043g0150 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.543+1566A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142197236 | ||||||
| chr3:142197350
|
C | G | 2 | a0001c0001t0044g0140a0001c0001t0045g0139 | 2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.543+1452G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142197350 | ||||||
| chr3:142197413
|
C | T | 137 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(134): Show | 138 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(135): Show |
intron_variant | MODIFIER | c.543+1389G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142197413 | ||||||
| chr3:142197818
|
T | C | 3 | a0001c0001t0001g0240a0001c0001t0003g0152a0001c0001t0025g0116 | 3 | HG02486.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.543+984A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142197818 | ||||||
| chr3:142197820
|
C | T | 3 | a0001c0001t0001g0121a0001c0001t0012g0120a0001c0001t0045g0139 | 3 | HG02056.hp1 HG02165.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.543+982G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142197820 | ||||||
| chr3:142197868
|
C | G | 3 | a0001c0001t0001g0240a0001c0001t0003g0152a0001c0001t0025g0116 | 3 | HG02486.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.543+934G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142197868 | ||||||
| chr3:142197978
|
G | A | 25 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0099others(22): Show | 26 | HG00639.hp1 HG01081.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.543+824C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142197978 | ||||||
| chr3:142198036
|
A | T | 8 | a0001c0001t0001g0063a0001c0001t0014g0041a0001c0001t0014g0125others(5): Show | 8 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.543+766T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142198036 | ||||||
| chr3:142198058
|
T | C | 2 | a0001c0001t0008g0215a0001c0001t0008g0231 | 2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.543+744A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142198058 | ||||||
| chr3:142198253
|
T | C | 1 | a0001c0001t0036g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.543+549A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142198253 | ||||||
| chr3:142198340
|
T | C | 1 | a0001c0002t0009g0251 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.543+462A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142198340 | ||||||
| chr3:142198343
|
C | T | 137 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(134): Show | 138 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(135): Show |
intron_variant | MODIFIER | c.543+459G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142198343 | ||||||
| chr3:142198441
|
C | T | 12 | a0001c0001t0001g0122a0001c0001t0003g0061a0001c0001t0003g0062others(9): Show | 12 | HG01496.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.543+361G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142198441 | ||||||
| chr3:142198714
|
T | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0104a0001c0001t0057g0103 | 4 | NA18956.hp2 NA18982.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+88A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142198714 | ||||||
| chr3:142198790
|
G | A | 1 | a0001c0001t0008g0215 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.543+12C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 5/15 | chr3 | 142198790 | ||||||
| chr3:142198968
|
T | C | 31 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0099others(28): Show | 32 | HG00639.hp1 HG01081.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.412-35A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142198968 | ||||||
| chr3:142198983
|
A | G | 1 | a0001c0001t0016g0131 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.412-50T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142198983 | ||||||
| chr3:142199009
|
G | T | 1 | a0001c0001t0046g0239 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.412-76C>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142199009 | ||||||
| chr3:142199124
|
A | G | 1 | a0001c0001t0046g0239 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.412-191T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142199124 | ||||||
| chr3:142199192
|
T | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0090a0001c0001t0001g0240others(2): Show | 6 | HG02280.hp2 HG02486.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.412-259A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142199192 | ||||||
| chr3:142199225
|
C | T | 1 | a0001c0001t0001g0178 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.412-292G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142199225 | ||||||
| chr3:142199601
|
T | C | 1 | a0001c0001t0001g0130 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.412-668A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142199601 | ||||||
| chr3:142199625
|
A | C | 1 | a0001c0001t0001g0074 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.412-692T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142199625 | ||||||
| chr3:142199857
|
A | T | 147 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(144): Show | 149 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(146): Show |
intron_variant | MODIFIER | c.412-924T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142199857 | ||||||
| chr3:142199864
|
T | C | 42 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0024others(39): Show | 42 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.412-931A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142199864 | ||||||
| chr3:142200087
|
CTA | C | 3 | a0001c0001t0003g0047a0001c0001t0036g0232a0001c0001t0087g0257 | 3 | HG00741.hp2 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.412-1156_412-1155d others(4): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142200087 | ||||||
| chr3:142200096
|
T | C | 6 | a0001c0001t0001g0063a0001c0001t0014g0041a0001c0001t0014g0125others(3): Show | 6 | HG00099.hp1 HG00642.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.412-1163A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142200096 | ||||||
| chr3:142200098
|
T | C | 23 | a0001c0001t0001g0063a0001c0001t0001g0122a0001c0001t0003g0061others(20): Show | 23 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.412-1165A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142200098 | ||||||
| chr3:142200098
|
T | TAC | 11 | a0001c0001t0001g0156a0001c0001t0007g0105a0001c0001t0044g0140others(8): Show | 11 | HG01099.hp1 HG02602.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.412-1167_412-1166d others(4): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142200098 | ||||||
| chr3:142200098
|
T | TACACAC | 17 | a0001c0001t0006g0029a0001c0001t0006g0030a0001c0001t0006g0142others(14): Show | 17 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.412-1171_412-1166d others(8): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142200098 | ||||||
| chr3:142200098
|
TACAC | T | 3 | a0001c0001t0001g0240a0001c0001t0003g0152a0001c0001t0025g0116 | 3 | HG02486.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.412-1169_412-1166d others(6): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142200098 | ||||||
| chr3:142200100
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.412-1167G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142200100 | ||||||
| chr3:142200245
|
T | C | 1 | a0001c0001t0011g0092 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.412-1312A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142200245 | ||||||
| chr3:142200610
|
C | T | 5 | a0001c0001t0013g0234a0001c0001t0013g0235a0001c0001t0013g0236others(2): Show | 5 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.412-1677G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142200610 | ||||||
| chr3:142200668
|
C | A | 1 | a0001c0001t0002g0025 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.412-1735G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142200668 | ||||||
| chr3:142200769
|
A | T | 1 | a0001c0001t0001g0198 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.412-1836T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142200769 | ||||||
| chr3:142201089
|
C | T | 41 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0024others(38): Show | 41 | HG00642.hp1 HG00738.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.412-2156G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142201089 | ||||||
| chr3:142201192
|
T | A | 1 | a0001c0001t0002g0025 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.412-2259A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142201192 | ||||||
| chr3:142201231
|
T | C | 17 | a0001c0001t0001g0156a0001c0001t0001g0230a0001c0001t0005g0072others(14): Show | 17 | HG01175.hp2 HG02559.hp1 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.412-2298A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142201231 | ||||||
| chr3:142201278
|
T | C | 1 | a0001c0001t0018g0086 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.412-2345A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142201278 | ||||||
| chr3:142201426
|
A | C | 4 | a0001c0001t0006g0030a0001c0001t0021g0034a0001c0001t0040g0037others(1): Show | 4 | HG01243.hp2 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.412-2493T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142201426 | ||||||
| chr3:142201592
|
G | A | 164 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(161): Show | 172 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.412-2659C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142201592 | ||||||
| chr3:142201614
|
A | C | 1 | a0001c0001t0064g0214 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.412-2681T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142201614 | ||||||
| chr3:142201627
|
C | T | 2 | a0001c0001t0079g0067a0001c0001t0080g0073 | 2 | HG00597.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.412-2694G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142201627 | ||||||
| chr3:142201631
|
T | C | 1 | a0001c0001t0011g0117 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.412-2698A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142201631 | ||||||
| chr3:142201719
|
C | T | 2 | a0001c0001t0015g0238a0001c0001t0015g0255 | 2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.412-2786G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142201719 | ||||||
| chr3:142201723
|
G | A | 2 | a0001c0001t0025g0116a0003c0005t0020g0203 | 2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.412-2790C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142201723 | ||||||
| chr3:142201725
|
C | A | 2 | a0001c0001t0015g0238a0001c0001t0015g0255 | 2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.412-2792G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142201725 | ||||||
| chr3:142201768
|
G | T | 172 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(169): Show | 180 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.412-2835C>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142201768 | ||||||
| chr3:142201997
|
G | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0063others(63): Show | 71 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.411+2698C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142201997 | ||||||
| chr3:142202017
|
G | C | 97 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0024others(94): Show | 100 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.411+2678C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142202017 | ||||||
| chr3:142202044
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.411+2651G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142202044 | ||||||
| chr3:142202743
|
G | A | 4 | a0001c0001t0001g0228a0001c0001t0004g0229a0001c0001t0027g0013others(1): Show | 4 | NA18950.hp2 NA18982.hp2 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.411+1952C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142202743 | ||||||
| chr3:142203300
|
T | A | 5 | a0001c0001t0003g0036a0001c0001t0021g0034a0001c0001t0028g0035others(2): Show | 5 | HG01243.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.411+1395A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142203300 | ||||||
| chr3:142203436
|
A | C | 1 | a0001c0002t0017g0216 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.411+1259T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142203436 | ||||||
| chr3:142203444
|
A | C | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.411+1251T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142203444 | ||||||
| chr3:142203501
|
G | A | 1 | a0001c0001t0008g0089 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.411+1194C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142203501 | ||||||
| chr3:142203568
|
A | C | 4 | a0001c0001t0003g0211a0001c0001t0003g0212a0001c0001t0006g0210others(1): Show | 4 | HG01255.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.411+1127T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142203568 | ||||||
| chr3:142203591
|
G | A | 15 | a0001c0001t0003g0152a0001c0001t0006g0029a0001c0001t0006g0142others(12): Show | 15 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.411+1104C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142203591 | ||||||
| chr3:142203731
|
G | A | 1 | a0001c0001t0002g0025 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.411+964C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142203731 | ||||||
| chr3:142203964
|
T | C | 1 | a0001c0001t0002g0025 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.411+731A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142203964 | ||||||
| chr3:142203982
|
T | C | 3 | a0001c0002t0009g0218a0001c0002t0009g0219a0001c0002t0053g0220 | 3 | HG02896.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.411+713A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142203982 | ||||||
| chr3:142204014
|
C | T | 1 | a0001c0001t0082g0221 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.411+681G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142204014 | ||||||
| chr3:142204095
|
T | G | 1 | a0001c0001t0012g0250 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.411+600A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142204095 | ||||||
| chr3:142204200
|
T | G | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.411+495A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142204200 | ||||||
| chr3:142204335
|
A | G | 2 | a0001c0001t0001g0124a0001c0001t0001g0135 | 2 | HG02074.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.411+360T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142204335 | ||||||
| chr3:142204380
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0090 | 3 | HG02280.hp2 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.411+315A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142204380 | ||||||
| chr3:142204526
|
C | G | 1 | a0001c0001t0004g0008 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.411+169G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142204526 | ||||||
| chr3:142204636
|
A | T | 1 | a0001c0001t0021g0163 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.411+59T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142204636 | ||||||
| chr3:142204641
|
C | T | 3 | a0001c0002t0009g0218a0001c0002t0009g0219a0001c0002t0053g0220 | 3 | HG02896.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.411+54G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142204641 | ||||||
| chr3:142204664
|
C | T | 160 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(157): Show | 169 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.411+31G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 4/15 | chr3 | 142204664 | ||||||
| chr3:142204940
|
T | C | 1 | a0001c0001t0021g0163 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.318-152A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142204940 | ||||||
| chr3:142205277
|
A | C | 1 | a0001c0001t0012g0045 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.318-489T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142205277 | ||||||
| chr3:142205451
|
C | G | 1 | a0001c0001t0002g0025 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.318-663G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142205451 | ||||||
| chr3:142205497
|
T | A | 15 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0228others(12): Show | 15 | HG00597.hp1 HG01175.hp2 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.318-709A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142205497 | ||||||
| chr3:142205834
|
A | G | 191 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(188): Show | 200 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.318-1046T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142205834 | ||||||
| chr3:142206025
|
G | C | 1 | a0001c0001t0004g0229 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.318-1237C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142206025 | ||||||
| chr3:142206027
|
T | C | 1 | a0001c0001t0011g0117 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.318-1239A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142206027 | ||||||
| chr3:142206100
|
C | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(128): Show | 140 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.318-1312G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142206100 | ||||||
| chr3:142206101
|
G | A | 1 | a0001c0001t0008g0233 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.318-1313C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142206101 | ||||||
| chr3:142206189
|
C | G | 1 | a0001c0002t0034g0044 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.318-1401G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142206189 | ||||||
| chr3:142206197
|
T | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(175): Show | 187 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.318-1409A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142206197 | ||||||
| chr3:142206289
|
T | G | 1 | a0001c0001t0087g0257 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.318-1501A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142206289 | ||||||
| chr3:142206354
|
G | A | 18 | a0001c0001t0001g0122a0001c0001t0003g0152a0001c0001t0006g0029others(15): Show | 18 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.318-1566C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142206354 | ||||||
| chr3:142206550
|
T | A | 1 | a0001c0001t0001g0063 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.318-1762A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142206550 | ||||||
| chr3:142206562
|
T | C | 15 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0228others(12): Show | 15 | HG00597.hp1 HG01175.hp2 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.318-1774A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142206562 | ||||||
| chr3:142206590
|
A | G | 178 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(175): Show | 187 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.318-1802T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142206590 | ||||||
| chr3:142206600
|
T | C | 3 | a0001c0002t0009g0218a0001c0002t0009g0219a0001c0002t0053g0220 | 3 | HG02896.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.318-1812A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142206600 | ||||||
| chr3:142206724
|
C | G | 177 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(174): Show | 186 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.318-1936G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142206724 | ||||||
| chr3:142206921
|
T | C | 3 | a0001c0002t0009g0218a0001c0002t0009g0219a0001c0002t0053g0220 | 3 | HG02896.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.318-2133A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142206921 | ||||||
| chr3:142207024
|
T | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(174): Show | 186 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.318-2236A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142207024 | ||||||
| chr3:142207283
|
C | T | 1 | a0001c0001t0058g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.318-2495G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142207283 | ||||||
| chr3:142207319
|
C | T | 1 | a0001c0001t0012g0120 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.318-2531G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142207319 | ||||||
| chr3:142207432
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.318-2644G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142207432 | ||||||
| chr3:142207653
|
C | G | 3 | a0001c0001t0001g0240a0001c0001t0008g0233a0001c0001t0036g0232 | 3 | HG01433.hp1 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.318-2865G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142207653 | ||||||
| chr3:142207676
|
C | A | 18 | a0001c0001t0001g0122a0001c0001t0003g0152a0001c0001t0006g0029others(15): Show | 18 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.318-2888G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142207676 | ||||||
| chr3:142207704
|
G | A | 34 | a0001c0001t0001g0007a0001c0001t0001g0099a0001c0001t0001g0100others(31): Show | 35 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.318-2916C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142207704 | ||||||
| chr3:142207794
|
C | A | 35 | a0001c0001t0001g0007a0001c0001t0001g0099a0001c0001t0001g0100others(32): Show | 36 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.318-3006G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142207794 | ||||||
| chr3:142207931
|
G | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(174): Show | 186 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.318-3143C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142207931 | ||||||
| chr3:142208244
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0090 | 3 | HG02280.hp2 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.318-3456C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142208244 | ||||||
| chr3:142208652
|
A | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(73): Show | 84 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.318-3864T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142208652 | ||||||
| chr3:142208795
|
G | A | 3 | a0001c0001t0001g0122a0001c0001t0044g0140a0001c0001t0045g0139 | 3 | HG02965.hp1 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.318-4007C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142208795 | ||||||
| chr3:142208872
|
G | A | 2 | a0001c0001t0008g0215a0001c0001t0064g0214 | 2 | HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.318-4084C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142208872 | ||||||
| chr3:142208875
|
C | T | 18 | a0001c0001t0001g0122a0001c0001t0003g0152a0001c0001t0006g0029others(15): Show | 18 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.318-4087G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142208875 | ||||||
| chr3:142208925
|
G | A | 1 | a0001c0001t0002g0025 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.318-4137C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142208925 | ||||||
| chr3:142208964
|
A | G | 10 | a0001c0001t0003g0211a0001c0001t0003g0212a0001c0001t0006g0210others(7): Show | 10 | HG01255.hp1 HG01891.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.318-4176T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142208964 | ||||||
| chr3:142209097
|
C | T | 1 | a0001c0001t0081g0065 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.318-4309G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142209097 | ||||||
| chr3:142209115
|
C | T | 1 | a0001c0001t0073g0026 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.318-4327G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142209115 | ||||||
| chr3:142209144
|
G | A | 18 | a0001c0001t0001g0122a0001c0001t0003g0152a0001c0001t0006g0029others(15): Show | 18 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.318-4356C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142209144 | ||||||
| chr3:142209148
|
C | CA | 16 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0228others(13): Show | 16 | HG00597.hp1 HG01175.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.318-4361dupT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142209148 | ||||||
| chr3:142209514
|
A | C | 4 | a0001c0001t0013g0234a0001c0001t0013g0235a0001c0001t0013g0236others(1): Show | 4 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.317+4012T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142209514 | ||||||
| chr3:142209552
|
A | G | 178 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(175): Show | 187 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.317+3974T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142209552 | ||||||
| chr3:142209709
|
T | C | 9 | a0001c0001t0001g0011a0001c0001t0001g0167a0001c0001t0001g0195others(6): Show | 10 | HG00408.hp2 HG00621.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.317+3817A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142209709 | ||||||
| chr3:142209809
|
C | T | 1 | a0001c0001t0003g0043 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.317+3717G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142209809 | ||||||
| chr3:142209897
|
T | C | 1 | a0001c0001t0005g0091 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.317+3629A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142209897 | ||||||
| chr3:142209927
|
A | T | 5 | a0001c0001t0003g0036a0001c0001t0021g0034a0001c0001t0028g0035others(2): Show | 5 | HG01243.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.317+3599T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142209927 | ||||||
| chr3:142209951
|
A | AT | 189 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(186): Show | 198 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.317+3574dupA | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142209951 | ||||||
| chr3:142210165
|
C | T | 1 | a0001c0001t0002g0064 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.317+3361G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142210165 | ||||||
| chr3:142210427
|
T | C | 1 | a0001c0001t0001g0240 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.317+3099A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142210427 | ||||||
| chr3:142210850
|
C | T | 3 | a0001c0001t0014g0041a0001c0001t0014g0125a0001c0001t0032g0042 | 3 | HG03831.hp2 HG03942.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.317+2676G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142210850 | ||||||
| chr3:142210930
|
C | CTCCACTT others(7): Show |
15 | a0001c0001t0003g0152a0001c0001t0006g0029a0001c0001t0006g0142others(12): Show | 15 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.317+2582_317+2595d others(16): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142210930 | ||||||
| chr3:142211020
|
A | G | 180 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(177): Show | 189 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.317+2506T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142211020 | ||||||
| chr3:142211164
|
G | C | 83 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0020others(80): Show | 84 | HG00597.hp1 HG00738.hp2 HG00741.hp2 others(81): Show |
intron_variant | MODIFIER | c.317+2362C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142211164 | ||||||
| chr3:142211464
|
A | C | 1 | a0001c0001t0001g0167 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.317+2062T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142211464 | ||||||
| chr3:142211492
|
T | C | 2 | a0001c0001t0001g0230a0001c0001t0008g0231 | 2 | HG01175.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.317+2034A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142211492 | ||||||
| chr3:142211571
|
C | A | 1 | a0001c0001t0041g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.317+1955G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142211571 | ||||||
| chr3:142211594
|
A | C | 180 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(177): Show | 189 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.317+1932T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142211594 | ||||||
| chr3:142212219
|
C | T | 2 | a0001c0001t0003g0040a0001c0001t0047g0039 | 2 | HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.317+1307G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142212219 | ||||||
| chr3:142212463
|
G | A | 84 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0020others(81): Show | 85 | HG00597.hp1 HG00738.hp2 HG00741.hp2 others(82): Show |
intron_variant | MODIFIER | c.317+1063C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142212463 | ||||||
| chr3:142212551
|
G | A | 84 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0020others(81): Show | 85 | HG00597.hp1 HG00738.hp2 HG00741.hp2 others(82): Show |
intron_variant | MODIFIER | c.317+975C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142212551 | ||||||
| chr3:142212630
|
A | C | 1 | a0001c0001t0008g0233 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.317+896T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142212630 | ||||||
| chr3:142212707
|
T | C | 1 | a0001c0001t0037g0147 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.317+819A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142212707 | ||||||
| chr3:142212753
|
TACTATAC others(4): Show |
T | 2 | a0001c0001t0006g0030a0001c0001t0046g0239 | 2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.317+762_317+772del others(11): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142212753 | ||||||
| chr3:142212793
|
A | T | 179 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(176): Show | 188 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.317+733T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142212793 | ||||||
| chr3:142212822
|
A | ATGTTTTC others(5): Show |
5 | a0001c0001t0011g0094a0001c0001t0025g0097a0001c0001t0048g0095others(2): Show | 5 | HG00738.hp1 HG01123.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.317+703_317+704ins others(12): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142212822 | ||||||
| chr3:142212822
|
A | ATGTTTTC others(6): Show |
1 | a0001c0001t0011g0092 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.317+703_317+704ins others(13): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142212822 | ||||||
| chr3:142212824
|
A | ATTTTCTT others(5): Show |
170 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(167): Show | 179 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.317+690_317+701dup others(12): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142212824 | ||||||
| chr3:142212824
|
A | G | 1 | a0001c0001t0009g0119 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.317+702T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142212824 | ||||||
| chr3:142212824
|
A | T | 6 | a0001c0001t0011g0092a0001c0001t0011g0094a0001c0001t0025g0097others(3): Show | 6 | HG00738.hp1 HG01123.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.317+702T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142212824 | ||||||
| chr3:142212839
|
T | TTCTTTTT others(6): Show |
5 | a0001c0001t0001g0134a0001c0001t0008g0215a0001c0001t0008g0233others(2): Show | 5 | HG01433.hp1 HG02074.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.317+686_317+687ins others(13): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142212839 | ||||||
| chr3:142212840
|
C | T | 4 | a0001c0001t0001g0134a0001c0001t0008g0215a0001c0001t0064g0214others(1): Show | 4 | HG02074.hp1 HG02615.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.317+686G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142212840 | ||||||
| chr3:142212940
|
T | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(176): Show | 188 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.317+586A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142212940 | ||||||
| chr3:142213055
|
C | T | 1 | a0003c0005t0020g0203 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.317+471G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142213055 | ||||||
| chr3:142213056
|
G | C | 5 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(2): Show | 5 | HG00438.hp2 HG01123.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.317+470C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142213056 | ||||||
| chr3:142213086
|
G | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(72): Show | 83 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.317+440C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142213086 | ||||||
| chr3:142213126
|
T | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(179): Show | 191 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.317+400A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142213126 | ||||||
| chr3:142213164
|
C | A | 4 | a0001c0001t0003g0211a0001c0001t0003g0212a0001c0001t0006g0210others(1): Show | 4 | HG01255.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.317+362G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142213164 | ||||||
| chr3:142213283
|
CGAAA | C | 5 | a0001c0001t0003g0036a0001c0001t0021g0034a0001c0001t0028g0035others(2): Show | 5 | HG01243.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.317+239_317+242del others(4): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142213283 | ||||||
| chr3:142213352
|
C | G | 1 | a0001c0001t0016g0131 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.317+174G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142213352 | ||||||
| chr3:142213514
|
G | A | 179 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(176): Show | 188 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.317+12C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 3/15 | chr3 | 142213514 | ||||||
| chr3:142213689
|
T | C | 37 | a0001c0001t0001g0007a0001c0001t0001g0099a0001c0001t0001g0100others(34): Show | 38 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.242-88A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 2/15 | chr3 | 142213689 | ||||||
| chr3:142213709
|
T | A | 86 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0020others(83): Show | 87 | HG00597.hp1 HG00738.hp2 HG00741.hp2 others(84): Show |
intron_variant | MODIFIER | c.242-108A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 2/15 | chr3 | 142213709 | ||||||
| chr3:142213711
|
G | A | 1 | a0001c0001t0007g0209 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.242-110C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 2/15 | chr3 | 142213711 | ||||||
| chr3:142213777
|
T | A | 56 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0020others(53): Show | 57 | HG00738.hp2 HG00741.hp2 HG01074.hp2 others(54): Show |
intron_variant | MODIFIER | c.242-176A>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 2/15 | chr3 | 142213777 | ||||||
| chr3:142214326
|
G | A | 1 | a0001c0002t0015g0252 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.242-725C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 2/15 | chr3 | 142214326 | ||||||
| chr3:142214377
|
T | C | 3 | a0001c0001t0002g0025a0001c0001t0015g0238a0001c0001t0015g0255 | 3 | HG02647.hp2 HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.242-776A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 2/15 | chr3 | 142214377 | ||||||
| chr3:142214459
|
G | A | 84 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0020others(81): Show | 85 | HG00597.hp1 HG00738.hp2 HG00741.hp2 others(82): Show |
intron_variant | MODIFIER | c.242-858C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 2/15 | chr3 | 142214459 | ||||||
| chr3:142214807
|
C | T | 86 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0020others(83): Show | 87 | HG00597.hp1 HG00738.hp2 HG00741.hp2 others(84): Show |
intron_variant | MODIFIER | c.241+792G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 2/15 | chr3 | 142214807 | ||||||
| chr3:142214945
|
T | C | 14 | a0001c0001t0003g0152a0001c0001t0006g0029a0001c0001t0006g0142others(11): Show | 14 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.241+654A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 2/15 | chr3 | 142214945 | ||||||
| chr3:142215072
|
C | G | 2 | a0001c0001t0004g0166a0001c0001t0005g0165 | 2 | NA18952.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.241+527G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 2/15 | chr3 | 142215072 | ||||||
| chr3:142215229
|
G | C | 2 | a0001c0001t0001g0121a0001c0001t0012g0120 | 2 | HG02056.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.241+370C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 2/15 | chr3 | 142215229 | ||||||
| chr3:142215495
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.241+104T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 2/15 | chr3 | 142215495 | ||||||
| chr3:142215551
|
C | CA | 17 | a0001c0001t0001g0122a0001c0001t0006g0029a0001c0001t0006g0142others(14): Show | 17 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.241+47dupT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 2/15 | chr3 | 142215551 | ||||||
| chr3:142216065
|
G | A | 2 | a0001c0001t0006g0030a0001c0001t0046g0239 | 2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.148-373C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142216065 | ||||||
| chr3:142216552
|
T | C | 28 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0228others(25): Show | 28 | HG00597.hp1 HG01175.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.148-860A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142216552 | ||||||
| chr3:142216578
|
C | T | 6 | a0001c0001t0006g0029a0001c0001t0011g0148a0001c0001t0020g0149others(3): Show | 6 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.148-886G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142216578 | ||||||
| chr3:142216797
|
T | C | 3 | a0001c0001t0002g0025a0001c0001t0015g0238a0001c0001t0015g0255 | 3 | HG02647.hp2 HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.148-1105A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142216797 | ||||||
| chr3:142216864
|
T | C | 4 | a0001c0001t0006g0029a0001c0001t0011g0148a0001c0001t0020g0149others(1): Show | 4 | HG01891.hp2 HG02257.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.148-1172A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142216864 | ||||||
| chr3:142217445
|
G | A | 1 | a0001c0001t0007g0123 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.148-1753C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142217445 | ||||||
| chr3:142217590
|
G | GA | 6 | a0001c0001t0006g0030a0001c0001t0013g0234a0001c0001t0013g0235others(3): Show | 6 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.148-1899dupT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142217590 | ||||||
| chr3:142217713
|
T | C | 3 | a0001c0001t0002g0025a0001c0001t0015g0238a0001c0001t0015g0255 | 3 | HG02647.hp2 HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.148-2021A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142217713 | ||||||
| chr3:142218111
|
C | A | 2 | a0001c0001t0001g0124a0001c0001t0001g0135 | 2 | HG02074.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.148-2419G>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142218111 | ||||||
| chr3:142218229
|
C | CA | 9 | a0001c0001t0001g0015a0001c0001t0001g0126a0001c0001t0006g0030others(6): Show | 9 | HG01891.hp1 HG02886.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.148-2538dupT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142218229 | ||||||
| chr3:142218304
|
G | A | 4 | a0001c0001t0013g0234a0001c0001t0013g0235a0001c0001t0013g0236others(1): Show | 4 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.148-2612C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142218304 | ||||||
| chr3:142218369
|
C | T | 1 | a0001c0001t0010g0033 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.148-2677G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142218369 | ||||||
| chr3:142218377
|
C | CA | 166 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(163): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.148-2686dupT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142218377 | ||||||
| chr3:142218377
|
C | CAA | 28 | a0001c0001t0001g0020a0001c0001t0001g0024a0001c0001t0001g0128others(25): Show | 28 | HG01255.hp1 HG01433.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.148-2687_148-2686d others(4): Show |
GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142218377 | ||||||
| chr3:142218413
|
G | A | 4 | a0001c0001t0016g0131a0001c0001t0016g0132a0001c0001t0016g0133others(1): Show | 4 | HG01074.hp2 HG03710.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.148-2721C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142218413 | ||||||
| chr3:142218469
|
A | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(154): Show | 166 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.148-2777T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142218469 | ||||||
| chr3:142218540
|
C | CA | 7 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0205others(4): Show | 7 | HG02074.hp1 HG02074.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.148-2849dupT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142218540 | ||||||
| chr3:142218735
|
G | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(154): Show | 166 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.148-3043C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142218735 | ||||||
| chr3:142218744
|
T | C | 1 | a0001c0001t0001g0206 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.148-3052A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142218744 | ||||||
| chr3:142218876
|
T | C | 3 | a0001c0001t0007g0209a0001c0001t0014g0208a0001c0001t0031g0207 | 3 | HG00099.hp1 HG00642.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.148-3184A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142218876 | ||||||
| chr3:142219038
|
A | G | 2 | a0001c0001t0008g0215a0001c0001t0064g0214 | 2 | HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.148-3346T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142219038 | ||||||
| chr3:142219111
|
T | C | 28 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0228others(25): Show | 28 | HG00597.hp1 HG01175.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.148-3419A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142219111 | ||||||
| chr3:142219650
|
T | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(154): Show | 166 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.148-3958A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142219650 | ||||||
| chr3:142219889
|
A | C | 1 | a0001c0001t0061g0032 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.148-4197T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142219889 | ||||||
| chr3:142220367
|
C | T | 148 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(145): Show | 157 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.148-4675G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142220367 | ||||||
| chr3:142220414
|
C | G | 1 | a0001c0001t0002g0031 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.148-4722G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142220414 | ||||||
| chr3:142220424
|
C | T | 6 | a0001c0001t0006g0030a0001c0001t0013g0234a0001c0001t0013g0235others(3): Show | 6 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.148-4732G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142220424 | ||||||
| chr3:142220756
|
T | G | 1 | a0001c0001t0049g0155 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.147+4553A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142220756 | ||||||
| chr3:142221085
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.147+4224A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142221085 | ||||||
| chr3:142221135
|
A | C | 1 | a0001c0001t0001g0241 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.147+4174T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142221135 | ||||||
| chr3:142221243
|
T | G | 1 | a0001c0001t0046g0239 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.147+4066A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142221243 | ||||||
| chr3:142221486
|
C | T | 28 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0228others(25): Show | 28 | HG00597.hp1 HG01175.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.147+3823G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142221486 | ||||||
| chr3:142221977
|
A | G | 1 | a0001c0001t0001g0156 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.147+3332T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142221977 | ||||||
| chr3:142222033
|
T | C | 2 | a0001c0001t0033g0153a0001c0001t0035g0154 | 2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.147+3276A>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142222033 | ||||||
| chr3:142222210
|
G | C | 2 | a0001c0001t0023g0137a0001c0001t0023g0138 | 2 | HG01496.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.147+3099C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142222210 | ||||||
| chr3:142222266
|
A | T | 176 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(173): Show | 185 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.147+3043T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142222266 | ||||||
| chr3:142222267
|
A | T | 4 | a0001c0001t0003g0211a0001c0001t0003g0212a0001c0001t0006g0210others(1): Show | 4 | HG01255.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+3042T>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142222267 | ||||||
| chr3:142222391
|
C | G | 4 | a0001c0001t0003g0211a0001c0001t0003g0212a0001c0001t0006g0210others(1): Show | 4 | HG01255.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+2918G>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142222391 | ||||||
| chr3:142222490
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.147+2819C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142222490 | ||||||
| chr3:142223018
|
C | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(146): Show | 158 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.147+2291G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142223018 | ||||||
| chr3:142223024
|
G | C | 1 | a0001c0001t0049g0155 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.147+2285C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142223024 | ||||||
| chr3:142223358
|
T | G | 185 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(182): Show | 194 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.147+1951A>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142223358 | ||||||
| chr3:142223524
|
G | C | 1 | a0001c0001t0004g0028 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.147+1785C>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142223524 | ||||||
| chr3:142223837
|
A | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 259 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.147+1472T>G | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142223837 | ||||||
| chr3:142224176
|
G | A | 2 | a0001c0002t0009g0251a0001c0002t0015g0252 | 2 | HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.147+1133C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142224176 | ||||||
| chr3:142224695
|
A | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(146): Show | 158 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.147+614T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142224695 | ||||||
| chr3:142224747
|
G | A | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.147+562C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142224747 | ||||||
| chr3:142224766
|
A | G | 1 | a0001c0001t0006g0029 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.147+543T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142224766 | ||||||
| chr3:142224771
|
A | G | 3 | a0001c0001t0004g0028a0001c0001t0056g0027a0001c0001t0073g0026 | 3 | HG02523.hp2 NA18612.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.147+538T>C | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142224771 | ||||||
| chr3:142224786
|
C | T | 1 | a0001c0001t0002g0025 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.147+523G>A | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142224786 | ||||||
| chr3:142224852
|
GA | G | 11 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0020others(8): Show | 11 | HG01192.hp2 HG02071.hp2 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.147+456delT | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142224852 | ||||||
| chr3:142224897
|
G | A | 1 | a0001c0001t0015g0255 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.147+412C>T | GK5 | ENSG00000175066.16 | transcript | ENST00000392993.7 | protein_coding | 1/15 | chr3 | 142224897 |