Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 79807 |
|---|---|
| ensemblid | ENSG00000138780.15 |
| hgncid | 25806 |
| symbol | GSTCD |
| name | glutathione S-transferase C-terminal domain containing |
| refseq_nuc | NM_001370181.1 |
| refseq_prot | NP_001357110.1 |
| ensembl_nuc | ENST00000515279.6 |
| ensembl_prot | ENSP00000422354.1 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 105708784 |
| end | 105847725 |
| strand | + |
| ver | v1.2 |
| region | chr4:105708784-105847725 |
| region5000 | chr4:105703784-105852725 |
| regionname0 | GSTCD_chr4_105708784_105847725 |
| regionname5000 | GSTCD_chr4_105703784_105852725 |
| 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 | 633 | 183 | 72 | 40 | 44 | 11 | 14 | 28 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0002 | 0/0 | 633 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0003 | 0/0 | 633 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| 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 | 1902 | 159 | 52 | 37 | 43 | 11 | 14 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| c0002 | 0/0 | 1902 | 22 | 19 | 3 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| c0003 | 0/0 | 1902 | 2 | 2 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| c0004 | 0/0 | 1902 | 1 | 0 | 0 | 0 | 1 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| c0005 | 0/0 | 1902 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| c0006 | 0/0 | 1902 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2403 | 58 | 9 | 17 | 19 | 6 | 7 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| t0002 | 0/1 | 2403 | 39 | 22 | 4 | 7 | 3 | 2 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| t0003 | 0/0 | 2403 | 37 | 14 | 6 | 13 | 1 | 3 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| t0004 | 0/0 | 2399 | 11 | 9 | 2 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| t0005 | 0/0 | 2404 | 7 | 2 | 4 | 0 | 1 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| t0006 | 0/0 | 2404 | 7 | 0 | 6 | 0 | 0 | 1 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| t0007 | 0/0 | 2403 | 3 | 3 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| t0008 | 0/0 | 2399 | 2 | 2 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| t0009 | 0/0 | 2403 | 2 | 2 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| t0010 | 0/0 | 2403 | 2 | 2 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| t0011 | 0/0 | 2404 | 2 | 1 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| t0012 | 0/0 | 2404 | 2 | 0 | 0 | 1 | 0 | 1 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| t0013 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| t0014 | 0/0 | 2404 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| t0015 | 0/0 | 2404 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| t0016 | 0/0 | 2399 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| t0017 | 0/0 | 2402 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| t0018 | 0/0 | 2403 | 1 | 0 | 0 | 0 | 1 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| t0019 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| t0020 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| t0021 | 0/0 | 2399 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| t0022 | 0/0 | 2403 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| t0023 | 0/0 | 2403 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| t0024 | 0/0 | 2403 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| t0025 | 1/0 | 2403 | 1 | 0 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| t0026 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| 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 | 2 | 0 | 0 | 0 | 2 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0004 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| 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 | 1902 | 159 | 52 | 37 | 43 | 11 | 14 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0001c0002 | 0/0 | 1902 | 22 | 19 | 3 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0001c0005 | 0/0 | 1902 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0001c0006 | 0/0 | 1902 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0002c0003 | 0/0 | 1902 | 2 | 2 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0003c0004 | 0/0 | 1902 | 1 | 0 | 0 | 0 | 1 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4304 | 57 | 9 | 17 | 18 | 6 | 7 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0001c0001t0002 | 0/1 | 4304 | 19 | 6 | 1 | 7 | 2 | 2 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0001c0001t0003 | 0/0 | 4304 | 37 | 14 | 6 | 13 | 1 | 3 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0001c0001t0004 | 0/0 | 4300 | 11 | 9 | 2 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0001c0001t0005 | 0/0 | 4305 | 7 | 2 | 4 | 0 | 1 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0001c0001t0006 | 0/0 | 4305 | 7 | 0 | 6 | 0 | 0 | 1 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0001c0001t0007 | 0/0 | 4304 | 3 | 3 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0001c0001t0008 | 0/0 | 4300 | 2 | 2 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0001c0001t0009 | 0/0 | 4304 | 2 | 2 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0001c0001t0011 | 0/0 | 4305 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0001c0001t0012 | 0/0 | 4305 | 2 | 0 | 0 | 1 | 0 | 1 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0001c0001t0013 | 0/0 | 4304 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0001c0001t0014 | 0/0 | 4305 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0001c0001t0015 | 0/0 | 4305 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0001c0001t0016 | 0/0 | 4300 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0001c0001t0017 | 0/0 | 4303 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0001c0001t0018 | 0/0 | 4304 | 1 | 0 | 0 | 0 | 1 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0001c0001t0019 | 0/0 | 4304 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0001c0001t0022 | 0/0 | 4304 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0001c0001t0023 | 0/0 | 4304 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0001c0001t0024 | 0/0 | 4304 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0001c0001t0025 | 1/0 | 4304 | 1 | 0 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0001c0002t0002 | 0/0 | 4304 | 19 | 16 | 3 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0001c0002t0011 | 0/0 | 4305 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0001c0002t0020 | 0/0 | 4304 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0001c0002t0026 | 0/0 | 4304 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0001c0005t0021 | 0/0 | 4300 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0001c0006t0001 | 0/0 | 4304 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0002c0003t0010 | 0/0 | 4304 | 2 | 2 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| a0003c0004t0002 | 0/0 | 4304 | 1 | 0 | 0 | 0 | 1 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | copy fasta | chr4 | 105703784 | 105852725 |
| 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 | 2 | 0 | 0 | 0 | 2 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0002g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0005g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0005g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0005g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0005g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0005g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0005g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0005g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0006g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0006g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0006g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0006g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0006g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0006g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0006g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0007g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0007g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0007g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0008g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0008g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0009g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0009g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0011g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0012g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0012g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0013g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0014g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0015g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0016g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0017g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0018g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0019g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0022g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0023g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0024g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0001t0025g0004 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0002t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0002t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0002t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0002t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0002t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0002t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0002t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0002t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0002t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0002t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0002t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0002t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0002t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0002t0011g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0002t0020g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0002t0026g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0005t0021g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0001c0006t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0002c0003t0010g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0002c0003t0010g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| a0003c0004t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG00280 | hp1 | a0001 | c0001 | t0018 | g0160 | EUR | FIN | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0039 | EUR | FIN | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | CHS | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | CHS | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | CHS | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG00639 | hp1 | a0001 | c0001 | t0006 | g0169 | AMR | PUR | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG00735 | hp1 | a0001 | c0001 | t0005 | g0182 | AMR | PUR | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG00741 | hp1 | a0001 | c0001 | t0006 | g0168 | AMR | PUR | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0086 | AMR | PUR | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0078 | AMR | PUR | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01081 | hp1 | a0001 | c0001 | t0017 | g0162 | AMR | PUR | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0121 | AMR | PUR | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01109 | hp2 | a0001 | c0001 | t0006 | g0171 | AMR | PUR | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0174 | AMR | PUR | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0139 | AMR | PUR | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01175 | hp2 | a0001 | c0001 | t0006 | g0172 | AMR | PUR | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0097 | AMR | PUR | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0102 | AMR | PUR | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0181 | AMR | PUR | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0133 | AMR | PUR | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0094 | AMR | CLM | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0104 | AMR | CLM | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01346 | hp1 | a0001 | c0001 | t0006 | g0166 | AMR | CLM | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0109 | AMR | CLM | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0175 | EUR | IBS | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0151 | EUR | IBS | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0047 | EUR | IBS | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0150 | EUR | IBS | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0176 | AFR | ACB | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | ACB | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0124 | AFR | ACB | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0089 | AMR | PEL | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01981 | hp1 | a0001 | c0001 | t0006 | g0173 | AMR | PEL | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02004 | hp2 | a0001 | c0001 | t0005 | g0167 | AMR | PEL | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | KHV | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02071 | hp1 | a0001 | c0001 | t0023 | g0050 | EAS | KHV | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | KHV | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | KHV | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02145 | hp1 | a0001 | c0002 | t0011 | g0138 | AFR | ACB | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02145 | hp2 | a0001 | c0001 | t0014 | g0105 | AFR | ACB | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | CDX | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02155 | hp2 | a0001 | c0006 | t0001 | g0045 | EAS | CDX | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0131 | AFR | ACB | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0125 | AFR | ACB | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | PEL | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0127 | AFR | ACB | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0132 | AFR | ACB | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | KHV | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0163 | AFR | GWD | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0137 | AFR | GWD | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0076 | AFR | GWD | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0143 | AFR | GWD | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0101 | AFR | GWD | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0083 | AFR | GWD | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0177 | AFR | GWD | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02809 | hp1 | a0001 | c0001 | t0008 | g0072 | AFR | GWD | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02809 | hp2 | a0001 | c0001 | t0007 | g0164 | AFR | GWD | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0087 | AFR | GWD | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02886 | hp2 | a0001 | c0001 | t0019 | g0066 | AFR | GWD | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0079 | AFR | GWD | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02896 | hp2 | a0001 | c0001 | t0009 | g0142 | AFR | GWD | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0116 | AFR | ESN | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | ESN | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0098 | AFR | ESN | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0073 | AFR | ESN | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0128 | AFR | ESN | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG03041 | hp1 | a0001 | c0002 | t0002 | g0088 | AFR | GWD | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0123 | AFR | GWD | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0135 | AFR | MSL | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0180 | AFR | MSL | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0122 | AFR | ESN | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG03139 | hp1 | a0001 | c0001 | t0009 | g0141 | AFR | ESN | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0082 | AFR | ESN | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG03195 | hp1 | a0001 | c0001 | t0016 | g0130 | AFR | ESN | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0080 | AFR | ESN | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0081 | AFR | MSL | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG03225 | hp2 | a0001 | c0002 | t0026 | g0090 | AFR | MSL | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0120 | AFR | MSL | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG03453 | hp2 | a0001 | c0001 | t0015 | g0183 | AFR | MSL | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG03486 | hp1 | a0001 | c0002 | t0020 | g0136 | AFR | MSL | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0092 | AFR | MSL | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG03516 | hp1 | a0001 | c0005 | t0021 | g0091 | AFR | ESN | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0075 | AFR | ESN | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0159 | AFR | GWD | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0129 | AFR | GWD | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0108 | SAS | PJL | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0152 | SAS | BEB | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | STU | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0165 | SAS | STU | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG04184 | hp1 | a0001 | c0001 | t0012 | g0049 | SAS | BEB | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG04184 | hp2 | a0001 | c0001 | t0006 | g0170 | SAS | BEB | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0178 | AFR | YRI | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0093 | AFR | YRI | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | YRI | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA18906 | hp2 | a0002 | c0003 | t0010 | g0126 | AFR | YRI | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA18972 | hp1 | a0001 | c0001 | t0022 | g0054 | EAS | JPT | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA18994 | hp1 | a0001 | c0001 | t0011 | g0147 | EAS | JPT | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA18994 | hp2 | a0001 | c0001 | t0012 | g0063 | EAS | JPT | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0184 | AFR | LWK | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA19030 | hp2 | a0002 | c0003 | t0010 | g0144 | AFR | LWK | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0074 | AFR | LWK | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0117 | AFR | LWK | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA19072 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA19087 | hp1 | a0001 | c0001 | t0024 | g0055 | EAS | JPT | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0077 | AFR | YRI | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0068 | AFR | ASW | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA20129 | hp2 | a0001 | c0001 | t0013 | g0070 | AFR | ASW | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA20752 | hp1 | a0003 | c0004 | t0002 | g0085 | EUR | TSI | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0115 | EUR | TSI | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0096 | AFR | ACB | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | MSL | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0069 | AFR | MSL | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0084 | AFR | USA | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | USA | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0099 | AFR | USA | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | USA | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0100 | AFR | LWK | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0179 | AFR | LWK | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0155 | REF | REF | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0025 | g0004 | REF | REF | GSTCD_chr4_105703784_105852725 | GSTCD | chr4 | 105703784 | 105852725 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:105718019
|
T | A | 1 | a0003 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.406T>A | p.Cys136Ser | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 2/12 | 660/4304 | 406/1902 | 136/633 | chr4 | 105718019 | ||
| chr4:105825770
|
G | A | 1 | a0002 | 2 | NA18906.hp2 NA19030.hp2 |
missense_variant | MODERATE | c.1500G>A | p.Met500Ile | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/12 | 1754/4304 | 1500/1902 | 500/633 | chr4 | 105825770 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:105719230
|
G | A | 1 | a0001c0005 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.597G>A | p.Lys199Lys | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/12 | 851/4304 | 597/1902 | 199/633 | chr4 | 105719230 | ||
| chr4:105726695
|
C | T | 1 | a0001c0006 | 1 | HG02155.hp2 | synonymous_variant | LOW | c.1011C>T | p.Ile337Ile | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/12 | 1265/4304 | 1011/1902 | 337/633 | chr4 | 105726695 | ||
| chr4:105729474
|
C | G | 3 | a0001c0002a0001c0005a0003c0004 | 24 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(21): Show |
synonymous_variant | LOW | c.1215C>G | p.Leu405Leu | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/12 | 1469/4304 | 1215/1902 | 405/633 | chr4 | 105729474 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:105708836
|
A | G | 1 | a0001c0002t0026 | 1 | HG03225.hp2 | 5_prime_UTR_variant | MODIFIER | c.-202A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/12 | 8778 | chr4 | 105708836 | |||||
| chr4:105708850
|
G | C | 11 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(8): Show | 72 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(69): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-188G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/12 | chr4 | 105708850 | ||||||
| chr4:105708862
|
T | A | 1 | a0001c0001t0008 | 2 | HG02809.hp1 HG02976.hp1 |
5_prime_UTR_variant | MODIFIER | c.-176T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/12 | 8752 | chr4 | 105708862 | |||||
| chr4:105708873
|
G | C | 23 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(20): Show | 122 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(119): Show |
5_prime_UTR_variant | MODIFIER | c.-165G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/12 | 8741 | chr4 | 105708873 | |||||
| chr4:105846057
|
G | C | 1 | a0001c0001t0013 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*480G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 12/12 | 480 | chr4 | 105846057 | |||||
| chr4:105846069
|
C | T | 7 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(4): Show | 30 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*492C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 12/12 | 492 | chr4 | 105846069 | |||||
| chr4:105846333
|
T | C | 28 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(25): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*756T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 12/12 | 756 | chr4 | 105846333 | |||||
| chr4:105846375
|
CAAAT | C | 4 | a0001c0001t0004a0001c0001t0008a0001c0001t0016others(1): Show | 15 | HG01070.hp2 HG01243.hp2 HG01884.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*815_*818delAAAT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 12/12 | 815 | INFO_REALIGN_3_PRIME | chr4 | 105846375 | ||||
| chr4:105846466
|
C | T | 3 | a0001c0001t0005a0001c0001t0006a0001c0001t0015 | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*889C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 12/12 | 889 | chr4 | 105846466 | |||||
| chr4:105846546
|
AT | A | 2 | a0001c0001t0017a0001c0001t0018 | 2 | HG00280.hp1 HG01081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*970delT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 12/12 | 970 | chr4 | 105846546 | |||||
| chr4:105846584
|
A | G | 1 | a0001c0001t0006 | 7 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1007A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 12/12 | 1007 | chr4 | 105846584 | |||||
| chr4:105846586
|
T | G | 1 | a0001c0001t0009 | 2 | HG02896.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1009T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 12/12 | 1009 | chr4 | 105846586 | |||||
| chr4:105846668
|
C | CT | 8 | a0001c0001t0005a0001c0001t0006a0001c0001t0011others(5): Show | 21 | HG00280.hp1 HG00639.hp1 HG00735.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1111dupT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 12/12 | 1112 | INFO_REALIGN_3_PRIME | chr4 | 105846668 | ||||
| chr4:105846693
|
C | G | 1 | a0001c0001t0016 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1116C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 12/12 | 1116 | chr4 | 105846693 | |||||
| chr4:105846929
|
A | G | 3 | a0001c0001t0005a0001c0001t0006a0001c0001t0015 | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1352A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 12/12 | 1352 | chr4 | 105846929 | |||||
| chr4:105846934
|
C | T | 1 | a0001c0001t0024 | 1 | NA19087.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1357C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 12/12 | 1357 | chr4 | 105846934 | |||||
| chr4:105847038
|
G | C | 1 | a0001c0001t0015 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1461G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 12/12 | 1461 | chr4 | 105847038 | |||||
| chr4:105847049
|
A | G | 1 | a0001c0002t0020 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1472A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 12/12 | 1472 | chr4 | 105847049 | |||||
| chr4:105847122
|
C | T | 1 | a0001c0001t0023 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1545C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 12/12 | 1545 | chr4 | 105847122 | |||||
| chr4:105847347
|
T | G | 1 | a0001c0001t0022 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1770T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 12/12 | 1770 | chr4 | 105847347 | |||||
| chr4:105847441
|
G | A | 1 | a0002c0003t0010 | 2 | NA18906.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1864G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 12/12 | 1864 | chr4 | 105847441 | |||||
| chr4:105847441
|
G | T | 3 | a0001c0001t0005a0001c0001t0006a0001c0001t0015 | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1864G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 12/12 | 1864 | chr4 | 105847441 | |||||
| chr4:105847632
|
G | A | 1 | a0001c0001t0019 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2055G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 12/12 | 2055 | chr4 | 105847632 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:105709546
|
A | T | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22+530A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105709546 | ||||||
| chr4:105709623
|
C | G | 1 | a0001c0001t0002g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-22+607C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105709623 | ||||||
| chr4:105709655
|
C | G | 3 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0178 | 3 | HG01884.hp1 HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-22+639C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105709655 | ||||||
| chr4:105709792
|
C | T | 118 | a0001c0001t0002g0071a0001c0001t0002g0145a0001c0001t0002g0146others(115): Show | 119 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.-22+776C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105709792 | ||||||
| chr4:105709965
|
G | GT | 11 | a0001c0001t0001g0067a0001c0001t0005g0167a0001c0001t0005g0174others(8): Show | 11 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-22+958dupT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 105709965 | |||||
| chr4:105709970
|
T | C | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22+954T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105709970 | ||||||
| chr4:105710152
|
A | G | 22 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0148others(19): Show | 22 | HG00280.hp1 HG01081.hp1 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.-22+1136A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105710152 | ||||||
| chr4:105710199
|
C | T | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-22+1183C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105710199 | ||||||
| chr4:105710232
|
A | AT | 50 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(47): Show | 51 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.-22+1239dupT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 105710232 | |||||
| chr4:105710232
|
A | ATT | 13 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0056others(10): Show | 13 | HG01069.hp2 HG01167.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.-22+1238_-22+1239d others(4): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 105710232 | |||||
| chr4:105710232
|
A | ATTT | 14 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0148others(11): Show | 14 | HG01516.hp1 HG01517.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.-22+1237_-22+1239d others(5): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 105710232 | |||||
| chr4:105710232
|
A | ATTTT | 37 | a0001c0001t0002g0157a0001c0001t0002g0158a0001c0001t0002g0161others(34): Show | 37 | HG00280.hp1 HG01069.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.-22+1236_-22+1239d others(6): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 105710232 | |||||
| chr4:105710232
|
A | ATTTTT | 41 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(38): Show | 42 | HG00408.hp2 HG00597.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.-22+1235_-22+1239d others(7): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 105710232 | |||||
| chr4:105710232
|
A | ATTTTTT | 10 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0003g0143others(7): Show | 10 | HG00438.hp2 HG01175.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-22+1234_-22+1239d others(8): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 105710232 | |||||
| chr4:105710234
|
T | TTA | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-22+1219_-22+1220i others(4): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 105710234 | |||||
| chr4:105710239
|
T | A | 8 | a0001c0001t0005g0167a0001c0001t0006g0166a0001c0001t0006g0168others(5): Show | 8 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-22+1223T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105710239 | ||||||
| chr4:105710241
|
T | A | 1 | a0001c0001t0005g0174 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-22+1225T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105710241 | ||||||
| chr4:105710267
|
C | G | 2 | a0001c0001t0005g0184a0001c0001t0015g0183 | 2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-22+1251C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105710267 | ||||||
| chr4:105710387
|
C | CT | 11 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0051others(8): Show | 11 | HG01081.hp2 HG01192.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.-22+1391dupT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 105710387 | |||||
| chr4:105710480
|
C | T | 1 | a0001c0001t0003g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-22+1464C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105710480 | ||||||
| chr4:105710481
|
G | A | 2 | a0001c0001t0008g0072a0001c0001t0008g0073 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-22+1465G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105710481 | ||||||
| chr4:105710527
|
C | T | 1 | a0001c0001t0003g0134 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-22+1511C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105710527 | ||||||
| chr4:105710531
|
T | C | 5 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG01070.hp2 HG02630.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22+1515T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105710531 | ||||||
| chr4:105710541
|
T | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0062 | 2 | HG00639.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.-22+1525T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105710541 | ||||||
| chr4:105710713
|
A | G | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-22+1697A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105710713 | ||||||
| chr4:105710978
|
T | C | 1 | a0001c0001t0001g0010 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-22+1962T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105710978 | ||||||
| chr4:105711023
|
T | A | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-22+2007T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105711023 | ||||||
| chr4:105711060
|
C | T | 1 | a0001c0001t0023g0050 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-22+2044C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105711060 | ||||||
| chr4:105711206
|
CAT | C | 12 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(9): Show | 12 | HG01070.hp2 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.-22+2193_-22+2194d others(4): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 105711206 | |||||
| chr4:105711256
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0012g0049 | 2 | HG04184.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.-22+2240A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105711256 | ||||||
| chr4:105711263
|
GTGTT | G | 24 | a0001c0002t0002g0079a0001c0002t0002g0080a0001c0002t0002g0081others(21): Show | 24 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(21): Show |
intron_variant | MODIFIER | c.-22+2251_-22+2254d others(6): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 105711263 | |||||
| chr4:105711279
|
A | G | 22 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0148others(19): Show | 22 | HG00280.hp1 HG01081.hp1 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.-22+2263A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105711279 | ||||||
| chr4:105711404
|
G | GT | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-22+2396dupT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 105711404 | |||||
| chr4:105711500
|
G | A | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-22+2484G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105711500 | ||||||
| chr4:105711532
|
G | A | 1 | a0001c0001t0001g0010 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-22+2516G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105711532 | ||||||
| chr4:105711872
|
A | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-22+2856A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105711872 | ||||||
| chr4:105711888
|
T | A | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-22+2872T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105711888 | ||||||
| chr4:105712027
|
A | G | 2 | a0001c0001t0008g0072a0001c0001t0008g0073 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-22+3011A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105712027 | ||||||
| chr4:105712510
|
T | C | 1 | a0001c0001t0003g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-22+3494T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105712510 | ||||||
| chr4:105713114
|
G | T | 41 | a0001c0001t0003g0002a0001c0001t0003g0069a0001c0001t0003g0094others(38): Show | 42 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.-22+4098G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105713114 | ||||||
| chr4:105713182
|
C | A | 1 | a0001c0001t0003g0139 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-22+4166C>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105713182 | ||||||
| chr4:105713201
|
CAA | C | 14 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(11): Show | 14 | HG01070.hp2 HG01243.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-22+4188_-22+4189d others(4): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 105713201 | |||||
| chr4:105713223
|
C | G | 1 | a0001c0001t0001g0047 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-22+4207C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105713223 | ||||||
| chr4:105713223
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-22+4207C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105713223 | ||||||
| chr4:105713532
|
A | G | 1 | a0001c0001t0003g0095 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-21-4061A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105713532 | ||||||
| chr4:105713579
|
T | C | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-21-4014T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105713579 | ||||||
| chr4:105714024
|
G | GA | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-21-3558dupA | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 105714024 | |||||
| chr4:105714400
|
A | G | 4 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(1): Show | 4 | HG01069.hp2 HG01167.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21-3193A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105714400 | ||||||
| chr4:105714420
|
C | T | 7 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(4): Show | 7 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.-21-3173C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105714420 | ||||||
| chr4:105714463
|
A | AT | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(15): Show | 18 | HG00140.hp1 HG00140.hp2 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.-21-3117dupT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 105714463 | |||||
| chr4:105714631
|
A | T | 1 | a0001c0001t0001g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-21-2962A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105714631 | ||||||
| chr4:105714637
|
AT | A | 48 | a0001c0001t0002g0071a0001c0001t0003g0002a0001c0001t0003g0068others(45): Show | 49 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.-21-2945delT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 105714637 | |||||
| chr4:105714637
|
ATT | A | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-21-2946_-21-2945d others(4): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 105714637 | |||||
| chr4:105714703
|
A | G | 12 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(9): Show | 12 | HG01070.hp2 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.-21-2890A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105714703 | ||||||
| chr4:105714745
|
A | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-21-2848A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105714745 | ||||||
| chr4:105714905
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-21-2688G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105714905 | ||||||
| chr4:105715441
|
A | G | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-21-2152A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105715441 | ||||||
| chr4:105715480
|
A | G | 12 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(9): Show | 12 | HG01109.hp1 HG01891.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-21-2113A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105715480 | ||||||
| chr4:105715542
|
ATTAT | A | 5 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG01070.hp2 HG02630.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21-2048_-21-2045d others(6): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 105715542 | |||||
| chr4:105715692
|
T | TAAAATAT others(313): Show |
1 | a0001c0001t0003g0129 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-21-1888_-21-1887i others(322): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 105715692 | |||||
| chr4:105715692
|
T | TAAAATAT others(314): Show |
7 | a0001c0001t0003g0115a0001c0001t0003g0116a0001c0001t0003g0117others(4): Show | 7 | HG02451.hp1 HG02965.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.-21-1888_-21-1887i others(323): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 105715692 | |||||
| chr4:105715692
|
T | TAAAATAT others(315): Show |
22 | a0001c0001t0003g0002a0001c0001t0003g0095a0001c0001t0003g0106others(19): Show | 23 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.-21-1888_-21-1887i others(324): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 105715692 | |||||
| chr4:105715692
|
T | TAAAATAT others(316): Show |
8 | a0001c0001t0003g0094a0001c0001t0003g0102a0001c0001t0003g0103others(5): Show | 8 | HG00438.hp2 HG01109.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.-21-1888_-21-1887i others(325): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 105715692 | |||||
| chr4:105716127
|
C | T | 1 | a0001c0001t0006g0173 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-21-1466C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105716127 | ||||||
| chr4:105716254
|
C | T | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-21-1339C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105716254 | ||||||
| chr4:105716533
|
C | T | 1 | a0001c0001t0023g0050 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-21-1060C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105716533 | ||||||
| chr4:105716695
|
C | T | 22 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0148others(19): Show | 22 | HG00280.hp1 HG01081.hp1 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.-21-898C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105716695 | ||||||
| chr4:105717099
|
T | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-21-494T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105717099 | ||||||
| chr4:105717149
|
A | G | 1 | a0001c0002t0026g0090 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-21-444A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105717149 | ||||||
| chr4:105717468
|
A | G | 1 | a0001c0001t0003g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-21-125A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105717468 | ||||||
| chr4:105717540
|
A | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-21-53A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 1/11 | chr4 | 105717540 | ||||||
| chr4:105718134
|
A | T | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.426+95A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 2/11 | chr4 | 105718134 | ||||||
| chr4:105718154
|
C | A | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.426+115C>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 2/11 | chr4 | 105718154 | ||||||
| chr4:105718378
|
G | A | 2 | a0001c0001t0008g0072a0001c0001t0008g0073 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.426+339G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 2/11 | chr4 | 105718378 | ||||||
| chr4:105718381
|
T | C | 1 | a0001c0001t0002g0157 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.426+342T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 2/11 | chr4 | 105718381 | ||||||
| chr4:105718555
|
A | G | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.427-505A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 2/11 | chr4 | 105718555 | ||||||
| chr4:105719027
|
C | A | 56 | a0001c0001t0003g0002a0001c0001t0003g0068a0001c0001t0003g0069others(53): Show | 57 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.427-33C>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 2/11 | chr4 | 105719027 | ||||||
| chr4:105719910
|
T | A | 1 | a0001c0001t0001g0052 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.894+383T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105719910 | ||||||
| chr4:105720068
|
G | A | 22 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0148others(19): Show | 22 | HG00280.hp1 HG01081.hp1 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.894+541G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105720068 | ||||||
| chr4:105720147
|
ATCTC | A | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.894+636_894+639del others(4): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 105720147 | |||||
| chr4:105720163
|
CTCTG | C | 56 | a0001c0001t0003g0002a0001c0001t0003g0068a0001c0001t0003g0069others(53): Show | 57 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.894+644_894+647del others(4): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 105720163 | |||||
| chr4:105720766
|
C | T | 41 | a0001c0001t0003g0002a0001c0001t0003g0069a0001c0001t0003g0094others(38): Show | 42 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.894+1239C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105720766 | ||||||
| chr4:105720898
|
T | G | 2 | a0001c0001t0002g0157a0001c0001t0002g0179 | 2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.894+1371T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105720898 | ||||||
| chr4:105720930
|
T | C | 4 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0148others(1): Show | 4 | NA18987.hp1 NA18990.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.894+1403T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105720930 | ||||||
| chr4:105720951
|
T | C | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.894+1424T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105720951 | ||||||
| chr4:105720980
|
CT | C | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.894+1463delT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 105720980 | |||||
| chr4:105721102
|
G | T | 1 | a0001c0001t0013g0070 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.894+1575G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105721102 | ||||||
| chr4:105721362
|
A | G | 1 | a0001c0001t0003g0121 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.894+1835A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105721362 | ||||||
| chr4:105721473
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.894+1946A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105721473 | ||||||
| chr4:105721754
|
A | G | 22 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0148others(19): Show | 22 | HG00280.hp1 HG01081.hp1 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.894+2227A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105721754 | ||||||
| chr4:105722004
|
G | A | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.894+2477G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105722004 | ||||||
| chr4:105722145
|
C | G | 3 | a0001c0001t0003g0069a0001c0001t0003g0135a0001c0001t0013g0070 | 3 | HG03098.hp1 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.894+2618C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105722145 | ||||||
| chr4:105722246
|
A | G | 24 | a0001c0002t0002g0079a0001c0002t0002g0080a0001c0002t0002g0081others(21): Show | 24 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(21): Show |
intron_variant | MODIFIER | c.894+2719A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105722246 | ||||||
| chr4:105722288
|
G | A | 118 | a0001c0001t0002g0071a0001c0001t0002g0145a0001c0001t0002g0146others(115): Show | 119 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.894+2761G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105722288 | ||||||
| chr4:105722661
|
T | A | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.894+3134T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105722661 | ||||||
| chr4:105722745
|
T | A | 1 | a0001c0001t0002g0149 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.894+3218T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105722745 | ||||||
| chr4:105722837
|
G | T | 1 | a0001c0001t0004g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.894+3310G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105722837 | ||||||
| chr4:105723400
|
G | T | 1 | a0001c0001t0004g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.895-3179G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105723400 | ||||||
| chr4:105723628
|
C | T | 4 | a0001c0002t0002g0100a0001c0002t0002g0101a0001c0002t0002g0137others(1): Show | 4 | HG02145.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.895-2951C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105723628 | ||||||
| chr4:105723712
|
A | T | 12 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(9): Show | 12 | HG01070.hp2 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.895-2867A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105723712 | ||||||
| chr4:105723885
|
G | T | 1 | a0001c0001t0007g0164 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.895-2694G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105723885 | ||||||
| chr4:105724080
|
A | G | 5 | a0001c0002t0002g0089a0001c0002t0002g0092a0001c0002t0002g0093others(2): Show | 5 | HG01975.hp2 HG02970.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.895-2499A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105724080 | ||||||
| chr4:105724207
|
T | C | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.895-2372T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105724207 | ||||||
| chr4:105724308
|
C | T | 1 | a0001c0001t0004g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.895-2271C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105724308 | ||||||
| chr4:105724413
|
A | T | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.895-2166A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105724413 | ||||||
| chr4:105724511
|
T | A | 12 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(9): Show | 12 | HG01070.hp2 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.895-2068T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105724511 | ||||||
| chr4:105724605
|
AC | A | 16 | a0001c0002t0002g0079a0001c0002t0002g0080a0001c0002t0002g0081others(13): Show | 16 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.895-1973delC | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105724605 | ||||||
| chr4:105724614
|
G | A | 72 | a0001c0001t0002g0071a0001c0001t0003g0002a0001c0001t0003g0068others(69): Show | 73 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.895-1965G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105724614 | ||||||
| chr4:105724624
|
AAACACAA others(8): Show |
A | 2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | HG00642.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.895-1951_895-1937d others(17): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 105724624 | |||||
| chr4:105725025
|
G | T | 2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | HG00642.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.895-1554G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105725025 | ||||||
| chr4:105725071
|
A | AATTGAAT | 41 | a0001c0001t0003g0002a0001c0001t0003g0069a0001c0001t0003g0094others(38): Show | 42 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.895-1505_895-1499d others(9): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 105725071 | |||||
| chr4:105725192
|
A | G | 11 | a0001c0001t0004g0132a0001c0001t0005g0167a0001c0001t0005g0174others(8): Show | 11 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.895-1387A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105725192 | ||||||
| chr4:105725361
|
A | G | 5 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG01070.hp2 HG02630.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.895-1218A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105725361 | ||||||
| chr4:105725589
|
AT | A | 12 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(9): Show | 12 | HG01070.hp2 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.895-982delT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 105725589 | |||||
| chr4:105725729
|
G | A | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.895-850G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105725729 | ||||||
| chr4:105725866
|
T | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.895-713T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105725866 | ||||||
| chr4:105725975
|
T | C | 38 | a0001c0001t0003g0002a0001c0001t0003g0094a0001c0001t0003g0095others(35): Show | 39 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.895-604T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105725975 | ||||||
| chr4:105726047
|
G | A | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.895-532G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105726047 | ||||||
| chr4:105726049
|
AAC | A | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.895-526_895-525del others(2): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 105726049 | |||||
| chr4:105726142
|
A | G | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.895-437A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105726142 | ||||||
| chr4:105726209
|
C | T | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.895-370C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105726209 | ||||||
| chr4:105726320
|
G | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(179): Show | 184 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.895-259G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105726320 | ||||||
| chr4:105726352
|
C | T | 2 | a0001c0001t0008g0072a0001c0001t0008g0073 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.895-227C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105726352 | ||||||
| chr4:105726432
|
A | G | 1 | a0001c0001t0004g0078 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.895-147A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105726432 | ||||||
| chr4:105726442
|
A | G | 5 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG01070.hp2 HG02630.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.895-137A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105726442 | ||||||
| chr4:105726464
|
CATT | C | 18 | a0001c0001t0003g0068a0001c0001t0003g0069a0001c0001t0003g0135others(15): Show | 18 | HG01070.hp2 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.895-114_895-112del others(3): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105726464 | ||||||
| chr4:105726522
|
C | T | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.895-57C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 3/11 | chr4 | 105726522 | ||||||
| chr4:105727088
|
C | CT | 69 | a0001c0001t0001g0035a0001c0001t0001g0047a0001c0001t0001g0057others(66): Show | 69 | HG00280.hp1 HG00735.hp1 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.1146+274dupT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 105727088 | |||||
| chr4:105727088
|
C | CTT | 50 | a0001c0001t0002g0071a0001c0001t0003g0002a0001c0001t0003g0094others(47): Show | 51 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.1146+273_1146+274d others(4): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 105727088 | |||||
| chr4:105727102
|
T | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | HG00642.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1146+272T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | chr4 | 105727102 | ||||||
| chr4:105727191
|
T | C | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1146+361T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | chr4 | 105727191 | ||||||
| chr4:105727441
|
T | C | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1146+611T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | chr4 | 105727441 | ||||||
| chr4:105727484
|
C | T | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1146+654C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | chr4 | 105727484 | ||||||
| chr4:105727644
|
T | A | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1146+814T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | chr4 | 105727644 | ||||||
| chr4:105727708
|
C | T | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1146+878C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | chr4 | 105727708 | ||||||
| chr4:105727753
|
T | C | 1 | a0001c0001t0006g0173 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1146+923T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | chr4 | 105727753 | ||||||
| chr4:105727888
|
C | T | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1146+1058C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | chr4 | 105727888 | ||||||
| chr4:105728532
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1147-874G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | chr4 | 105728532 | ||||||
| chr4:105728592
|
T | C | 1 | a0001c0001t0002g0158 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1147-814T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | chr4 | 105728592 | ||||||
| chr4:105728658
|
C | T | 2 | a0001c0001t0003g0069a0001c0001t0013g0070 | 2 | HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1147-748C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | chr4 | 105728658 | ||||||
| chr4:105728669
|
C | CTAGATA | 8 | a0001c0001t0002g0071a0001c0001t0002g0157a0001c0001t0002g0161others(5): Show | 8 | HG00280.hp1 HG01081.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1147-728_1147-723d others(8): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 105728669 | |||||
| chr4:105728669
|
C | CTAGATAT others(5): Show |
10 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0122others(7): Show | 10 | HG01109.hp1 HG01167.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.1147-734_1147-723d others(14): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 105728669 | |||||
| chr4:105728669
|
C | CTAGATAT others(11): Show |
2 | a0001c0001t0008g0072a0001c0001t0008g0073 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1147-723_1147-722i others(20): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 105728669 | |||||
| chr4:105728680
|
T | TATAG | 23 | a0001c0002t0002g0079a0001c0002t0002g0080a0001c0002t0002g0081others(20): Show | 23 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.1147-723_1147-722i others(6): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 105728680 | |||||
| chr4:105728680
|
T | TATAGATA others(23): Show |
1 | a0001c0001t0004g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1147-723_1147-722i others(32): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 105728680 | |||||
| chr4:105728680
|
T | TATAGATA others(11): Show |
21 | a0001c0001t0003g0115a0001c0001t0003g0123a0001c0001t0003g0124others(18): Show | 21 | HG00639.hp1 HG00741.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.1147-723_1147-722i others(20): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 105728680 | |||||
| chr4:105728680
|
T | TATAGATA others(17): Show |
12 | a0001c0001t0003g0068a0001c0001t0003g0106a0001c0001t0003g0107others(9): Show | 12 | HG00597.hp2 HG01175.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1147-723_1147-722i others(26): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 105728680 | |||||
| chr4:105728680
|
T | TATAGATA others(23): Show |
16 | a0001c0001t0003g0002a0001c0001t0003g0095a0001c0001t0003g0102others(13): Show | 17 | HG00408.hp2 HG00438.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.1147-723_1147-722i others(32): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 105728680 | |||||
| chr4:105728680
|
T | TATAGATA others(29): Show |
3 | a0001c0001t0003g0094a0001c0001t0003g0104a0003c0004t0002g0085 | 3 | HG01256.hp2 HG01258.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1147-723_1147-722i others(38): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 105728680 | |||||
| chr4:105728680
|
T | TATAGATA others(5): Show |
2 | a0001c0001t0007g0164a0002c0003t0010g0144 | 2 | HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1147-723_1147-722i others(14): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 105728680 | |||||
| chr4:105728680
|
T | TATAGATA others(11): Show |
1 | a0001c0001t0005g0184 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1147-723_1147-722i others(20): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 105728680 | |||||
| chr4:105728680
|
T | TATAGATA others(17): Show |
4 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(1): Show | 4 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1147-723_1147-722i others(26): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 105728680 | |||||
| chr4:105728680
|
T | TATAGATA others(23): Show |
1 | a0001c0001t0003g0069 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1147-723_1147-722i others(32): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 105728680 | |||||
| chr4:105728680
|
TATATAG | T | 60 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(57): Show | 61 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1147-694_1147-689d others(8): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 105728680 | |||||
| chr4:105728684
|
T | A | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1147-722T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | chr4 | 105728684 | ||||||
| chr4:105728684
|
T | G | 14 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0148others(11): Show | 14 | HG01516.hp1 HG01517.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.1147-722T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | chr4 | 105728684 | ||||||
| chr4:105728686
|
G | GAT | 21 | a0001c0002t0002g0079a0001c0002t0002g0080a0001c0002t0002g0081others(18): Show | 21 | HG01975.hp2 HG02109.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.1147-716_1147-715d others(4): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 105728686 | |||||
| chr4:105728686
|
G | T | 15 | a0001c0001t0002g0071a0001c0001t0002g0145a0001c0001t0002g0146others(12): Show | 15 | HG01516.hp1 HG01517.hp1 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.1147-720G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | chr4 | 105728686 | ||||||
| chr4:105728689
|
A | ATC | 3 | a0001c0002t0002g0086a0001c0002t0002g0087a0001c0002t0002g0097 | 3 | HG01069.hp1 HG01192.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1147-716_1147-715i others(4): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 105728689 | |||||
| chr4:105728694
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01081.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1147-712T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | chr4 | 105728694 | ||||||
| chr4:105728840
|
A | G | 2 | a0001c0001t0008g0072a0001c0001t0008g0073 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1147-566A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | chr4 | 105728840 | ||||||
| chr4:105728881
|
A | G | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1147-525A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | chr4 | 105728881 | ||||||
| chr4:105728959
|
G | A | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1147-447G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | chr4 | 105728959 | ||||||
| chr4:105729032
|
T | A | 5 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG01070.hp2 HG02630.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1147-374T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | chr4 | 105729032 | ||||||
| chr4:105729220
|
G | A | 1 | a0001c0001t0004g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1147-186G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | chr4 | 105729220 | ||||||
| chr4:105729368
|
A | G | 3 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0178 | 3 | HG01884.hp1 HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1147-38A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 4/11 | chr4 | 105729368 | ||||||
| chr4:105729620
|
G | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01081.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1240+121G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105729620 | ||||||
| chr4:105729777
|
G | C | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1240+278G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105729777 | ||||||
| chr4:105729841
|
C | A | 1 | a0001c0001t0001g0011 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1240+342C>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105729841 | ||||||
| chr4:105729887
|
T | G | 1 | a0001c0001t0001g0035 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1240+388T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105729887 | ||||||
| chr4:105729910
|
C | T | 1 | a0001c0001t0001g0033 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1240+411C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105729910 | ||||||
| chr4:105729918
|
G | A | 1 | a0001c0001t0013g0070 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1240+419G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105729918 | ||||||
| chr4:105729977
|
A | C | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | NA18942.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1240+478A>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105729977 | ||||||
| chr4:105730033
|
G | A | 1 | a0001c0002t0020g0136 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1240+534G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105730033 | ||||||
| chr4:105730094
|
A | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+595A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105730094 | ||||||
| chr4:105730122
|
A | T | 1 | a0001c0002t0002g0137 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1240+623A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105730122 | ||||||
| chr4:105730159
|
T | C | 1 | a0001c0001t0001g0041 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1240+660T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105730159 | ||||||
| chr4:105730191
|
C | T | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+692C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105730191 | ||||||
| chr4:105730291
|
A | G | 1 | a0001c0002t0002g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1240+792A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105730291 | ||||||
| chr4:105730299
|
C | A | 1 | a0001c0002t0002g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1240+800C>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105730299 | ||||||
| chr4:105730364
|
G | T | 1 | a0001c0002t0002g0097 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1240+865G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105730364 | ||||||
| chr4:105730480
|
T | G | 2 | a0001c0001t0008g0072a0001c0001t0008g0073 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1240+981T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105730480 | ||||||
| chr4:105730545
|
G | C | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1240+1046G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105730545 | ||||||
| chr4:105730558
|
T | A | 1 | a0001c0001t0003g0120 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1240+1059T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105730558 | ||||||
| chr4:105730672
|
A | T | 44 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(41): Show | 45 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.1240+1173A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105730672 | ||||||
| chr4:105730684
|
C | T | 44 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(41): Show | 45 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.1240+1185C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105730684 | ||||||
| chr4:105730784
|
T | G | 1 | a0001c0001t0003g0125 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1240+1285T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105730784 | ||||||
| chr4:105730796
|
G | T | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+1297G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105730796 | ||||||
| chr4:105730806
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1240+1307A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105730806 | ||||||
| chr4:105730896
|
A | G | 1 | a0001c0001t0004g0178 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1240+1397A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105730896 | ||||||
| chr4:105730951
|
T | C | 1 | a0001c0001t0003g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1240+1452T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105730951 | ||||||
| chr4:105730980
|
A | G | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1240+1481A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105730980 | ||||||
| chr4:105731096
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1240+1597G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105731096 | ||||||
| chr4:105731224
|
G | A | 1 | a0001c0001t0001g0012 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1240+1725G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105731224 | ||||||
| chr4:105731315
|
C | G | 3 | a0001c0001t0003g0069a0001c0001t0003g0135a0001c0001t0013g0070 | 3 | HG03098.hp1 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1240+1816C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105731315 | ||||||
| chr4:105731321
|
C | T | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+1822C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105731321 | ||||||
| chr4:105731448
|
T | G | 1 | a0001c0001t0001g0037 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1240+1949T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105731448 | ||||||
| chr4:105731463
|
A | C | 1 | a0001c0001t0001g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1240+1964A>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105731463 | ||||||
| chr4:105731527
|
C | CTGTT | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+2031_1240+203 others(8): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105731527 | |||||
| chr4:105731627
|
C | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+2128C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105731627 | ||||||
| chr4:105731751
|
G | A | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1240+2252G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105731751 | ||||||
| chr4:105731975
|
G | A | 2 | a0001c0001t0008g0072a0001c0001t0008g0073 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1240+2476G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105731975 | ||||||
| chr4:105732110
|
G | A | 41 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(38): Show | 42 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.1240+2611G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105732110 | ||||||
| chr4:105732164
|
T | C | 1 | a0001c0005t0021g0091 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1240+2665T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105732164 | ||||||
| chr4:105732166
|
T | C | 3 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0178 | 3 | HG01884.hp1 HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1240+2667T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105732166 | ||||||
| chr4:105732293
|
A | G | 1 | a0001c0001t0004g0177 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1240+2794A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105732293 | ||||||
| chr4:105732317
|
G | C | 1 | a0001c0001t0004g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1240+2818G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105732317 | ||||||
| chr4:105732477
|
A | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+2978A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105732477 | ||||||
| chr4:105732485
|
G | T | 1 | a0001c0001t0004g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1240+2986G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105732485 | ||||||
| chr4:105732498
|
T | C | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+2999T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105732498 | ||||||
| chr4:105732527
|
G | A | 14 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(11): Show | 14 | HG01070.hp2 HG01243.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1240+3028G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105732527 | ||||||
| chr4:105732659
|
T | A | 62 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(59): Show | 63 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.1240+3160T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105732659 | ||||||
| chr4:105732709
|
C | T | 12 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(9): Show | 12 | HG01070.hp2 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1240+3210C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105732709 | ||||||
| chr4:105732722
|
C | T | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+3223C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105732722 | ||||||
| chr4:105732770
|
T | C | 1 | a0001c0001t0004g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1240+3271T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105732770 | ||||||
| chr4:105732785
|
G | T | 1 | a0001c0001t0003g0069 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1240+3286G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105732785 | ||||||
| chr4:105732887
|
T | C | 1 | a0001c0001t0016g0130 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1240+3388T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105732887 | ||||||
| chr4:105732939
|
C | T | 1 | a0001c0001t0002g0065 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1240+3440C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105732939 | ||||||
| chr4:105732985
|
T | C | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1240+3486T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105732985 | ||||||
| chr4:105733053
|
C | G | 2 | a0001c0001t0007g0163a0001c0001t0007g0164 | 2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1240+3554C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105733053 | ||||||
| chr4:105733144
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | NA18942.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1240+3645C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105733144 | ||||||
| chr4:105733173
|
G | A | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+3674G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105733173 | ||||||
| chr4:105733205
|
T | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(155): Show | 160 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1240+3706T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105733205 | ||||||
| chr4:105733255
|
C | G | 7 | a0001c0002t0002g0079a0001c0002t0002g0080a0001c0002t0002g0081others(4): Show | 7 | HG02109.hp2 HG02723.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240+3756C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105733255 | ||||||
| chr4:105733472
|
G | T | 1 | a0001c0001t0001g0030 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1240+3973G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105733472 | ||||||
| chr4:105733506
|
C | T | 1 | a0001c0001t0013g0070 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1240+4007C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105733506 | ||||||
| chr4:105733521
|
A | C | 1 | a0001c0001t0001g0046 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1240+4022A>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105733521 | ||||||
| chr4:105733687
|
G | A | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1240+4188G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105733687 | ||||||
| chr4:105733734
|
G | A | 4 | a0001c0001t0003g0116a0001c0001t0003g0117a0001c0001t0003g0139others(1): Show | 4 | HG01175.hp1 HG02145.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1240+4235G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105733734 | ||||||
| chr4:105733753
|
C | T | 1 | a0001c0001t0003g0120 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1240+4254C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105733753 | ||||||
| chr4:105733754
|
G | A | 1 | a0001c0001t0003g0121 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1240+4255G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105733754 | ||||||
| chr4:105733816
|
G | A | 62 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(59): Show | 63 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.1240+4317G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105733816 | ||||||
| chr4:105733824
|
G | C | 1 | a0001c0001t0003g0002 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1240+4325G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105733824 | ||||||
| chr4:105733826
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0003g0002 | 3 | HG01361.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1240+4327G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105733826 | ||||||
| chr4:105733830
|
T | G | 1 | a0001c0001t0003g0002 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1240+4331T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105733830 | ||||||
| chr4:105734092
|
C | T | 12 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(9): Show | 12 | HG01070.hp2 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1240+4593C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105734092 | ||||||
| chr4:105734277
|
C | T | 3 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0158 | 3 | HG02015.hp2 HG02071.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1240+4778C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105734277 | ||||||
| chr4:105734278
|
G | A | 3 | a0001c0001t0003g0069a0001c0001t0003g0135a0001c0001t0013g0070 | 3 | HG03098.hp1 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1240+4779G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105734278 | ||||||
| chr4:105734326
|
A | G | 2 | a0001c0001t0004g0131a0001c0001t0016g0130 | 2 | HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1240+4827A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105734326 | ||||||
| chr4:105734480
|
A | G | 175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(172): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.1240+4981A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105734480 | ||||||
| chr4:105734562
|
T | C | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+5063T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105734562 | ||||||
| chr4:105734614
|
T | C | 1 | a0001c0001t0003g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1240+5115T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105734614 | ||||||
| chr4:105734673
|
T | C | 74 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(71): Show | 75 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.1240+5174T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105734673 | ||||||
| chr4:105734689
|
C | T | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1240+5190C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105734689 | ||||||
| chr4:105734800
|
C | T | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+5301C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105734800 | ||||||
| chr4:105734919
|
A | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+5420A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105734919 | ||||||
| chr4:105735041
|
G | A | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+5542G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105735041 | ||||||
| chr4:105735063
|
G | A | 1 | a0001c0002t0002g0088 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1240+5564G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105735063 | ||||||
| chr4:105735066
|
C | T | 62 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(59): Show | 63 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.1240+5567C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105735066 | ||||||
| chr4:105735177
|
C | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(158): Show | 163 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.1240+5678C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105735177 | ||||||
| chr4:105735312
|
G | A | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1240+5813G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105735312 | ||||||
| chr4:105735397
|
G | A | 1 | a0001c0001t0003g0115 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1240+5898G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105735397 | ||||||
| chr4:105735451
|
C | T | 3 | a0001c0001t0004g0131a0001c0001t0004g0132a0001c0001t0016g0130 | 3 | HG02257.hp2 HG02451.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1240+5952C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105735451 | ||||||
| chr4:105735457
|
C | T | 59 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(56): Show | 60 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.1240+5958C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105735457 | ||||||
| chr4:105735517
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1240+6018A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105735517 | ||||||
| chr4:105735622
|
C | T | 1 | a0001c0001t0003g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1240+6123C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105735622 | ||||||
| chr4:105735811
|
G | A | 1 | a0001c0001t0001g0042 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1240+6312G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105735811 | ||||||
| chr4:105735849
|
A | G | 1 | a0003c0004t0002g0085 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1240+6350A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105735849 | ||||||
| chr4:105735994
|
G | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(158): Show | 163 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.1240+6495G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105735994 | ||||||
| chr4:105736034
|
TTGGTTTT others(8): Show |
T | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+6538_1240+655 others(19): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105736034 | |||||
| chr4:105736156
|
A | C | 1 | a0001c0001t0003g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1240+6657A>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105736156 | ||||||
| chr4:105736311
|
C | A | 1 | a0001c0001t0003g0127 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1240+6812C>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105736311 | ||||||
| chr4:105736501
|
T | G | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1240+7002T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105736501 | ||||||
| chr4:105736511
|
TATG | T | 2 | a0001c0001t0008g0072a0001c0001t0008g0073 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1240+7015_1240+701 others(7): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105736511 | |||||
| chr4:105736814
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1240+7315G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105736814 | ||||||
| chr4:105737060
|
A | T | 41 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(38): Show | 42 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.1240+7561A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105737060 | ||||||
| chr4:105737092
|
T | A | 62 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(59): Show | 63 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.1240+7593T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105737092 | ||||||
| chr4:105737405
|
G | A | 1 | a0001c0001t0016g0130 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1240+7906G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105737405 | ||||||
| chr4:105737501
|
G | A | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+8002G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105737501 | ||||||
| chr4:105737655
|
T | A | 1 | a0001c0001t0001g0033 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1240+8156T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105737655 | ||||||
| chr4:105737678
|
C | T | 3 | a0001c0001t0003g0069a0001c0001t0003g0135a0001c0001t0013g0070 | 3 | HG03098.hp1 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1240+8179C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105737678 | ||||||
| chr4:105737759
|
A | C | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1240+8260A>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105737759 | ||||||
| chr4:105738188
|
C | A | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1240+8689C>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105738188 | ||||||
| chr4:105738562
|
C | T | 13 | a0001c0001t0003g0095a0001c0001t0003g0103a0001c0001t0003g0106others(10): Show | 13 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(10): Show |
intron_variant | MODIFIER | c.1240+9063C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105738562 | ||||||
| chr4:105738624
|
T | G | 1 | a0001c0001t0004g0075 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1240+9125T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105738624 | ||||||
| chr4:105738883
|
G | A | 1 | a0001c0001t0004g0177 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1240+9384G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105738883 | ||||||
| chr4:105738889
|
G | A | 1 | a0001c0001t0004g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1240+9390G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105738889 | ||||||
| chr4:105739167
|
A | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+9668A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105739167 | ||||||
| chr4:105739452
|
T | C | 27 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(24): Show | 28 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.1240+9953T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105739452 | ||||||
| chr4:105739458
|
G | A | 1 | a0001c0001t0013g0070 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1240+9959G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105739458 | ||||||
| chr4:105739494
|
T | A | 13 | a0001c0001t0003g0095a0001c0001t0003g0103a0001c0001t0003g0106others(10): Show | 13 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(10): Show |
intron_variant | MODIFIER | c.1240+9995T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105739494 | ||||||
| chr4:105739710
|
T | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0052 | 2 | NA18987.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1240+10211T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105739710 | ||||||
| chr4:105739792
|
A | C | 1 | a0001c0001t0002g0152 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1240+10293A>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105739792 | ||||||
| chr4:105739801
|
C | T | 12 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(9): Show | 12 | HG01070.hp2 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1240+10302C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105739801 | ||||||
| chr4:105739886
|
C | T | 2 | a0001c0001t0008g0072a0001c0001t0008g0073 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1240+10387C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105739886 | ||||||
| chr4:105740037
|
G | A | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1240+10538G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105740037 | ||||||
| chr4:105740307
|
G | T | 1 | a0001c0001t0003g0125 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1240+10808G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105740307 | ||||||
| chr4:105740368
|
C | A | 1 | a0001c0001t0002g0155 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1240+10869C>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105740368 | ||||||
| chr4:105740407
|
G | T | 1 | a0001c0001t0003g0121 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1240+10908G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105740407 | ||||||
| chr4:105740489
|
G | A | 1 | a0001c0002t0002g0088 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1240+10990G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105740489 | ||||||
| chr4:105740639
|
C | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02630.hp2 HG02970.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1240+11140C>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105740639 | ||||||
| chr4:105740813
|
A | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+11314A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105740813 | ||||||
| chr4:105740847
|
A | G | 71 | a0001c0001t0003g0002a0001c0001t0003g0068a0001c0001t0003g0069others(68): Show | 72 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.1240+11348A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105740847 | ||||||
| chr4:105740961
|
G | A | 72 | a0001c0001t0002g0071a0001c0001t0003g0002a0001c0001t0003g0068others(69): Show | 73 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.1240+11462G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105740961 | ||||||
| chr4:105740999
|
C | A | 1 | a0001c0001t0002g0155 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1240+11500C>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105740999 | ||||||
| chr4:105741139
|
A | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(1): Show | 4 | HG02630.hp2 HG02970.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1240+11640A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105741139 | ||||||
| chr4:105741142
|
T | C | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1240+11643T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105741142 | ||||||
| chr4:105741184
|
C | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0027a0001c0001t0001g0028others(2): Show | 6 | HG00642.hp2 HG01515.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1240+11685C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105741184 | ||||||
| chr4:105741506
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1240+12007A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105741506 | ||||||
| chr4:105741528
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1240+12029G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105741528 | ||||||
| chr4:105741535
|
G | C | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+12036G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105741535 | ||||||
| chr4:105741789
|
C | T | 65 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(62): Show | 66 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.1240+12290C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105741789 | ||||||
| chr4:105741819
|
T | C | 3 | a0001c0001t0003g0120a0001c0001t0003g0121a0001c0001t0003g0143 | 3 | HG01109.hp1 HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1240+12320T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105741819 | ||||||
| chr4:105741823
|
A | T | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1240+12324A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105741823 | ||||||
| chr4:105741955
|
AG | A | 12 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(9): Show | 12 | HG01070.hp2 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1240+12460delG | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105741955 | |||||
| chr4:105742077
|
C | T | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+12578C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105742077 | ||||||
| chr4:105742163
|
G | C | 1 | a0001c0001t0003g0108 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1240+12664G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105742163 | ||||||
| chr4:105742221
|
T | C | 1 | a0001c0001t0004g0074 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1240+12722T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105742221 | ||||||
| chr4:105742322
|
T | A | 1 | a0001c0001t0001g0016 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1240+12823T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105742322 | ||||||
| chr4:105742384
|
T | C | 65 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(62): Show | 66 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.1240+12885T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105742384 | ||||||
| chr4:105742476
|
C | T | 1 | a0001c0001t0004g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1240+12977C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105742476 | ||||||
| chr4:105742500
|
C | T | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+13001C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105742500 | ||||||
| chr4:105742707
|
CT | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(103): Show | 108 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.1240+13225delT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105742707 | |||||
| chr4:105742762
|
T | C | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1240+13263T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105742762 | ||||||
| chr4:105742822
|
C | T | 2 | a0001c0001t0008g0072a0001c0001t0008g0073 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1240+13323C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105742822 | ||||||
| chr4:105742875
|
T | A | 2 | a0001c0001t0003g0069a0001c0001t0013g0070 | 2 | HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1240+13376T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105742875 | ||||||
| chr4:105742954
|
T | C | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1240+13455T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105742954 | ||||||
| chr4:105742988
|
T | C | 1 | a0001c0001t0006g0168 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1240+13489T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105742988 | ||||||
| chr4:105742989
|
G | A | 1 | a0001c0001t0006g0168 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1240+13490G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105742989 | ||||||
| chr4:105743007
|
TGCCGCGA others(18): Show |
T | 3 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0002g0165 | 3 | HG01516.hp1 HG01517.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1240+13514_1240+13 others(31): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105743007 | |||||
| chr4:105743032
|
C | T | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+13533C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105743032 | ||||||
| chr4:105743054
|
A | T | 65 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(62): Show | 66 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.1240+13555A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105743054 | ||||||
| chr4:105743098
|
C | T | 1 | a0001c0001t0016g0130 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1240+13599C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105743098 | ||||||
| chr4:105743141
|
G | A | 1 | a0001c0002t0026g0090 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1240+13642G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105743141 | ||||||
| chr4:105743172
|
G | C | 1 | a0001c0001t0001g0027 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1240+13673G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105743172 | ||||||
| chr4:105743197
|
C | G | 1 | a0001c0001t0002g0157 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1240+13698C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105743197 | ||||||
| chr4:105743215
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0017g0162a0003c0004t0002g0085 | 3 | HG01070.hp1 HG01081.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1240+13716A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105743215 | ||||||
| chr4:105743230
|
A | G | 20 | a0001c0001t0001g0003a0001c0001t0004g0133a0001c0001t0004g0176others(17): Show | 20 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.1240+13731A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105743230 | ||||||
| chr4:105743239
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0051 | 2 | NA18983.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1240+13740C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105743239 | ||||||
| chr4:105743242
|
A | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(118): Show | 122 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1240+13743A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105743242 | ||||||
| chr4:105743267
|
T | C | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+13768T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105743267 | ||||||
| chr4:105743398
|
C | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(117): Show | 121 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.1240+13899C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105743398 | ||||||
| chr4:105743611
|
T | G | 3 | a0001c0002t0002g0086a0001c0002t0002g0087a0001c0002t0002g0097 | 3 | HG01069.hp1 HG01192.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1240+14112T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105743611 | ||||||
| chr4:105743653
|
C | CT | 15 | a0001c0001t0001g0044a0001c0001t0002g0071a0001c0001t0002g0148others(12): Show | 15 | HG00597.hp1 HG01175.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1240+14180dupT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105743653 | |||||
| chr4:105743653
|
C | CTT | 6 | a0001c0001t0004g0075a0001c0001t0004g0077a0001c0001t0004g0078others(3): Show | 6 | HG01070.hp2 HG02451.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240+14179_1240+14 others(8): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105743653 | |||||
| chr4:105743653
|
CT | C | 37 | a0001c0001t0001g0043a0001c0001t0001g0061a0001c0001t0002g0157others(34): Show | 37 | HG00639.hp1 HG00741.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.1240+14180delT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105743653 | |||||
| chr4:105743653
|
CTT | C | 6 | a0001c0001t0005g0175a0001c0001t0005g0180a0001c0001t0005g0181others(3): Show | 6 | HG00735.hp1 HG01243.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.1240+14179_1240+14 others(8): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105743653 | |||||
| chr4:105743679
|
T | A | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1240+14180T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105743679 | ||||||
| chr4:105743714
|
G | A | 1 | a0001c0001t0004g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1240+14215G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105743714 | ||||||
| chr4:105743733
|
A | G | 1 | a0001c0002t0020g0136 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1240+14234A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105743733 | ||||||
| chr4:105743862
|
G | A | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+14363G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105743862 | ||||||
| chr4:105743956
|
G | A | 2 | a0001c0001t0002g0157a0001c0001t0002g0179 | 2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1240+14457G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105743956 | ||||||
| chr4:105744838
|
T | A | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1240+15339T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105744838 | ||||||
| chr4:105744886
|
AT | A | 62 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(59): Show | 63 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.1240+15389delT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105744886 | |||||
| chr4:105745154
|
C | T | 2 | a0001c0001t0009g0141a0001c0001t0009g0142 | 2 | HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1240+15655C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105745154 | ||||||
| chr4:105745178
|
C | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+15679C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105745178 | ||||||
| chr4:105745202
|
T | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(158): Show | 163 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.1240+15703T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105745202 | ||||||
| chr4:105745234
|
C | A | 1 | a0001c0001t0002g0156 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1240+15735C>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105745234 | ||||||
| chr4:105745423
|
A | G | 41 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(38): Show | 42 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.1240+15924A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105745423 | ||||||
| chr4:105745575
|
C | T | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+16076C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105745575 | ||||||
| chr4:105745616
|
T | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(102): Show | 106 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1240+16117T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105745616 | ||||||
| chr4:105745645
|
T | C | 1 | a0001c0001t0004g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1240+16146T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105745645 | ||||||
| chr4:105746125
|
C | G | 1 | a0001c0001t0004g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1240+16626C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105746125 | ||||||
| chr4:105746682
|
C | T | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1240+17183C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105746682 | ||||||
| chr4:105746868
|
T | C | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1240+17369T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105746868 | ||||||
| chr4:105747131
|
T | C | 1 | a0001c0001t0001g0010 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1240+17632T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105747131 | ||||||
| chr4:105747149
|
G | T | 3 | a0001c0001t0003g0124a0001c0001t0003g0128a0001c0001t0003g0129 | 3 | HG01891.hp2 HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1240+17650G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105747149 | ||||||
| chr4:105747201
|
A | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(158): Show | 163 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.1240+17702A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105747201 | ||||||
| chr4:105747389
|
G | A | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+17890G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105747389 | ||||||
| chr4:105747552
|
G | A | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1240+18053G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105747552 | ||||||
| chr4:105747670
|
T | C | 1 | a0001c0001t0004g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1240+18171T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105747670 | ||||||
| chr4:105747866
|
C | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(84): Show | 88 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.1240+18367C>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105747866 | ||||||
| chr4:105747889
|
T | TTTG | 160 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(157): Show | 162 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.1240+18402_1240+18 others(9): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105747889 | |||||
| chr4:105748137
|
C | T | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1240+18638C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105748137 | ||||||
| chr4:105748187
|
G | A | 41 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(38): Show | 42 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.1240+18688G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105748187 | ||||||
| chr4:105748195
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1240+18696G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105748195 | ||||||
| chr4:105748437
|
G | A | 24 | a0001c0002t0002g0079a0001c0002t0002g0080a0001c0002t0002g0081others(21): Show | 24 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(21): Show |
intron_variant | MODIFIER | c.1240+18938G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105748437 | ||||||
| chr4:105748808
|
AAGTT | A | 62 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(59): Show | 63 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.1240+19312_1240+19 others(10): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105748808 | |||||
| chr4:105749181
|
GAA | G | 127 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(124): Show | 129 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1240+19684_1240+19 others(8): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105749181 | |||||
| chr4:105749185
|
C | CAT | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+19686_1240+19 others(8): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105749185 | ||||||
| chr4:105749202
|
T | C | 2 | a0001c0001t0008g0072a0001c0001t0008g0073 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1240+19703T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105749202 | ||||||
| chr4:105749336
|
A | T | 12 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(9): Show | 12 | HG01070.hp2 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1240+19837A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105749336 | ||||||
| chr4:105749401
|
A | T | 128 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(125): Show | 130 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.1240+19902A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105749401 | ||||||
| chr4:105749432
|
G | C | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+19933G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105749432 | ||||||
| chr4:105749466
|
G | A | 4 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0115others(1): Show | 4 | HG01884.hp2 HG02886.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+19967G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105749466 | ||||||
| chr4:105749493
|
A | G | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+19994A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105749493 | ||||||
| chr4:105749548
|
C | T | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+20049C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105749548 | ||||||
| chr4:105749609
|
C | CA | 17 | a0001c0001t0002g0153a0001c0001t0003g0135a0001c0001t0005g0167others(14): Show | 17 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.1240+20126dupA | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105749609 | |||||
| chr4:105750056
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1240+20557G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105750056 | ||||||
| chr4:105750186
|
G | A | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1240+20687G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105750186 | ||||||
| chr4:105750229
|
C | T | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1240+20730C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105750229 | ||||||
| chr4:105750235
|
G | C | 1 | a0001c0001t0001g0017 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1240+20736G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105750235 | ||||||
| chr4:105750316
|
C | T | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1240+20817C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105750316 | ||||||
| chr4:105750317
|
G | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0062 | 2 | HG00639.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1240+20818G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105750317 | ||||||
| chr4:105750460
|
C | CA | 7 | a0001c0001t0004g0133a0001c0001t0004g0176a0001c0001t0004g0177others(4): Show | 7 | HG01243.hp2 HG01884.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1240+20980dupA | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105750460 | |||||
| chr4:105750725
|
C | T | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1240+21226C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105750725 | ||||||
| chr4:105750835
|
A | G | 1 | a0001c0005t0021g0091 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1240+21336A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105750835 | ||||||
| chr4:105750912
|
G | A | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+21413G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105750912 | ||||||
| chr4:105751041
|
T | C | 65 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(62): Show | 66 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.1240+21542T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105751041 | ||||||
| chr4:105751350
|
T | A | 4 | a0001c0001t0004g0133a0001c0001t0004g0176a0001c0001t0004g0177others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+21851T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105751350 | ||||||
| chr4:105751354
|
T | G | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1240+21855T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105751354 | ||||||
| chr4:105751406
|
A | G | 4 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0035others(1): Show | 4 | HG02015.hp1 HG02080.hp2 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+21907A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105751406 | ||||||
| chr4:105751701
|
T | C | 1 | a0001c0001t0004g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1240+22202T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105751701 | ||||||
| chr4:105751734
|
AAGG | A | 62 | a0001c0001t0003g0002a0001c0001t0003g0094a0001c0001t0003g0095others(59): Show | 63 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.1240+22238_1240+22 others(9): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105751734 | |||||
| chr4:105751773
|
A | G | 1 | a0001c0001t0003g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1240+22274A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105751773 | ||||||
| chr4:105752171
|
G | A | 156 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(153): Show | 158 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.1240+22672G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105752171 | ||||||
| chr4:105752171
|
G | T | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+22672G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105752171 | ||||||
| chr4:105752486
|
T | A | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1240+22987T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105752486 | ||||||
| chr4:105752736
|
T | C | 1 | a0001c0001t0003g0115 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1240+23237T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105752736 | ||||||
| chr4:105752896
|
G | T | 1 | a0001c0002t0002g0088 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1240+23397G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105752896 | ||||||
| chr4:105753113
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1240+23614C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105753113 | ||||||
| chr4:105753511
|
T | C | 65 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(62): Show | 66 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.1240+24012T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105753511 | ||||||
| chr4:105753947
|
G | A | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+24448G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105753947 | ||||||
| chr4:105753964
|
A | AT | 14 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(11): Show | 14 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.1240+24477dupT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105753964 | |||||
| chr4:105753994
|
G | T | 2 | a0001c0001t0005g0184a0001c0001t0015g0183 | 2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1240+24495G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105753994 | ||||||
| chr4:105754484
|
TTTTA | T | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+24987_1240+24 others(10): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105754484 | |||||
| chr4:105754757
|
G | A | 5 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG01070.hp2 HG02630.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+25258G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105754757 | ||||||
| chr4:105754789
|
A | T | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+25290A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105754789 | ||||||
| chr4:105754893
|
T | A | 2 | a0001c0001t0008g0072a0001c0001t0008g0073 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1240+25394T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105754893 | ||||||
| chr4:105755056
|
CAAAA | C | 5 | a0001c0001t0002g0161a0001c0001t0003g0135a0001c0001t0004g0076others(2): Show | 5 | HG00280.hp1 HG01070.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240+25597_1240+25 others(10): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105755056 | |||||
| chr4:105755056
|
CAAAAA | C | 7 | a0001c0001t0002g0149a0001c0001t0002g0157a0001c0001t0002g0179others(4): Show | 7 | HG01081.hp1 HG02451.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.1240+25596_1240+25 others(11): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105755056 | |||||
| chr4:105755056
|
CAAAAAAA others(1): Show |
C | 5 | a0001c0001t0002g0145a0001c0001t0002g0148a0001c0001t0002g0150others(2): Show | 5 | HG01517.hp1 HG02071.hp2 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240+25593_1240+25 others(14): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105755056 | |||||
| chr4:105755056
|
CAAAAAAA others(2): Show |
C | 7 | a0001c0001t0002g0146a0001c0001t0002g0151a0001c0001t0002g0152others(4): Show | 7 | HG01516.hp1 HG02015.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240+25592_1240+25 others(15): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105755056 | |||||
| chr4:105755056
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1240+25591_1240+25 others(16): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105755056 | |||||
| chr4:105755056
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0004g0133a0001c0001t0008g0072 | 2 | HG01243.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1240+25590_1240+25 others(17): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105755056 | |||||
| chr4:105755056
|
CAAAAAAA others(5): Show |
C | 7 | a0001c0001t0001g0036a0001c0001t0004g0176a0001c0001t0004g0177others(4): Show | 7 | HG01069.hp1 HG01884.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240+25589_1240+25 others(18): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105755056 | |||||
| chr4:105755056
|
CAAAAAAA others(6): Show |
C | 23 | a0001c0001t0001g0040a0001c0001t0002g0064a0001c0001t0003g0106others(20): Show | 23 | HG01109.hp1 HG01175.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.1240+25588_1240+25 others(19): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105755056 | |||||
| chr4:105755056
|
CAAAAAAA others(7): Show |
C | 49 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(46): Show | 50 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.1240+25587_1240+25 others(20): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105755056 | |||||
| chr4:105755056
|
CAAAAAAA others(8): Show |
C | 65 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(62): Show | 66 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.1240+25586_1240+25 others(21): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105755056 | |||||
| chr4:105755056
|
CAAAAAAA others(9): Show |
C | 3 | a0001c0001t0001g0039a0001c0001t0005g0174a0001c0001t0005g0175 | 3 | HG00280.hp2 HG01167.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1240+25585_1240+25 others(22): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105755056 | |||||
| chr4:105755056
|
CAAAAAAA others(13): Show |
C | 1 | a0001c0001t0004g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1240+25581_1240+25 others(26): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105755056 | |||||
| chr4:105755078
|
A | T | 13 | a0001c0001t0005g0167a0001c0001t0005g0180a0001c0001t0005g0181others(10): Show | 13 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.1240+25579A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105755078 | ||||||
| chr4:105755079
|
A | T | 2 | a0001c0001t0005g0174a0001c0001t0005g0175 | 2 | HG01167.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1240+25580A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105755079 | ||||||
| chr4:105755084
|
A | T | 13 | a0001c0001t0005g0167a0001c0001t0005g0180a0001c0001t0005g0181others(10): Show | 13 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.1240+25585A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105755084 | ||||||
| chr4:105755085
|
A | T | 2 | a0001c0001t0005g0174a0001c0001t0005g0175 | 2 | HG01167.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1240+25586A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105755085 | ||||||
| chr4:105755144
|
A | G | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1240+25645A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105755144 | ||||||
| chr4:105755241
|
CAAGGTAG others(9): Show |
C | 1 | a0001c0001t0004g0078 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1240+25755_1240+25 others(22): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105755241 | |||||
| chr4:105755609
|
G | A | 128 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(125): Show | 130 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.1240+26110G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105755609 | ||||||
| chr4:105755844
|
ACTATAAA others(123): Show |
A | 1 | a0001c0001t0004g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1240+26346_1240+26 others(6): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105755844 | ||||||
| chr4:105755975
|
A | T | 1 | a0001c0001t0004g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1240+26476A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105755975 | ||||||
| chr4:105755986
|
C | T | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1240+26487C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105755986 | ||||||
| chr4:105756227
|
G | A | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+26728G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105756227 | ||||||
| chr4:105756384
|
A | T | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+26885A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105756384 | ||||||
| chr4:105756396
|
G | A | 1 | a0001c0001t0003g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1240+26897G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105756396 | ||||||
| chr4:105756495
|
T | TAC | 4 | a0001c0001t0001g0053a0001c0001t0002g0153a0001c0001t0002g0157others(1): Show | 4 | HG01361.hp2 HG06807.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1240+27027_1240+27 others(8): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105756495 | |||||
| chr4:105756495
|
T | TACAC | 6 | a0001c0001t0002g0071a0001c0001t0002g0179a0001c0001t0003g0068others(3): Show | 6 | HG01884.hp1 HG02723.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1240+27025_1240+27 others(10): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105756495 | |||||
| chr4:105756495
|
T | TACACACA others(1): Show |
3 | a0001c0001t0004g0074a0001c0001t0004g0131a0001c0001t0004g0132 | 3 | HG02257.hp2 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1240+27021_1240+27 others(14): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105756495 | |||||
| chr4:105756495
|
T | TACACACA others(3): Show |
1 | a0001c0001t0004g0078 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1240+27019_1240+27 others(16): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105756495 | |||||
| chr4:105756495
|
T | TACACACA others(5): Show |
3 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0077 | 3 | HG02630.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1240+27017_1240+27 others(18): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105756495 | |||||
| chr4:105756495
|
T | TACACACA others(9): Show |
1 | a0001c0001t0016g0130 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1240+27013_1240+27 others(22): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105756495 | |||||
| chr4:105756495
|
T | TACACACA others(11): Show |
1 | a0001c0001t0004g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1240+27011_1240+27 others(24): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105756495 | |||||
| chr4:105756495
|
TAC | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(100): Show | 105 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.1240+27027_1240+27 others(8): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105756495 | |||||
| chr4:105756495
|
TACAC | T | 3 | a0001c0001t0001g0052a0001c0001t0003g0115a0001c0002t0002g0088 | 3 | HG03041.hp1 NA18990.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1240+27025_1240+27 others(10): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105756495 | |||||
| chr4:105756495
|
TACACACA others(1): Show |
T | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+27021_1240+27 others(14): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105756495 | |||||
| chr4:105756526
|
ACG | A | 5 | a0001c0002t0002g0100a0001c0002t0002g0101a0001c0002t0002g0137others(2): Show | 5 | HG02145.hp1 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+27028_1240+27 others(8): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105756526 | ||||||
| chr4:105756564
|
A | G | 1 | a0001c0001t0008g0073 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1240+27065A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105756564 | ||||||
| chr4:105756576
|
GTGTGTAT others(3): Show |
G | 1 | a0001c0001t0004g0074 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1240+27079_1240+27 others(16): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105756576 | |||||
| chr4:105756580
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1240+27081G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105756580 | ||||||
| chr4:105756580
|
GTA | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(78): Show | 82 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1240+27102_1240+27 others(8): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105756580 | |||||
| chr4:105756580
|
GTATA | G | 7 | a0001c0001t0001g0010a0001c0001t0004g0075a0001c0001t0004g0076others(4): Show | 7 | HG01070.hp2 HG01243.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240+27100_1240+27 others(10): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105756580 | |||||
| chr4:105756582
|
A | G | 68 | a0001c0001t0002g0152a0001c0001t0002g0156a0001c0001t0003g0002others(65): Show | 69 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.1240+27083A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105756582 | ||||||
| chr4:105756584
|
A | G | 19 | a0001c0001t0001g0029a0001c0001t0003g0068a0001c0001t0004g0131others(16): Show | 19 | HG00642.hp2 HG01884.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1240+27085A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105756584 | ||||||
| chr4:105756586
|
A | G | 12 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0077others(9): Show | 12 | HG01070.hp2 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1240+27087A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105756586 | ||||||
| chr4:105756588
|
A | G | 2 | a0001c0001t0004g0132a0003c0004t0002g0085 | 2 | HG02451.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1240+27089A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105756588 | ||||||
| chr4:105756599
|
TATA | T | 4 | a0001c0002t0002g0100a0001c0002t0002g0101a0001c0002t0011g0138others(1): Show | 4 | HG02145.hp1 HG02717.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1240+27104_1240+27 others(9): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105756599 | |||||
| chr4:105756842
|
C | T | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+27343C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105756842 | ||||||
| chr4:105757402
|
C | G | 1 | a0001c0001t0005g0167 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1240+27903C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105757402 | ||||||
| chr4:105757443
|
C | G | 1 | a0001c0001t0001g0057 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1240+27944C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105757443 | ||||||
| chr4:105757583
|
G | A | 3 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0178 | 3 | HG01884.hp1 HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1240+28084G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105757583 | ||||||
| chr4:105757801
|
T | C | 2 | a0001c0001t0008g0072a0001c0001t0008g0073 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1240+28302T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105757801 | ||||||
| chr4:105758116
|
G | A | 8 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(5): Show | 8 | HG01070.hp2 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1240+28617G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105758116 | ||||||
| chr4:105758440
|
G | A | 36 | a0001c0001t0003g0002a0001c0001t0003g0094a0001c0001t0003g0095others(33): Show | 37 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.1240+28941G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105758440 | ||||||
| chr4:105758508
|
A | G | 2 | a0001c0001t0008g0072a0001c0001t0008g0073 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1240+29009A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105758508 | ||||||
| chr4:105758535
|
A | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+29036A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105758535 | ||||||
| chr4:105758656
|
T | C | 4 | a0001c0001t0003g0116a0001c0001t0003g0117a0001c0001t0003g0139others(1): Show | 4 | HG01175.hp1 HG02145.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1240+29157T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105758656 | ||||||
| chr4:105758691
|
G | A | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+29192G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105758691 | ||||||
| chr4:105758728
|
G | C | 1 | a0001c0001t0003g0124 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1240+29229G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105758728 | ||||||
| chr4:105758933
|
G | A | 1 | a0001c0001t0003g0102 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1240+29434G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105758933 | ||||||
| chr4:105759116
|
T | C | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+29617T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105759116 | ||||||
| chr4:105759206
|
G | A | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+29707G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105759206 | ||||||
| chr4:105759294
|
G | A | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+29795G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105759294 | ||||||
| chr4:105759320
|
T | C | 1 | a0001c0001t0004g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1240+29821T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105759320 | ||||||
| chr4:105759346
|
A | ATCT | 8 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(5): Show | 8 | HG01070.hp2 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1240+29848_1240+29 others(9): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105759346 | |||||
| chr4:105759607
|
G | A | 41 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(38): Show | 42 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.1240+30108G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105759607 | ||||||
| chr4:105759879
|
A | G | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1240+30380A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105759879 | ||||||
| chr4:105759982
|
C | T | 1 | a0001c0002t0002g0088 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1240+30483C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105759982 | ||||||
| chr4:105760022
|
A | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+30523A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105760022 | ||||||
| chr4:105760094
|
T | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(140): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1240+30595T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105760094 | ||||||
| chr4:105760126
|
G | A | 16 | a0001c0002t0002g0079a0001c0002t0002g0080a0001c0002t0002g0081others(13): Show | 16 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.1240+30627G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105760126 | ||||||
| chr4:105760152
|
GA | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+30663delA | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105760152 | |||||
| chr4:105760167
|
CA | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(142): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1240+30687delA | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105760167 | |||||
| chr4:105760167
|
CAA | C | 8 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(5): Show | 8 | HG01070.hp2 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1240+30686_1240+30 others(8): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105760167 | |||||
| chr4:105760180
|
A | C | 127 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(124): Show | 129 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1240+30681A>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105760180 | ||||||
| chr4:105760293
|
C | T | 1 | a0001c0001t0018g0160 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1240+30794C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105760293 | ||||||
| chr4:105760461
|
G | C | 1 | a0001c0001t0004g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1240+30962G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105760461 | ||||||
| chr4:105760572
|
G | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0062 | 2 | HG00639.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1240+31073G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105760572 | ||||||
| chr4:105760996
|
A | AT | 7 | a0001c0001t0003g0109a0001c0001t0003g0119a0001c0001t0003g0139others(4): Show | 7 | HG00438.hp2 HG01175.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240+31522dupT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105760996 | |||||
| chr4:105760996
|
AT | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(89): Show | 93 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.1240+31522delT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105760996 | |||||
| chr4:105760996
|
ATT | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0020a0001c0001t0001g0061others(4): Show | 7 | HG01167.hp2 HG01975.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240+31521_1240+31 others(8): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105760996 | |||||
| chr4:105760996
|
ATTTTTT | A | 14 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(11): Show | 14 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.1240+31517_1240+31 others(12): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105760996 | |||||
| chr4:105761096
|
C | T | 1 | a0001c0001t0023g0050 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1240+31597C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105761096 | ||||||
| chr4:105761186
|
T | C | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1240+31687T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105761186 | ||||||
| chr4:105761192
|
T | C | 5 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG01070.hp2 HG02630.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+31693T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105761192 | ||||||
| chr4:105761279
|
T | C | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+31780T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105761279 | ||||||
| chr4:105761362
|
T | C | 65 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(62): Show | 66 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.1240+31863T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105761362 | ||||||
| chr4:105761492
|
G | A | 1 | a0003c0004t0002g0085 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1240+31993G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105761492 | ||||||
| chr4:105761663
|
C | G | 1 | a0003c0004t0002g0085 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1240+32164C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105761663 | ||||||
| chr4:105761674
|
G | A | 4 | a0001c0001t0001g0015a0001c0001t0004g0075a0001c0001t0004g0076others(1): Show | 4 | HG02630.hp1 HG02630.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+32175G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105761674 | ||||||
| chr4:105761718
|
G | T | 7 | a0001c0002t0002g0088a0001c0002t0002g0100a0001c0002t0002g0101others(4): Show | 7 | HG02145.hp1 HG02622.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1240+32219G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105761718 | ||||||
| chr4:105761799
|
C | T | 1 | a0001c0001t0004g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1240+32300C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105761799 | ||||||
| chr4:105761839
|
T | C | 1 | a0001c0001t0002g0157 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1240+32340T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105761839 | ||||||
| chr4:105761964
|
G | A | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+32465G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105761964 | ||||||
| chr4:105762294
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1240+32795C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105762294 | ||||||
| chr4:105762335
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1240+32836G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105762335 | ||||||
| chr4:105762462
|
G | A | 1 | a0001c0001t0001g0001 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1240+32963G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105762462 | ||||||
| chr4:105762530
|
G | A | 2 | a0001c0001t0004g0131a0001c0001t0004g0132 | 2 | HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1240+33031G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105762530 | ||||||
| chr4:105762865
|
G | A | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(5): Show | 8 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(5): Show |
intron_variant | MODIFIER | c.1240+33366G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105762865 | ||||||
| chr4:105763047
|
T | G | 41 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(38): Show | 42 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.1240+33548T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105763047 | ||||||
| chr4:105763065
|
A | G | 1 | a0001c0001t0001g0007 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1240+33566A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105763065 | ||||||
| chr4:105763227
|
A | T | 1 | a0001c0001t0001g0016 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1240+33728A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105763227 | ||||||
| chr4:105763388
|
G | A | 143 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(140): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1240+33889G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105763388 | ||||||
| chr4:105763510
|
C | T | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(158): Show | 163 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.1240+34011C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105763510 | ||||||
| chr4:105763708
|
C | G | 1 | a0001c0001t0006g0173 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1240+34209C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105763708 | ||||||
| chr4:105763771
|
T | C | 1 | a0001c0001t0003g0115 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1240+34272T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105763771 | ||||||
| chr4:105763821
|
A | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(155): Show | 160 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1240+34322A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105763821 | ||||||
| chr4:105763850
|
T | C | 3 | a0001c0001t0003g0069a0001c0001t0003g0135a0001c0001t0013g0070 | 3 | HG03098.hp1 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1240+34351T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105763850 | ||||||
| chr4:105763873
|
C | A | 3 | a0001c0001t0004g0131a0001c0001t0004g0132a0001c0001t0016g0130 | 3 | HG02257.hp2 HG02451.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1240+34374C>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105763873 | ||||||
| chr4:105764371
|
G | A | 6 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(3): Show | 6 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1240+34872G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105764371 | ||||||
| chr4:105764388
|
A | G | 4 | a0001c0001t0004g0133a0001c0001t0004g0176a0001c0001t0004g0177others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+34889A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105764388 | ||||||
| chr4:105764400
|
A | G | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+34901A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105764400 | ||||||
| chr4:105764414
|
A | C | 1 | a0001c0001t0016g0130 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1240+34915A>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105764414 | ||||||
| chr4:105764476
|
T | C | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+34977T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105764476 | ||||||
| chr4:105764533
|
CT | C | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+35037delT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105764533 | |||||
| chr4:105764668
|
C | A | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+35169C>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105764668 | ||||||
| chr4:105764919
|
C | T | 2 | a0001c0001t0003g0124a0001c0001t0003g0128 | 2 | HG01891.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1240+35420C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105764919 | ||||||
| chr4:105764939
|
T | G | 1 | a0001c0001t0001g0001 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1240+35440T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105764939 | ||||||
| chr4:105765340
|
G | C | 1 | a0001c0001t0013g0070 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1240+35841G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105765340 | ||||||
| chr4:105765704
|
T | C | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1240+36205T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105765704 | ||||||
| chr4:105766106
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1240+36607C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105766106 | ||||||
| chr4:105766576
|
A | G | 128 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(125): Show | 130 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.1240+37077A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105766576 | ||||||
| chr4:105766802
|
A | T | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+37303A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105766802 | ||||||
| chr4:105766853
|
T | C | 1 | a0001c0001t0002g0154 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1240+37354T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105766853 | ||||||
| chr4:105766887
|
C | CTT | 9 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0031others(6): Show | 9 | HG01069.hp2 HG01070.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.1240+37412_1240+37 others(8): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105766887 | |||||
| chr4:105766887
|
C | CTTT | 56 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(53): Show | 57 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.1240+37411_1240+37 others(9): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105766887 | |||||
| chr4:105766887
|
C | CTTTT | 9 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0019others(6): Show | 9 | HG00438.hp1 HG00642.hp1 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.1240+37410_1240+37 others(10): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105766887 | |||||
| chr4:105766887
|
C | CTTTTTTT others(6): Show |
1 | a0001c0002t0002g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1240+37401_1240+37 others(19): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105766887 | |||||
| chr4:105766887
|
C | CTTTTTTT others(7): Show |
1 | a0001c0002t0002g0086 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1240+37400_1240+37 others(20): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105766887 | |||||
| chr4:105766887
|
C | CTTTTTTT others(8): Show |
1 | a0001c0002t0002g0097 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1240+37399_1240+37 others(21): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105766887 | |||||
| chr4:105766887
|
C | CTTTTTTT others(9): Show |
1 | a0001c0002t0002g0087 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1240+37398_1240+37 others(22): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105766887 | |||||
| chr4:105766887
|
C | CTTTTTTT others(10): Show |
9 | a0001c0001t0003g0116a0001c0001t0003g0117a0001c0001t0003g0139others(6): Show | 9 | HG01175.hp1 HG02109.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1240+37397_1240+37 others(23): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105766887 | |||||
| chr4:105766887
|
C | CTTTTTTT others(11): Show |
4 | a0001c0001t0002g0071a0001c0001t0009g0141a0001c0001t0009g0142others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1240+37396_1240+37 others(24): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105766887 | |||||
| chr4:105766887
|
C | CTTTTTTT others(12): Show |
3 | a0001c0001t0003g0122a0001c0001t0003g0125a0001c0002t0002g0083 | 3 | HG02258.hp2 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1240+37395_1240+37 others(25): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105766887 | |||||
| chr4:105766887
|
C | CTTTTTTT others(13): Show |
4 | a0001c0001t0003g0123a0001c0001t0003g0124a0001c0001t0003g0129others(1): Show | 4 | HG01891.hp2 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+37394_1240+37 others(26): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105766887 | |||||
| chr4:105766887
|
C | CTTTTTTT others(14): Show |
2 | a0001c0001t0003g0120a0001c0001t0003g0121 | 2 | HG01109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1240+37393_1240+37 others(27): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105766887 | |||||
| chr4:105766887
|
C | CTTTTTTT others(15): Show |
1 | a0001c0002t0002g0088 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1240+37392_1240+37 others(28): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105766887 | |||||
| chr4:105766887
|
C | CTTTTTTT others(18): Show |
1 | a0003c0004t0002g0085 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1240+37389_1240+37 others(31): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105766887 | |||||
| chr4:105766887
|
C | CTTTTTTT others(19): Show |
1 | a0001c0001t0003g0143 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1240+37413_1240+37 others(32): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105766887 | |||||
| chr4:105766887
|
C | CTTTTTTT others(21): Show |
2 | a0001c0002t0002g0137a0001c0002t0011g0138 | 2 | HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1240+37413_1240+37 others(34): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105766887 | |||||
| chr4:105766887
|
C | CTTTTTTT others(24): Show |
1 | a0001c0002t0002g0101 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1240+37413_1240+37 others(37): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105766887 | |||||
| chr4:105766887
|
CT | C | 8 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0161others(5): Show | 8 | HG01243.hp2 HG01884.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1240+37413delT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105766887 | |||||
| chr4:105766887
|
CTT | C | 14 | a0001c0001t0003g0068a0001c0001t0003g0127a0001c0001t0004g0074others(11): Show | 14 | HG00735.hp1 HG01243.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1240+37412_1240+37 others(8): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105766887 | |||||
| chr4:105766887
|
CTTTTTTT | C | 23 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(20): Show | 24 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.1240+37407_1240+37 others(13): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105766887 | |||||
| chr4:105766887
|
CTTTTTTT others(2): Show |
C | 5 | a0001c0002t0002g0089a0001c0002t0002g0092a0001c0002t0002g0093others(2): Show | 5 | HG01975.hp2 HG02970.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+37405_1240+37 others(15): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105766887 | |||||
| chr4:105766929
|
A | G | 16 | a0001c0002t0002g0079a0001c0002t0002g0080a0001c0002t0002g0081others(13): Show | 16 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.1240+37430A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105766929 | ||||||
| chr4:105767040
|
G | A | 1 | a0001c0001t0002g0156 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1240+37541G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105767040 | ||||||
| chr4:105767198
|
G | C | 12 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(9): Show | 12 | HG01070.hp2 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1240+37699G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105767198 | ||||||
| chr4:105767201
|
T | G | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1240+37702T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105767201 | ||||||
| chr4:105767217
|
A | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(155): Show | 160 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1240+37718A>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105767217 | ||||||
| chr4:105767372
|
T | C | 1 | a0001c0001t0003g0139 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1240+37873T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105767372 | ||||||
| chr4:105767436
|
T | C | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1240+37937T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105767436 | ||||||
| chr4:105767494
|
TTTATTA | T | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(158): Show | 163 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.1240+37996_1240+38 others(12): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105767494 | ||||||
| chr4:105767505
|
T | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(158): Show | 163 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.1240+38006T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105767505 | ||||||
| chr4:105767509
|
T | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(158): Show | 163 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.1240+38010T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105767509 | ||||||
| chr4:105767510
|
AGGTT | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(158): Show | 163 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.1240+38012_1240+38 others(10): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105767510 | ||||||
| chr4:105767747
|
A | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+38248A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105767747 | ||||||
| chr4:105767819
|
T | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(140): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1240+38320T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105767819 | ||||||
| chr4:105767931
|
TG | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(124): Show | 129 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1240+38433delG | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105767931 | ||||||
| chr4:105767932
|
G | T | 1 | a0001c0001t0001g0012 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1240+38433G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105767932 | ||||||
| chr4:105768028
|
TA | T | 9 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(6): Show | 9 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1240+38539delA | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105768028 | |||||
| chr4:105768038
|
A | T | 6 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(3): Show | 6 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1240+38539A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105768038 | ||||||
| chr4:105768105
|
G | A | 1 | a0001c0001t0012g0049 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1240+38606G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105768105 | ||||||
| chr4:105768255
|
C | A | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1240+38756C>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105768255 | ||||||
| chr4:105768265
|
C | T | 1 | a0001c0002t0002g0088 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1240+38766C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105768265 | ||||||
| chr4:105768417
|
G | A | 3 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0178 | 3 | HG01884.hp1 HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1240+38918G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105768417 | ||||||
| chr4:105768420
|
G | A | 1 | a0001c0001t0002g0165 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1240+38921G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105768420 | ||||||
| chr4:105768693
|
A | G | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+39194A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105768693 | ||||||
| chr4:105768889
|
A | G | 14 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0148others(11): Show | 14 | HG01516.hp1 HG01517.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.1240+39390A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105768889 | ||||||
| chr4:105769199
|
A | G | 143 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(140): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1240+39700A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105769199 | ||||||
| chr4:105769231
|
GCGCA | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+39734_1240+39 others(10): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105769231 | |||||
| chr4:105769233
|
G | GATCACA | 4 | a0001c0001t0004g0132a0001c0001t0004g0176a0001c0001t0004g0177others(1): Show | 4 | HG01884.hp1 HG02451.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+39734_1240+39 others(12): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105769233 | ||||||
| chr4:105769233
|
G | GATCACAC others(3): Show |
1 | a0001c0001t0004g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1240+39734_1240+39 others(16): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105769233 | ||||||
| chr4:105769233
|
G | GATCACAC others(7): Show |
1 | a0001c0001t0004g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1240+39734_1240+39 others(20): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105769233 | ||||||
| chr4:105769233
|
GCA | G | 24 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0148others(21): Show | 24 | HG00280.hp1 HG01081.hp1 HG01516.hp1 others(21): Show |
intron_variant | MODIFIER | c.1240+39774_1240+39 others(8): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105769233 | |||||
| chr4:105769233
|
GCACA | G | 4 | a0001c0001t0003g0095a0001c0001t0003g0108a0001c0001t0003g0121others(1): Show | 4 | HG01109.hp1 HG03710.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+39772_1240+39 others(10): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105769233 | |||||
| chr4:105769233
|
GCACACA | G | 45 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0023others(42): Show | 46 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.1240+39770_1240+39 others(12): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105769233 | |||||
| chr4:105769233
|
GCACACAC others(1): Show |
G | 61 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(58): Show | 62 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.1240+39768_1240+39 others(14): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105769233 | |||||
| chr4:105769233
|
GCACACAC others(3): Show |
G | 17 | a0001c0001t0002g0071a0001c0002t0002g0079a0001c0002t0002g0080others(14): Show | 17 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.1240+39766_1240+39 others(16): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105769233 | |||||
| chr4:105769234
|
C | A | 4 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0077others(1): Show | 4 | HG01070.hp2 HG02630.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+39735C>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105769234 | ||||||
| chr4:105769235
|
A | T | 4 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0077others(1): Show | 4 | HG01070.hp2 HG02630.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+39736A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105769235 | ||||||
| chr4:105769237
|
A | G | 3 | a0001c0001t0002g0157a0001c0001t0002g0179a0001c0001t0003g0135 | 3 | HG03098.hp1 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1240+39738A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105769237 | ||||||
| chr4:105769241
|
A | G | 1 | a0001c0001t0003g0069 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1240+39742A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105769241 | ||||||
| chr4:105769243
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0062 | 2 | HG00639.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1240+39744A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105769243 | ||||||
| chr4:105769271
|
A | C | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1240+39772A>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105769271 | ||||||
| chr4:105769309
|
C | G | 1 | a0001c0001t0001g0021 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1240+39810C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105769309 | ||||||
| chr4:105769355
|
G | A | 1 | a0001c0001t0004g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1240+39856G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105769355 | ||||||
| chr4:105769517
|
A | G | 1 | a0001c0001t0002g0152 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1240+40018A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105769517 | ||||||
| chr4:105770012
|
G | T | 5 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG01070.hp2 HG02630.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+40513G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105770012 | ||||||
| chr4:105770359
|
CT | C | 80 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(77): Show | 81 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.1240+40871delT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105770359 | |||||
| chr4:105770456
|
G | C | 41 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(38): Show | 42 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.1240+40957G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105770456 | ||||||
| chr4:105770478
|
C | T | 1 | a0001c0001t0003g0129 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1240+40979C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105770478 | ||||||
| chr4:105771186
|
C | T | 5 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG01070.hp2 HG02630.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+41687C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105771186 | ||||||
| chr4:105771316
|
G | C | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+41817G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105771316 | ||||||
| chr4:105771324
|
A | G | 18 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0178others(15): Show | 18 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.1240+41825A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105771324 | ||||||
| chr4:105771621
|
T | G | 1 | a0001c0002t0020g0136 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1240+42122T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105771621 | ||||||
| chr4:105771787
|
C | T | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+42288C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105771787 | ||||||
| chr4:105771799
|
A | G | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+42300A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105771799 | ||||||
| chr4:105771828
|
G | A | 1 | a0001c0001t0002g0152 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1240+42329G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105771828 | ||||||
| chr4:105772209
|
A | G | 2 | a0001c0001t0004g0075a0001c0001t0004g0077 | 2 | HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1240+42710A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105772209 | ||||||
| chr4:105772267
|
C | T | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1240+42768C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105772267 | ||||||
| chr4:105772351
|
A | T | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0030others(2): Show | 5 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+42852A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105772351 | ||||||
| chr4:105772965
|
C | T | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1240+43466C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105772965 | ||||||
| chr4:105773017
|
T | A | 1 | a0001c0001t0018g0160 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1240+43518T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105773017 | ||||||
| chr4:105773061
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1240+43562G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105773061 | ||||||
| chr4:105773163
|
C | A | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1240+43664C>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105773163 | ||||||
| chr4:105773311
|
C | T | 3 | a0001c0002t0002g0086a0001c0002t0002g0087a0001c0002t0002g0097 | 3 | HG01069.hp1 HG01192.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1240+43812C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105773311 | ||||||
| chr4:105773327
|
T | C | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1240+43828T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105773327 | ||||||
| chr4:105773456
|
G | A | 1 | a0001c0001t0004g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1240+43957G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105773456 | ||||||
| chr4:105773464
|
T | C | 62 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(59): Show | 63 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.1240+43965T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105773464 | ||||||
| chr4:105773490
|
A | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+43991A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105773490 | ||||||
| chr4:105773831
|
G | A | 41 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(38): Show | 42 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.1240+44332G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105773831 | ||||||
| chr4:105773899
|
T | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(158): Show | 163 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.1240+44400T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105773899 | ||||||
| chr4:105773911
|
G | A | 1 | a0001c0001t0002g0158 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1240+44412G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105773911 | ||||||
| chr4:105774001
|
T | C | 4 | a0001c0001t0003g0116a0001c0001t0003g0117a0001c0001t0003g0139others(1): Show | 4 | HG01175.hp1 HG02145.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1240+44502T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105774001 | ||||||
| chr4:105774334
|
GCATTTAG others(2): Show |
G | 3 | a0001c0001t0003g0069a0001c0001t0003g0135a0001c0001t0013g0070 | 3 | HG03098.hp1 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1240+44842_1240+44 others(15): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105774334 | |||||
| chr4:105774521
|
C | T | 1 | a0001c0001t0011g0147 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1240+45022C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105774521 | ||||||
| chr4:105774648
|
T | C | 1 | a0001c0001t0004g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1240+45149T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105774648 | ||||||
| chr4:105774733
|
C | T | 4 | a0001c0001t0004g0133a0001c0001t0004g0176a0001c0001t0004g0177others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+45234C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105774733 | ||||||
| chr4:105774734
|
G | A | 1 | a0001c0001t0003g0002 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1240+45235G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105774734 | ||||||
| chr4:105774817
|
T | C | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1240+45318T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105774817 | ||||||
| chr4:105775003
|
AG | A | 127 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(124): Show | 129 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1240+45506delG | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105775003 | |||||
| chr4:105775090
|
T | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+45591T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105775090 | ||||||
| chr4:105775103
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1240+45604A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105775103 | ||||||
| chr4:105775106
|
G | A | 2 | a0001c0001t0008g0072a0001c0001t0008g0073 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1240+45607G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105775106 | ||||||
| chr4:105775167
|
G | A | 1 | a0001c0001t0001g0010 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1240+45668G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105775167 | ||||||
| chr4:105775239
|
A | G | 1 | a0001c0001t0013g0070 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1240+45740A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105775239 | ||||||
| chr4:105775273
|
T | G | 1 | a0001c0001t0022g0054 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1240+45774T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105775273 | ||||||
| chr4:105775319
|
G | A | 127 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(124): Show | 129 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1240+45820G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105775319 | ||||||
| chr4:105775421
|
A | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(180): Show | 185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.1240+45922A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105775421 | ||||||
| chr4:105775506
|
T | G | 1 | a0001c0002t0002g0079 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1240+46007T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105775506 | ||||||
| chr4:105775599
|
A | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1240+46100A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105775599 | ||||||
| chr4:105775620
|
G | C | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1240+46121G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105775620 | ||||||
| chr4:105775757
|
A | G | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+46258A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105775757 | ||||||
| chr4:105775898
|
T | C | 5 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG01070.hp2 HG02630.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+46399T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105775898 | ||||||
| chr4:105776097
|
G | A | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1240+46598G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105776097 | ||||||
| chr4:105776126
|
G | A | 1 | a0001c0001t0003g0120 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1240+46627G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105776126 | ||||||
| chr4:105776143
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1240+46644G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105776143 | ||||||
| chr4:105776237
|
C | T | 12 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(9): Show | 12 | HG01070.hp2 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1241-46717C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105776237 | ||||||
| chr4:105776238
|
G | A | 2 | a0001c0001t0005g0174a0001c0001t0005g0175 | 2 | HG01167.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1241-46716G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105776238 | ||||||
| chr4:105776352
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1241-46602T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105776352 | ||||||
| chr4:105776416
|
C | T | 1 | a0001c0001t0002g0065 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1241-46538C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105776416 | ||||||
| chr4:105776548
|
T | G | 1 | a0001c0001t0003g0108 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1241-46406T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105776548 | ||||||
| chr4:105776619
|
G | A | 1 | a0001c0001t0004g0177 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1241-46335G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105776619 | ||||||
| chr4:105776655
|
T | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(155): Show | 160 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1241-46299T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105776655 | ||||||
| chr4:105776782
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1241-46172G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105776782 | ||||||
| chr4:105777286
|
A | ATG | 4 | a0001c0002t0002g0100a0001c0002t0002g0101a0001c0002t0002g0137others(1): Show | 4 | HG02145.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1241-45660_1241-45 others(8): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105777286 | |||||
| chr4:105777294
|
G | A | 1 | a0001c0001t0002g0165 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1241-45660G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105777294 | ||||||
| chr4:105777543
|
C | A | 128 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(125): Show | 130 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.1241-45411C>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105777543 | ||||||
| chr4:105777735
|
T | C | 51 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(48): Show | 51 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.1241-45219T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105777735 | ||||||
| chr4:105777931
|
T | C | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1241-45023T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105777931 | ||||||
| chr4:105778201
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1241-44753G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105778201 | ||||||
| chr4:105778615
|
C | T | 1 | a0001c0001t0003g0115 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1241-44339C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105778615 | ||||||
| chr4:105778655
|
A | G | 3 | a0001c0001t0004g0131a0001c0001t0004g0132a0001c0001t0016g0130 | 3 | HG02257.hp2 HG02451.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1241-44299A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105778655 | ||||||
| chr4:105778786
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1241-44168A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105778786 | ||||||
| chr4:105779444
|
A | G | 1 | a0002c0003t0010g0126 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1241-43510A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105779444 | ||||||
| chr4:105779652
|
A | G | 2 | a0001c0001t0008g0072a0001c0001t0008g0073 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1241-43302A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105779652 | ||||||
| chr4:105779665
|
C | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1241-43289C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105779665 | ||||||
| chr4:105779720
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1241-43234C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105779720 | ||||||
| chr4:105780047
|
C | G | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1241-42907C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105780047 | ||||||
| chr4:105780261
|
A | G | 2 | a0001c0001t0001g0026a0001c0001t0012g0063 | 2 | NA18983.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1241-42693A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105780261 | ||||||
| chr4:105780315
|
G | A | 1 | a0003c0004t0002g0085 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1241-42639G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105780315 | ||||||
| chr4:105780339
|
G | T | 2 | a0001c0001t0003g0069a0001c0001t0013g0070 | 2 | HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1241-42615G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105780339 | ||||||
| chr4:105780380
|
T | C | 1 | a0001c0001t0003g0115 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1241-42574T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105780380 | ||||||
| chr4:105780522
|
A | T | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1241-42432A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105780522 | ||||||
| chr4:105780608
|
T | A | 12 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(9): Show | 12 | HG01070.hp2 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1241-42346T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105780608 | ||||||
| chr4:105781231
|
C | T | 1 | a0001c0001t0005g0182 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1241-41723C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105781231 | ||||||
| chr4:105781239
|
A | T | 2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | HG00642.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1241-41715A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105781239 | ||||||
| chr4:105781411
|
C | CT | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1241-41528dupT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105781411 | |||||
| chr4:105781434
|
T | C | 1 | a0002c0003t0010g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1241-41520T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105781434 | ||||||
| chr4:105781542
|
C | T | 1 | a0001c0001t0003g0069 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1241-41412C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105781542 | ||||||
| chr4:105781793
|
CT | C | 11 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(8): Show | 11 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1241-41153delT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105781793 | |||||
| chr4:105782215
|
C | T | 6 | a0001c0001t0004g0132a0001c0001t0005g0180a0001c0001t0005g0181others(3): Show | 6 | HG00735.hp1 HG01243.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1241-40739C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105782215 | ||||||
| chr4:105782237
|
C | T | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1241-40717C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105782237 | ||||||
| chr4:105782352
|
G | A | 1 | a0001c0001t0023g0050 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1241-40602G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105782352 | ||||||
| chr4:105782386
|
A | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1241-40568A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105782386 | ||||||
| chr4:105782400
|
A | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1241-40554A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105782400 | ||||||
| chr4:105782458
|
G | A | 1 | a0001c0001t0004g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1241-40496G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105782458 | ||||||
| chr4:105782475
|
G | C | 4 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(1): Show | 4 | HG01069.hp2 HG01167.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1241-40479G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105782475 | ||||||
| chr4:105782593
|
C | CT | 18 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0077others(15): Show | 18 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.1241-40351dupT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105782593 | |||||
| chr4:105782738
|
A | T | 1 | a0001c0001t0001g0028 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1241-40216A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105782738 | ||||||
| chr4:105782819
|
G | A | 1 | a0001c0001t0004g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1241-40135G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105782819 | ||||||
| chr4:105783009
|
A | G | 41 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(38): Show | 42 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.1241-39945A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105783009 | ||||||
| chr4:105783207
|
C | A | 2 | a0001c0001t0008g0072a0001c0001t0008g0073 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1241-39747C>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105783207 | ||||||
| chr4:105783245
|
G | C | 2 | a0001c0001t0008g0072a0001c0001t0008g0073 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1241-39709G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105783245 | ||||||
| chr4:105783370
|
A | G | 1 | a0001c0001t0016g0130 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1241-39584A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105783370 | ||||||
| chr4:105783574
|
A | G | 65 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(62): Show | 66 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.1241-39380A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105783574 | ||||||
| chr4:105783591
|
T | C | 1 | a0001c0001t0002g0065 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1241-39363T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105783591 | ||||||
| chr4:105783616
|
A | G | 175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(172): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.1241-39338A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105783616 | ||||||
| chr4:105783873
|
T | C | 1 | a0001c0001t0003g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1241-39081T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105783873 | ||||||
| chr4:105783939
|
A | G | 1 | a0001c0001t0003g0122 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1241-39015A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105783939 | ||||||
| chr4:105784182
|
G | A | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1241-38772G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105784182 | ||||||
| chr4:105784206
|
C | G | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241-38748C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105784206 | ||||||
| chr4:105784237
|
A | G | 1 | a0001c0001t0001g0001 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1241-38717A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105784237 | ||||||
| chr4:105784562
|
G | T | 1 | a0001c0001t0001g0043 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1241-38392G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105784562 | ||||||
| chr4:105784706
|
T | C | 62 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(59): Show | 63 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.1241-38248T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105784706 | ||||||
| chr4:105784783
|
A | G | 2 | a0001c0001t0001g0026a0001c0001t0012g0063 | 2 | NA18983.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1241-38171A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105784783 | ||||||
| chr4:105784854
|
G | A | 3 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0178 | 3 | HG01884.hp1 HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1241-38100G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105784854 | ||||||
| chr4:105785351
|
T | A | 1 | a0001c0001t0003g0118 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1241-37603T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105785351 | ||||||
| chr4:105785391
|
T | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(158): Show | 163 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.1241-37563T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105785391 | ||||||
| chr4:105785818
|
A | T | 1 | a0001c0001t0009g0142 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1241-37136A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105785818 | ||||||
| chr4:105785875
|
G | A | 158 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(155): Show | 160 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1241-37079G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105785875 | ||||||
| chr4:105785899
|
C | T | 62 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(59): Show | 63 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.1241-37055C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105785899 | ||||||
| chr4:105785941
|
TTGCACC | T | 3 | a0001c0001t0003g0124a0001c0001t0003g0128a0001c0001t0003g0129 | 3 | HG01891.hp2 HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1241-37008_1241-37 others(12): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105785941 | |||||
| chr4:105786069
|
A | G | 175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(172): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.1241-36885A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105786069 | ||||||
| chr4:105786140
|
T | C | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1241-36814T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105786140 | ||||||
| chr4:105786173
|
AAGCAATA others(9788): Show |
A | 3 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0178 | 3 | HG01884.hp1 HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1241-36777_1241-26 others(6): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105786173 | |||||
| chr4:105786469
|
C | A | 1 | a0001c0001t0016g0130 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1241-36485C>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105786469 | ||||||
| chr4:105786662
|
A | G | 1 | a0001c0001t0006g0173 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1241-36292A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105786662 | ||||||
| chr4:105786888
|
C | T | 1 | a0001c0001t0019g0066 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1241-36066C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105786888 | ||||||
| chr4:105786973
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1241-35981G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105786973 | ||||||
| chr4:105787028
|
T | G | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-35926T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105787028 | ||||||
| chr4:105787082
|
AT | A | 2 | a0001c0001t0008g0072a0001c0001t0008g0073 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1241-35871delT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105787082 | ||||||
| chr4:105787192
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1241-35762C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105787192 | ||||||
| chr4:105787220
|
G | A | 1 | a0001c0001t0003g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1241-35734G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105787220 | ||||||
| chr4:105787607
|
C | T | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241-35347C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105787607 | ||||||
| chr4:105787628
|
C | T | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1241-35326C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105787628 | ||||||
| chr4:105787822
|
A | G | 1 | a0001c0001t0003g0129 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1241-35132A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105787822 | ||||||
| chr4:105787847
|
C | T | 2 | a0001c0001t0009g0141a0001c0001t0009g0142 | 2 | HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1241-35107C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105787847 | ||||||
| chr4:105787862
|
A | G | 1 | a0001c0001t0003g0114 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1241-35092A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105787862 | ||||||
| chr4:105788325
|
ATAGT | A | 65 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(62): Show | 66 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.1241-34626_1241-34 others(10): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105788325 | |||||
| chr4:105788426
|
T | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(152): Show | 157 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1241-34528T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105788426 | ||||||
| chr4:105788935
|
A | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1241-34019A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105788935 | ||||||
| chr4:105789297
|
G | T | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1241-33657G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105789297 | ||||||
| chr4:105789453
|
G | A | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-33501G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105789453 | ||||||
| chr4:105789496
|
T | C | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241-33458T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105789496 | ||||||
| chr4:105789803
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1241-33151C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105789803 | ||||||
| chr4:105790259
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1241-32695G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105790259 | ||||||
| chr4:105790267
|
T | C | 2 | a0002c0003t0010g0126a0002c0003t0010g0144 | 2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1241-32687T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105790267 | ||||||
| chr4:105790492
|
A | G | 2 | a0001c0001t0009g0141a0001c0001t0009g0142 | 2 | HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1241-32462A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105790492 | ||||||
| chr4:105790666
|
C | A | 1 | a0001c0001t0001g0044 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1241-32288C>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105790666 | ||||||
| chr4:105790690
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1241-32264T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105790690 | ||||||
| chr4:105790836
|
T | A | 3 | a0001c0001t0001g0029a0001c0001t0008g0072a0001c0001t0008g0073 | 3 | HG00642.hp2 HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1241-32118T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105790836 | ||||||
| chr4:105790855
|
G | A | 1 | a0001c0001t0002g0152 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1241-32099G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105790855 | ||||||
| chr4:105790934
|
C | G | 1 | a0001c0001t0001g0016 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1241-32020C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105790934 | ||||||
| chr4:105790972
|
G | A | 1 | a0001c0001t0002g0153 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1241-31982G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105790972 | ||||||
| chr4:105791047
|
A | G | 2 | a0001c0001t0005g0174a0001c0001t0005g0175 | 2 | HG01167.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1241-31907A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105791047 | ||||||
| chr4:105791082
|
A | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(152): Show | 157 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1241-31872A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105791082 | ||||||
| chr4:105791122
|
G | A | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1241-31832G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105791122 | ||||||
| chr4:105791189
|
C | T | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241-31765C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105791189 | ||||||
| chr4:105791220
|
C | T | 1 | a0001c0001t0004g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1241-31734C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105791220 | ||||||
| chr4:105791388
|
G | A | 9 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(6): Show | 9 | HG01070.hp2 HG01243.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1241-31566G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105791388 | ||||||
| chr4:105791392
|
C | CA | 9 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0077others(6): Show | 9 | HG01070.hp2 HG02257.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1241-31545dupA | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105791392 | |||||
| chr4:105791409
|
AG | A | 13 | a0001c0001t0005g0167a0001c0001t0005g0175a0001c0001t0005g0180others(10): Show | 13 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.1241-31544delG | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105791409 | ||||||
| chr4:105791410
|
G | A | 1 | a0001c0001t0005g0184 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1241-31544G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105791410 | ||||||
| chr4:105791787
|
ATT | A | 62 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(59): Show | 63 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.1241-31166_1241-31 others(8): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105791787 | ||||||
| chr4:105791820
|
G | A | 6 | a0001c0002t0002g0100a0001c0002t0002g0101a0001c0002t0002g0137others(3): Show | 6 | HG02145.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1241-31134G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105791820 | ||||||
| chr4:105792333
|
G | A | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1241-30621G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105792333 | ||||||
| chr4:105792417
|
G | C | 2 | a0001c0001t0001g0010a0001c0001t0012g0049 | 2 | HG04184.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.1241-30537G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105792417 | ||||||
| chr4:105792516
|
G | A | 143 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(140): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1241-30438G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105792516 | ||||||
| chr4:105792678
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1241-30276G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105792678 | ||||||
| chr4:105792790
|
G | T | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-30164G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105792790 | ||||||
| chr4:105792841
|
G | T | 143 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(140): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1241-30113G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105792841 | ||||||
| chr4:105793178
|
G | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(174): Show | 179 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.1241-29776G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105793178 | ||||||
| chr4:105793215
|
A | G | 1 | a0001c0001t0003g0118 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1241-29739A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105793215 | ||||||
| chr4:105793283
|
G | A | 1 | a0001c0001t0004g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1241-29671G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105793283 | ||||||
| chr4:105793343
|
A | T | 1 | a0001c0001t0013g0070 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1241-29611A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105793343 | ||||||
| chr4:105793390
|
G | T | 1 | a0001c0001t0016g0130 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1241-29564G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105793390 | ||||||
| chr4:105793408
|
G | GT | 38 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(35): Show | 39 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.1241-29535dupT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105793408 | |||||
| chr4:105793418
|
T | A | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1241-29536T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105793418 | ||||||
| chr4:105793419
|
T | A | 85 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(82): Show | 86 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.1241-29535T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105793419 | ||||||
| chr4:105793419
|
T | TA | 7 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(4): Show | 7 | HG00735.hp1 HG01243.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1241-29527dupA | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105793419 | |||||
| chr4:105793420
|
A | T | 4 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0019g0066others(1): Show | 4 | HG01884.hp2 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1241-29534A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105793420 | ||||||
| chr4:105793674
|
C | T | 1 | a0001c0001t0006g0173 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1241-29280C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105793674 | ||||||
| chr4:105793991
|
T | A | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1241-28963T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105793991 | ||||||
| chr4:105794332
|
A | G | 65 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(62): Show | 66 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.1241-28622A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105794332 | ||||||
| chr4:105794601
|
A | T | 1 | a0001c0001t0003g0002 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1241-28353A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105794601 | ||||||
| chr4:105794813
|
A | G | 1 | a0001c0001t0007g0159 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1241-28141A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105794813 | ||||||
| chr4:105794821
|
TTTTATCT others(9): Show |
T | 13 | a0001c0001t0003g0121a0001c0001t0003g0124a0001c0001t0003g0128others(10): Show | 13 | HG01109.hp1 HG01192.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1241-28115_1241-28 others(22): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105794821 | |||||
| chr4:105794823
|
T | C | 1 | a0001c0001t0004g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1241-28131T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105794823 | ||||||
| chr4:105794823
|
TTATCTAT others(13): Show |
T | 25 | a0001c0001t0002g0064a0001c0001t0003g0002a0001c0001t0003g0094others(22): Show | 26 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.1241-28115_1241-28 others(26): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105794823 | |||||
| chr4:105794823
|
TTATCTAT others(17): Show |
T | 17 | a0001c0001t0003g0109a0001c0001t0003g0110a0001c0001t0003g0113others(14): Show | 17 | HG01175.hp1 HG01361.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.1241-28115_1241-28 others(30): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105794823 | |||||
| chr4:105794823
|
TTATCTAT others(21): Show |
T | 4 | a0001c0001t0003g0115a0001c0001t0019g0066a0001c0002t0011g0138others(1): Show | 4 | HG02145.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1241-28115_1241-28 others(34): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105794823 | |||||
| chr4:105794823
|
TTATCTAT others(25): Show |
T | 2 | a0001c0001t0002g0065a0001c0002t0026g0090 | 2 | HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1241-28115_1241-28 others(38): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105794823 | |||||
| chr4:105794823
|
TTATCTAT others(29): Show |
T | 1 | a0001c0002t0002g0088 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1241-28115_1241-28 others(42): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105794823 | |||||
| chr4:105794827
|
CTATCTAT others(5): Show |
C | 6 | a0001c0001t0003g0123a0001c0001t0003g0129a0001c0001t0005g0180others(3): Show | 6 | HG00735.hp1 HG01243.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1241-28115_1241-28 others(18): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105794827 | |||||
| chr4:105794835
|
CTATT | C | 4 | a0001c0001t0006g0166a0001c0001t0006g0168a0001c0001t0006g0169others(1): Show | 4 | HG00639.hp1 HG00741.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.1241-28115_1241-28 others(10): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105794835 | |||||
| chr4:105794839
|
T | C | 5 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0006g0171others(2): Show | 5 | HG01109.hp2 HG01167.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-28115T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105794839 | ||||||
| chr4:105794839
|
TTATC | T | 38 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(35): Show | 38 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.1241-28063_1241-28 others(10): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105794839 | |||||
| chr4:105794839
|
TTATCTAT others(1): Show |
T | 19 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0021others(16): Show | 19 | HG01081.hp1 HG02015.hp2 HG02071.hp2 others(16): Show |
intron_variant | MODIFIER | c.1241-28067_1241-28 others(14): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105794839 | |||||
| chr4:105794839
|
TTATCTAT others(5): Show |
T | 1 | a0001c0001t0004g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1241-28071_1241-28 others(18): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105794839 | |||||
| chr4:105794839
|
TTATCTAT others(9): Show |
T | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1241-28075_1241-28 others(22): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105794839 | |||||
| chr4:105794843
|
C | T | 6 | a0001c0001t0004g0078a0001c0001t0005g0167a0001c0001t0005g0174others(3): Show | 6 | HG01070.hp2 HG01109.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.1241-28111C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105794843 | ||||||
| chr4:105794847
|
C | T | 7 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(4): Show | 7 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.1241-28107C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105794847 | ||||||
| chr4:105794889
|
A | ATCTATCT others(5): Show |
1 | a0001c0001t0001g0056 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1241-28060_1241-28 others(18): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105794889 | |||||
| chr4:105794889
|
A | ATCTATCT others(1): Show |
4 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0040others(1): Show | 4 | HG01361.hp2 HG02630.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1241-28060_1241-28 others(14): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105794889 | |||||
| chr4:105794889
|
A | ATCTG | 12 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(9): Show | 13 | HG00280.hp2 HG00408.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.1241-28062_1241-28 others(10): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105794889 | |||||
| chr4:105794889
|
A | G | 46 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(43): Show | 46 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.1241-28065A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105794889 | ||||||
| chr4:105794916
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1241-28038G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105794916 | ||||||
| chr4:105794920
|
A | G | 1 | a0001c0001t0003g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1241-28034A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105794920 | ||||||
| chr4:105794967
|
C | T | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1241-27987C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105794967 | ||||||
| chr4:105795316
|
T | C | 1 | a0001c0001t0003g0069 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1241-27638T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105795316 | ||||||
| chr4:105795348
|
ATAG | A | 129 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(126): Show | 131 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1241-27601_1241-27 others(9): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105795348 | |||||
| chr4:105795370
|
T | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1241-27584T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105795370 | ||||||
| chr4:105795395
|
A | AT | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1241-27553dupT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105795395 | |||||
| chr4:105795741
|
T | G | 1 | a0001c0001t0001g0038 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1241-27213T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105795741 | ||||||
| chr4:105796382
|
T | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1241-26572T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105796382 | ||||||
| chr4:105796640
|
A | G | 144 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(141): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1241-26314A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105796640 | ||||||
| chr4:105796733
|
T | C | 1 | a0001c0001t0004g0076 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1241-26221T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105796733 | ||||||
| chr4:105796788
|
A | C | 65 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(62): Show | 66 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.1241-26166A>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105796788 | ||||||
| chr4:105796995
|
G | C | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1241-25959G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105796995 | ||||||
| chr4:105797045
|
C | CGT | 3 | a0001c0001t0002g0071a0001c0002t0002g0084a0002c0003t0010g0126 | 3 | HG02965.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1241-25909_1241-25 others(8): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105797045 | ||||||
| chr4:105797045
|
C | CGTGT | 21 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(18): Show | 22 | HG01109.hp1 HG01361.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1241-25909_1241-25 others(10): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105797045 | ||||||
| chr4:105797045
|
C | CGTGTGT | 33 | a0001c0001t0003g0094a0001c0001t0003g0095a0001c0001t0003g0102others(30): Show | 33 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1241-25909_1241-25 others(12): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105797045 | ||||||
| chr4:105797045
|
C | CGTGTGTG others(1): Show |
5 | a0001c0001t0003g0118a0001c0001t0003g0120a0001c0001t0003g0127others(2): Show | 5 | HG02451.hp1 HG03139.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1241-25909_1241-25 others(14): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105797045 | ||||||
| chr4:105797045
|
CAT | C | 4 | a0001c0001t0003g0116a0001c0001t0003g0117a0001c0001t0003g0139others(1): Show | 4 | HG01175.hp1 HG02145.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1241-25908_1241-25 others(8): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105797045 | ||||||
| chr4:105797046
|
A | ATG | 13 | a0001c0001t0001g0035a0001c0001t0001g0047a0001c0001t0004g0074others(10): Show | 13 | HG00741.hp1 HG01070.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.1241-25876_1241-25 others(8): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105797046 | |||||
| chr4:105797046
|
A | ATGTG | 10 | a0001c0001t0001g0029a0001c0001t0001g0057a0001c0001t0004g0131others(7): Show | 10 | HG00642.hp2 HG00735.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1241-25878_1241-25 others(10): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105797046 | |||||
| chr4:105797046
|
A | ATGTGTG | 12 | a0001c0001t0003g0068a0001c0001t0004g0075a0001c0001t0004g0076others(9): Show | 12 | HG00639.hp1 HG01109.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.1241-25880_1241-25 others(12): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105797046 | |||||
| chr4:105797046
|
A | G | 62 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0002g0071others(59): Show | 63 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.1241-25908A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105797046 | ||||||
| chr4:105797046
|
ATG | A | 7 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0148others(4): Show | 7 | HG02015.hp2 HG02071.hp2 NA18987.hp1 others(4): Show |
intron_variant | MODIFIER | c.1241-25876_1241-25 others(8): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105797046 | |||||
| chr4:105797046
|
ATGTG | A | 4 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(1): Show | 4 | HG01069.hp2 HG01167.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1241-25878_1241-25 others(10): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105797046 | |||||
| chr4:105797046
|
ATGTGTGT others(5): Show |
A | 1 | a0001c0001t0001g0017 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1241-25886_1241-25 others(18): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105797046 | |||||
| chr4:105797080
|
A | G | 1 | a0001c0006t0001g0045 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1241-25874A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105797080 | ||||||
| chr4:105797096
|
G | A | 13 | a0001c0001t0001g0039a0001c0001t0002g0157a0001c0001t0002g0179others(10): Show | 13 | HG00280.hp2 HG00639.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.1241-25858G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105797096 | ||||||
| chr4:105797159
|
G | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(141): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1241-25795G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105797159 | ||||||
| chr4:105797355
|
T | C | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1241-25599T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105797355 | ||||||
| chr4:105797441
|
A | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0025others(1): Show | 4 | HG00438.hp1 NA18959.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.1241-25513A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105797441 | ||||||
| chr4:105797514
|
TA | T | 16 | a0001c0001t0003g0115a0001c0001t0005g0167a0001c0001t0005g0174others(13): Show | 16 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.1241-25430delA | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105797514 | |||||
| chr4:105797651
|
G | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(177): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1241-25303G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105797651 | ||||||
| chr4:105797730
|
C | T | 1 | a0001c0001t0004g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1241-25224C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105797730 | ||||||
| chr4:105797760
|
C | CT | 7 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0150others(4): Show | 7 | HG01517.hp1 HG02622.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1241-25162dupT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105797760 | |||||
| chr4:105797760
|
C | CTTTTTTT others(14): Show |
1 | a0001c0001t0003g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1241-25182_1241-25 others(27): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105797760 | |||||
| chr4:105797760
|
CTTT | C | 13 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(10): Show | 13 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.1241-25164_1241-25 others(9): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105797760 | |||||
| chr4:105797760
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0019g0066a0001c0002t0002g0081 | 2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1241-25172_1241-25 others(17): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105797760 | |||||
| chr4:105797760
|
CTTTTTTT others(5): Show |
C | 123 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(120): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.1241-25173_1241-25 others(18): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105797760 | |||||
| chr4:105797760
|
CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0001g0003a0001c0001t0001g0061a0001c0001t0003g0117 | 3 | HG01070.hp1 HG01167.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1241-25174_1241-25 others(19): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105797760 | |||||
| chr4:105797760
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0016g0130 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1241-25175_1241-25 others(20): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105797760 | |||||
| chr4:105797838
|
G | A | 1 | a0001c0001t0003g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1241-25116G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105797838 | ||||||
| chr4:105797970
|
T | C | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1241-24984T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105797970 | ||||||
| chr4:105798024
|
A | T | 1 | a0001c0001t0004g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1241-24930A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105798024 | ||||||
| chr4:105798035
|
A | G | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241-24919A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105798035 | ||||||
| chr4:105798059
|
T | C | 1 | a0001c0001t0004g0074 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1241-24895T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105798059 | ||||||
| chr4:105798081
|
T | C | 3 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0077 | 3 | HG02630.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1241-24873T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105798081 | ||||||
| chr4:105798208
|
T | G | 1 | a0001c0001t0001g0020 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1241-24746T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105798208 | ||||||
| chr4:105798432
|
A | G | 41 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(38): Show | 42 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.1241-24522A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105798432 | ||||||
| chr4:105798648
|
A | G | 1 | a0001c0001t0001g0051 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1241-24306A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105798648 | ||||||
| chr4:105798732
|
G | GTGTGCAA others(15): Show |
144 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(141): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1241-24221_1241-24 others(28): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105798732 | |||||
| chr4:105798816
|
G | T | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241-24138G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105798816 | ||||||
| chr4:105798962
|
A | G | 1 | a0001c0001t0001g0026 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1241-23992A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105798962 | ||||||
| chr4:105799047
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1241-23907T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105799047 | ||||||
| chr4:105799246
|
A | G | 1 | a0001c0001t0007g0159 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1241-23708A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105799246 | ||||||
| chr4:105799501
|
C | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(155): Show | 160 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1241-23453C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105799501 | ||||||
| chr4:105799567
|
G | A | 1 | a0001c0001t0003g0140 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1241-23387G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105799567 | ||||||
| chr4:105799809
|
C | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1241-23145C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105799809 | ||||||
| chr4:105799810
|
G | A | 2 | a0001c0001t0003g0116a0001c0001t0003g0117 | 2 | HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1241-23144G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105799810 | ||||||
| chr4:105799814
|
C | CA | 69 | a0001c0001t0001g0032a0001c0001t0002g0065a0001c0001t0003g0002others(66): Show | 70 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.1241-23124dupA | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105799814 | |||||
| chr4:105799814
|
CAA | C | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1241-23125_1241-23 others(8): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105799814 | |||||
| chr4:105800113
|
G | A | 51 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(48): Show | 51 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.1241-22841G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105800113 | ||||||
| chr4:105800133
|
G | A | 1 | a0001c0001t0003g0122 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1241-22821G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105800133 | ||||||
| chr4:105800231
|
G | A | 1 | a0001c0001t0004g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1241-22723G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105800231 | ||||||
| chr4:105800727
|
C | T | 1 | a0001c0002t0011g0138 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1241-22227C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105800727 | ||||||
| chr4:105800845
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1241-22109T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105800845 | ||||||
| chr4:105800860
|
A | T | 1 | a0001c0001t0002g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1241-22094A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105800860 | ||||||
| chr4:105800980
|
T | C | 1 | a0001c0001t0001g0003 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1241-21974T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105800980 | ||||||
| chr4:105801054
|
A | T | 1 | a0001c0001t0001g0011 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1241-21900A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105801054 | ||||||
| chr4:105801141
|
C | A | 63 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(60): Show | 64 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.1241-21813C>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105801141 | ||||||
| chr4:105801218
|
A | G | 8 | a0001c0002t0002g0086a0001c0002t0002g0087a0001c0002t0002g0089others(5): Show | 8 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.1241-21736A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105801218 | ||||||
| chr4:105801360
|
A | T | 1 | a0001c0001t0003g0102 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1241-21594A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105801360 | ||||||
| chr4:105801632
|
A | C | 65 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(62): Show | 66 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.1241-21322A>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105801632 | ||||||
| chr4:105802335
|
G | A | 8 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(5): Show | 8 | HG01070.hp2 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1241-20619G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105802335 | ||||||
| chr4:105802340
|
G | A | 175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(172): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.1241-20614G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105802340 | ||||||
| chr4:105802585
|
T | C | 1 | a0001c0002t0002g0093 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1241-20369T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105802585 | ||||||
| chr4:105802597
|
T | G | 1 | a0001c0002t0002g0093 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1241-20357T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105802597 | ||||||
| chr4:105802646
|
T | C | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1241-20308T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105802646 | ||||||
| chr4:105803109
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1241-19845G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105803109 | ||||||
| chr4:105803171
|
C | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(155): Show | 160 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1241-19783C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105803171 | ||||||
| chr4:105803307
|
A | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1241-19647A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105803307 | ||||||
| chr4:105803363
|
C | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(158): Show | 163 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.1241-19591C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105803363 | ||||||
| chr4:105803376
|
G | T | 1 | a0001c0001t0012g0063 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1241-19578G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105803376 | ||||||
| chr4:105803631
|
C | T | 1 | a0001c0001t0022g0054 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1241-19323C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105803631 | ||||||
| chr4:105803877
|
C | T | 177 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(174): Show | 179 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.1241-19077C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105803877 | ||||||
| chr4:105803983
|
T | A | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241-18971T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105803983 | ||||||
| chr4:105803984
|
A | G | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1241-18970A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105803984 | ||||||
| chr4:105804073
|
T | C | 1 | a0001c0001t0003g0119 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1241-18881T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105804073 | ||||||
| chr4:105804547
|
T | C | 1 | a0001c0002t0002g0088 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1241-18407T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105804547 | ||||||
| chr4:105804647
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1241-18307C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105804647 | ||||||
| chr4:105805234
|
A | C | 13 | a0001c0001t0002g0064a0001c0001t0003g0120a0001c0001t0003g0121others(10): Show | 13 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1241-17720A>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105805234 | ||||||
| chr4:105805407
|
G | C | 4 | a0001c0001t0004g0133a0001c0001t0004g0176a0001c0001t0004g0177others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1241-17547G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105805407 | ||||||
| chr4:105805491
|
C | T | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1241-17463C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105805491 | ||||||
| chr4:105805839
|
A | G | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1241-17115A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105805839 | ||||||
| chr4:105806171
|
A | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(155): Show | 160 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1241-16783A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105806171 | ||||||
| chr4:105806410
|
G | T | 1 | a0001c0001t0001g0038 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1241-16544G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105806410 | ||||||
| chr4:105806560
|
T | C | 1 | a0001c0001t0001g0033 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1241-16394T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105806560 | ||||||
| chr4:105806641
|
G | A | 1 | a0001c0001t0001g0033 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1241-16313G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105806641 | ||||||
| chr4:105806819
|
T | C | 1 | a0001c0001t0001g0025 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1241-16135T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105806819 | ||||||
| chr4:105807311
|
T | C | 1 | a0001c0001t0001g0025 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1241-15643T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105807311 | ||||||
| chr4:105807857
|
G | A | 1 | a0001c0001t0004g0074 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1241-15097G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105807857 | ||||||
| chr4:105807896
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1241-15058G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105807896 | ||||||
| chr4:105808101
|
T | C | 1 | a0001c0001t0018g0160 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1241-14853T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105808101 | ||||||
| chr4:105808418
|
T | A | 1 | a0001c0001t0001g0030 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1241-14536T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105808418 | ||||||
| chr4:105808759
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1241-14195A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105808759 | ||||||
| chr4:105808776
|
C | T | 17 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(14): Show | 17 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.1241-14178C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105808776 | ||||||
| chr4:105808871
|
A | G | 4 | a0001c0001t0003g0116a0001c0001t0003g0117a0001c0001t0003g0139others(1): Show | 4 | HG01175.hp1 HG02145.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1241-14083A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105808871 | ||||||
| chr4:105809185
|
C | G | 13 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(10): Show | 13 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.1241-13769C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105809185 | ||||||
| chr4:105809298
|
G | A | 4 | a0001c0001t0004g0133a0001c0001t0004g0176a0001c0001t0004g0177others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1241-13656G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105809298 | ||||||
| chr4:105809506
|
G | A | 129 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(126): Show | 131 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1241-13448G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105809506 | ||||||
| chr4:105809553
|
C | A | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1241-13401C>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105809553 | ||||||
| chr4:105809862
|
G | C | 62 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(59): Show | 63 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.1241-13092G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105809862 | ||||||
| chr4:105810057
|
G | A | 1 | a0001c0001t0003g0069 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1241-12897G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105810057 | ||||||
| chr4:105810085
|
G | C | 1 | a0001c0001t0003g0139 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1241-12869G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105810085 | ||||||
| chr4:105810139
|
G | C | 2 | a0001c0001t0008g0072a0001c0001t0008g0073 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1241-12815G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105810139 | ||||||
| chr4:105810253
|
A | G | 129 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(126): Show | 131 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1241-12701A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105810253 | ||||||
| chr4:105811026
|
T | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(126): Show | 131 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1241-11928T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105811026 | ||||||
| chr4:105811202
|
A | C | 65 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(62): Show | 66 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.1241-11752A>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105811202 | ||||||
| chr4:105811613
|
G | A | 3 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0178 | 3 | HG01884.hp1 HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1241-11341G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105811613 | ||||||
| chr4:105811772
|
A | G | 5 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG01070.hp2 HG02630.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-11182A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105811772 | ||||||
| chr4:105811800
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1241-11154G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105811800 | ||||||
| chr4:105812161
|
A | G | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-10793A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105812161 | ||||||
| chr4:105812223
|
C | T | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1241-10731C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105812223 | ||||||
| chr4:105812351
|
T | C | 1 | a0001c0001t0004g0176 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1241-10603T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105812351 | ||||||
| chr4:105812505
|
C | G | 2 | a0001c0001t0017g0162a0001c0001t0018g0160 | 2 | HG00280.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1241-10449C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105812505 | ||||||
| chr4:105812585
|
C | G | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1241-10369C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105812585 | ||||||
| chr4:105812661
|
A | T | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1241-10293A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105812661 | ||||||
| chr4:105812878
|
T | C | 3 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0011g0147 | 3 | NA18990.hp1 NA18994.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1241-10076T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105812878 | ||||||
| chr4:105812928
|
CAGTA | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0052 | 2 | NA18987.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1241-10023_1241-10 others(10): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105812928 | |||||
| chr4:105813189
|
A | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1241-9765A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105813189 | ||||||
| chr4:105813527
|
C | G | 12 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(9): Show | 12 | HG01070.hp2 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1241-9427C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105813527 | ||||||
| chr4:105813598
|
T | G | 4 | a0001c0001t0004g0133a0001c0001t0004g0176a0001c0001t0004g0177others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1241-9356T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105813598 | ||||||
| chr4:105813657
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1241-9297A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105813657 | ||||||
| chr4:105814378
|
C | T | 1 | a0001c0001t0018g0160 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1241-8576C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105814378 | ||||||
| chr4:105814379
|
G | A | 1 | a0001c0001t0003g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1241-8575G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105814379 | ||||||
| chr4:105814437
|
A | G | 1 | a0001c0001t0001g0009 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1241-8517A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105814437 | ||||||
| chr4:105814465
|
A | T | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1241-8489A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105814465 | ||||||
| chr4:105814473
|
C | T | 5 | a0001c0002t0002g0089a0001c0002t0002g0092a0001c0002t0002g0093others(2): Show | 5 | HG01975.hp2 HG02970.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-8481C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105814473 | ||||||
| chr4:105814487
|
C | T | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1241-8467C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105814487 | ||||||
| chr4:105814505
|
C | T | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241-8449C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105814505 | ||||||
| chr4:105814587
|
G | A | 1 | a0001c0001t0004g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1241-8367G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105814587 | ||||||
| chr4:105814606
|
T | C | 1 | a0001c0001t0003g0115 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1241-8348T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105814606 | ||||||
| chr4:105814695
|
G | A | 12 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(9): Show | 12 | HG01070.hp2 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1241-8259G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105814695 | ||||||
| chr4:105814972
|
T | C | 1 | a0001c0001t0003g0121 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1241-7982T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105814972 | ||||||
| chr4:105815051
|
A | G | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-7903A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105815051 | ||||||
| chr4:105815185
|
C | T | 1 | a0001c0001t0002g0065 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1241-7769C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105815185 | ||||||
| chr4:105815198
|
G | A | 65 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(62): Show | 66 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.1241-7756G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105815198 | ||||||
| chr4:105815223
|
T | G | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1241-7731T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105815223 | ||||||
| chr4:105815690
|
G | T | 5 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG01070.hp2 HG02630.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-7264G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105815690 | ||||||
| chr4:105815779
|
T | C | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1241-7175T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105815779 | ||||||
| chr4:105815949
|
A | G | 1 | a0001c0005t0021g0091 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1241-7005A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105815949 | ||||||
| chr4:105815977
|
G | A | 1 | a0001c0001t0003g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1241-6977G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105815977 | ||||||
| chr4:105815980
|
T | C | 2 | a0001c0001t0008g0072a0001c0001t0008g0073 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1241-6974T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105815980 | ||||||
| chr4:105816183
|
T | C | 1 | a0001c0001t0013g0070 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1241-6771T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105816183 | ||||||
| chr4:105816225
|
G | A | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241-6729G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105816225 | ||||||
| chr4:105816331
|
A | G | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1241-6623A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105816331 | ||||||
| chr4:105816352
|
T | A | 12 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(9): Show | 12 | HG01070.hp2 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1241-6602T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105816352 | ||||||
| chr4:105816639
|
G | A | 63 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(60): Show | 64 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.1241-6315G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105816639 | ||||||
| chr4:105816833
|
C | A | 2 | a0001c0002t0002g0087a0001c0002t0002g0097 | 2 | HG01192.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1241-6121C>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105816833 | ||||||
| chr4:105816924
|
C | T | 1 | a0001c0001t0003g0123 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1241-6030C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105816924 | ||||||
| chr4:105817003
|
A | G | 1 | a0001c0001t0004g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1241-5951A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105817003 | ||||||
| chr4:105817093
|
G | A | 1 | a0001c0001t0002g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1241-5861G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105817093 | ||||||
| chr4:105817492
|
G | A | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1241-5462G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105817492 | ||||||
| chr4:105817603
|
A | G | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241-5351A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105817603 | ||||||
| chr4:105817648
|
A | G | 144 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(141): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1241-5306A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105817648 | ||||||
| chr4:105818217
|
G | A | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241-4737G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105818217 | ||||||
| chr4:105818310
|
TAGG | T | 72 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(69): Show | 73 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.1241-4641_1241-463 others(7): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105818310 | |||||
| chr4:105818352
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01081.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1241-4602G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105818352 | ||||||
| chr4:105818436
|
G | T | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1241-4518G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105818436 | ||||||
| chr4:105818816
|
A | G | 144 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(141): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1241-4138A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105818816 | ||||||
| chr4:105819185
|
T | A | 14 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0148others(11): Show | 14 | HG01516.hp1 HG01517.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.1241-3769T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105819185 | ||||||
| chr4:105819335
|
C | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(155): Show | 160 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1241-3619C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105819335 | ||||||
| chr4:105819610
|
T | C | 7 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(4): Show | 7 | HG00438.hp1 NA18959.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.1241-3344T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105819610 | ||||||
| chr4:105819830
|
C | T | 2 | a0001c0001t0008g0072a0001c0001t0008g0073 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1241-3124C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105819830 | ||||||
| chr4:105819986
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1241-2968A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105819986 | ||||||
| chr4:105820006
|
G | A | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241-2948G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105820006 | ||||||
| chr4:105820131
|
A | AT | 6 | a0001c0001t0003g0068a0001c0001t0005g0180a0001c0001t0005g0181others(3): Show | 6 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1241-2812dupT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105820131 | |||||
| chr4:105820267
|
C | T | 14 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0148others(11): Show | 14 | HG01516.hp1 HG01517.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.1241-2687C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105820267 | ||||||
| chr4:105820564
|
C | G | 1 | a0001c0002t0002g0101 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1241-2390C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105820564 | ||||||
| chr4:105820705
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1241-2249C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105820705 | ||||||
| chr4:105820735
|
C | A | 2 | a0001c0001t0003g0103a0001c0001t0003g0111 | 2 | NA18942.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1241-2219C>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105820735 | ||||||
| chr4:105820817
|
T | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(141): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1241-2137T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105820817 | ||||||
| chr4:105820881
|
A | AT | 129 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(126): Show | 131 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1241-2072dupT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 105820881 | |||||
| chr4:105821059
|
T | C | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241-1895T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105821059 | ||||||
| chr4:105821106
|
A | G | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(139): Show | 144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1241-1848A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105821106 | ||||||
| chr4:105821705
|
C | T | 1 | a0001c0001t0013g0070 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1241-1249C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105821705 | ||||||
| chr4:105821721
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1241-1233G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105821721 | ||||||
| chr4:105821801
|
A | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(126): Show | 131 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1241-1153A>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105821801 | ||||||
| chr4:105821806
|
A | G | 1 | a0001c0001t0003g0110 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1241-1148A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105821806 | ||||||
| chr4:105822010
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1241-944G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105822010 | ||||||
| chr4:105822735
|
G | C | 1 | a0001c0001t0003g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1241-219G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105822735 | ||||||
| chr4:105822807
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1241-147T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105822807 | ||||||
| chr4:105822943
|
G | A | 1 | a0001c0001t0007g0163 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1241-11G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 5/11 | chr4 | 105822943 | ||||||
| chr4:105823324
|
T | G | 1 | a0001c0001t0004g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1401+49T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 7/11 | chr4 | 105823324 | ||||||
| chr4:105823900
|
C | T | 3 | a0001c0001t0003g0069a0001c0001t0003g0135a0001c0001t0013g0070 | 3 | HG03098.hp1 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1401+625C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 7/11 | chr4 | 105823900 | ||||||
| chr4:105823954
|
T | C | 1 | a0001c0001t0002g0065 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1401+679T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 7/11 | chr4 | 105823954 | ||||||
| chr4:105824248
|
A | G | 129 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(126): Show | 131 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1401+973A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 7/11 | chr4 | 105824248 | ||||||
| chr4:105824594
|
T | C | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1402-1078T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 7/11 | chr4 | 105824594 | ||||||
| chr4:105824684
|
C | G | 1 | a0001c0001t0003g0139 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1402-988C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 7/11 | chr4 | 105824684 | ||||||
| chr4:105824791
|
T | C | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1402-881T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 7/11 | chr4 | 105824791 | ||||||
| chr4:105824855
|
A | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1402-817A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 7/11 | chr4 | 105824855 | ||||||
| chr4:105824908
|
C | T | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1402-764C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 7/11 | chr4 | 105824908 | ||||||
| chr4:105824926
|
C | T | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1402-746C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 7/11 | chr4 | 105824926 | ||||||
| chr4:105825030
|
C | T | 4 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0115others(1): Show | 4 | HG01884.hp2 HG02886.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1402-642C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 7/11 | chr4 | 105825030 | ||||||
| chr4:105825100
|
ATTGG | A | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1402-541_1402-538d others(6): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 105825100 | |||||
| chr4:105825131
|
G | GGTTGGTT others(1): Show |
5 | a0001c0001t0003g0116a0001c0001t0003g0117a0001c0001t0003g0139others(2): Show | 5 | HG01175.hp1 HG02145.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1402-538_1402-537i others(10): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 105825131 | |||||
| chr4:105825135
|
T | G | 7 | a0001c0001t0001g0026a0001c0001t0001g0053a0001c0001t0002g0071others(4): Show | 7 | HG01361.hp2 HG02257.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.1402-537T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 7/11 | chr4 | 105825135 | ||||||
| chr4:105825146
|
T | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(88): Show | 92 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.1402-526T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 7/11 | chr4 | 105825146 | ||||||
| chr4:105825146
|
T | TTGTC | 38 | a0001c0001t0001g0010a0001c0001t0001g0032a0001c0001t0002g0064others(35): Show | 39 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.1402-524_1402-523i others(6): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 105825146 | |||||
| chr4:105825208
|
T | A | 1 | a0001c0001t0001g0011 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1402-464T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 7/11 | chr4 | 105825208 | ||||||
| chr4:105825374
|
C | T | 1 | a0001c0002t0002g0079 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1402-298C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 7/11 | chr4 | 105825374 | ||||||
| chr4:105825412
|
G | T | 1 | a0001c0001t0003g0110 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1402-260G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 7/11 | chr4 | 105825412 | ||||||
| chr4:105825421
|
C | A | 1 | a0001c0001t0003g0110 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1402-251C>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 7/11 | chr4 | 105825421 | ||||||
| chr4:105825490
|
T | G | 4 | a0001c0001t0004g0133a0001c0001t0004g0176a0001c0001t0004g0177others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1402-182T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 7/11 | chr4 | 105825490 | ||||||
| chr4:105825525
|
A | G | 1 | a0001c0001t0003g0139 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1402-147A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 7/11 | chr4 | 105825525 | ||||||
| chr4:105826031
|
T | G | 1 | a0001c0001t0003g0002 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1530+231T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105826031 | ||||||
| chr4:105826275
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1530+475G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105826275 | ||||||
| chr4:105826339
|
A | G | 1 | a0001c0001t0002g0152 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1530+539A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105826339 | ||||||
| chr4:105826402
|
T | C | 2 | a0001c0001t0002g0157a0001c0001t0002g0179 | 2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1530+602T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105826402 | ||||||
| chr4:105826421
|
G | A | 14 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0148others(11): Show | 14 | HG01516.hp1 HG01517.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.1530+621G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105826421 | ||||||
| chr4:105826589
|
C | T | 4 | a0001c0001t0004g0133a0001c0001t0004g0176a0001c0001t0004g0177others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1530+789C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105826589 | ||||||
| chr4:105827018
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1530+1218C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105827018 | ||||||
| chr4:105827296
|
C | T | 2 | a0001c0001t0008g0072a0001c0001t0008g0073 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1530+1496C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105827296 | ||||||
| chr4:105827606
|
G | C | 1 | a0001c0001t0001g0010 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1530+1806G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105827606 | ||||||
| chr4:105827650
|
A | C | 1 | a0001c0001t0003g0095 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1530+1850A>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105827650 | ||||||
| chr4:105827903
|
A | T | 1 | a0001c0001t0004g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1530+2103A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105827903 | ||||||
| chr4:105828028
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1530+2228G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105828028 | ||||||
| chr4:105828137
|
G | A | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1530+2337G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105828137 | ||||||
| chr4:105828155
|
A | C | 1 | a0001c0001t0001g0036 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1530+2355A>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105828155 | ||||||
| chr4:105828436
|
T | A | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1530+2636T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105828436 | ||||||
| chr4:105828700
|
G | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(126): Show | 131 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1530+2900G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105828700 | ||||||
| chr4:105828865
|
G | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(141): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1530+3065G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105828865 | ||||||
| chr4:105828872
|
G | A | 1 | a0001c0001t0002g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1530+3072G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105828872 | ||||||
| chr4:105829057
|
C | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(124): Show | 129 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1530+3257C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105829057 | ||||||
| chr4:105829094
|
G | A | 12 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(9): Show | 12 | HG01070.hp2 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1530+3294G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105829094 | ||||||
| chr4:105829187
|
TA | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0020others(3): Show | 6 | HG01975.hp1 HG02809.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1530+3407delA | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 105829187 | |||||
| chr4:105829204
|
A | G | 1 | a0001c0001t0004g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1530+3404A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105829204 | ||||||
| chr4:105829219
|
A | G | 16 | a0001c0001t0001g0024a0001c0001t0005g0167a0001c0001t0005g0174others(13): Show | 16 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.1530+3419A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105829219 | ||||||
| chr4:105829330
|
A | G | 1 | a0001c0002t0002g0093 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1530+3530A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105829330 | ||||||
| chr4:105829373
|
G | A | 1 | a0001c0001t0005g0181 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1530+3573G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105829373 | ||||||
| chr4:105829527
|
C | T | 64 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(61): Show | 65 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.1530+3727C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105829527 | ||||||
| chr4:105829871
|
T | C | 127 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(124): Show | 129 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1530+4071T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105829871 | ||||||
| chr4:105829978
|
A | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1530+4178A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105829978 | ||||||
| chr4:105830074
|
C | A | 63 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(60): Show | 64 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.1530+4274C>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105830074 | ||||||
| chr4:105830561
|
T | G | 1 | a0001c0001t0003g0069 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1531-3900T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105830561 | ||||||
| chr4:105830644
|
C | T | 5 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(2): Show | 5 | HG01070.hp2 HG02630.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1531-3817C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105830644 | ||||||
| chr4:105830645
|
G | A | 64 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(61): Show | 65 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.1531-3816G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105830645 | ||||||
| chr4:105830866
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1531-3595G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105830866 | ||||||
| chr4:105831183
|
A | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1531-3278A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105831183 | ||||||
| chr4:105831432
|
A | G | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1531-3029A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105831432 | ||||||
| chr4:105831617
|
C | T | 2 | a0001c0001t0009g0141a0001c0001t0009g0142 | 2 | HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1531-2844C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105831617 | ||||||
| chr4:105831636
|
T | C | 1 | a0001c0002t0002g0096 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1531-2825T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105831636 | ||||||
| chr4:105831896
|
G | A | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1531-2565G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105831896 | ||||||
| chr4:105832179
|
T | C | 1 | a0001c0001t0013g0070 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1531-2282T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105832179 | ||||||
| chr4:105832223
|
C | A | 1 | a0001c0001t0001g0044 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1531-2238C>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105832223 | ||||||
| chr4:105832239
|
A | T | 1 | a0001c0001t0001g0042 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1531-2222A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105832239 | ||||||
| chr4:105832256
|
G | GT | 10 | a0001c0001t0003g0116a0001c0001t0003g0117a0001c0002t0002g0086others(7): Show | 10 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.1531-2196dupT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 105832256 | |||||
| chr4:105832525
|
ACT | A | 3 | a0001c0001t0004g0131a0001c0001t0004g0132a0001c0001t0016g0130 | 3 | HG02257.hp2 HG02451.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1531-1933_1531-193 others(6): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 105832525 | |||||
| chr4:105832688
|
A | C | 62 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(59): Show | 63 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.1531-1773A>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105832688 | ||||||
| chr4:105832695
|
T | C | 7 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0148others(4): Show | 7 | HG02015.hp2 HG02071.hp2 NA18987.hp1 others(4): Show |
intron_variant | MODIFIER | c.1531-1766T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105832695 | ||||||
| chr4:105833074
|
G | C | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1531-1387G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105833074 | ||||||
| chr4:105833190
|
C | G | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1531-1271C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105833190 | ||||||
| chr4:105833388
|
G | A | 2 | a0001c0001t0008g0072a0001c0001t0008g0073 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1531-1073G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105833388 | ||||||
| chr4:105833420
|
G | C | 3 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182 | 3 | HG00735.hp1 HG01243.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1531-1041G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105833420 | ||||||
| chr4:105833457
|
C | CGA | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1531-1004_1531-100 others(6): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105833457 | ||||||
| chr4:105833463
|
C | CA | 6 | a0001c0001t0002g0071a0001c0001t0005g0180a0001c0001t0005g0181others(3): Show | 6 | HG00735.hp1 HG01243.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1531-984dupA | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 105833463 | |||||
| chr4:105833740
|
T | TTATAGTA others(8): Show |
31 | a0001c0001t0002g0071a0001c0001t0004g0074a0001c0001t0004g0075others(28): Show | 31 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.1531-716_1531-702d others(17): Show |
GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 105833740 | |||||
| chr4:105833940
|
T | A | 1 | a0001c0001t0002g0157 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1531-521T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105833940 | ||||||
| chr4:105833945
|
AG | A | 30 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(27): Show | 30 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.1531-513delG | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 105833945 | |||||
| chr4:105833953
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0062 | 2 | HG00639.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1531-508A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105833953 | ||||||
| chr4:105834260
|
A | C | 1 | a0001c0001t0001g0032 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1531-201A>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105834260 | ||||||
| chr4:105834267
|
C | T | 18 | a0001c0001t0003g0116a0001c0001t0003g0117a0001c0002t0002g0079others(15): Show | 18 | HG01069.hp1 HG01192.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.1531-194C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105834267 | ||||||
| chr4:105834287
|
T | A | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1531-174T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 8/11 | chr4 | 105834287 | ||||||
| chr4:105834839
|
G | A | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1664+245G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 9/11 | chr4 | 105834839 | ||||||
| chr4:105834879
|
A | T | 1 | a0001c0001t0003g0002 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1664+285A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 9/11 | chr4 | 105834879 | ||||||
| chr4:105834894
|
C | T | 1 | a0001c0001t0002g0149 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1664+300C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 9/11 | chr4 | 105834894 | ||||||
| chr4:105834908
|
A | G | 1 | a0001c0001t0002g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1664+314A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 9/11 | chr4 | 105834908 | ||||||
| chr4:105835195
|
G | A | 64 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(61): Show | 65 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.1664+601G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 9/11 | chr4 | 105835195 | ||||||
| chr4:105835457
|
G | A | 1 | a0001c0002t0002g0081 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1664+863G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 9/11 | chr4 | 105835457 | ||||||
| chr4:105835505
|
A | C | 1 | a0001c0001t0016g0130 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1664+911A>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 9/11 | chr4 | 105835505 | ||||||
| chr4:105835692
|
G | C | 3 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0077 | 3 | HG02630.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1664+1098G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 9/11 | chr4 | 105835692 | ||||||
| chr4:105835720
|
T | C | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1664+1126T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 9/11 | chr4 | 105835720 | ||||||
| chr4:105835785
|
C | T | 4 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0002g0155others(1): Show | 4 | HG01516.hp1 HG01517.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1664+1191C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 9/11 | chr4 | 105835785 | ||||||
| chr4:105835832
|
A | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1664+1238A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 9/11 | chr4 | 105835832 | ||||||
| chr4:105836139
|
T | C | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1664+1545T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 9/11 | chr4 | 105836139 | ||||||
| chr4:105836215
|
A | C | 30 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(27): Show | 30 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.1664+1621A>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 9/11 | chr4 | 105836215 | ||||||
| chr4:105836216
|
C | A | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1664+1622C>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 9/11 | chr4 | 105836216 | ||||||
| chr4:105836237
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1665-1622G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 9/11 | chr4 | 105836237 | ||||||
| chr4:105836278
|
C | T | 17 | a0001c0001t0001g0009a0001c0001t0001g0062a0001c0001t0003g0116others(14): Show | 17 | HG00639.hp2 HG00735.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.1665-1581C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 9/11 | chr4 | 105836278 | ||||||
| chr4:105836279
|
G | A | 2 | a0001c0001t0008g0072a0001c0001t0008g0073 | 2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1665-1580G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 9/11 | chr4 | 105836279 | ||||||
| chr4:105836404
|
A | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(158): Show | 163 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.1665-1455A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 9/11 | chr4 | 105836404 | ||||||
| chr4:105836446
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1665-1413G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 9/11 | chr4 | 105836446 | ||||||
| chr4:105836527
|
T | A | 1 | a0001c0001t0002g0157 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1665-1332T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 9/11 | chr4 | 105836527 | ||||||
| chr4:105836533
|
T | G | 2 | a0001c0001t0001g0026a0001c0001t0012g0063 | 2 | NA18983.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1665-1326T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 9/11 | chr4 | 105836533 | ||||||
| chr4:105836899
|
T | C | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1665-960T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 9/11 | chr4 | 105836899 | ||||||
| chr4:105836973
|
A | G | 3 | a0001c0001t0014g0105a0001c0002t0002g0101a0001c0002t0002g0137 | 3 | HG02145.hp2 HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1665-886A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 9/11 | chr4 | 105836973 | ||||||
| chr4:105837248
|
A | G | 64 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(61): Show | 65 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.1665-611A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 9/11 | chr4 | 105837248 | ||||||
| chr4:105837442
|
C | G | 1 | a0001c0005t0021g0091 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1665-417C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 9/11 | chr4 | 105837442 | ||||||
| chr4:105837496
|
A | C | 1 | a0001c0005t0021g0091 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1665-363A>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 9/11 | chr4 | 105837496 | ||||||
| chr4:105837524
|
C | G | 1 | a0001c0001t0001g0003 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1665-335C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 9/11 | chr4 | 105837524 | ||||||
| chr4:105837593
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG01081.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1665-266T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 9/11 | chr4 | 105837593 | ||||||
| chr4:105837925
|
A | G | 7 | a0001c0001t0014g0105a0001c0002t0002g0081a0001c0002t0002g0088others(4): Show | 7 | HG02145.hp2 HG02622.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1695+36A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 10/11 | chr4 | 105837925 | ||||||
| chr4:105838220
|
G | A | 4 | a0001c0001t0004g0133a0001c0001t0004g0176a0001c0001t0004g0177others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+331G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 10/11 | chr4 | 105838220 | ||||||
| chr4:105838651
|
G | A | 1 | a0001c0001t0003g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1695+762G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 10/11 | chr4 | 105838651 | ||||||
| chr4:105838652
|
A | T | 1 | a0001c0001t0003g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1695+763A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 10/11 | chr4 | 105838652 | ||||||
| chr4:105838805
|
A | G | 1 | a0001c0001t0003g0112 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1695+916A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 10/11 | chr4 | 105838805 | ||||||
| chr4:105838985
|
G | C | 1 | a0001c0002t0020g0136 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1695+1096G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 10/11 | chr4 | 105838985 | ||||||
| chr4:105839041
|
A | T | 62 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(59): Show | 63 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.1695+1152A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 10/11 | chr4 | 105839041 | ||||||
| chr4:105839129
|
G | T | 1 | a0001c0001t0023g0050 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1695+1240G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 10/11 | chr4 | 105839129 | ||||||
| chr4:105839135
|
A | G | 1 | a0001c0005t0021g0091 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1695+1246A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 10/11 | chr4 | 105839135 | ||||||
| chr4:105839774
|
G | A | 15 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(12): Show | 15 | HG01070.hp2 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1695+1885G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 10/11 | chr4 | 105839774 | ||||||
| chr4:105840165
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1696-1900A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 10/11 | chr4 | 105840165 | ||||||
| chr4:105840259
|
C | G | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1696-1806C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 10/11 | chr4 | 105840259 | ||||||
| chr4:105840355
|
T | A | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1696-1710T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 10/11 | chr4 | 105840355 | ||||||
| chr4:105840416
|
GT | G | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1696-1641delT | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105840416 | |||||
| chr4:105840659
|
C | T | 1 | a0001c0001t0002g0148 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1696-1406C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 10/11 | chr4 | 105840659 | ||||||
| chr4:105840680
|
A | G | 63 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(60): Show | 64 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.1696-1385A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 10/11 | chr4 | 105840680 | ||||||
| chr4:105841087
|
G | A | 7 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0021others(4): Show | 7 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1696-978G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 10/11 | chr4 | 105841087 | ||||||
| chr4:105841126
|
C | T | 15 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(12): Show | 15 | HG01070.hp2 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1696-939C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 10/11 | chr4 | 105841126 | ||||||
| chr4:105841192
|
C | T | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1696-873C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 10/11 | chr4 | 105841192 | ||||||
| chr4:105841205
|
T | A | 3 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182 | 3 | HG00735.hp1 HG01243.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1696-860T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 10/11 | chr4 | 105841205 | ||||||
| chr4:105841292
|
G | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(91): Show | 95 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.1696-773G>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 10/11 | chr4 | 105841292 | ||||||
| chr4:105841323
|
CA | C | 12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0005g0167others(9): Show | 12 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1696-730delA | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105841323 | |||||
| chr4:105841572
|
T | A | 1 | a0001c0002t0002g0099 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1696-493T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 10/11 | chr4 | 105841572 | ||||||
| chr4:105841665
|
G | A | 1 | a0001c0001t0013g0070 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1696-400G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 10/11 | chr4 | 105841665 | ||||||
| chr4:105841674
|
G | GA | 94 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(91): Show | 95 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.1696-382dupA | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 105841674 | |||||
| chr4:105841698
|
A | G | 2 | a0001c0001t0004g0075a0001c0001t0004g0077 | 2 | HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1696-367A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 10/11 | chr4 | 105841698 | ||||||
| chr4:105841743
|
C | T | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1696-322C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 10/11 | chr4 | 105841743 | ||||||
| chr4:105841928
|
A | C | 15 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(12): Show | 15 | HG01070.hp2 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1696-137A>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 10/11 | chr4 | 105841928 | ||||||
| chr4:105842287
|
T | G | 2 | a0001c0001t0002g0157a0001c0001t0002g0179 | 2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1765+153T>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 11/11 | chr4 | 105842287 | ||||||
| chr4:105842521
|
T | C | 1 | a0001c0001t0013g0070 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1765+387T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 11/11 | chr4 | 105842521 | ||||||
| chr4:105842654
|
A | T | 30 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(27): Show | 30 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.1765+520A>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 11/11 | chr4 | 105842654 | ||||||
| chr4:105842732
|
T | C | 1 | a0001c0001t0003g0110 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1765+598T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 11/11 | chr4 | 105842732 | ||||||
| chr4:105842823
|
G | T | 5 | a0001c0001t0005g0180a0001c0001t0005g0181a0001c0001t0005g0182others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1765+689G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 11/11 | chr4 | 105842823 | ||||||
| chr4:105843141
|
G | A | 1 | a0001c0001t0004g0177 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1765+1007G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 11/11 | chr4 | 105843141 | ||||||
| chr4:105843901
|
T | C | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1766-1540T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 11/11 | chr4 | 105843901 | ||||||
| chr4:105843906
|
G | T | 10 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1766-1535G>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 11/11 | chr4 | 105843906 | ||||||
| chr4:105843967
|
C | T | 37 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0003g0002others(34): Show | 38 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.1766-1474C>T | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 11/11 | chr4 | 105843967 | ||||||
| chr4:105844194
|
C | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1766-1247C>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 11/11 | chr4 | 105844194 | ||||||
| chr4:105844368
|
C | A | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1766-1073C>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 11/11 | chr4 | 105844368 | ||||||
| chr4:105844432
|
G | A | 1 | a0001c0001t0003g0124 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1766-1009G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 11/11 | chr4 | 105844432 | ||||||
| chr4:105844656
|
T | A | 30 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(27): Show | 30 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.1766-785T>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 11/11 | chr4 | 105844656 | ||||||
| chr4:105844758
|
G | A | 30 | a0001c0001t0004g0074a0001c0001t0004g0075a0001c0001t0004g0076others(27): Show | 30 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.1766-683G>A | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 11/11 | chr4 | 105844758 | ||||||
| chr4:105845273
|
T | C | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1766-168T>C | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 11/11 | chr4 | 105845273 | ||||||
| chr4:105845339
|
A | G | 15 | a0001c0001t0005g0167a0001c0001t0005g0174a0001c0001t0005g0175others(12): Show | 15 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1766-102A>G | GSTCD | ENSG00000138780.15 | transcript | ENST00000515279.6 | protein_coding | 11/11 | chr4 | 105845339 |