| geneid | 389207 |
|---|---|
| ensemblid | ENSG00000215203.3 |
| hgncid | 31673 |
| symbol | GRXCR1 |
| name | glutaredoxin and cysteine rich domain containing 1 |
| refseq_nuc | NM_001080476.3 |
| refseq_prot | NP_001073945.1 |
| ensembl_nuc | ENST00000399770.3 |
| ensembl_prot | ENSP00000382670.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 42892713 |
| end | 43030658 |
| strand | + |
| ver | v1.2 |
| region | chr4:42892713-43030658 |
| region5000 | chr4:42887713-43035658 |
| regionname0 | GRXCR1_chr4_42892713_43030658 |
| regionname5000 | GRXCR1_chr4_42887713_43035658 |
| 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 | 1/0 | 290 | 216 | 68 | 44 | 75 | 10 | 18 | 63 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| a0002 | 0/0 | 290 | 67 | 1 | 13 | 45 | 0 | 8 | 33 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| a0003 | 0/1 | 290 | 53 | 21 | 5 | 25 | 0 | 1 | 18 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| a0004 | 0/0 | 290 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| a0005 | 0/0 | 290 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| 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 | 1/0 | 873 | 213 | 65 | 44 | 75 | 10 | 18 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| c0002 | 0/0 | 873 | 67 | 1 | 13 | 45 | 0 | 8 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| c0003 | 0/1 | 873 | 52 | 20 | 5 | 25 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| c0004 | 0/0 | 873 | 3 | 3 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| c0005 | 0/0 | 873 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| c0006 | 0/0 | 873 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| c0007 | 0/0 | 873 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| 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 | 673 | 153 | 22 | 22 | 88 | 6 | 15 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| t0002 | 1/1 | 673 | 98 | 43 | 21 | 21 | 2 | 9 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| t0003 | 0/0 | 673 | 39 | 8 | 4 | 25 | 0 | 2 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| t0004 | 0/0 | 673 | 39 | 12 | 14 | 11 | 2 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| t0005 | 0/0 | 673 | 2 | 2 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| t0006 | 0/0 | 673 | 2 | 2 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| t0007 | 0/0 | 673 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| t0008 | 0/0 | 673 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| t0009 | 0/0 | 673 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| t0010 | 0/0 | 673 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| t0011 | 0/0 | 673 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0079 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0300 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| 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 | 1/0 | 873 | 213 | 65 | 44 | 75 | 10 | 18 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| a0001c0004 | 0/0 | 873 | 3 | 3 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| a0002c0002 | 0/0 | 873 | 67 | 1 | 13 | 45 | 0 | 8 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| a0003c0003 | 0/1 | 873 | 52 | 20 | 5 | 25 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| a0003c0005 | 0/0 | 873 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| a0004c0007 | 0/0 | 873 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| a0005c0006 | 0/0 | 873 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1545 | 64 | 13 | 10 | 26 | 6 | 9 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| a0001c0001t0002 | 1/0 | 1545 | 64 | 27 | 16 | 12 | 2 | 6 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| a0001c0001t0003 | 0/0 | 1545 | 39 | 8 | 4 | 25 | 0 | 2 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| a0001c0001t0004 | 0/0 | 1545 | 39 | 12 | 14 | 11 | 2 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| a0001c0001t0005 | 0/0 | 1545 | 2 | 2 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| a0001c0001t0006 | 0/0 | 1545 | 2 | 2 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| a0001c0001t0008 | 0/0 | 1545 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| a0001c0001t0009 | 0/0 | 1545 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| a0001c0001t0010 | 0/0 | 1545 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| a0001c0004t0002 | 0/0 | 1545 | 3 | 3 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| a0002c0002t0001 | 0/0 | 1545 | 55 | 0 | 11 | 39 | 0 | 5 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| a0002c0002t0002 | 0/0 | 1545 | 11 | 1 | 1 | 6 | 0 | 3 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| a0002c0002t0007 | 0/0 | 1545 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| a0003c0003t0001 | 0/0 | 1545 | 34 | 9 | 1 | 23 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| a0003c0003t0002 | 0/1 | 1545 | 18 | 11 | 4 | 2 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| a0003c0005t0002 | 0/0 | 1545 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| a0004c0007t0002 | 0/0 | 1545 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| a0005c0006t0011 | 0/0 | 1545 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | copy fasta | chr4 | 42887713 | 43035658 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0079 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0006g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0008g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0009g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0001t0010g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0004t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0004t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0001c0004t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0002c0002t0007g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0002g0300 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0003t0002g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0003c0005t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0004c0007t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| a0005c0006t0011g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0056 | EUR | GBR | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0077 | EUR | GBR | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | FIN | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0168 | EUR | FIN | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0220 | EAS | CHS | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG00423 | hp2 | a0004 | c0007 | t0002 | g0114 | EAS | CHS | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0274 | EAS | CHS | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0266 | EAS | CHS | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0276 | EAS | CHS | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0251 | EAS | CHS | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0180 | EAS | CHS | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0238 | EAS | CHS | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | CHS | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | CHS | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0252 | EAS | CHS | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG00733 | hp1 | a0003 | c0003 | t0002 | g0322 | AMR | PUR | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0203 | AMR | PUR | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0198 | AMR | PUR | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0199 | AMR | PUR | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0184 | AMR | PUR | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0222 | AMR | PUR | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0183 | AMR | PUR | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0174 | AMR | PUR | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0173 | AMR | PUR | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0172 | AMR | PUR | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01192 | hp2 | a0003 | c0003 | t0001 | g0290 | AMR | PUR | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01243 | hp1 | a0003 | c0003 | t0002 | g0323 | AMR | PUR | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0191 | AMR | CLM | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0247 | AMR | CLM | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | CLM | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0244 | AMR | CLM | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | CLM | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0193 | AMR | CLM | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | CLM | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0248 | AMR | CLM | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01496 | hp1 | a0002 | c0002 | t0007 | g0226 | AMR | CLM | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | CLM | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0052 | EUR | IBS | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | IBS | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0033 | EUR | IBS | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0278 | AFR | ACB | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01891 | hp1 | a0003 | c0003 | t0002 | g0335 | AFR | ACB | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0144 | AFR | ACB | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0233 | AMR | PEL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0242 | AMR | PEL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0255 | AMR | PEL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0189 | AMR | PEL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0267 | AMR | PEL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0241 | AMR | PEL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0240 | AMR | PEL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0162 | AMR | PEL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0170 | AMR | PEL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01978 | hp2 | a0003 | c0003 | t0002 | g0301 | AMR | PEL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01981 | hp1 | a0003 | c0003 | t0002 | g0305 | AMR | PEL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0169 | AMR | PEL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PEL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0206 | EAS | KHV | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0259 | EAS | KHV | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02027 | hp1 | a0003 | c0003 | t0001 | g0312 | EAS | KHV | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0280 | EAS | KHV | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0106 | AFR | ACB | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | ACB | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02056 | hp1 | a0003 | c0003 | t0001 | g0316 | EAS | KHV | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02056 | hp2 | a0003 | c0003 | t0002 | g0328 | EAS | KHV | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | KHV | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0213 | EAS | KHV | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | KHV | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02132 | hp2 | a0003 | c0003 | t0001 | g0307 | EAS | KHV | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | KHV | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | KHV | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | ACB | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0257 | EAS | CDX | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02155 | hp2 | a0003 | c0003 | t0001 | g0304 | EAS | CDX | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0221 | EAS | CDX | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02165 | hp2 | a0003 | c0003 | t0001 | g0315 | EAS | CDX | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02257 | hp1 | a0003 | c0003 | t0002 | g0303 | AFR | ACB | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0136 | AFR | ACB | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0256 | AMR | PEL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0176 | AMR | PEL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02280 | hp1 | a0003 | c0003 | t0002 | g0314 | AFR | ACB | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0140 | AFR | ACB | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0177 | AMR | PEL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0253 | AMR | PEL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | KHV | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02523 | hp2 | a0003 | c0003 | t0002 | g0308 | EAS | KHV | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0003 | AFR | GWD | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02572 | hp2 | a0003 | c0005 | t0002 | g0332 | AFR | GWD | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0158 | AFR | GWD | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | GWD | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0141 | AFR | GWD | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0138 | AFR | GWD | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | GWD | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02717 | hp2 | a0003 | c0003 | t0001 | g0317 | AFR | GWD | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02723 | hp2 | a0003 | c0003 | t0002 | g0336 | AFR | GWD | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0134 | SAS | PJL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02738 | hp1 | a0002 | c0002 | t0002 | g0271 | SAS | PJL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | GWD | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02809 | hp2 | a0001 | c0004 | t0002 | g0091 | AFR | GWD | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0159 | AFR | GWD | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02895 | hp1 | a0003 | c0003 | t0001 | g0326 | AFR | GWD | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0128 | AFR | GWD | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0157 | AFR | GWD | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02922 | hp1 | a0003 | c0003 | t0002 | g0297 | AFR | ESN | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0281 | AFR | ESN | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ESN | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | ESN | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0137 | AFR | ESN | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | ESN | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | ESN | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03041 | hp1 | a0003 | c0003 | t0001 | g0331 | AFR | GWD | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0131 | AFR | GWD | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03098 | hp1 | a0003 | c0003 | t0002 | g0334 | AFR | MSL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | MSL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03130 | hp1 | a0001 | c0004 | t0002 | g0087 | AFR | ESN | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0142 | AFR | ESN | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0160 | AFR | ESN | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | ESN | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0282 | AFR | MSL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | MSL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03225 | hp1 | a0003 | c0003 | t0002 | g0324 | AFR | MSL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | MSL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03453 | hp2 | a0003 | c0003 | t0001 | g0337 | AFR | MSL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03486 | hp1 | a0002 | c0002 | t0002 | g0225 | AFR | MSL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0139 | AFR | MSL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0223 | SAS | PJL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03491 | hp1 | a0003 | c0003 | t0001 | g0299 | SAS | PJL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0038 | SAS | PJL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03516 | hp1 | a0003 | c0003 | t0002 | g0291 | AFR | ESN | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03516 | hp2 | a0003 | c0003 | t0001 | g0295 | AFR | ESN | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0211 | AFR | MSL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | MSL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03669 | hp2 | a0005 | c0006 | t0011 | g0283 | SAS | PJL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0254 | SAS | STU | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | STU | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0229 | SAS | BEB | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0275 | SAS | BEB | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0230 | SAS | BEB | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0246 | SAS | BEB | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0037 | SAS | STU | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG04115 | hp2 | a0001 | c0001 | t0010 | g0284 | SAS | STU | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0277 | SAS | STU | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0135 | SAS | STU | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18522 | hp2 | a0003 | c0003 | t0001 | g0306 | AFR | YRI | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | YRI | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0130 | AFR | YRI | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0152 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0219 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18944 | hp1 | a0003 | c0003 | t0001 | g0286 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0148 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18945 | hp2 | a0003 | c0003 | t0001 | g0310 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0243 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18949 | hp1 | a0003 | c0003 | t0001 | g0298 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18950 | hp1 | a0003 | c0003 | t0001 | g0311 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0204 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0269 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18964 | hp2 | a0003 | c0003 | t0001 | g0319 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18965 | hp1 | a0003 | c0003 | t0001 | g0293 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18970 | hp1 | a0003 | c0003 | t0001 | g0294 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18973 | hp2 | a0003 | c0003 | t0001 | g0292 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0239 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18980 | hp2 | a0003 | c0003 | t0001 | g0296 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18984 | hp1 | a0001 | c0001 | t0004 | g0210 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18984 | hp2 | a0002 | c0002 | t0002 | g0215 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18985 | hp2 | a0001 | c0001 | t0009 | g0040 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18992 | hp1 | a0003 | c0003 | t0001 | g0313 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18993 | hp2 | a0003 | c0003 | t0001 | g0288 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18994 | hp1 | a0003 | c0003 | t0001 | g0289 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18995 | hp2 | a0003 | c0003 | t0001 | g0309 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18998 | hp1 | a0003 | c0003 | t0001 | g0320 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19000 | hp2 | a0003 | c0003 | t0001 | g0321 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0147 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0245 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0258 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19011 | hp1 | a0003 | c0003 | t0001 | g0287 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19012 | hp2 | a0003 | c0003 | t0001 | g0338 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0156 | AFR | LWK | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | LWK | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0155 | AFR | LWK | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0108 | AFR | LWK | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0270 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0250 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0179 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0205 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19072 | hp2 | a0002 | c0002 | t0002 | g0265 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0279 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0166 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19081 | hp1 | a0003 | c0003 | t0001 | g0325 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0232 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0214 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0237 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | YRI | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0161 | AFR | YRI | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0171 | AFR | ASW | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0192 | AFR | ASW | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0133 | EUR | TSI | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | TSI | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0053 | SAS | GIH | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | GIH | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0197 | AMR | CLM | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0165 | AMR | CLM | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02109 | hp1 | a0003 | c0003 | t0002 | g0302 | AFR | ACB | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02109 | hp2 | a0003 | c0003 | t0001 | g0330 | AFR | ACB | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02559 | hp1 | a0003 | c0003 | t0002 | g0327 | AFR | ACB | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0143 | AFR | ACB | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | MSL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG03471 | hp2 | a0003 | c0003 | t0001 | g0318 | AFR | MSL | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG06807 | hp1 | a0001 | c0001 | t0006 | g0016 | AFR | USA | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| HG06807 | hp2 | a0003 | c0003 | t0001 | g0333 | AFR | USA | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA20300 | hp1 | a0001 | c0004 | t0002 | g0088 | AFR | USA | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | USA | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA21309 | hp1 | a0003 | c0003 | t0002 | g0329 | AFR | LWK | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0209 | AFR | LWK | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0002 | g0300 | REF | REF | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0079 | REF | REF | GRXCR1_chr4_42887713_43035658 | GRXCR1 | chr4 | 42887713 | 43035658 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:42893291
|
G | A | 1 | a0003 | 53 | HG00733.hp1 HG01192.hp2 HG01243.hp1 others(50): Show |
missense_variant | MODERATE | c.25G>A | p.Glu9Lys | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/4 | 579/1545 | 25/873 | 9/290 | chr4 | 42893291 | ||
| chr4:42893406
|
C | T | 1 | a0002 | 67 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(64): Show |
missense_variant | MODERATE | c.140C>T | p.Ala47Val | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/4 | 694/1545 | 140/873 | 47/290 | chr4 | 42893406 | ||
| chr4:42893456
|
G | A | 1 | a0005 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.190G>A | p.Gly64Ser | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/4 | 744/1545 | 190/873 | 64/290 | chr4 | 42893456 | ||
| chr4:42893555
|
G | A | 1 | a0004 | 1 | HG00423.hp2 | missense_variant | MODERATE | c.289G>A | p.Val97Ile | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/4 | 843/1545 | 289/873 | 97/290 | chr4 | 42893555 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:43030444
|
C | T | 2 | a0001c0004a0003c0005 | 4 | HG02572.hp2 HG02809.hp2 HG03130.hp1 others(1): Show |
synonymous_variant | LOW | c.777C>T | p.Ser259Ser | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 4/4 | 1331/1545 | 777/873 | 259/290 | chr4 | 43030444 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:42892741
|
T | C | 3 | a0001c0001t0003a0001c0001t0004a0001c0001t0005 | 80 | HG00323.hp2 HG00609.hp2 HG00673.hp1 others(77): Show |
5_prime_UTR_variant | MODIFIER | c.-526T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/4 | 526 | chr4 | 42892741 | |||||
| chr4:42892805
|
G | T | 2 | a0001c0001t0010a0005c0006t0011 | 2 | HG03669.hp2 HG04115.hp2 |
5_prime_UTR_variant | MODIFIER | c.-462G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/4 | 462 | chr4 | 42892805 | |||||
| chr4:42892884
|
G | A | 1 | a0002c0002t0007 | 1 | HG01496.hp1 | 5_prime_UTR_variant | MODIFIER | c.-383G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/4 | 383 | chr4 | 42892884 | |||||
| chr4:42892964
|
C | T | 1 | a0001c0001t0009 | 1 | NA18985.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-303C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/4 | chr4 | 42892964 | ||||||
| chr4:42893015
|
A | G | 1 | a0001c0001t0006 | 2 | HG02572.hp1 HG06807.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-252A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/4 | chr4 | 42893015 | ||||||
| chr4:42893076
|
C | T | 1 | a0001c0001t0008 | 1 | HG02055.hp1 | 5_prime_UTR_variant | MODIFIER | c.-191C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/4 | 191 | chr4 | 42893076 | |||||
| chr4:42893123
|
G | A | 1 | a0001c0001t0006 | 2 | HG02572.hp1 HG06807.hp1 |
5_prime_UTR_variant | MODIFIER | c.-144G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/4 | 144 | chr4 | 42893123 | |||||
| chr4:42893159
|
G | C | 2 | a0001c0001t0010a0005c0006t0011 | 2 | HG03669.hp2 HG04115.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-108G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/4 | chr4 | 42893159 | ||||||
| chr4:43030581
|
A | G | 1 | a0001c0001t0005 | 2 | HG02896.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*41A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 4/4 | 41 | chr4 | 43030581 | |||||
| chr4:43030595
|
G | A | 7 | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(4): Show | 195 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*55G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 4/4 | 55 | chr4 | 43030595 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:42893698
|
A | G | 53 | a0003c0003t0001g0286a0003c0003t0001g0287a0003c0003t0001g0288others(50): Show | 53 | HG00733.hp1 HG01192.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.384+48A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42893698 | ||||||
| chr4:42893789
|
T | C | 2 | a0001c0001t0002g0001a0001c0001t0002g0002 | 2 | HG01167.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.384+139T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42893789 | ||||||
| chr4:42893854
|
G | A | 68 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(65): Show | 68 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.384+204G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42893854 | ||||||
| chr4:42894012
|
A | G | 54 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0023others(51): Show | 54 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.384+362A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42894012 | ||||||
| chr4:42894050
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.384+400C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42894050 | ||||||
| chr4:42894095
|
C | T | 206 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(203): Show | 206 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.384+445C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42894095 | ||||||
| chr4:42894127
|
C | T | 299 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(296): Show | 299 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(296): Show |
intron_variant | MODIFIER | c.384+477C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42894127 | ||||||
| chr4:42894143
|
C | T | 2 | a0001c0001t0010g0284a0005c0006t0011g0283 | 2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.384+493C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42894143 | ||||||
| chr4:42894174
|
A | G | 38 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0045others(35): Show | 38 | HG00140.hp1 HG00639.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.384+524A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42894174 | ||||||
| chr4:42894179
|
T | G | 1 | a0001c0001t0001g0017 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.384+529T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42894179 | ||||||
| chr4:42894345
|
G | A | 1 | a0001c0001t0002g0033 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.384+695G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42894345 | ||||||
| chr4:42894367
|
TAAC | T | 14 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(11): Show | 14 | HG01168.hp1 HG01169.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.384+720_384+722del others(3): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42894367 | |||||
| chr4:42894441
|
A | T | 2 | a0001c0001t0010g0284a0005c0006t0011g0283 | 2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.384+791A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42894441 | ||||||
| chr4:42894693
|
AG | A | 54 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0023others(51): Show | 54 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.384+1045delG | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42894693 | |||||
| chr4:42894857
|
C | T | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070 | 3 | HG01109.hp2 HG01515.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.384+1207C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42894857 | ||||||
| chr4:42895067
|
G | A | 17 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(14): Show | 17 | HG00423.hp2 HG00438.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.384+1417G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42895067 | ||||||
| chr4:42895126
|
A | G | 1 | a0003c0003t0001g0338 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.384+1476A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42895126 | ||||||
| chr4:42895225
|
C | T | 14 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(11): Show | 14 | HG01168.hp1 HG01169.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.384+1575C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42895225 | ||||||
| chr4:42895376
|
T | C | 1 | a0001c0001t0001g0034 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.384+1726T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42895376 | ||||||
| chr4:42895508
|
C | A | 1 | a0001c0001t0001g0071 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.384+1858C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42895508 | ||||||
| chr4:42895826
|
C | G | 54 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0023others(51): Show | 54 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.384+2176C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42895826 | ||||||
| chr4:42895837
|
A | G | 2 | a0001c0001t0002g0281a0001c0001t0002g0282 | 2 | HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.384+2187A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42895837 | ||||||
| chr4:42896253
|
A | T | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.384+2603A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42896253 | ||||||
| chr4:42896276
|
C | T | 54 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0023others(51): Show | 54 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.384+2626C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42896276 | ||||||
| chr4:42896379
|
G | A | 8 | a0001c0001t0003g0149a0001c0001t0003g0150a0001c0001t0003g0151others(5): Show | 8 | NA18941.hp2 NA18942.hp1 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.384+2729G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42896379 | ||||||
| chr4:42896436
|
AG | A | 64 | a0001c0001t0003g0149a0001c0001t0003g0150a0001c0001t0003g0151others(61): Show | 64 | HG00323.hp2 HG00609.hp2 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.384+2787delG | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42896436 | ||||||
| chr4:42896763
|
G | T | 2 | a0002c0002t0001g0279a0002c0002t0001g0280 | 2 | HG02027.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.384+3113G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42896763 | ||||||
| chr4:42896770
|
A | G | 1 | a0002c0002t0001g0280 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.384+3120A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42896770 | ||||||
| chr4:42896947
|
A | T | 2 | a0001c0001t0010g0284a0005c0006t0011g0283 | 2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.384+3297A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42896947 | ||||||
| chr4:42896961
|
GA | G | 19 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(16): Show | 19 | HG00423.hp2 HG00438.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.384+3312delA | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42896961 | ||||||
| chr4:42897061
|
A | C | 68 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(65): Show | 68 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.384+3411A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42897061 | ||||||
| chr4:42897205
|
A | C | 1 | a0001c0001t0006g0016 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.384+3555A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42897205 | ||||||
| chr4:42897301
|
C | T | 1 | a0001c0001t0004g0210 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.384+3651C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42897301 | ||||||
| chr4:42897344
|
G | C | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | NA18951.hp1 NA18952.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.384+3694G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42897344 | ||||||
| chr4:42897362
|
C | A | 2 | a0001c0001t0010g0284a0005c0006t0011g0283 | 2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.384+3712C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42897362 | ||||||
| chr4:42897409
|
T | C | 68 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(65): Show | 68 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.384+3759T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42897409 | ||||||
| chr4:42897410
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.384+3760G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42897410 | ||||||
| chr4:42897513
|
A | T | 1 | a0001c0001t0001g0125 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.384+3863A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42897513 | ||||||
| chr4:42897571
|
T | C | 2 | a0001c0001t0010g0284a0005c0006t0011g0283 | 2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.384+3921T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42897571 | ||||||
| chr4:42897592
|
TAGTATGT others(13): Show |
T | 2 | a0001c0001t0001g0017a0001c0001t0010g0284 | 2 | HG01255.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.384+3963_384+3982d others(22): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42897592 | |||||
| chr4:42897688
|
C | T | 295 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(292): Show | 295 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.384+4038C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42897688 | ||||||
| chr4:42897709
|
C | T | 1 | a0001c0001t0001g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.384+4059C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42897709 | ||||||
| chr4:42897808
|
A | C | 68 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(65): Show | 68 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.384+4158A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42897808 | ||||||
| chr4:42897897
|
A | G | 295 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(292): Show | 295 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.384+4247A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42897897 | ||||||
| chr4:42897921
|
C | CTAT | 5 | a0001c0001t0001g0075a0001c0001t0002g0076a0003c0003t0001g0337others(2): Show | 5 | HG01891.hp1 HG01993.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.384+4306_384+4308d others(5): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42897921 | |||||
| chr4:42897921
|
CTAT | C | 17 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(14): Show | 17 | HG02055.hp1 HG02132.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.384+4306_384+4308d others(5): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42897921 | |||||
| chr4:42897921
|
CTATTAT | C | 5 | a0001c0001t0002g0107a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.384+4303_384+4308d others(8): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42897921 | |||||
| chr4:42897921
|
CTATTATT others(5): Show |
C | 1 | a0001c0001t0002g0108 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.384+4297_384+4308d others(14): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42897921 | |||||
| chr4:42897933
|
T | A | 7 | a0001c0001t0003g0159a0001c0001t0003g0160a0001c0001t0003g0161others(4): Show | 7 | HG02615.hp1 HG02886.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.384+4283T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42897933 | ||||||
| chr4:42897938
|
ATTATTAT others(14): Show |
A | 58 | a0001c0001t0003g0149a0001c0001t0003g0150a0001c0001t0003g0151others(55): Show | 58 | HG00323.hp2 HG00609.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.384+4296_384+4316d others(23): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42897938 | |||||
| chr4:42897941
|
ATTATTAT others(11): Show |
A | 16 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(13): Show | 16 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.384+4299_384+4316d others(20): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42897941 | |||||
| chr4:42897944
|
ATTATTAT others(8): Show |
A | 10 | a0001c0001t0001g0125a0001c0001t0001g0212a0001c0001t0002g0036others(7): Show | 10 | HG02083.hp1 HG02135.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.384+4302_384+4316d others(17): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42897944 | |||||
| chr4:42897947
|
ATTATTAT others(5): Show |
A | 129 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0023others(126): Show | 129 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.384+4305_384+4316d others(14): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42897947 | |||||
| chr4:42897950
|
ATTATTAT others(2): Show |
A | 25 | a0001c0001t0001g0032a0001c0001t0001g0110a0001c0001t0001g0111others(22): Show | 25 | HG00423.hp2 HG00438.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.384+4308_384+4316d others(11): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42897950 | |||||
| chr4:42897953
|
ATTATTC | A | 9 | a0001c0001t0001g0123a0001c0001t0001g0146a0001c0001t0002g0145others(6): Show | 9 | HG02818.hp2 HG02922.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.384+4309_384+4314d others(8): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42897953 | |||||
| chr4:42897956
|
ATTC | A | 31 | a0001c0001t0001g0067a0001c0001t0001g0124a0001c0001t0003g0159others(28): Show | 31 | HG00733.hp1 HG01255.hp2 HG01981.hp1 others(28): Show |
intron_variant | MODIFIER | c.384+4309_384+4311d others(5): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42897956 | |||||
| chr4:42897959
|
C | A | 17 | a0001c0001t0002g0278a0003c0003t0001g0325a0003c0003t0001g0326others(14): Show | 17 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.384+4309C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42897959 | ||||||
| chr4:42897964
|
T | G | 20 | a0001c0001t0003g0130a0001c0001t0003g0132a0001c0001t0003g0134others(17): Show | 20 | HG01192.hp2 HG01891.hp2 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.384+4314T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42897964 | ||||||
| chr4:42898170
|
C | A | 2 | a0001c0001t0010g0284a0005c0006t0011g0283 | 2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.384+4520C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42898170 | ||||||
| chr4:42898239
|
A | G | 54 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0023others(51): Show | 54 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.384+4589A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42898239 | ||||||
| chr4:42898244
|
A | G | 21 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(18): Show | 21 | HG00423.hp2 HG00438.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.384+4594A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42898244 | ||||||
| chr4:42898251
|
ATCT | A | 83 | a0001c0001t0001g0212a0001c0001t0002g0281a0001c0001t0002g0282others(80): Show | 83 | HG00323.hp2 HG00609.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.384+4604_384+4606d others(5): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42898251 | |||||
| chr4:42898261
|
A | T | 2 | a0003c0003t0002g0300a0003c0003t0002g0334 | 2 | HG03098.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.384+4611A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42898261 | ||||||
| chr4:42898450
|
T | TG | 54 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0023others(51): Show | 54 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.384+4803dupG | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42898450 | |||||
| chr4:42898465
|
C | A | 2 | a0001c0001t0003g0130a0001c0001t0004g0131 | 2 | HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.384+4815C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42898465 | ||||||
| chr4:42898473
|
C | T | 2 | a0001c0001t0010g0284a0005c0006t0011g0283 | 2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.384+4823C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42898473 | ||||||
| chr4:42898493
|
C | T | 2 | a0001c0001t0010g0284a0005c0006t0011g0283 | 2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.384+4843C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42898493 | ||||||
| chr4:42898517
|
G | A | 1 | a0003c0003t0001g0290 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.384+4867G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42898517 | ||||||
| chr4:42898545
|
A | C | 56 | a0001c0001t0003g0149a0001c0001t0003g0150a0001c0001t0003g0151others(53): Show | 56 | HG00323.hp2 HG00609.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.384+4895A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42898545 | ||||||
| chr4:42898564
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.384+4914C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42898564 | ||||||
| chr4:42898703
|
A | G | 3 | a0001c0001t0001g0212a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | HG02145.hp2 HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.384+5053A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42898703 | ||||||
| chr4:42898734
|
C | A | 1 | a0001c0001t0002g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.384+5084C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42898734 | ||||||
| chr4:42898792
|
G | T | 1 | a0002c0002t0001g0276 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.384+5142G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42898792 | ||||||
| chr4:42898804
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.384+5154T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42898804 | ||||||
| chr4:42898811
|
T | TTC | 53 | a0003c0003t0001g0286a0003c0003t0001g0287a0003c0003t0001g0288others(50): Show | 53 | HG00733.hp1 HG01192.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.384+5163_384+5164d others(4): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42898811 | |||||
| chr4:42898848
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0032 | 2 | HG03654.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.384+5198C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42898848 | ||||||
| chr4:42899009
|
A | G | 1 | a0001c0001t0003g0208 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.384+5359A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42899009 | ||||||
| chr4:42899063
|
C | T | 1 | a0003c0003t0002g0322 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.384+5413C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42899063 | ||||||
| chr4:42899110
|
A | G | 1 | a0001c0001t0003g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.384+5460A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42899110 | ||||||
| chr4:42899200
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.384+5550C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42899200 | ||||||
| chr4:42899418
|
A | G | 4 | a0001c0001t0002g0092a0001c0001t0002g0093a0001c0001t0002g0107others(1): Show | 4 | HG02809.hp1 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.384+5768A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42899418 | ||||||
| chr4:42899488
|
G | T | 3 | a0001c0001t0001g0212a0001c0001t0002g0281a0001c0001t0002g0282 | 3 | HG02145.hp2 HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.384+5838G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42899488 | ||||||
| chr4:42899511
|
A | G | 2 | a0003c0003t0001g0320a0003c0003t0001g0321 | 2 | NA18998.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.384+5861A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42899511 | ||||||
| chr4:42899617
|
C | G | 56 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(53): Show | 56 | HG00733.hp1 HG01109.hp2 HG01192.hp2 others(53): Show |
intron_variant | MODIFIER | c.384+5967C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42899617 | ||||||
| chr4:42899712
|
C | T | 2 | a0001c0001t0010g0284a0005c0006t0011g0283 | 2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.384+6062C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42899712 | ||||||
| chr4:42899819
|
G | A | 2 | a0001c0001t0002g0001a0001c0001t0002g0002 | 2 | HG01167.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.384+6169G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42899819 | ||||||
| chr4:42899836
|
A | T | 69 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(66): Show | 69 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.384+6186A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42899836 | ||||||
| chr4:42899910
|
G | A | 1 | a0002c0002t0001g0214 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.384+6260G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42899910 | ||||||
| chr4:42900630
|
T | C | 1 | a0001c0001t0001g0110 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.384+6980T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42900630 | ||||||
| chr4:42900637
|
A | G | 67 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(64): Show | 67 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.384+6987A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42900637 | ||||||
| chr4:42900650
|
T | C | 82 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(79): Show | 82 | HG00423.hp2 HG00438.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.384+7000T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42900650 | ||||||
| chr4:42900717
|
A | G | 53 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0023others(50): Show | 53 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.384+7067A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42900717 | ||||||
| chr4:42900743
|
T | A | 1 | a0001c0001t0001g0111 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.384+7093T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42900743 | ||||||
| chr4:42900751
|
A | G | 4 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.384+7101A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42900751 | ||||||
| chr4:42900912
|
T | C | 37 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0045others(34): Show | 37 | HG00140.hp1 HG00639.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.384+7262T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42900912 | ||||||
| chr4:42900989
|
A | C | 1 | a0001c0001t0002g0014 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.384+7339A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42900989 | ||||||
| chr4:42901066
|
T | G | 1 | a0003c0003t0002g0302 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.384+7416T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42901066 | ||||||
| chr4:42901129
|
T | C | 2 | a0001c0001t0010g0284a0005c0006t0011g0283 | 2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.384+7479T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42901129 | ||||||
| chr4:42901392
|
G | A | 67 | a0002c0002t0001g0213a0002c0002t0001g0214a0002c0002t0001g0216others(64): Show | 67 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.384+7742G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42901392 | ||||||
| chr4:42901543
|
C | T | 327 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(324): Show | 327 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(324): Show |
intron_variant | MODIFIER | c.384+7893C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42901543 | ||||||
| chr4:42901550
|
C | T | 67 | a0002c0002t0001g0213a0002c0002t0001g0214a0002c0002t0001g0216others(64): Show | 67 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.384+7900C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42901550 | ||||||
| chr4:42901594
|
C | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(8): Show | 11 | HG01168.hp1 HG01169.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.384+7944C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42901594 | ||||||
| chr4:42901645
|
T | C | 53 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0023others(50): Show | 53 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.384+7995T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42901645 | ||||||
| chr4:42901662
|
T | C | 67 | a0002c0002t0001g0213a0002c0002t0001g0214a0002c0002t0001g0216others(64): Show | 67 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.384+8012T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42901662 | ||||||
| chr4:42901689
|
C | G | 82 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(79): Show | 82 | HG00423.hp2 HG00438.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.384+8039C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42901689 | ||||||
| chr4:42901709
|
G | A | 67 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(64): Show | 67 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.384+8059G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42901709 | ||||||
| chr4:42901990
|
T | C | 76 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(73): Show | 76 | HG00423.hp2 HG00438.hp1 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.384+8340T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42901990 | ||||||
| chr4:42902018
|
C | T | 67 | a0002c0002t0001g0213a0002c0002t0001g0214a0002c0002t0001g0216others(64): Show | 67 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.384+8368C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42902018 | ||||||
| chr4:42902137
|
A | G | 2 | a0001c0001t0010g0284a0005c0006t0011g0283 | 2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.384+8487A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42902137 | ||||||
| chr4:42902421
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.384+8771G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42902421 | ||||||
| chr4:42902460
|
TC | T | 7 | a0002c0002t0001g0216a0002c0002t0001g0217a0002c0002t0001g0218others(4): Show | 7 | HG00423.hp1 HG00544.hp2 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.384+8811delC | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42902460 | ||||||
| chr4:42902479
|
C | T | 1 | a0003c0003t0001g0319 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.384+8829C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42902479 | ||||||
| chr4:42902489
|
C | T | 53 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0023others(50): Show | 53 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.384+8839C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42902489 | ||||||
| chr4:42902516
|
T | C | 1 | a0002c0002t0001g0221 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.384+8866T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42902516 | ||||||
| chr4:42902534
|
T | C | 2 | a0003c0003t0001g0290a0003c0003t0002g0301 | 2 | HG01192.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.384+8884T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42902534 | ||||||
| chr4:42902534
|
T | TG | 69 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(66): Show | 69 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.384+8886dupG | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42902534 | |||||
| chr4:42902595
|
T | C | 2 | a0003c0003t0002g0303a0003c0003t0002g0324 | 2 | HG02257.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.384+8945T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42902595 | ||||||
| chr4:42902642
|
T | G | 67 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(64): Show | 67 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.384+8992T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42902642 | ||||||
| chr4:42902756
|
G | T | 2 | a0001c0001t0010g0284a0005c0006t0011g0283 | 2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.384+9106G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42902756 | ||||||
| chr4:42902817
|
T | C | 2 | a0001c0001t0010g0284a0005c0006t0011g0283 | 2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.384+9167T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42902817 | ||||||
| chr4:42902839
|
A | C | 1 | a0003c0003t0001g0318 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.384+9189A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42902839 | ||||||
| chr4:42902892
|
G | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.384+9242G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42902892 | ||||||
| chr4:42902900
|
C | A | 1 | a0002c0002t0001g0279 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.384+9250C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42902900 | ||||||
| chr4:42902902
|
T | C | 53 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0023others(50): Show | 53 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.384+9252T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42902902 | ||||||
| chr4:42903060
|
CA | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(8): Show | 11 | HG01168.hp1 HG01169.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.384+9411delA | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42903060 | ||||||
| chr4:42903148
|
TGGCTTTA others(681): Show |
T | 67 | a0002c0002t0001g0213a0002c0002t0001g0214a0002c0002t0001g0216others(64): Show | 67 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.384+9499_384+10186 others(3): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42903148 | ||||||
| chr4:42903308
|
A | AT | 17 | a0001c0001t0001g0105a0001c0001t0001g0122a0001c0001t0001g0146others(14): Show | 17 | HG02055.hp2 HG02056.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.384+9686dupT | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42903308 | |||||
| chr4:42903308
|
AT | A | 71 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(68): Show | 71 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.384+9686delT | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42903308 | |||||
| chr4:42903308
|
ATT | A | 18 | a0001c0001t0001g0039a0001c0001t0001g0111a0001c0001t0001g0120others(15): Show | 18 | HG00673.hp1 HG01069.hp1 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.384+9685_384+9686d others(4): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42903308 | |||||
| chr4:42903308
|
ATTT | A | 58 | a0001c0001t0001g0019a0001c0001t0001g0109a0001c0001t0001g0110others(55): Show | 58 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.384+9684_384+9686d others(5): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42903308 | |||||
| chr4:42903308
|
ATTTT | A | 8 | a0001c0001t0001g0124a0001c0001t0002g0086a0001c0001t0003g0163others(5): Show | 8 | HG01123.hp2 HG01975.hp2 HG03669.hp2 others(5): Show |
intron_variant | MODIFIER | c.384+9683_384+9686d others(6): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42903308 | |||||
| chr4:42903308
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0002g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.384+9676_384+9686d others(13): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42903308 | |||||
| chr4:42903308
|
ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.384+9673_384+9686d others(16): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42903308 | |||||
| chr4:42903337
|
A | T | 1 | a0003c0003t0001g0338 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.384+9687A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42903337 | ||||||
| chr4:42903373
|
A | G | 25 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(22): Show | 25 | HG00323.hp1 HG00733.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.384+9723A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42903373 | ||||||
| chr4:42903374
|
T | C | 25 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(22): Show | 25 | HG00323.hp1 HG00733.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.384+9724T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42903374 | ||||||
| chr4:42903437
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.384+9787A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42903437 | ||||||
| chr4:42903457
|
A | G | 5 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.384+9807A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42903457 | ||||||
| chr4:42903478
|
A | AT | 5 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(2): Show | 5 | HG02132.hp1 NA18951.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.384+9834dupT | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42903478 | |||||
| chr4:42903534
|
T | G | 3 | a0001c0001t0006g0003a0001c0001t0006g0016a0003c0003t0001g0306 | 3 | HG02572.hp1 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.384+9884T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42903534 | ||||||
| chr4:42903541
|
A | T | 1 | a0003c0003t0001g0306 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.384+9891A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42903541 | ||||||
| chr4:42903555
|
G | A | 4 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.384+9905G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42903555 | ||||||
| chr4:42903664
|
C | A | 2 | a0001c0001t0001g0125a0001c0001t0004g0166 | 2 | NA18964.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.384+10014C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42903664 | ||||||
| chr4:42903717
|
C | T | 15 | a0001c0001t0001g0006a0001c0001t0001g0285a0001c0001t0002g0013others(12): Show | 15 | HG01192.hp2 HG01978.hp2 HG02300.hp2 others(12): Show |
intron_variant | MODIFIER | c.384+10067C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42903717 | ||||||
| chr4:42903784
|
C | G | 2 | a0001c0001t0002g0101a0001c0001t0002g0102 | 2 | NA18997.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.384+10134C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42903784 | ||||||
| chr4:42903952
|
G | A | 3 | a0001c0001t0001g0212a0001c0001t0002g0086a0003c0003t0002g0327 | 3 | HG02145.hp2 HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.384+10302G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42903952 | ||||||
| chr4:42904044
|
T | C | 52 | a0001c0001t0001g0068a0001c0001t0001g0110a0001c0001t0002g0021others(49): Show | 52 | HG00323.hp2 HG00609.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.384+10394T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42904044 | ||||||
| chr4:42904082
|
C | T | 3 | a0001c0001t0001g0212a0001c0001t0002g0086a0003c0003t0002g0327 | 3 | HG02145.hp2 HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.384+10432C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42904082 | ||||||
| chr4:42904083
|
A | G | 203 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(200): Show | 203 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.384+10433A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42904083 | ||||||
| chr4:42904105
|
T | C | 1 | a0001c0001t0002g0086 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.384+10455T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42904105 | ||||||
| chr4:42904239
|
G | T | 1 | a0001c0001t0003g0161 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.384+10589G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42904239 | ||||||
| chr4:42904302
|
C | T | 67 | a0002c0002t0001g0213a0002c0002t0001g0214a0002c0002t0001g0216others(64): Show | 67 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.384+10652C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42904302 | ||||||
| chr4:42904336
|
T | C | 2 | a0001c0001t0003g0191a0001c0001t0004g0192 | 2 | HG01346.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.384+10686T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42904336 | ||||||
| chr4:42904367
|
A | G | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.384+10717A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42904367 | ||||||
| chr4:42904404
|
G | C | 200 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(197): Show | 200 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.384+10754G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42904404 | ||||||
| chr4:42904487
|
A | C | 1 | a0002c0002t0001g0275 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.384+10837A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42904487 | ||||||
| chr4:42904610
|
T | C | 333 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(330): Show | 333 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.384+10960T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42904610 | ||||||
| chr4:42904636
|
A | G | 50 | a0001c0001t0001g0068a0001c0001t0002g0065a0001c0001t0002g0083others(47): Show | 50 | HG00323.hp2 HG00609.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.384+10986A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42904636 | ||||||
| chr4:42904637
|
T | C | 200 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(197): Show | 200 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.384+10987T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42904637 | ||||||
| chr4:42904725
|
A | T | 56 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0046others(53): Show | 56 | HG00621.hp2 HG00639.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.384+11075A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42904725 | ||||||
| chr4:42904741
|
A | G | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.384+11091A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42904741 | ||||||
| chr4:42904788
|
AG | A | 6 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0057others(3): Show | 6 | HG02015.hp1 HG02056.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.384+11139delG | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42904788 | ||||||
| chr4:42904798
|
C | A | 1 | a0001c0001t0002g0041 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.384+11148C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42904798 | ||||||
| chr4:42904869
|
A | T | 1 | a0001c0001t0001g0077 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.384+11219A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42904869 | ||||||
| chr4:42904870
|
C | A | 1 | a0001c0001t0001g0077 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.384+11220C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42904870 | ||||||
| chr4:42904892
|
G | A | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.384+11242G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42904892 | ||||||
| chr4:42905004
|
A | G | 58 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0046others(55): Show | 58 | HG00621.hp2 HG00639.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.384+11354A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42905004 | ||||||
| chr4:42905110
|
C | T | 2 | a0001c0001t0010g0284a0003c0003t0002g0324 | 2 | HG03225.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.384+11460C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42905110 | ||||||
| chr4:42905180
|
A | G | 100 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0024others(97): Show | 100 | HG00140.hp1 HG00323.hp1 HG00733.hp2 others(97): Show |
intron_variant | MODIFIER | c.384+11530A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42905180 | ||||||
| chr4:42905345
|
C | T | 9 | a0001c0001t0003g0163a0001c0001t0003g0164a0001c0001t0003g0186others(6): Show | 9 | HG01934.hp2 NA18946.hp2 NA18950.hp2 others(6): Show |
intron_variant | MODIFIER | c.384+11695C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42905345 | ||||||
| chr4:42905348
|
A | C | 1 | a0001c0001t0002g0107 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.384+11698A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42905348 | ||||||
| chr4:42905447
|
G | A | 1 | a0003c0003t0002g0335 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.384+11797G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42905447 | ||||||
| chr4:42905579
|
C | T | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.384+11929C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42905579 | ||||||
| chr4:42905786
|
C | A | 16 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(13): Show | 16 | HG01168.hp1 HG01169.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.384+12136C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42905786 | ||||||
| chr4:42905862
|
A | G | 1 | a0001c0001t0002g0107 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.384+12212A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42905862 | ||||||
| chr4:42905876
|
T | C | 1 | a0002c0002t0001g0222 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.384+12226T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42905876 | ||||||
| chr4:42905897
|
A | G | 58 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0046others(55): Show | 58 | HG00621.hp2 HG00639.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.384+12247A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42905897 | ||||||
| chr4:42905937
|
G | A | 1 | a0001c0001t0002g0108 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.384+12287G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42905937 | ||||||
| chr4:42905967
|
T | C | 1 | a0001c0001t0002g0108 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.384+12317T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42905967 | ||||||
| chr4:42906054
|
C | A | 1 | a0002c0002t0002g0215 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.384+12404C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42906054 | ||||||
| chr4:42906068
|
ATCTT | A | 3 | a0001c0001t0001g0212a0001c0001t0002g0086a0003c0003t0002g0327 | 3 | HG02145.hp2 HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.384+12422_384+1242 others(8): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42906068 | |||||
| chr4:42906212
|
T | G | 3 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0003g0203 | 3 | HG00733.hp2 HG03654.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.384+12562T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42906212 | ||||||
| chr4:42906329
|
A | G | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.384+12679A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42906329 | ||||||
| chr4:42906340
|
G | T | 28 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0077others(25): Show | 28 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.384+12690G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42906340 | ||||||
| chr4:42906356
|
C | T | 1 | a0001c0001t0004g0162 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.384+12706C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42906356 | ||||||
| chr4:42906408
|
G | A | 3 | a0001c0001t0001g0212a0001c0001t0002g0086a0003c0003t0002g0327 | 3 | HG02145.hp2 HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.384+12758G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42906408 | ||||||
| chr4:42906414
|
T | C | 2 | a0001c0001t0002g0145a0001c0001t0005g0211 | 2 | HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.384+12764T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42906414 | ||||||
| chr4:42906455
|
T | C | 1 | a0001c0001t0003g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.384+12805T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42906455 | ||||||
| chr4:42906708
|
A | G | 1 | a0001c0001t0005g0157 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.384+13058A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42906708 | ||||||
| chr4:42906777
|
C | A | 1 | a0001c0001t0002g0108 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.384+13127C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42906777 | ||||||
| chr4:42906778
|
T | C | 100 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0024others(97): Show | 100 | HG00140.hp1 HG00323.hp1 HG00733.hp2 others(97): Show |
intron_variant | MODIFIER | c.384+13128T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42906778 | ||||||
| chr4:42907122
|
G | A | 1 | a0001c0001t0002g0014 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.384+13472G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42907122 | ||||||
| chr4:42907261
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.384+13611G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42907261 | ||||||
| chr4:42907339
|
C | G | 1 | a0001c0001t0002g0278 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.384+13689C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42907339 | ||||||
| chr4:42907422
|
C | G | 1 | a0001c0001t0003g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.384+13772C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42907422 | ||||||
| chr4:42907503
|
A | C | 333 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(330): Show | 333 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.384+13853A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42907503 | ||||||
| chr4:42907640
|
C | G | 1 | a0002c0002t0001g0277 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.384+13990C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42907640 | ||||||
| chr4:42907669
|
C | T | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.384+14019C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42907669 | ||||||
| chr4:42907762
|
T | G | 1 | a0001c0001t0002g0278 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.384+14112T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42907762 | ||||||
| chr4:42907770
|
A | C | 1 | a0001c0001t0002g0278 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.384+14120A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42907770 | ||||||
| chr4:42907784
|
G | A | 1 | a0001c0001t0002g0108 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.384+14134G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42907784 | ||||||
| chr4:42907962
|
C | T | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.384+14312C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42907962 | ||||||
| chr4:42907976
|
C | A | 2 | a0001c0001t0003g0143a0001c0001t0004g0137 | 2 | HG02559.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.384+14326C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42907976 | ||||||
| chr4:42907985
|
A | G | 1 | a0001c0001t0002g0108 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.384+14335A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42907985 | ||||||
| chr4:42908030
|
G | T | 1 | a0001c0001t0001g0067 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.384+14380G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42908030 | ||||||
| chr4:42908073
|
A | T | 58 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0046others(55): Show | 58 | HG00621.hp2 HG00639.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.384+14423A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42908073 | ||||||
| chr4:42908259
|
A | T | 19 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0024others(16): Show | 19 | HG00140.hp1 HG00323.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.384+14609A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42908259 | ||||||
| chr4:42908312
|
G | A | 1 | a0001c0001t0003g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.384+14662G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42908312 | ||||||
| chr4:42908321
|
C | A | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.384+14671C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42908321 | ||||||
| chr4:42908342
|
G | C | 1 | a0002c0002t0001g0223 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.384+14692G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42908342 | ||||||
| chr4:42908405
|
T | A | 132 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0019others(129): Show | 132 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.384+14755T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42908405 | ||||||
| chr4:42908546
|
T | C | 1 | a0001c0001t0003g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.384+14896T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42908546 | ||||||
| chr4:42908572
|
C | T | 1 | a0001c0001t0005g0157 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.384+14922C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42908572 | ||||||
| chr4:42908746
|
C | G | 1 | a0001c0001t0003g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.384+15096C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42908746 | ||||||
| chr4:42908774
|
A | C | 1 | a0001c0001t0002g0108 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.384+15124A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42908774 | ||||||
| chr4:42909037
|
A | T | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.384+15387A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42909037 | ||||||
| chr4:42909047
|
G | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(14): Show | 17 | HG01168.hp1 HG01169.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.384+15397G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42909047 | ||||||
| chr4:42909107
|
C | T | 2 | a0001c0001t0002g0013a0003c0003t0002g0329 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.384+15457C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42909107 | ||||||
| chr4:42909186
|
G | A | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.384+15536G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42909186 | ||||||
| chr4:42909278
|
C | T | 3 | a0001c0001t0001g0212a0001c0001t0002g0086a0003c0003t0002g0327 | 3 | HG02145.hp2 HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.384+15628C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42909278 | ||||||
| chr4:42909338
|
A | G | 1 | a0001c0001t0003g0190 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.384+15688A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42909338 | ||||||
| chr4:42909350
|
G | C | 1 | a0001c0001t0003g0167 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.384+15700G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42909350 | ||||||
| chr4:42909360
|
T | C | 3 | a0001c0001t0003g0143a0001c0001t0004g0137a0001c0001t0004g0138 | 3 | HG02559.hp2 HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.384+15710T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42909360 | ||||||
| chr4:42909645
|
C | T | 8 | a0001c0001t0003g0132a0001c0001t0003g0134a0001c0001t0003g0135others(5): Show | 8 | HG02074.hp1 HG02257.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.384+15995C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42909645 | ||||||
| chr4:42909836
|
G | T | 47 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0046others(44): Show | 47 | HG00621.hp2 HG00639.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.384+16186G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42909836 | ||||||
| chr4:42909890
|
G | T | 1 | a0001c0001t0001g0125 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.384+16240G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42909890 | ||||||
| chr4:42910050
|
G | A | 333 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(330): Show | 333 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.384+16400G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42910050 | ||||||
| chr4:42910127
|
G | C | 67 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0046others(64): Show | 67 | HG00621.hp2 HG00639.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.384+16477G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42910127 | ||||||
| chr4:42910242
|
T | G | 5 | a0001c0001t0004g0168a0001c0001t0004g0169a0001c0001t0004g0170others(2): Show | 5 | HG00323.hp2 HG01978.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.384+16592T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42910242 | ||||||
| chr4:42910244
|
G | C | 1 | a0001c0001t0002g0043 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.384+16594G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42910244 | ||||||
| chr4:42910273
|
G | A | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.384+16623G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42910273 | ||||||
| chr4:42910377
|
T | C | 1 | a0002c0002t0001g0224 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.384+16727T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42910377 | ||||||
| chr4:42910436
|
T | G | 1 | a0001c0001t0001g0017 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.384+16786T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42910436 | ||||||
| chr4:42910495
|
G | A | 50 | a0001c0001t0001g0068a0001c0001t0002g0065a0001c0001t0002g0083others(47): Show | 50 | HG00323.hp2 HG00609.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.384+16845G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42910495 | ||||||
| chr4:42910497
|
T | C | 3 | a0001c0001t0001g0212a0001c0001t0002g0086a0003c0003t0002g0327 | 3 | HG02145.hp2 HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.384+16847T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42910497 | ||||||
| chr4:42910516
|
G | A | 1 | a0002c0002t0002g0225 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.384+16866G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42910516 | ||||||
| chr4:42910557
|
A | G | 63 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0046others(60): Show | 63 | HG00621.hp2 HG00639.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.384+16907A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42910557 | ||||||
| chr4:42910569
|
A | T | 1 | a0001c0001t0001g0077 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.384+16919A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42910569 | ||||||
| chr4:42910604
|
C | T | 1 | a0002c0002t0001g0275 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.384+16954C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42910604 | ||||||
| chr4:42910670
|
A | G | 68 | a0002c0002t0001g0213a0002c0002t0001g0214a0002c0002t0001g0216others(65): Show | 68 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.384+17020A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42910670 | ||||||
| chr4:42910691
|
C | G | 1 | a0001c0004t0002g0091 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.384+17041C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42910691 | ||||||
| chr4:42910734
|
A | G | 2 | a0001c0001t0002g0001a0001c0001t0002g0002 | 2 | HG01167.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.384+17084A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42910734 | ||||||
| chr4:42910742
|
C | T | 3 | a0001c0001t0001g0212a0001c0001t0002g0086a0003c0003t0002g0327 | 3 | HG02145.hp2 HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.384+17092C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42910742 | ||||||
| chr4:42910816
|
G | A | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.384+17166G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42910816 | ||||||
| chr4:42910885
|
C | T | 63 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0046others(60): Show | 63 | HG00621.hp2 HG00639.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.384+17235C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42910885 | ||||||
| chr4:42910890
|
G | A | 5 | a0001c0001t0001g0068a0001c0001t0004g0172a0001c0001t0004g0173others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.384+17240G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42910890 | ||||||
| chr4:42910935
|
G | A | 1 | a0001c0001t0003g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.384+17285G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42910935 | ||||||
| chr4:42911080
|
G | T | 1 | a0001c0001t0001g0125 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.384+17430G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42911080 | ||||||
| chr4:42911155
|
C | T | 2 | a0001c0001t0002g0001a0001c0001t0002g0002 | 2 | HG01167.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.384+17505C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42911155 | ||||||
| chr4:42911273
|
T | C | 263 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(260): Show | 263 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.384+17623T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42911273 | ||||||
| chr4:42911374
|
A | G | 2 | a0001c0001t0002g0145a0001c0001t0005g0211 | 2 | HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.384+17724A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42911374 | ||||||
| chr4:42911376
|
T | A | 1 | a0001c0001t0002g0044 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.384+17726T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42911376 | ||||||
| chr4:42911428
|
T | C | 333 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(330): Show | 333 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.384+17778T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42911428 | ||||||
| chr4:42911978
|
T | C | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.384+18328T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42911978 | ||||||
| chr4:42911998
|
C | T | 5 | a0001c0001t0001g0090a0001c0001t0002g0089a0001c0004t0002g0087others(2): Show | 5 | HG02809.hp2 HG03130.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.384+18348C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42911998 | ||||||
| chr4:42912002
|
G | A | 2 | a0001c0001t0002g0001a0001c0001t0002g0002 | 2 | HG01167.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.384+18352G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42912002 | ||||||
| chr4:42912084
|
C | G | 64 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0046others(61): Show | 64 | HG00621.hp2 HG00639.hp2 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.384+18434C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42912084 | ||||||
| chr4:42912245
|
G | T | 1 | a0003c0003t0002g0327 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.384+18595G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42912245 | ||||||
| chr4:42912290
|
C | A | 7 | a0001c0001t0003g0132a0001c0001t0003g0134a0001c0001t0003g0135others(4): Show | 7 | HG02074.hp1 HG02257.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.384+18640C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42912290 | ||||||
| chr4:42912418
|
A | T | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.384+18768A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42912418 | ||||||
| chr4:42912548
|
C | A | 62 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0046others(59): Show | 62 | HG00621.hp2 HG00639.hp2 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.384+18898C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42912548 | ||||||
| chr4:42912569
|
G | A | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.384+18919G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42912569 | ||||||
| chr4:42912623
|
T | C | 50 | a0001c0001t0001g0068a0001c0001t0002g0065a0001c0001t0002g0083others(47): Show | 50 | HG00323.hp2 HG00609.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.384+18973T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42912623 | ||||||
| chr4:42912692
|
A | G | 3 | a0002c0002t0001g0274a0003c0003t0001g0298a0003c0003t0001g0338 | 3 | HG00438.hp2 NA18949.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.384+19042A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42912692 | ||||||
| chr4:42912695
|
G | A | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.384+19045G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42912695 | ||||||
| chr4:42912734
|
A | C | 69 | a0002c0002t0001g0213a0002c0002t0001g0214a0002c0002t0001g0216others(66): Show | 69 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.384+19084A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42912734 | ||||||
| chr4:42912893
|
T | C | 65 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0046others(62): Show | 65 | HG00621.hp2 HG00639.hp2 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.384+19243T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42912893 | ||||||
| chr4:42913206
|
G | T | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.384+19556G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42913206 | ||||||
| chr4:42913304
|
G | C | 1 | a0001c0001t0002g0094 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.384+19654G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42913304 | ||||||
| chr4:42913435
|
C | T | 3 | a0001c0001t0001g0212a0001c0001t0002g0086a0003c0003t0002g0327 | 3 | HG02145.hp2 HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.384+19785C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42913435 | ||||||
| chr4:42913519
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.384+19869C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42913519 | ||||||
| chr4:42913714
|
T | G | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.384+20064T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42913714 | ||||||
| chr4:42913752
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0069 | 2 | HG00735.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.384+20102G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42913752 | ||||||
| chr4:42913895
|
T | C | 198 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(195): Show | 198 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.384+20245T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42913895 | ||||||
| chr4:42914179
|
C | G | 1 | a0001c0001t0002g0014 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.384+20529C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42914179 | ||||||
| chr4:42914379
|
A | G | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.384+20729A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42914379 | ||||||
| chr4:42914403
|
A | G | 61 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0046others(58): Show | 61 | HG00621.hp2 HG00639.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.384+20753A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42914403 | ||||||
| chr4:42914429
|
A | G | 2 | a0001c0001t0002g0001a0001c0001t0002g0002 | 2 | HG01167.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.384+20779A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42914429 | ||||||
| chr4:42914494
|
A | T | 1 | a0003c0003t0002g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.384+20844A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42914494 | ||||||
| chr4:42914582
|
G | T | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.384+20932G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42914582 | ||||||
| chr4:42914712
|
CCCCACCC others(4): Show |
C | 3 | a0001c0001t0003g0194a0001c0001t0003g0195a0001c0001t0003g0196 | 3 | NA18941.hp1 NA18957.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.384+21069_384+2107 others(15): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42914712 | |||||
| chr4:42914779
|
A | G | 1 | a0001c0001t0002g0063 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.384+21129A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42914779 | ||||||
| chr4:42914961
|
A | G | 330 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(327): Show | 330 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.384+21311A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42914961 | ||||||
| chr4:42914983
|
G | A | 1 | a0003c0003t0002g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.384+21333G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42914983 | ||||||
| chr4:42915080
|
G | A | 1 | a0003c0003t0001g0307 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.384+21430G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42915080 | ||||||
| chr4:42915245
|
C | T | 330 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(327): Show | 330 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.384+21595C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42915245 | ||||||
| chr4:42915273
|
G | A | 1 | a0003c0003t0002g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.384+21623G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42915273 | ||||||
| chr4:42915311
|
G | A | 3 | a0001c0001t0001g0212a0001c0001t0002g0086a0003c0003t0002g0327 | 3 | HG02145.hp2 HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.384+21661G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42915311 | ||||||
| chr4:42915415
|
G | A | 1 | a0003c0003t0002g0305 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.384+21765G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42915415 | ||||||
| chr4:42915416
|
G | A | 17 | a0001c0001t0001g0019a0001c0001t0001g0109a0001c0001t0001g0110others(14): Show | 17 | HG00423.hp2 HG00438.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.384+21766G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42915416 | ||||||
| chr4:42915853
|
T | G | 65 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0046others(62): Show | 65 | HG00621.hp2 HG00639.hp2 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.384+22203T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42915853 | ||||||
| chr4:42916009
|
C | G | 2 | a0002c0002t0001g0272a0002c0002t0001g0273 | 2 | NA18985.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.384+22359C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42916009 | ||||||
| chr4:42916047
|
A | C | 3 | a0001c0001t0001g0212a0001c0001t0002g0086a0003c0003t0002g0327 | 3 | HG02145.hp2 HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.384+22397A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42916047 | ||||||
| chr4:42916053
|
G | A | 330 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(327): Show | 330 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.384+22403G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42916053 | ||||||
| chr4:42916088
|
A | G | 1 | a0003c0003t0001g0294 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.384+22438A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42916088 | ||||||
| chr4:42916099
|
G | GA | 189 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(186): Show | 189 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.384+22461dupA | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42916099 | |||||
| chr4:42916099
|
GA | G | 72 | a0001c0001t0001g0005a0001c0001t0001g0212a0001c0001t0002g0086others(69): Show | 72 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.384+22461delA | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42916099 | |||||
| chr4:42916126
|
G | A | 1 | a0003c0003t0002g0297 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.384+22476G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42916126 | ||||||
| chr4:42916136
|
A | G | 2 | a0001c0001t0004g0155a0001c0001t0004g0156 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.384+22486A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42916136 | ||||||
| chr4:42916398
|
A | G | 1 | a0001c0001t0002g0108 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.384+22748A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42916398 | ||||||
| chr4:42916431
|
A | G | 2 | a0001c0001t0002g0281a0001c0001t0002g0282 | 2 | HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.384+22781A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42916431 | ||||||
| chr4:42916639
|
G | T | 60 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0046others(57): Show | 60 | HG00621.hp2 HG00639.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.384+22989G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42916639 | ||||||
| chr4:42916650
|
G | A | 61 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0046others(58): Show | 61 | HG00621.hp2 HG00639.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.384+23000G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42916650 | ||||||
| chr4:42916840
|
C | T | 7 | a0001c0001t0003g0132a0001c0001t0003g0134a0001c0001t0003g0135others(4): Show | 7 | HG02074.hp1 HG02257.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.384+23190C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42916840 | ||||||
| chr4:42916902
|
G | A | 1 | a0003c0003t0002g0297 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.384+23252G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42916902 | ||||||
| chr4:42917153
|
T | C | 1 | a0003c0003t0002g0297 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.384+23503T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42917153 | ||||||
| chr4:42917230
|
T | C | 1 | a0001c0001t0002g0086 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.384+23580T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42917230 | ||||||
| chr4:42917244
|
T | C | 1 | a0003c0003t0002g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.384+23594T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42917244 | ||||||
| chr4:42917289
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.384+23639C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42917289 | ||||||
| chr4:42917302
|
C | T | 1 | a0003c0003t0001g0315 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.384+23652C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42917302 | ||||||
| chr4:42917339
|
G | T | 60 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0046others(57): Show | 60 | HG00621.hp2 HG00639.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.384+23689G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42917339 | ||||||
| chr4:42917453
|
T | G | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.384+23803T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42917453 | ||||||
| chr4:42917504
|
A | G | 196 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(193): Show | 196 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.384+23854A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42917504 | ||||||
| chr4:42917512
|
C | T | 1 | a0002c0002t0001g0223 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.384+23862C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42917512 | ||||||
| chr4:42917623
|
G | A | 50 | a0001c0001t0001g0068a0001c0001t0002g0065a0001c0001t0002g0083others(47): Show | 50 | HG00323.hp2 HG00609.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.384+23973G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42917623 | ||||||
| chr4:42917862
|
G | A | 2 | a0001c0001t0002g0092a0001c0001t0002g0093 | 2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.384+24212G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42917862 | ||||||
| chr4:42918134
|
G | A | 41 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0146others(38): Show | 41 | HG01243.hp1 HG01891.hp1 HG01981.hp1 others(38): Show |
intron_variant | MODIFIER | c.384+24484G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42918134 | ||||||
| chr4:42918186
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.384+24536T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42918186 | ||||||
| chr4:42918199
|
A | G | 1 | a0001c0001t0003g0185 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.384+24549A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42918199 | ||||||
| chr4:42918369
|
T | A | 15 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(12): Show | 15 | HG01168.hp1 HG01169.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.384+24719T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42918369 | ||||||
| chr4:42918588
|
A | G | 2 | a0001c0001t0001g0095a0001c0001t0001g0100 | 2 | HG03490.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.384+24938A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42918588 | ||||||
| chr4:42918676
|
T | C | 3 | a0001c0001t0003g0149a0001c0001t0004g0147a0001c0001t0004g0148 | 3 | NA18945.hp1 NA18965.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.384+25026T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42918676 | ||||||
| chr4:42918807
|
A | C | 2 | a0001c0001t0010g0284a0005c0006t0011g0283 | 2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.384+25157A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42918807 | ||||||
| chr4:42918923
|
G | C | 59 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0046others(56): Show | 59 | HG00621.hp2 HG00639.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.384+25273G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42918923 | ||||||
| chr4:42919191
|
G | T | 4 | a0001c0001t0002g0145a0001c0001t0005g0211a0001c0001t0010g0284others(1): Show | 4 | HG02976.hp2 HG03579.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.384+25541G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42919191 | ||||||
| chr4:42919286
|
C | G | 1 | a0001c0001t0004g0205 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.384+25636C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42919286 | ||||||
| chr4:42919316
|
A | T | 3 | a0003c0003t0001g0326a0003c0003t0001g0331a0003c0003t0001g0337 | 3 | HG02895.hp1 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.384+25666A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42919316 | ||||||
| chr4:42919342
|
C | T | 97 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0024others(94): Show | 97 | HG00140.hp1 HG00323.hp1 HG00733.hp2 others(94): Show |
intron_variant | MODIFIER | c.384+25692C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42919342 | ||||||
| chr4:42919474
|
T | G | 1 | a0001c0001t0001g0112 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.384+25824T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42919474 | ||||||
| chr4:42919497
|
T | A | 5 | a0001c0001t0001g0090a0001c0001t0002g0089a0001c0004t0002g0087others(2): Show | 5 | HG02809.hp2 HG03130.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.384+25847T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42919497 | ||||||
| chr4:42919511
|
A | G | 68 | a0002c0002t0001g0214a0002c0002t0001g0216a0002c0002t0001g0217others(65): Show | 68 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.384+25861A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42919511 | ||||||
| chr4:42919523
|
T | G | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.384+25873T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42919523 | ||||||
| chr4:42919730
|
T | A | 1 | a0002c0002t0001g0227 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.384+26080T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42919730 | ||||||
| chr4:42919739
|
C | G | 1 | a0002c0002t0002g0271 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.384+26089C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42919739 | ||||||
| chr4:42919770
|
T | A | 1 | a0001c0001t0004g0155 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.384+26120T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42919770 | ||||||
| chr4:42919787
|
G | T | 2 | a0003c0003t0001g0320a0003c0003t0001g0321 | 2 | NA18998.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.384+26137G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42919787 | ||||||
| chr4:42919824
|
A | G | 2 | a0001c0001t0003g0209a0001c0001t0005g0157 | 2 | HG02896.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.384+26174A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42919824 | ||||||
| chr4:42919921
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.384+26271G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42919921 | ||||||
| chr4:42919930
|
G | T | 1 | a0002c0002t0001g0220 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.384+26280G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42919930 | ||||||
| chr4:42919983
|
C | A | 61 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0046others(58): Show | 61 | HG00621.hp2 HG00639.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.384+26333C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42919983 | ||||||
| chr4:42920029
|
C | T | 50 | a0001c0001t0001g0068a0001c0001t0002g0065a0001c0001t0002g0083others(47): Show | 50 | HG00323.hp2 HG00609.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.384+26379C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42920029 | ||||||
| chr4:42920337
|
C | T | 68 | a0002c0002t0001g0214a0002c0002t0001g0216a0002c0002t0001g0217others(65): Show | 68 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.384+26687C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42920337 | ||||||
| chr4:42920363
|
C | CA | 59 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0046others(56): Show | 59 | HG00621.hp2 HG00639.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.384+26715dupA | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42920363 | |||||
| chr4:42920438
|
G | A | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.384+26788G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42920438 | ||||||
| chr4:42920468
|
A | G | 1 | a0002c0002t0002g0270 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.384+26818A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42920468 | ||||||
| chr4:42920473
|
T | A | 3 | a0001c0001t0004g0142a0003c0003t0002g0291a0003c0003t0002g0302 | 3 | HG02109.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.384+26823T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42920473 | ||||||
| chr4:42920533
|
G | T | 1 | a0002c0002t0001g0269 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.384+26883G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42920533 | ||||||
| chr4:42920538
|
G | T | 2 | a0001c0001t0002g0145a0001c0001t0005g0211 | 2 | HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.384+26888G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42920538 | ||||||
| chr4:42920602
|
T | A | 1 | a0001c0001t0002g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.384+26952T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42920602 | ||||||
| chr4:42920679
|
C | T | 1 | a0001c0001t0002g0085 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.384+27029C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42920679 | ||||||
| chr4:42920686
|
C | T | 48 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0046others(45): Show | 48 | HG00621.hp2 HG00639.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.384+27036C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42920686 | ||||||
| chr4:42920848
|
T | G | 1 | a0003c0003t0002g0300 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.384+27198T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42920848 | ||||||
| chr4:42920900
|
T | G | 2 | a0001c0001t0002g0145a0001c0001t0005g0211 | 2 | HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.384+27250T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42920900 | ||||||
| chr4:42920909
|
C | T | 3 | a0001c0001t0002g0020a0001c0001t0002g0022a0005c0006t0011g0283 | 3 | HG02895.hp2 HG02897.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.384+27259C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42920909 | ||||||
| chr4:42920917
|
ATTCAAG | A | 97 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0024others(94): Show | 97 | HG00140.hp1 HG00323.hp1 HG00733.hp2 others(94): Show |
intron_variant | MODIFIER | c.384+27276_384+2728 others(10): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42920917 | |||||
| chr4:42921050
|
T | C | 1 | a0003c0005t0002g0332 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.384+27400T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42921050 | ||||||
| chr4:42921493
|
C | G | 261 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(258): Show | 261 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.384+27843C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42921493 | ||||||
| chr4:42921537
|
G | A | 1 | a0001c0001t0002g0007 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.384+27887G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42921537 | ||||||
| chr4:42921546
|
C | T | 3 | a0001c0001t0001g0212a0001c0001t0002g0086a0003c0003t0002g0327 | 3 | HG02145.hp2 HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.384+27896C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42921546 | ||||||
| chr4:42921591
|
C | G | 68 | a0002c0002t0001g0214a0002c0002t0001g0216a0002c0002t0001g0217others(65): Show | 68 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.384+27941C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42921591 | ||||||
| chr4:42921679
|
G | C | 1 | a0001c0001t0004g0156 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.384+28029G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42921679 | ||||||
| chr4:42921726
|
C | T | 23 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0109others(20): Show | 23 | HG00423.hp2 HG00438.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.384+28076C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42921726 | ||||||
| chr4:42921780
|
G | A | 327 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(324): Show | 327 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(324): Show |
intron_variant | MODIFIER | c.384+28130G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42921780 | ||||||
| chr4:42921943
|
T | C | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.384+28293T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42921943 | ||||||
| chr4:42921976
|
C | T | 1 | a0003c0003t0002g0324 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.384+28326C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42921976 | ||||||
| chr4:42922180
|
T | C | 50 | a0001c0001t0001g0068a0001c0001t0002g0065a0001c0001t0002g0083others(47): Show | 50 | HG00323.hp2 HG00609.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.384+28530T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42922180 | ||||||
| chr4:42922270
|
T | G | 50 | a0001c0001t0001g0068a0001c0001t0002g0065a0001c0001t0002g0083others(47): Show | 50 | HG00323.hp2 HG00609.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.384+28620T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42922270 | ||||||
| chr4:42922408
|
C | T | 68 | a0002c0002t0001g0214a0002c0002t0001g0216a0002c0002t0001g0217others(65): Show | 68 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.384+28758C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42922408 | ||||||
| chr4:42922437
|
G | A | 1 | a0003c0003t0001g0299 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.384+28787G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42922437 | ||||||
| chr4:42922460
|
G | A | 1 | a0002c0002t0001g0272 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.384+28810G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42922460 | ||||||
| chr4:42922496
|
T | C | 3 | a0001c0001t0001g0096a0001c0001t0003g0130a0001c0001t0003g0144 | 3 | HG01891.hp2 HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.384+28846T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42922496 | ||||||
| chr4:42922595
|
T | G | 202 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(199): Show | 202 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.384+28945T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42922595 | ||||||
| chr4:42922734
|
T | C | 1 | a0002c0002t0001g0228 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.384+29084T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42922734 | ||||||
| chr4:42922788
|
T | C | 1 | a0001c0001t0003g0132 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.384+29138T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42922788 | ||||||
| chr4:42922824
|
C | A | 2 | a0001c0001t0003g0209a0001c0001t0005g0157 | 2 | HG02896.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.384+29174C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42922824 | ||||||
| chr4:42922836
|
A | G | 131 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.384+29186A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42922836 | ||||||
| chr4:42922944
|
C | T | 6 | a0001c0001t0002g0145a0001c0001t0004g0169a0001c0001t0004g0170others(3): Show | 6 | HG01978.hp1 HG01993.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.384+29294C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42922944 | ||||||
| chr4:42922945
|
A | G | 202 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(199): Show | 202 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.384+29295A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42922945 | ||||||
| chr4:42922971
|
T | C | 19 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0024others(16): Show | 19 | HG00140.hp1 HG00323.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.384+29321T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42922971 | ||||||
| chr4:42922982
|
G | A | 1 | a0001c0001t0003g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.384+29332G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42922982 | ||||||
| chr4:42923051
|
A | G | 1 | a0001c0001t0002g0108 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.384+29401A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42923051 | ||||||
| chr4:42923067
|
A | T | 12 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 12 | HG01884.hp2 HG02109.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.384+29417A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42923067 | ||||||
| chr4:42923126
|
C | T | 1 | a0001c0001t0001g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.384+29476C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42923126 | ||||||
| chr4:42923144
|
C | T | 1 | a0003c0003t0002g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.384+29494C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42923144 | ||||||
| chr4:42923311
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.384+29661C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42923311 | ||||||
| chr4:42923402
|
A | T | 1 | a0001c0001t0001g0082 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.384+29752A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42923402 | ||||||
| chr4:42923481
|
A | G | 1 | a0002c0002t0001g0268 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.384+29831A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42923481 | ||||||
| chr4:42923614
|
A | T | 205 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(202): Show | 205 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.384+29964A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42923614 | ||||||
| chr4:42923711
|
C | A | 1 | a0001c0001t0001g0113 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.384+30061C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42923711 | ||||||
| chr4:42923734
|
G | A | 2 | a0001c0001t0002g0001a0001c0001t0002g0002 | 2 | HG01167.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.384+30084G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42923734 | ||||||
| chr4:42923777
|
T | A | 4 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.384+30127T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42923777 | ||||||
| chr4:42923815
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0285a0003c0003t0001g0290others(1): Show | 4 | HG01192.hp2 HG01978.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.384+30165G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42923815 | ||||||
| chr4:42923915
|
G | C | 1 | a0001c0001t0001g0056 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.384+30265G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42923915 | ||||||
| chr4:42924005
|
T | C | 42 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0046others(39): Show | 42 | HG00423.hp2 HG00621.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.384+30355T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42924005 | ||||||
| chr4:42924022
|
C | T | 14 | a0001c0001t0002g0013a0001c0001t0002g0044a0001c0001t0003g0132others(11): Show | 14 | HG00639.hp2 HG02074.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.384+30372C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42924022 | ||||||
| chr4:42924080
|
A | G | 1 | a0003c0003t0002g0297 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.384+30430A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42924080 | ||||||
| chr4:42924085
|
A | T | 2 | a0001c0001t0003g0153a0001c0001t0003g0154 | 2 | NA18948.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.384+30435A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42924085 | ||||||
| chr4:42924303
|
A | G | 7 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(4): Show | 7 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.384+30653A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42924303 | ||||||
| chr4:42924444
|
G | A | 3 | a0001c0001t0003g0159a0001c0001t0003g0160a0001c0001t0003g0161 | 3 | HG02886.hp1 HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.384+30794G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42924444 | ||||||
| chr4:42924681
|
G | C | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.384+31031G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42924681 | ||||||
| chr4:42924919
|
T | A | 1 | a0001c0001t0005g0157 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.384+31269T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42924919 | ||||||
| chr4:42925002
|
G | T | 1 | a0002c0002t0001g0277 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.384+31352G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42925002 | ||||||
| chr4:42925061
|
GA | G | 21 | a0001c0001t0001g0012a0001c0001t0001g0069a0001c0001t0001g0075others(18): Show | 21 | HG01884.hp1 HG01981.hp2 HG01993.hp2 others(18): Show |
intron_variant | MODIFIER | c.384+31423delA | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42925061 | |||||
| chr4:42925063
|
A | G | 1 | a0003c0003t0001g0325 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.384+31413A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42925063 | ||||||
| chr4:42925107
|
A | G | 1 | a0003c0003t0002g0297 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.384+31457A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42925107 | ||||||
| chr4:42925110
|
T | C | 7 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(4): Show | 7 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.384+31460T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42925110 | ||||||
| chr4:42925165
|
C | T | 1 | a0001c0001t0002g0094 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.384+31515C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42925165 | ||||||
| chr4:42925208
|
G | A | 1 | a0002c0002t0002g0270 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.384+31558G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42925208 | ||||||
| chr4:42925365
|
T | G | 3 | a0002c0002t0001g0221a0002c0002t0001g0231a0002c0002t0001g0232 | 3 | HG02165.hp1 NA19083.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.384+31715T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42925365 | ||||||
| chr4:42925388
|
A | G | 2 | a0001c0001t0001g0012a0001c0001t0002g0282 | 2 | HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.384+31738A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42925388 | ||||||
| chr4:42925401
|
A | T | 2 | a0001c0001t0004g0183a0001c0001t0004g0184 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.384+31751A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42925401 | ||||||
| chr4:42925530
|
T | C | 97 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(94): Show | 97 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.384+31880T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42925530 | ||||||
| chr4:42925573
|
C | T | 1 | a0001c0001t0002g0281 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.384+31923C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42925573 | ||||||
| chr4:42925662
|
G | T | 42 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0046others(39): Show | 42 | HG00423.hp2 HG00621.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.384+32012G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42925662 | ||||||
| chr4:42925681
|
C | T | 1 | a0001c0001t0002g0055 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.384+32031C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42925681 | ||||||
| chr4:42925915
|
G | C | 4 | a0002c0002t0001g0234a0002c0002t0001g0235a0002c0002t0001g0236others(1): Show | 4 | NA18957.hp1 NA19011.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.384+32265G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42925915 | ||||||
| chr4:42926071
|
A | G | 1 | a0001c0001t0001g0071 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.384+32421A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42926071 | ||||||
| chr4:42926076
|
C | A | 1 | a0003c0003t0001g0319 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.384+32426C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42926076 | ||||||
| chr4:42926077
|
G | A | 1 | a0003c0003t0002g0328 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.384+32427G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42926077 | ||||||
| chr4:42926229
|
T | A | 1 | a0003c0003t0002g0300 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.384+32579T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42926229 | ||||||
| chr4:42926301
|
C | T | 1 | a0001c0001t0002g0054 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.384+32651C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42926301 | ||||||
| chr4:42926447
|
C | A | 10 | a0001c0001t0001g0075a0001c0001t0002g0076a0001c0001t0002g0080others(7): Show | 10 | HG01993.hp2 HG02074.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.384+32797C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42926447 | ||||||
| chr4:42926485
|
G | T | 1 | a0001c0001t0002g0085 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.384+32835G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42926485 | ||||||
| chr4:42926494
|
G | GTT | 42 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0046others(39): Show | 42 | HG00423.hp2 HG00621.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.384+32853_384+3285 others(6): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42926494 | |||||
| chr4:42926494
|
G | T | 92 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(89): Show | 92 | HG00140.hp1 HG00323.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.384+32844G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42926494 | ||||||
| chr4:42926494
|
GT | G | 10 | a0001c0001t0001g0075a0001c0001t0002g0076a0001c0001t0002g0080others(7): Show | 10 | HG01993.hp2 HG02074.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.384+32854delT | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42926494 | |||||
| chr4:42926630
|
TG | T | 18 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(15): Show | 18 | HG02074.hp1 HG02132.hp1 HG03490.hp2 others(15): Show |
intron_variant | MODIFIER | c.384+32981delG | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42926630 | ||||||
| chr4:42926744
|
A | T | 1 | a0001c0001t0005g0211 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.384+33094A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42926744 | ||||||
| chr4:42926791
|
A | C | 2 | a0001c0001t0002g0107a0001c0001t0002g0108 | 2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.384+33141A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42926791 | ||||||
| chr4:42926824
|
A | G | 3 | a0001c0001t0001g0077a0001c0001t0002g0281a0003c0005t0002g0332 | 3 | HG00140.hp2 HG02572.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.384+33174A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42926824 | ||||||
| chr4:42927245
|
G | A | 1 | a0002c0002t0001g0238 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.384+33595G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42927245 | ||||||
| chr4:42927304
|
G | A | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG03704.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.384+33654G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42927304 | ||||||
| chr4:42927552
|
A | G | 7 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(4): Show | 7 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.384+33902A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42927552 | ||||||
| chr4:42927753
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.384+34103A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42927753 | ||||||
| chr4:42927881
|
T | C | 4 | a0001c0001t0002g0080a0001c0001t0004g0136a0001c0001t0006g0003others(1): Show | 4 | HG02145.hp1 HG02257.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.384+34231T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42927881 | ||||||
| chr4:42928257
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.384+34607G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42928257 | ||||||
| chr4:42928309
|
A | G | 2 | a0001c0001t0001g0212a0001c0001t0002g0145 | 2 | HG02145.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.385-34583A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42928309 | ||||||
| chr4:42928377
|
C | T | 1 | a0001c0001t0002g0108 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.385-34515C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42928377 | ||||||
| chr4:42928390
|
G | A | 1 | a0001c0001t0002g0108 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.385-34502G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42928390 | ||||||
| chr4:42928434
|
T | C | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.385-34458T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42928434 | ||||||
| chr4:42928561
|
A | G | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.385-34331A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42928561 | ||||||
| chr4:42928675
|
T | C | 2 | a0001c0001t0001g0212a0001c0001t0002g0145 | 2 | HG02145.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.385-34217T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42928675 | ||||||
| chr4:42928750
|
G | T | 1 | a0004c0007t0002g0114 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.385-34142G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42928750 | ||||||
| chr4:42928907
|
T | C | 7 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(4): Show | 7 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.385-33985T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42928907 | ||||||
| chr4:42928940
|
A | G | 25 | a0001c0001t0001g0012a0001c0001t0001g0075a0001c0001t0002g0076others(22): Show | 25 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.385-33952A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42928940 | ||||||
| chr4:42929011
|
T | C | 1 | a0001c0001t0002g0108 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.385-33881T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42929011 | ||||||
| chr4:42929034
|
C | T | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.385-33858C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42929034 | ||||||
| chr4:42929127
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.385-33765G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42929127 | ||||||
| chr4:42929457
|
G | A | 1 | a0001c0001t0002g0278 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.385-33435G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42929457 | ||||||
| chr4:42929557
|
G | A | 13 | a0001c0001t0001g0012a0001c0001t0002g0108a0001c0001t0002g0126others(10): Show | 13 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.385-33335G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42929557 | ||||||
| chr4:42929585
|
G | C | 1 | a0001c0001t0003g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.385-33307G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42929585 | ||||||
| chr4:42929587
|
G | A | 2 | a0001c0001t0001g0075a0001c0001t0002g0076 | 2 | HG01993.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.385-33305G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42929587 | ||||||
| chr4:42929673
|
C | T | 2 | a0001c0001t0006g0003a0001c0001t0006g0016 | 2 | HG02572.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.385-33219C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42929673 | ||||||
| chr4:42929774
|
A | C | 1 | a0003c0003t0001g0306 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.385-33118A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42929774 | ||||||
| chr4:42929816
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.385-33076G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42929816 | ||||||
| chr4:42929817
|
C | T | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.385-33075C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42929817 | ||||||
| chr4:42929917
|
A | G | 11 | a0001c0001t0001g0012a0001c0001t0002g0126a0001c0001t0002g0127others(8): Show | 11 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.385-32975A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42929917 | ||||||
| chr4:42929944
|
A | G | 2 | a0001c0001t0002g0086a0003c0003t0002g0327 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.385-32948A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42929944 | ||||||
| chr4:42930089
|
C | T | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.385-32803C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42930089 | ||||||
| chr4:42930189
|
A | G | 1 | a0001c0001t0002g0108 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.385-32703A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42930189 | ||||||
| chr4:42930286
|
C | G | 7 | a0001c0001t0001g0112a0001c0001t0001g0117a0001c0001t0001g0118others(4): Show | 7 | HG00438.hp1 NA18971.hp1 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.385-32606C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42930286 | ||||||
| chr4:42930476
|
T | C | 7 | a0001c0001t0001g0121a0001c0001t0001g0122a0003c0003t0001g0292others(4): Show | 7 | HG02027.hp1 NA18945.hp2 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.385-32416T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42930476 | ||||||
| chr4:42930482
|
T | G | 2 | a0001c0001t0002g0086a0003c0003t0002g0327 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.385-32410T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42930482 | ||||||
| chr4:42930507
|
C | T | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.385-32385C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42930507 | ||||||
| chr4:42930602
|
C | A | 2 | a0001c0001t0001g0012a0001c0001t0002g0282 | 2 | HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.385-32290C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42930602 | ||||||
| chr4:42930788
|
G | A | 2 | a0001c0001t0001g0212a0001c0001t0002g0145 | 2 | HG02145.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.385-32104G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42930788 | ||||||
| chr4:42930838
|
T | A | 1 | a0003c0003t0001g0315 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.385-32054T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42930838 | ||||||
| chr4:42930850
|
A | G | 1 | a0002c0002t0001g0275 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.385-32042A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42930850 | ||||||
| chr4:42930854
|
C | A | 5 | a0001c0001t0003g0150a0001c0001t0003g0151a0001c0001t0003g0153others(2): Show | 5 | NA18942.hp1 NA18948.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.385-32038C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42930854 | ||||||
| chr4:42930911
|
A | G | 2 | a0001c0001t0002g0086a0003c0003t0002g0327 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.385-31981A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42930911 | ||||||
| chr4:42931024
|
A | G | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.385-31868A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42931024 | ||||||
| chr4:42931029
|
T | C | 1 | a0001c0001t0005g0157 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.385-31863T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42931029 | ||||||
| chr4:42931059
|
C | CT | 14 | a0001c0001t0001g0006a0001c0001t0001g0075a0001c0001t0002g0076others(11): Show | 14 | HG00544.hp1 HG01192.hp2 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.385-31823dupT | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42931059 | |||||
| chr4:42931069
|
T | C | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.385-31823T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42931069 | ||||||
| chr4:42931252
|
T | C | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.385-31640T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42931252 | ||||||
| chr4:42931479
|
T | G | 28 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0077others(25): Show | 28 | HG00140.hp2 HG00438.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.385-31413T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42931479 | ||||||
| chr4:42931526
|
C | G | 12 | a0001c0001t0003g0182a0002c0002t0001g0227a0002c0002t0001g0228others(9): Show | 12 | HG02015.hp2 HG02155.hp1 NA18944.hp2 others(9): Show |
intron_variant | MODIFIER | c.385-31366C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42931526 | ||||||
| chr4:42931527
|
C | T | 1 | a0003c0003t0001g0312 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.385-31365C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42931527 | ||||||
| chr4:42931576
|
A | AT | 97 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0019others(94): Show | 97 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.385-31307dupT | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42931576 | |||||
| chr4:42931820
|
C | T | 17 | a0001c0001t0001g0012a0001c0001t0001g0077a0001c0001t0002g0086others(14): Show | 17 | HG00140.hp2 HG01243.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.385-31072C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42931820 | ||||||
| chr4:42931841
|
C | T | 82 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(79): Show | 82 | HG00323.hp1 HG00621.hp1 HG00733.hp2 others(79): Show |
intron_variant | MODIFIER | c.385-31051C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42931841 | ||||||
| chr4:42931936
|
G | T | 1 | a0001c0001t0001g0112 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.385-30956G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42931936 | ||||||
| chr4:42932000
|
G | A | 29 | a0001c0001t0001g0019a0001c0001t0001g0056a0001c0001t0001g0110others(26): Show | 29 | HG00140.hp1 HG00438.hp1 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.385-30892G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932000 | ||||||
| chr4:42932100
|
G | A | 1 | a0001c0001t0002g0033 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.385-30792G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932100 | ||||||
| chr4:42932452
|
T | TTTGCTTT others(3): Show |
335 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(332): Show | 335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.385-30436_385-3043 others(14): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932452 | |||||
| chr4:42932513
|
C | A | 1 | a0003c0003t0002g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.385-30379C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932513 | ||||||
| chr4:42932577
|
C | CAT | 7 | a0001c0001t0001g0082a0001c0001t0001g0111a0001c0001t0002g0018others(4): Show | 7 | HG01981.hp1 HG02165.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.385-30273_385-3027 others(6): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932577 | |||||
| chr4:42932577
|
C | CATAT | 4 | a0001c0001t0001g0112a0001c0001t0002g0083a0001c0001t0009g0040others(1): Show | 4 | HG00438.hp1 HG02055.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.385-30275_385-3027 others(8): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932577 | |||||
| chr4:42932577
|
C | CATATAT | 6 | a0001c0001t0001g0017a0001c0001t0002g0020a0001c0001t0002g0022others(3): Show | 6 | HG01255.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.385-30277_385-3027 others(10): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932577 | |||||
| chr4:42932577
|
C | CATATATA others(1): Show |
3 | a0001c0001t0003g0194a0001c0001t0004g0156a0001c0001t0008g0106 | 3 | HG02055.hp1 NA19030.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.385-30279_385-3027 others(12): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932577 | |||||
| chr4:42932577
|
C | CATATATA others(3): Show |
2 | a0001c0001t0001g0071a0001c0001t0003g0195 | 2 | NA18941.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.385-30281_385-3027 others(14): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932577 | |||||
| chr4:42932577
|
C | CATATATA others(5): Show |
3 | a0001c0001t0001g0120a0001c0001t0003g0196a0003c0003t0001g0296 | 3 | NA18957.hp2 NA18980.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.385-30283_385-3027 others(16): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932577 | |||||
| chr4:42932577
|
CAT | C | 5 | a0001c0001t0001g0034a0001c0001t0002g0108a0001c0001t0004g0180others(2): Show | 5 | HG00609.hp2 HG02109.hp2 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.385-30273_385-3027 others(6): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932577 | |||||
| chr4:42932577
|
CATAT | C | 8 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0001t0002g0078others(5): Show | 8 | HG00140.hp2 HG01515.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.385-30275_385-3027 others(8): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932577 | |||||
| chr4:42932577
|
CATATATA others(1): Show |
C | 4 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0003g0150others(1): Show | 4 | HG03654.hp1 NA19087.hp2 NA19088.hp2 others(1): Show |
intron_variant | MODIFIER | c.385-30279_385-3027 others(12): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932577 | |||||
| chr4:42932577
|
CATATATA others(5): Show |
C | 1 | a0003c0003t0001g0320 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.385-30283_385-3027 others(16): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932577 | |||||
| chr4:42932577
|
CATATATA others(11): Show |
C | 1 | a0001c0001t0001g0075 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.385-30289_385-3027 others(22): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932577 | |||||
| chr4:42932587
|
TATATATA others(8): Show |
T | 4 | a0001c0001t0002g0044a0001c0001t0004g0142a0003c0003t0002g0291others(1): Show | 4 | HG00639.hp2 HG03130.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-30304_385-3029 others(19): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932587 | ||||||
| chr4:42932587
|
TATATATA others(10): Show |
T | 2 | a0003c0003t0001g0317a0003c0003t0002g0302 | 2 | HG02109.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.385-30304_385-3028 others(21): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932587 | ||||||
| chr4:42932587
|
TATATATA others(14): Show |
T | 2 | a0001c0001t0002g0013a0001c0001t0003g0209 | 2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.385-30304_385-3028 others(25): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932587 | ||||||
| chr4:42932590
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.385-30302A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932590 | ||||||
| chr4:42932591
|
T | G | 1 | a0001c0001t0001g0006 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.385-30301T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932591 | ||||||
| chr4:42932593
|
T | A | 1 | a0001c0001t0001g0006 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.385-30299T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932593 | ||||||
| chr4:42932594
|
A | C | 1 | a0001c0001t0001g0006 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.385-30298A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932594 | ||||||
| chr4:42932596
|
A | C | 1 | a0001c0001t0001g0006 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.385-30296A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932596 | ||||||
| chr4:42932597
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.385-30295T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932597 | ||||||
| chr4:42932597
|
TATATATA others(27): Show |
T | 1 | a0002c0002t0001g0275 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.385-30293_385-3026 others(38): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932597 | |||||
| chr4:42932598
|
A | C | 1 | a0001c0001t0001g0006 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.385-30294A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932598 | ||||||
| chr4:42932599
|
TATATATA others(15): Show |
T | 2 | a0001c0001t0004g0165a0003c0003t0002g0322 | 2 | HG00733.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.385-30291_385-3027 others(26): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932599 | |||||
| chr4:42932599
|
TATATATA others(25): Show |
T | 2 | a0001c0001t0002g0001a0001c0001t0002g0002 | 2 | HG01167.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.385-30291_385-3026 others(36): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932599 | |||||
| chr4:42932601
|
T | TATATATA others(9): Show |
1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.385-30276_385-3027 others(20): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932601 | |||||
| chr4:42932603
|
TATATATA others(15): Show |
T | 2 | a0001c0001t0002g0059a0001c0001t0003g0202 | 2 | HG01433.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.385-30287_385-3026 others(26): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932603 | |||||
| chr4:42932603
|
TATATATA others(17): Show |
T | 1 | a0001c0001t0003g0163 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.385-30287_385-3026 others(28): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932603 | |||||
| chr4:42932603
|
TATATATA others(19): Show |
T | 1 | a0001c0001t0002g0036 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.385-30287_385-3026 others(30): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932603 | |||||
| chr4:42932603
|
TATATATA others(23): Show |
T | 1 | a0003c0003t0002g0324 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.385-30287_385-3025 others(34): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932603 | |||||
| chr4:42932604
|
A | C | 1 | a0001c0001t0001g0006 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.385-30288A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932604 | ||||||
| chr4:42932605
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.385-30287T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932605 | ||||||
| chr4:42932605
|
T | G | 4 | a0001c0001t0002g0044a0001c0001t0004g0142a0003c0003t0002g0291others(1): Show | 4 | HG00639.hp2 HG03130.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-30287T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932605 | ||||||
| chr4:42932605
|
TATATATA others(9): Show |
T | 2 | a0001c0001t0002g0048a0001c0001t0002g0086 | 2 | HG01496.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.385-30285_385-3027 others(20): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932605 | |||||
| chr4:42932605
|
TATATATA others(11): Show |
T | 1 | a0001c0001t0002g0063 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.385-30285_385-3026 others(22): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932605 | |||||
| chr4:42932605
|
TATATATA others(13): Show |
T | 1 | a0001c0004t0002g0087 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.385-30285_385-3026 others(24): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932605 | |||||
| chr4:42932605
|
TATATATA others(15): Show |
T | 4 | a0001c0001t0001g0058a0001c0004t0002g0088a0002c0002t0002g0239others(1): Show | 4 | HG00423.hp2 HG02074.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-30285_385-3026 others(26): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932605 | |||||
| chr4:42932607
|
T | G | 6 | a0001c0001t0002g0044a0001c0001t0004g0142a0003c0003t0001g0317others(3): Show | 6 | HG00639.hp2 HG02109.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.385-30285T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932607 | ||||||
| chr4:42932607
|
TATATATA others(9): Show |
T | 1 | a0001c0001t0006g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.385-30283_385-3026 others(20): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932607 | |||||
| chr4:42932607
|
TATATATA others(11): Show |
T | 2 | a0001c0001t0002g0054a0001c0001t0002g0066 | 2 | HG01192.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.385-30283_385-3026 others(22): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932607 | |||||
| chr4:42932607
|
TATATATA others(13): Show |
T | 1 | a0001c0001t0002g0049 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.385-30283_385-3026 others(24): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932607 | |||||
| chr4:42932607
|
TATATATA others(15): Show |
T | 5 | a0001c0001t0002g0033a0001c0001t0002g0037a0001c0001t0004g0207others(2): Show | 5 | HG01516.hp1 HG04115.hp1 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.385-30283_385-3026 others(26): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932607 | |||||
| chr4:42932609
|
T | G | 6 | a0001c0001t0002g0044a0001c0001t0004g0142a0003c0003t0001g0317others(3): Show | 6 | HG00639.hp2 HG02109.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.385-30283T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932609 | ||||||
| chr4:42932609
|
TATATATA others(5): Show |
T | 1 | a0002c0002t0002g0270 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.385-30281_385-3027 others(16): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932609 | |||||
| chr4:42932609
|
TATATATA others(7): Show |
T | 1 | a0001c0001t0004g0133 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.385-30281_385-3026 others(18): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932609 | |||||
| chr4:42932609
|
TATATATA others(9): Show |
T | 1 | a0001c0001t0003g0132 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.385-30281_385-3026 others(20): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932609 | |||||
| chr4:42932609
|
TATATATA others(11): Show |
T | 5 | a0001c0001t0001g0067a0001c0001t0002g0035a0001c0001t0002g0038others(2): Show | 5 | HG01243.hp2 HG01255.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.385-30281_385-3026 others(22): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932609 | |||||
| chr4:42932609
|
TATATATA others(15): Show |
T | 3 | a0001c0001t0002g0051a0001c0001t0002g0060a0002c0002t0002g0229 | 3 | HG01069.hp2 HG01109.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.385-30281_385-3026 others(26): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932609 | |||||
| chr4:42932611
|
T | G | 8 | a0001c0001t0002g0013a0001c0001t0002g0044a0001c0001t0003g0209others(5): Show | 8 | HG00639.hp2 HG02109.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.385-30281T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932611 | ||||||
| chr4:42932611
|
TATATATA others(3): Show |
T | 3 | a0001c0001t0004g0147a0001c0001t0004g0176a0001c0001t0004g0177 | 3 | HG02273.hp2 HG02293.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.385-30279_385-3027 others(14): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932611 | |||||
| chr4:42932611
|
TATATATA others(5): Show |
T | 1 | a0001c0001t0004g0148 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.385-30279_385-3026 others(16): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932611 | |||||
| chr4:42932611
|
TATATATA others(7): Show |
T | 2 | a0001c0001t0002g0052a0001c0001t0002g0081 | 2 | HG01515.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.385-30279_385-3026 others(18): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932611 | |||||
| chr4:42932611
|
TATATATA others(9): Show |
T | 5 | a0001c0001t0002g0007a0001c0001t0002g0041a0001c0001t0002g0053others(2): Show | 5 | HG01168.hp2 NA18981.hp2 NA19081.hp2 others(2): Show |
intron_variant | MODIFIER | c.385-30279_385-3026 others(20): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932611 | |||||
| chr4:42932611
|
TATATATA others(15): Show |
T | 2 | a0001c0004t0002g0091a0003c0003t0002g0308 | 2 | HG02523.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.385-30279_385-3025 others(26): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932611 | |||||
| chr4:42932613
|
T | G | 10 | a0001c0001t0002g0013a0001c0001t0002g0044a0001c0001t0002g0078others(7): Show | 10 | HG00639.hp2 HG01346.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.385-30279T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932613 | ||||||
| chr4:42932613
|
TATATATA others(1): Show |
T | 6 | a0001c0001t0003g0135a0001c0001t0003g0178a0002c0002t0001g0233others(3): Show | 6 | HG01928.hp1 HG04228.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.385-30277_385-3027 others(12): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932613 | |||||
| chr4:42932613
|
TATATATA others(3): Show |
T | 3 | a0001c0001t0001g0068a0001c0001t0003g0151a0001c0001t0003g0153 | 3 | HG01109.hp2 NA18942.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.385-30277_385-3026 others(14): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932613 | |||||
| chr4:42932613
|
TATATATA others(5): Show |
T | 6 | a0001c0001t0002g0043a0001c0001t0003g0149a0001c0001t0004g0173others(3): Show | 6 | HG01070.hp1 HG01071.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.385-30277_385-3026 others(16): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932613 | |||||
| chr4:42932613
|
TATATATA others(7): Show |
T | 1 | a0003c0003t0002g0327 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.385-30277_385-3026 others(18): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932613 | |||||
| chr4:42932613
|
TATATATA others(9): Show |
T | 4 | a0001c0001t0001g0146a0001c0001t0002g0042a0001c0001t0004g0169others(1): Show | 4 | HG00544.hp1 HG01993.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.385-30277_385-3026 others(20): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932613 | |||||
| chr4:42932613
|
TATATATA others(13): Show |
T | 1 | a0002c0002t0002g0230 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.385-30277_385-3025 others(24): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932613 | |||||
| chr4:42932613
|
TATATATA others(15): Show |
T | 1 | a0002c0002t0001g0227 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.385-30277_385-3025 others(26): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932613 | |||||
| chr4:42932615
|
T | G | 13 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0044others(10): Show | 13 | HG00639.hp2 HG01346.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.385-30277T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932615 | ||||||
| chr4:42932615
|
TATATAGA others(1): Show |
T | 4 | a0001c0001t0004g0179a0002c0002t0001g0222a0002c0002t0001g0257others(1): Show | 4 | HG01070.hp2 HG02027.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-30275_385-3026 others(12): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932615 | |||||
| chr4:42932615
|
TATATAGA others(3): Show |
T | 3 | a0002c0002t0001g0241a0002c0002t0001g0269a0003c0003t0001g0293 | 3 | HG01952.hp2 NA18959.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.385-30275_385-3026 others(14): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932615 | |||||
| chr4:42932615
|
TATATAGA others(5): Show |
T | 6 | a0001c0001t0002g0085a0001c0001t0004g0138a0002c0002t0001g0213others(3): Show | 6 | HG00621.hp2 HG01496.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.385-30275_385-3026 others(16): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932615 | |||||
| chr4:42932615
|
TATATAGA others(7): Show |
T | 3 | a0001c0001t0003g0140a0001c0001t0004g0139a0002c0002t0001g0267 | 3 | HG01952.hp1 HG02280.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.385-30275_385-3026 others(18): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932615 | |||||
| chr4:42932615
|
TATATAGA others(9): Show |
T | 1 | a0003c0003t0002g0328 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.385-30275_385-3026 others(20): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932615 | |||||
| chr4:42932615
|
TATATAGA others(11): Show |
T | 3 | a0001c0001t0001g0061a0001c0001t0002g0062a0001c0001t0004g0170 | 3 | HG01361.hp1 HG01978.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.385-30275_385-3025 others(22): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932615 | |||||
| chr4:42932617
|
T | G | 18 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0044others(15): Show | 18 | HG00639.hp2 HG01346.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.385-30275T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932617 | ||||||
| chr4:42932617
|
T | TAGAGAGA others(5): Show |
1 | a0001c0001t0001g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.385-30274_385-3027 others(16): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932617 | |||||
| chr4:42932617
|
TATAG | T | 4 | a0001c0001t0001g0045a0001c0001t0002g0094a0002c0002t0001g0258others(1): Show | 4 | HG00735.hp1 HG02615.hp2 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-30273_385-3027 others(8): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932617 | |||||
| chr4:42932617
|
TATAGAG | T | 9 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0125others(6): Show | 9 | HG00438.hp2 HG01361.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.385-30273_385-3026 others(10): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932617 | |||||
| chr4:42932617
|
TATAGAGA others(1): Show |
T | 6 | a0001c0001t0002g0128a0001c0001t0002g0129a0001c0001t0003g0186others(3): Show | 6 | HG00423.hp1 HG01975.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.385-30273_385-3026 others(12): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932617 | |||||
| chr4:42932617
|
TATAGAGA others(3): Show |
T | 9 | a0001c0001t0002g0107a0001c0001t0003g0167a0001c0001t0003g0208others(6): Show | 9 | HG00323.hp2 HG01358.hp2 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.385-30273_385-3026 others(14): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932617 | |||||
| chr4:42932617
|
TATAGAGA others(5): Show |
T | 1 | a0001c0001t0004g0152 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.385-30273_385-3026 others(16): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932617 | |||||
| chr4:42932617
|
TATAGAGA others(7): Show |
T | 1 | a0001c0001t0003g0203 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.385-30273_385-3026 others(18): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932617 | |||||
| chr4:42932617
|
TATAGAGA others(9): Show |
T | 4 | a0001c0001t0001g0064a0001c0001t0002g0055a0001c0001t0004g0205others(1): Show | 4 | NA19004.hp1 NA19004.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-30273_385-3025 others(20): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932617 | |||||
| chr4:42932617
|
TATAGAGA others(11): Show |
T | 1 | a0001c0001t0001g0039 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.385-30273_385-3025 others(22): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932617 | |||||
| chr4:42932619
|
T | G | 29 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0023others(26): Show | 29 | HG00639.hp2 HG01099.hp1 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.385-30273T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932619 | ||||||
| chr4:42932619
|
T | TAG | 3 | a0001c0001t0001g0095a0001c0001t0003g0159a0001c0001t0004g0141 | 3 | HG02630.hp1 HG02886.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.385-30228_385-3022 others(6): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932619 | |||||
| chr4:42932619
|
T | TAGAGAG | 3 | a0001c0001t0001g0212a0001c0001t0002g0030a0001c0001t0002g0031 | 3 | HG01167.hp1 HG01169.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.385-30232_385-3022 others(10): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932619 | |||||
| chr4:42932619
|
T | TAGAGAGA others(3): Show |
2 | a0001c0001t0001g0072a0001c0001t0001g0116 | 2 | HG03654.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.385-30236_385-3022 others(14): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932619 | |||||
| chr4:42932619
|
T | TATAGAG | 3 | a0002c0002t0001g0251a0003c0003t0001g0325a0003c0003t0002g0300 | 3 | HG00609.hp1 NA19081.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.385-30272_385-3027 others(10): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932619 | |||||
| chr4:42932619
|
T | TATAGAGA others(5): Show |
1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.385-30272_385-3027 others(16): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932619 | |||||
| chr4:42932619
|
T | TATAGAGA others(7): Show |
1 | a0001c0001t0001g0056 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.385-30272_385-3027 others(18): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932619 | |||||
| chr4:42932619
|
T | TATATAGA others(3): Show |
1 | a0001c0001t0001g0113 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.385-30272_385-3027 others(14): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932619 | |||||
| chr4:42932619
|
T | TATATAGA others(5): Show |
1 | a0001c0001t0002g0278 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.385-30272_385-3027 others(16): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932619 | |||||
| chr4:42932619
|
T | TATATATA others(3): Show |
3 | a0001c0001t0001g0015a0001c0001t0001g0074a0002c0002t0001g0272 | 3 | NA18522.hp1 NA18952.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.385-30272_385-3027 others(14): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932619 | |||||
| chr4:42932619
|
T | TATATATA others(5): Show |
2 | a0001c0001t0001g0073a0001c0001t0001g0103 | 2 | HG02132.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.385-30272_385-3027 others(16): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932619 | |||||
| chr4:42932619
|
T | TATATATA others(7): Show |
1 | a0001c0001t0001g0123 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.385-30272_385-3027 others(18): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932619 | |||||
| chr4:42932619
|
T | TATATATA others(9): Show |
1 | a0001c0001t0001g0105 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.385-30272_385-3027 others(20): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932619 | |||||
| chr4:42932619
|
T | TATATATA others(3): Show |
2 | a0001c0001t0001g0097a0001c0001t0002g0282 | 2 | HG03209.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.385-30272_385-3027 others(14): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932619 | |||||
| chr4:42932619
|
T | TATATATA others(5): Show |
1 | a0001c0001t0001g0100 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.385-30272_385-3027 others(16): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932619 | |||||
| chr4:42932619
|
T | TATATATA others(7): Show |
1 | a0003c0003t0001g0304 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.385-30272_385-3027 others(18): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932619 | |||||
| chr4:42932619
|
T | TATATATA others(5): Show |
1 | a0001c0001t0001g0124 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.385-30272_385-3027 others(16): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932619 | |||||
| chr4:42932619
|
T | TATATATA others(7): Show |
2 | a0001c0001t0001g0098a0001c0001t0001g0117 | 2 | HG03704.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.385-30272_385-3027 others(18): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932619 | |||||
| chr4:42932619
|
T | TATATATA others(11): Show |
1 | a0001c0001t0001g0099 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.385-30272_385-3027 others(22): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932619 | |||||
| chr4:42932619
|
T | TATATATA others(13): Show |
1 | a0001c0001t0001g0118 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.385-30272_385-3027 others(24): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932619 | |||||
| chr4:42932619
|
TAG | T | 13 | a0001c0001t0001g0069a0001c0001t0001g0285a0001c0001t0002g0047others(10): Show | 13 | HG00673.hp1 HG00673.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.385-30228_385-3022 others(6): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932619 | |||||
| chr4:42932619
|
TAGAG | T | 19 | a0001c0001t0001g0011a0001c0001t0001g0046a0001c0001t0002g0065others(16): Show | 19 | HG00735.hp2 HG01192.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.385-30230_385-3022 others(8): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932619 | |||||
| chr4:42932619
|
TAGAGAG | T | 13 | a0001c0001t0001g0025a0001c0001t0001g0109a0001c0001t0002g0089others(10): Show | 13 | HG00323.hp1 HG00621.hp1 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.385-30232_385-3022 others(10): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932619 | |||||
| chr4:42932619
|
TAGAGAGA others(1): Show |
T | 20 | a0001c0001t0001g0024a0001c0001t0002g0093a0001c0001t0003g0185others(17): Show | 20 | HG01123.hp1 HG01346.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.385-30234_385-3022 others(12): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932619 | |||||
| chr4:42932619
|
TAGAGAGA others(3): Show |
T | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0090others(7): Show | 10 | HG00544.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.385-30236_385-3022 others(14): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932619 | |||||
| chr4:42932619
|
TAGAGAGA others(5): Show |
T | 4 | a0001c0001t0001g0010a0001c0001t0003g0181a0001c0001t0003g0190others(1): Show | 4 | HG02083.hp2 HG03139.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-30238_385-3022 others(16): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932619 | |||||
| chr4:42932619
|
TAGAGAGA others(7): Show |
T | 5 | a0001c0001t0001g0096a0001c0001t0002g0021a0001c0001t0003g0130others(2): Show | 5 | HG02723.hp1 HG03453.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.385-30240_385-3022 others(18): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932619 | |||||
| chr4:42932619
|
TAGAGAGA others(9): Show |
T | 3 | a0001c0001t0002g0092a0001c0001t0004g0204a0001c0001t0004g0210 | 3 | HG03471.hp1 NA18952.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.385-30242_385-3022 others(20): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42932619 | |||||
| chr4:42932621
|
G | T | 30 | a0001c0001t0001g0006a0001c0001t0001g0082a0001c0001t0001g0110others(27): Show | 30 | HG00438.hp1 HG01891.hp1 HG01934.hp1 others(27): Show |
intron_variant | MODIFIER | c.385-30271G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932621 | ||||||
| chr4:42932623
|
G | T | 33 | a0001c0001t0001g0082a0001c0001t0001g0112a0001c0001t0001g0285others(30): Show | 33 | HG00438.hp1 HG00673.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.385-30269G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932623 | ||||||
| chr4:42932625
|
G | T | 42 | a0001c0001t0001g0011a0001c0001t0001g0046a0001c0001t0001g0082others(39): Show | 42 | HG00438.hp1 HG00735.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.385-30267G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932625 | ||||||
| chr4:42932627
|
G | T | 37 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0046others(34): Show | 37 | HG00323.hp1 HG00438.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.385-30265G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932627 | ||||||
| chr4:42932629
|
G | T | 29 | a0001c0001t0001g0011a0001c0001t0001g0046a0001c0001t0001g0109others(26): Show | 29 | HG00621.hp1 HG00639.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.385-30263G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932629 | ||||||
| chr4:42932631
|
G | T | 20 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0046others(17): Show | 20 | HG00544.hp2 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.385-30261G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932631 | ||||||
| chr4:42932633
|
G | T | 10 | a0001c0001t0001g0010a0001c0001t0001g0046a0001c0001t0001g0090others(7): Show | 10 | HG00621.hp1 HG01981.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.385-30259G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932633 | ||||||
| chr4:42932635
|
G | T | 7 | a0001c0001t0001g0046a0001c0001t0001g0096a0001c0001t0003g0130others(4): Show | 7 | HG00621.hp1 HG02083.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.385-30257G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932635 | ||||||
| chr4:42932637
|
G | T | 4 | a0001c0001t0001g0046a0001c0001t0001g0096a0001c0001t0002g0092others(1): Show | 4 | HG02723.hp1 HG03471.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-30255G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932637 | ||||||
| chr4:42932639
|
G | T | 2 | a0001c0001t0001g0096a0003c0003t0001g0299 | 2 | HG02723.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.385-30253G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932639 | ||||||
| chr4:42932664
|
A | G | 10 | a0001c0001t0002g0014a0001c0001t0003g0132a0001c0001t0003g0134others(7): Show | 10 | HG02074.hp1 HG02257.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.385-30228A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932664 | ||||||
| chr4:42932671
|
C | T | 2 | a0001c0001t0002g0281a0003c0005t0002g0332 | 2 | HG02572.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.385-30221C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932671 | ||||||
| chr4:42932676
|
C | T | 1 | a0003c0003t0002g0329 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.385-30216C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932676 | ||||||
| chr4:42932763
|
A | G | 2 | a0001c0001t0002g0063a0001c0001t0002g0085 | 2 | HG00621.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.385-30129A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932763 | ||||||
| chr4:42932938
|
A | G | 185 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(182): Show | 185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.385-29954A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932938 | ||||||
| chr4:42932954
|
C | A | 1 | a0001c0001t0001g0212 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.385-29938C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42932954 | ||||||
| chr4:42933020
|
C | T | 2 | a0001c0001t0002g0086a0003c0003t0002g0327 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.385-29872C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42933020 | ||||||
| chr4:42933100
|
G | A | 7 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(4): Show | 7 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.385-29792G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42933100 | ||||||
| chr4:42933103
|
T | A | 28 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0056others(25): Show | 28 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.385-29789T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42933103 | ||||||
| chr4:42933146
|
A | T | 1 | a0004c0007t0002g0114 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.385-29746A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42933146 | ||||||
| chr4:42933152
|
G | A | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.385-29740G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42933152 | ||||||
| chr4:42933155
|
A | G | 28 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0056others(25): Show | 28 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.385-29737A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42933155 | ||||||
| chr4:42933156
|
C | T | 11 | a0001c0001t0001g0012a0001c0001t0002g0126a0001c0001t0002g0127others(8): Show | 11 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.385-29736C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42933156 | ||||||
| chr4:42933200
|
C | A | 1 | a0002c0002t0001g0224 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.385-29692C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42933200 | ||||||
| chr4:42933537
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0069 | 2 | HG00735.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.385-29355C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42933537 | ||||||
| chr4:42933631
|
G | A | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.385-29261G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42933631 | ||||||
| chr4:42933733
|
C | G | 30 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0056others(27): Show | 30 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.385-29159C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42933733 | ||||||
| chr4:42933938
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.385-28954C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42933938 | ||||||
| chr4:42933978
|
G | T | 2 | a0001c0001t0003g0167a0001c0001t0003g0185 | 2 | HG02135.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.385-28914G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42933978 | ||||||
| chr4:42934087
|
A | G | 2 | a0001c0001t0001g0075a0001c0001t0002g0076 | 2 | HG01993.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.385-28805A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42934087 | ||||||
| chr4:42934179
|
C | T | 5 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0171others(2): Show | 5 | HG01978.hp1 HG01981.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.385-28713C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42934179 | ||||||
| chr4:42934180
|
A | G | 42 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0019others(39): Show | 42 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.385-28712A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42934180 | ||||||
| chr4:42934240
|
T | TTA | 240 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(237): Show | 240 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(237): Show |
intron_variant | MODIFIER | c.385-28636_385-2863 others(6): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42934240 | |||||
| chr4:42934240
|
T | TTATA | 56 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0039others(53): Show | 56 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.385-28638_385-2863 others(8): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42934240 | |||||
| chr4:42934240
|
TTA | T | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | NA18951.hp1 NA18952.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.385-28636_385-2863 others(6): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42934240 | |||||
| chr4:42934472
|
A | G | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.385-28420A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42934472 | ||||||
| chr4:42934540
|
A | C | 1 | a0003c0003t0001g0317 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.385-28352A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42934540 | ||||||
| chr4:42934595
|
A | C | 1 | a0001c0001t0002g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.385-28297A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42934595 | ||||||
| chr4:42934643
|
A | G | 2 | a0001c0001t0002g0086a0003c0003t0002g0327 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.385-28249A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42934643 | ||||||
| chr4:42934667
|
A | G | 1 | a0001c0001t0003g0194 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.385-28225A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42934667 | ||||||
| chr4:42934673
|
T | C | 3 | a0001c0001t0001g0056a0001c0001t0003g0191a0001c0001t0004g0192 | 3 | HG00140.hp1 HG01346.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.385-28219T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42934673 | ||||||
| chr4:42934802
|
G | A | 7 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(4): Show | 7 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.385-28090G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42934802 | ||||||
| chr4:42934809
|
T | C | 27 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0056others(24): Show | 27 | HG00140.hp1 HG00438.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.385-28083T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42934809 | ||||||
| chr4:42934866
|
A | G | 1 | a0001c0001t0002g0044 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.385-28026A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42934866 | ||||||
| chr4:42935033
|
C | A | 87 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(84): Show | 87 | HG00323.hp1 HG00733.hp2 HG01099.hp1 others(84): Show |
intron_variant | MODIFIER | c.385-27859C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42935033 | ||||||
| chr4:42935045
|
A | G | 2 | a0001c0001t0002g0080a0001c0001t0004g0136 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.385-27847A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42935045 | ||||||
| chr4:42935068
|
C | T | 64 | a0001c0001t0001g0034a0001c0001t0001g0111a0001c0001t0001g0125others(61): Show | 64 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.385-27824C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42935068 | ||||||
| chr4:42935142
|
G | T | 1 | a0002c0002t0002g0265 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.385-27750G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42935142 | ||||||
| chr4:42935199
|
A | G | 1 | a0002c0002t0001g0224 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.385-27693A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42935199 | ||||||
| chr4:42935424
|
G | A | 1 | a0001c0001t0005g0157 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.385-27468G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42935424 | ||||||
| chr4:42935438
|
T | C | 7 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(4): Show | 7 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.385-27454T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42935438 | ||||||
| chr4:42935474
|
C | G | 27 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0056others(24): Show | 27 | HG00140.hp1 HG00438.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.385-27418C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42935474 | ||||||
| chr4:42935495
|
T | G | 1 | a0001c0001t0002g0052 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.385-27397T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42935495 | ||||||
| chr4:42935568
|
T | C | 42 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0019others(39): Show | 42 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.385-27324T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42935568 | ||||||
| chr4:42935662
|
G | A | 4 | a0001c0001t0001g0012a0001c0001t0002g0278a0003c0003t0002g0297others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-27230G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42935662 | ||||||
| chr4:42935740
|
G | C | 2 | a0001c0001t0004g0155a0001c0001t0004g0156 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.385-27152G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42935740 | ||||||
| chr4:42935753
|
AT | A | 87 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(84): Show | 87 | HG00323.hp1 HG00733.hp2 HG01099.hp1 others(84): Show |
intron_variant | MODIFIER | c.385-27136delT | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42935753 | |||||
| chr4:42935788
|
C | T | 1 | a0001c0001t0003g0132 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.385-27104C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42935788 | ||||||
| chr4:42935863
|
C | T | 1 | a0001c0001t0002g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.385-27029C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42935863 | ||||||
| chr4:42935864
|
G | A | 131 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(128): Show | 131 | HG00323.hp1 HG00423.hp2 HG00621.hp2 others(128): Show |
intron_variant | MODIFIER | c.385-27028G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42935864 | ||||||
| chr4:42935873
|
T | C | 10 | a0001c0001t0002g0014a0001c0001t0002g0080a0001c0001t0003g0132others(7): Show | 10 | HG02074.hp1 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.385-27019T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42935873 | ||||||
| chr4:42935875
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.385-27017A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42935875 | ||||||
| chr4:42935911
|
C | T | 12 | a0001c0001t0001g0012a0001c0001t0002g0126a0001c0001t0002g0127others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.385-26981C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42935911 | ||||||
| chr4:42935913
|
C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0285a0003c0003t0001g0290others(1): Show | 4 | HG01192.hp2 HG01978.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.385-26979C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42935913 | ||||||
| chr4:42935922
|
A | G | 2 | a0001c0001t0001g0212a0001c0001t0002g0145 | 2 | HG02145.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.385-26970A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42935922 | ||||||
| chr4:42935944
|
T | G | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.385-26948T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42935944 | ||||||
| chr4:42935954
|
C | T | 8 | a0001c0001t0002g0013a0001c0001t0002g0044a0001c0001t0003g0209others(5): Show | 8 | HG00639.hp2 HG02109.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.385-26938C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42935954 | ||||||
| chr4:42936003
|
T | G | 41 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0058others(38): Show | 41 | HG00423.hp2 HG00621.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.385-26889T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42936003 | ||||||
| chr4:42936026
|
T | C | 87 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(84): Show | 87 | HG00323.hp1 HG00733.hp2 HG01099.hp1 others(84): Show |
intron_variant | MODIFIER | c.385-26866T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42936026 | ||||||
| chr4:42936115
|
G | A | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.385-26777G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42936115 | ||||||
| chr4:42936223
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.385-26669A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42936223 | ||||||
| chr4:42936440
|
T | A | 8 | a0001c0001t0001g0146a0001c0001t0002g0092a0001c0001t0002g0093others(5): Show | 8 | HG02280.hp2 HG02559.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.385-26452T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42936440 | ||||||
| chr4:42936581
|
A | T | 11 | a0001c0001t0002g0014a0001c0001t0002g0080a0001c0001t0003g0132others(8): Show | 11 | HG02074.hp1 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.385-26311A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42936581 | ||||||
| chr4:42936603
|
C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0285a0003c0003t0001g0290others(1): Show | 4 | HG01192.hp2 HG01978.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.385-26289C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42936603 | ||||||
| chr4:42936677
|
T | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.385-26215T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42936677 | ||||||
| chr4:42936717
|
T | A | 1 | a0001c0001t0002g0049 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.385-26175T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42936717 | ||||||
| chr4:42936733
|
G | C | 1 | a0002c0002t0002g0270 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.385-26159G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42936733 | ||||||
| chr4:42936759
|
G | A | 41 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0058others(38): Show | 41 | HG00423.hp2 HG00621.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.385-26133G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42936759 | ||||||
| chr4:42936817
|
G | C | 41 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0058others(38): Show | 41 | HG00423.hp2 HG00621.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.385-26075G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42936817 | ||||||
| chr4:42936982
|
T | G | 30 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0056others(27): Show | 30 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.385-25910T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42936982 | ||||||
| chr4:42936984
|
T | C | 8 | a0001c0001t0002g0013a0001c0001t0002g0044a0001c0001t0003g0209others(5): Show | 8 | HG00639.hp2 HG02109.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.385-25908T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42936984 | ||||||
| chr4:42936996
|
A | G | 1 | a0001c0001t0004g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.385-25896A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42936996 | ||||||
| chr4:42937105
|
G | T | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.385-25787G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42937105 | ||||||
| chr4:42937275
|
TTTTTTA | T | 334 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(331): Show | 334 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.385-25599_385-2559 others(10): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42937275 | |||||
| chr4:42937339
|
TG | T | 8 | a0001c0001t0002g0013a0001c0001t0002g0044a0001c0001t0003g0209others(5): Show | 8 | HG00639.hp2 HG02109.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.385-25552delG | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42937339 | ||||||
| chr4:42937342
|
G | T | 8 | a0001c0001t0002g0013a0001c0001t0002g0044a0001c0001t0003g0209others(5): Show | 8 | HG00639.hp2 HG02109.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.385-25550G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42937342 | ||||||
| chr4:42937342
|
GT | G | 53 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0019others(50): Show | 53 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.385-25542delT | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42937342 | |||||
| chr4:42937353
|
G | A | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.385-25539G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42937353 | ||||||
| chr4:42937364
|
A | G | 28 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0056others(25): Show | 28 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.385-25528A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42937364 | ||||||
| chr4:42937388
|
C | G | 11 | a0001c0001t0001g0012a0001c0001t0002g0126a0001c0001t0002g0127others(8): Show | 11 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.385-25504C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42937388 | ||||||
| chr4:42937397
|
G | A | 1 | a0001c0001t0003g0130 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.385-25495G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42937397 | ||||||
| chr4:42937441
|
G | C | 42 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0058others(39): Show | 42 | HG00423.hp2 HG00621.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.385-25451G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42937441 | ||||||
| chr4:42937594
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.385-25298G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42937594 | ||||||
| chr4:42937675
|
C | T | 64 | a0001c0001t0001g0034a0001c0001t0001g0111a0001c0001t0001g0125others(61): Show | 64 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.385-25217C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42937675 | ||||||
| chr4:42937736
|
A | C | 7 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(4): Show | 7 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.385-25156A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42937736 | ||||||
| chr4:42938020
|
G | A | 88 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(85): Show | 88 | HG00323.hp1 HG00733.hp2 HG01099.hp1 others(85): Show |
intron_variant | MODIFIER | c.385-24872G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42938020 | ||||||
| chr4:42938032
|
T | A | 11 | a0001c0001t0001g0012a0001c0001t0002g0126a0001c0001t0002g0127others(8): Show | 11 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.385-24860T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42938032 | ||||||
| chr4:42938131
|
C | A | 1 | a0001c0001t0003g0208 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.385-24761C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42938131 | ||||||
| chr4:42938164
|
T | C | 5 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0171others(2): Show | 5 | HG01978.hp1 HG01981.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.385-24728T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42938164 | ||||||
| chr4:42938170
|
T | A | 8 | a0001c0001t0002g0080a0001c0001t0003g0132a0001c0001t0003g0134others(5): Show | 8 | HG02074.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.385-24722T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42938170 | ||||||
| chr4:42938173
|
G | A | 30 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0056others(27): Show | 30 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.385-24719G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42938173 | ||||||
| chr4:42938188
|
C | T | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.385-24704C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42938188 | ||||||
| chr4:42938222
|
C | A | 2 | a0001c0001t0001g0075a0001c0001t0002g0076 | 2 | HG01993.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.385-24670C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42938222 | ||||||
| chr4:42938385
|
C | T | 1 | a0002c0002t0001g0277 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.385-24507C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42938385 | ||||||
| chr4:42938386
|
G | A | 4 | a0001c0001t0001g0012a0001c0001t0002g0278a0003c0003t0002g0297others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-24506G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42938386 | ||||||
| chr4:42938628
|
A | G | 3 | a0001c0004t0002g0087a0001c0004t0002g0088a0001c0004t0002g0091 | 3 | HG02809.hp2 HG03130.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.385-24264A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42938628 | ||||||
| chr4:42938794
|
C | T | 184 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(181): Show | 184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.385-24098C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42938794 | ||||||
| chr4:42938848
|
T | C | 1 | a0002c0002t0001g0241 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.385-24044T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42938848 | ||||||
| chr4:42938851
|
C | T | 41 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0058others(38): Show | 41 | HG00423.hp2 HG00621.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.385-24041C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42938851 | ||||||
| chr4:42938861
|
C | T | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.385-24031C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42938861 | ||||||
| chr4:42938868
|
G | GT | 43 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0056others(40): Show | 43 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.385-24013dupT | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42938868 | |||||
| chr4:42938869
|
T | A | 2 | a0001c0001t0001g0075a0001c0001t0002g0076 | 2 | HG01993.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.385-24023T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42938869 | ||||||
| chr4:42938907
|
T | C | 1 | a0001c0001t0002g0037 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.385-23985T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42938907 | ||||||
| chr4:42939075
|
T | G | 8 | a0001c0001t0002g0013a0001c0001t0002g0044a0001c0001t0003g0209others(5): Show | 8 | HG00639.hp2 HG02109.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.385-23817T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42939075 | ||||||
| chr4:42939111
|
A | G | 8 | a0001c0001t0001g0082a0001c0001t0002g0020a0001c0001t0002g0022others(5): Show | 8 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.385-23781A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42939111 | ||||||
| chr4:42939123
|
C | T | 3 | a0001c0001t0002g0001a0001c0001t0002g0002a0003c0003t0002g0324 | 3 | HG01167.hp2 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.385-23769C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42939123 | ||||||
| chr4:42939166
|
C | T | 2 | a0001c0001t0002g0014a0001c0001t0004g0158 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.385-23726C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42939166 | ||||||
| chr4:42939208
|
G | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0285a0003c0003t0001g0290others(1): Show | 4 | HG01192.hp2 HG01978.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.385-23684G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42939208 | ||||||
| chr4:42939316
|
A | G | 334 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(331): Show | 334 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.385-23576A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42939316 | ||||||
| chr4:42939335
|
A | AT | 50 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0019others(47): Show | 50 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.385-23553dupT | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42939335 | |||||
| chr4:42939343
|
C | T | 1 | a0002c0002t0001g0216 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.385-23549C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42939343 | ||||||
| chr4:42939356
|
C | A | 1 | a0001c0001t0002g0094 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.385-23536C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42939356 | ||||||
| chr4:42939392
|
C | A | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.385-23500C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42939392 | ||||||
| chr4:42939430
|
G | T | 1 | a0001c0001t0003g0150 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.385-23462G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42939430 | ||||||
| chr4:42939597
|
T | C | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(7): Show | 10 | HG00323.hp1 HG00733.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.385-23295T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42939597 | ||||||
| chr4:42939709
|
A | G | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.385-23183A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42939709 | ||||||
| chr4:42939722
|
C | G | 1 | a0001c0001t0003g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.385-23170C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42939722 | ||||||
| chr4:42939878
|
T | C | 2 | a0001c0001t0001g0075a0001c0001t0002g0076 | 2 | HG01993.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.385-23014T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42939878 | ||||||
| chr4:42939896
|
C | A | 1 | a0001c0001t0001g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.385-22996C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42939896 | ||||||
| chr4:42939924
|
T | C | 1 | a0001c0001t0005g0211 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.385-22968T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42939924 | ||||||
| chr4:42940018
|
G | A | 26 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0056others(23): Show | 26 | HG00140.hp1 HG00438.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.385-22874G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42940018 | ||||||
| chr4:42940033
|
C | T | 88 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(85): Show | 88 | HG00140.hp1 HG00323.hp1 HG00733.hp2 others(85): Show |
intron_variant | MODIFIER | c.385-22859C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42940033 | ||||||
| chr4:42940053
|
G | A | 2 | a0003c0003t0001g0320a0003c0003t0001g0321 | 2 | NA18998.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.385-22839G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42940053 | ||||||
| chr4:42940157
|
G | A | 7 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(4): Show | 7 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.385-22735G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42940157 | ||||||
| chr4:42940180
|
TG | T | 3 | a0001c0001t0002g0014a0001c0001t0004g0158a0001c0001t0005g0157 | 3 | HG02615.hp1 HG02886.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.385-22709delG | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42940180 | |||||
| chr4:42940206
|
C | G | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.385-22686C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42940206 | ||||||
| chr4:42940412
|
C | A | 4 | a0001c0001t0001g0012a0001c0001t0002g0278a0003c0003t0002g0297others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-22480C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42940412 | ||||||
| chr4:42940448
|
C | T | 41 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0058others(38): Show | 41 | HG00423.hp2 HG00621.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.385-22444C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42940448 | ||||||
| chr4:42940492
|
C | T | 184 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(181): Show | 184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.385-22400C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42940492 | ||||||
| chr4:42940593
|
A | C | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.385-22299A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42940593 | ||||||
| chr4:42940609
|
G | A | 50 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0019others(47): Show | 50 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.385-22283G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42940609 | ||||||
| chr4:42940652
|
A | T | 50 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0019others(47): Show | 50 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.385-22240A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42940652 | ||||||
| chr4:42940680
|
A | G | 7 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(4): Show | 7 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.385-22212A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42940680 | ||||||
| chr4:42940767
|
C | T | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.385-22125C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42940767 | ||||||
| chr4:42940787
|
T | G | 1 | a0003c0005t0002g0332 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.385-22105T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42940787 | ||||||
| chr4:42940886
|
A | T | 1 | a0001c0001t0002g0101 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.385-22006A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42940886 | ||||||
| chr4:42940902
|
A | G | 1 | a0003c0003t0002g0297 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.385-21990A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42940902 | ||||||
| chr4:42940918
|
C | G | 1 | a0001c0001t0001g0110 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.385-21974C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42940918 | ||||||
| chr4:42940995
|
G | A | 8 | a0001c0001t0002g0013a0001c0001t0002g0044a0001c0001t0003g0209others(5): Show | 8 | HG00639.hp2 HG02109.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.385-21897G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42940995 | ||||||
| chr4:42940996
|
A | G | 8 | a0001c0001t0002g0013a0001c0001t0002g0044a0001c0001t0003g0209others(5): Show | 8 | HG00639.hp2 HG02109.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.385-21896A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42940996 | ||||||
| chr4:42941055
|
T | C | 3 | a0001c0001t0001g0075a0001c0001t0002g0076a0002c0002t0001g0276 | 3 | HG00544.hp2 HG01993.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.385-21837T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42941055 | ||||||
| chr4:42941160
|
G | A | 41 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0058others(38): Show | 41 | HG00423.hp2 HG00621.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.385-21732G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42941160 | ||||||
| chr4:42941187
|
TGTAA | T | 36 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0056others(33): Show | 36 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.385-21702_385-2169 others(8): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42941187 | |||||
| chr4:42941273
|
T | A | 1 | a0003c0003t0002g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.385-21619T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42941273 | ||||||
| chr4:42941320
|
G | T | 2 | a0001c0001t0002g0086a0003c0003t0002g0327 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.385-21572G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42941320 | ||||||
| chr4:42941347
|
A | G | 1 | a0003c0003t0001g0317 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.385-21545A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42941347 | ||||||
| chr4:42941505
|
C | T | 2 | a0001c0001t0001g0075a0001c0001t0002g0076 | 2 | HG01993.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.385-21387C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42941505 | ||||||
| chr4:42941546
|
C | G | 1 | a0001c0001t0004g0162 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.385-21346C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42941546 | ||||||
| chr4:42941596
|
A | C | 36 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0056others(33): Show | 36 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.385-21296A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42941596 | ||||||
| chr4:42941727
|
T | C | 1 | a0001c0001t0001g0121 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.385-21165T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42941727 | ||||||
| chr4:42941904
|
A | T | 336 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(333): Show | 336 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.385-20988A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42941904 | ||||||
| chr4:42941905
|
A | T | 1 | a0002c0002t0001g0279 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.385-20987A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42941905 | ||||||
| chr4:42941923
|
G | C | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | NA18981.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.385-20969G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42941923 | ||||||
| chr4:42941948
|
A | G | 2 | a0001c0001t0002g0086a0003c0003t0002g0327 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.385-20944A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42941948 | ||||||
| chr4:42941988
|
A | C | 1 | a0001c0001t0002g0052 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.385-20904A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42941988 | ||||||
| chr4:42942132
|
T | C | 2 | a0001c0001t0002g0086a0003c0003t0002g0327 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.385-20760T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42942132 | ||||||
| chr4:42942134
|
G | A | 2 | a0001c0001t0002g0030a0001c0001t0002g0031 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.385-20758G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42942134 | ||||||
| chr4:42942411
|
G | A | 1 | a0001c0001t0008g0106 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.385-20481G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42942411 | ||||||
| chr4:42942453
|
G | T | 1 | a0001c0001t0005g0157 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.385-20439G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42942453 | ||||||
| chr4:42942527
|
C | A | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.385-20365C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42942527 | ||||||
| chr4:42942548
|
G | A | 53 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0019others(50): Show | 53 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.385-20344G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42942548 | ||||||
| chr4:42942640
|
C | G | 86 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(83): Show | 86 | HG00323.hp1 HG00733.hp2 HG01099.hp1 others(83): Show |
intron_variant | MODIFIER | c.385-20252C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42942640 | ||||||
| chr4:42942980
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.385-19912C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42942980 | ||||||
| chr4:42943059
|
A | T | 36 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0056others(33): Show | 36 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.385-19833A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42943059 | ||||||
| chr4:42943078
|
G | A | 2 | a0001c0001t0001g0075a0001c0001t0002g0076 | 2 | HG01993.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.385-19814G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42943078 | ||||||
| chr4:42943139
|
A | T | 2 | a0001c0001t0002g0014a0001c0001t0004g0158 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.385-19753A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42943139 | ||||||
| chr4:42943252
|
A | C | 4 | a0001c0001t0001g0012a0001c0001t0002g0278a0003c0003t0002g0297others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-19640A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42943252 | ||||||
| chr4:42943470
|
C | G | 38 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0056others(35): Show | 38 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.385-19422C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42943470 | ||||||
| chr4:42943475
|
G | A | 1 | a0003c0003t0001g0338 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.385-19417G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42943475 | ||||||
| chr4:42943547
|
C | G | 197 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(194): Show | 197 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.385-19345C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42943547 | ||||||
| chr4:42943877
|
T | C | 7 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(4): Show | 7 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.385-19015T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42943877 | ||||||
| chr4:42943939
|
A | G | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.385-18953A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42943939 | ||||||
| chr4:42943942
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.385-18950C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42943942 | ||||||
| chr4:42943952
|
A | G | 2 | a0001c0001t0001g0212a0001c0001t0002g0145 | 2 | HG02145.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.385-18940A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42943952 | ||||||
| chr4:42943963
|
G | A | 52 | a0001c0001t0001g0012a0001c0001t0001g0039a0001c0001t0001g0046others(49): Show | 52 | HG00423.hp2 HG00621.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.385-18929G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42943963 | ||||||
| chr4:42944165
|
A | C | 9 | a0001c0001t0001g0067a0001c0001t0002g0035a0001c0001t0002g0038others(6): Show | 9 | HG01192.hp1 HG01243.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.385-18727A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42944165 | ||||||
| chr4:42944179
|
G | T | 1 | a0001c0001t0001g0077 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.385-18713G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42944179 | ||||||
| chr4:42944364
|
G | A | 8 | a0001c0001t0002g0013a0001c0001t0002g0044a0001c0001t0003g0209others(5): Show | 8 | HG00639.hp2 HG02109.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.385-18528G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42944364 | ||||||
| chr4:42944400
|
A | G | 2 | a0001c0001t0002g0086a0003c0003t0002g0327 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.385-18492A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42944400 | ||||||
| chr4:42944467
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.385-18425G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42944467 | ||||||
| chr4:42944592
|
T | C | 1 | a0001c0001t0002g0059 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.385-18300T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42944592 | ||||||
| chr4:42944603
|
G | T | 1 | a0001c0001t0001g0100 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.385-18289G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42944603 | ||||||
| chr4:42944607
|
T | C | 1 | a0001c0001t0002g0041 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.385-18285T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42944607 | ||||||
| chr4:42944622
|
C | T | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.385-18270C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42944622 | ||||||
| chr4:42944793
|
A | T | 1 | a0001c0001t0004g0210 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.385-18099A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42944793 | ||||||
| chr4:42944812
|
C | T | 5 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0171others(2): Show | 5 | HG01978.hp1 HG01981.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.385-18080C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42944812 | ||||||
| chr4:42944866
|
G | A | 41 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0058others(38): Show | 41 | HG00423.hp2 HG00621.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.385-18026G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42944866 | ||||||
| chr4:42945048
|
T | C | 197 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(194): Show | 197 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.385-17844T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42945048 | ||||||
| chr4:42945123
|
G | A | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.385-17769G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42945123 | ||||||
| chr4:42945124
|
C | T | 39 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0056others(36): Show | 39 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.385-17768C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42945124 | ||||||
| chr4:42945125
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.385-17767G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42945125 | ||||||
| chr4:42945175
|
C | A | 2 | a0001c0001t0002g0020a0001c0001t0002g0022 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.385-17717C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42945175 | ||||||
| chr4:42945205
|
C | G | 2 | a0001c0001t0001g0075a0001c0001t0002g0076 | 2 | HG01993.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.385-17687C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42945205 | ||||||
| chr4:42945245
|
C | T | 8 | a0001c0001t0002g0080a0001c0001t0003g0132a0001c0001t0003g0134others(5): Show | 8 | HG02074.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.385-17647C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42945245 | ||||||
| chr4:42945291
|
G | T | 41 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0058others(38): Show | 41 | HG00423.hp2 HG00621.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.385-17601G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42945291 | ||||||
| chr4:42945336
|
G | T | 8 | a0001c0001t0002g0013a0001c0001t0002g0044a0001c0001t0003g0209others(5): Show | 8 | HG00639.hp2 HG02109.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.385-17556G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42945336 | ||||||
| chr4:42945465
|
C | T | 1 | a0003c0003t0001g0293 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.385-17427C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42945465 | ||||||
| chr4:42945509
|
A | T | 2 | a0001c0001t0001g0075a0001c0001t0002g0076 | 2 | HG01993.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.385-17383A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42945509 | ||||||
| chr4:42945666
|
G | A | 197 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(194): Show | 197 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.385-17226G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42945666 | ||||||
| chr4:42945690
|
T | G | 38 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0056others(35): Show | 38 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.385-17202T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42945690 | ||||||
| chr4:42945934
|
T | C | 3 | a0001c0001t0002g0278a0003c0003t0002g0297a0003c0003t0002g0334 | 3 | HG01884.hp1 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.385-16958T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42945934 | ||||||
| chr4:42946024
|
T | C | 1 | a0002c0002t0001g0252 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.385-16868T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42946024 | ||||||
| chr4:42946146
|
C | A | 3 | a0001c0001t0002g0278a0003c0003t0002g0297a0003c0003t0002g0334 | 3 | HG01884.hp1 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.385-16746C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42946146 | ||||||
| chr4:42946228
|
A | T | 1 | a0001c0001t0001g0095 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.385-16664A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42946228 | ||||||
| chr4:42946281
|
A | AG | 100 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(97): Show | 100 | HG00323.hp1 HG00733.hp2 HG01099.hp1 others(97): Show |
intron_variant | MODIFIER | c.385-16610dupG | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42946281 | |||||
| chr4:42946374
|
T | C | 1 | a0001c0001t0003g0186 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.385-16518T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42946374 | ||||||
| chr4:42946533
|
T | G | 52 | a0001c0001t0001g0012a0001c0001t0001g0039a0001c0001t0001g0046others(49): Show | 52 | HG00423.hp2 HG00621.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.385-16359T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42946533 | ||||||
| chr4:42946580
|
T | C | 2 | a0001c0001t0002g0086a0003c0003t0002g0327 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.385-16312T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42946580 | ||||||
| chr4:42946854
|
A | G | 6 | a0001c0001t0001g0082a0001c0001t0002g0020a0001c0001t0002g0022others(3): Show | 6 | HG01891.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.385-16038A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42946854 | ||||||
| chr4:42946901
|
C | G | 1 | a0003c0003t0001g0304 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.385-15991C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42946901 | ||||||
| chr4:42946959
|
G | T | 101 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(98): Show | 101 | HG00323.hp1 HG00733.hp2 HG01099.hp1 others(98): Show |
intron_variant | MODIFIER | c.385-15933G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42946959 | ||||||
| chr4:42946999
|
T | C | 2 | a0001c0001t0002g0030a0001c0001t0002g0031 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.385-15893T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42946999 | ||||||
| chr4:42947282
|
G | A | 42 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0056others(39): Show | 42 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.385-15610G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42947282 | ||||||
| chr4:42947345
|
A | G | 1 | a0003c0003t0002g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.385-15547A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42947345 | ||||||
| chr4:42947395
|
C | T | 1 | a0001c0001t0002g0107 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.385-15497C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42947395 | ||||||
| chr4:42947490
|
T | A | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.385-15402T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42947490 | ||||||
| chr4:42947491
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.385-15401G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42947491 | ||||||
| chr4:42947533
|
T | C | 2 | a0001c0001t0004g0174a0001c0001t0004g0199 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.385-15359T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42947533 | ||||||
| chr4:42947675
|
G | T | 1 | a0001c0001t0005g0157 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.385-15217G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42947675 | ||||||
| chr4:42947697
|
G | A | 1 | a0001c0001t0002g0107 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.385-15195G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42947697 | ||||||
| chr4:42947723
|
A | G | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.385-15169A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42947723 | ||||||
| chr4:42947738
|
AT | A | 3 | a0001c0001t0002g0278a0003c0003t0002g0297a0003c0003t0002g0334 | 3 | HG01884.hp1 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.385-15148delT | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42947738 | |||||
| chr4:42947816
|
A | G | 2 | a0001c0001t0002g0086a0003c0003t0002g0327 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.385-15076A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42947816 | ||||||
| chr4:42947827
|
A | C | 8 | a0001c0001t0002g0013a0001c0001t0002g0044a0001c0001t0003g0209others(5): Show | 8 | HG00639.hp2 HG02109.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.385-15065A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42947827 | ||||||
| chr4:42947953
|
T | C | 296 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(293): Show | 296 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.385-14939T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42947953 | ||||||
| chr4:42948000
|
G | T | 1 | a0001c0001t0001g0027 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.385-14892G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42948000 | ||||||
| chr4:42948041
|
C | T | 2 | a0001c0001t0001g0075a0001c0001t0002g0076 | 2 | HG01993.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.385-14851C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42948041 | ||||||
| chr4:42948049
|
T | C | 9 | a0001c0001t0002g0014a0001c0001t0002g0126a0001c0001t0002g0127others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.385-14843T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42948049 | ||||||
| chr4:42948138
|
A | G | 139 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(136): Show | 139 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.385-14754A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42948138 | ||||||
| chr4:42948234
|
CT | C | 144 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(141): Show | 144 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.385-14644delT | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42948234 | |||||
| chr4:42948234
|
CTT | C | 152 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(149): Show | 152 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.385-14645_385-1464 others(6): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42948234 | |||||
| chr4:42948318
|
G | A | 3 | a0001c0001t0002g0278a0003c0003t0002g0297a0003c0003t0002g0334 | 3 | HG01884.hp1 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.385-14574G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42948318 | ||||||
| chr4:42948594
|
A | T | 296 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(293): Show | 296 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.385-14298A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42948594 | ||||||
| chr4:42948658
|
A | G | 36 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0056others(33): Show | 36 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.385-14234A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42948658 | ||||||
| chr4:42948661
|
T | C | 98 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(95): Show | 98 | HG00323.hp1 HG00733.hp2 HG01099.hp1 others(95): Show |
intron_variant | MODIFIER | c.385-14231T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42948661 | ||||||
| chr4:42948706
|
G | A | 5 | a0001c0001t0001g0146a0001c0001t0002g0092a0001c0001t0002g0093others(2): Show | 5 | HG02280.hp2 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.385-14186G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42948706 | ||||||
| chr4:42948851
|
G | A | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.385-14041G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42948851 | ||||||
| chr4:42948927
|
A | T | 1 | a0001c0001t0002g0047 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.385-13965A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42948927 | ||||||
| chr4:42949019
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.385-13873C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42949019 | ||||||
| chr4:42949080
|
G | A | 8 | a0001c0001t0002g0013a0001c0001t0002g0044a0001c0001t0003g0209others(5): Show | 8 | HG00639.hp2 HG02109.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.385-13812G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42949080 | ||||||
| chr4:42949094
|
G | A | 1 | a0003c0003t0002g0297 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.385-13798G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42949094 | ||||||
| chr4:42949158
|
C | A | 27 | a0001c0001t0001g0019a0001c0001t0001g0056a0001c0001t0001g0071others(24): Show | 27 | HG00140.hp1 HG00438.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.385-13734C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42949158 | ||||||
| chr4:42949182
|
C | T | 1 | a0003c0003t0001g0306 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.385-13710C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42949182 | ||||||
| chr4:42949209
|
C | A | 2 | a0001c0001t0002g0278a0001c0001t0005g0157 | 2 | HG01884.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.385-13683C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42949209 | ||||||
| chr4:42949211
|
A | C | 25 | a0001c0001t0003g0193a0001c0001t0004g0142a0001c0001t0010g0284others(22): Show | 25 | HG01361.hp2 HG01981.hp1 HG02015.hp2 others(22): Show |
intron_variant | MODIFIER | c.385-13681A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42949211 | ||||||
| chr4:42949296
|
T | C | 2 | a0001c0001t0002g0086a0003c0003t0002g0327 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.385-13596T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42949296 | ||||||
| chr4:42949354
|
C | CA | 53 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0045others(50): Show | 53 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.385-13516dupA | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42949354 | |||||
| chr4:42949354
|
C | CAA | 18 | a0001c0001t0001g0069a0001c0001t0003g0193a0002c0002t0001g0228others(15): Show | 18 | HG00621.hp1 HG00673.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.385-13517_385-1351 others(6): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42949354 | |||||
| chr4:42949354
|
CA | C | 31 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0056others(28): Show | 31 | HG00140.hp1 HG00438.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.385-13516delA | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42949354 | |||||
| chr4:42949354
|
CAA | C | 50 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0039others(47): Show | 50 | HG00140.hp2 HG00639.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.385-13517_385-1351 others(6): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42949354 | |||||
| chr4:42949354
|
CAAA | C | 81 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(78): Show | 81 | HG00733.hp2 HG01109.hp2 HG01884.hp2 others(78): Show |
intron_variant | MODIFIER | c.385-13518_385-1351 others(7): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42949354 | |||||
| chr4:42949354
|
CAAAA | C | 7 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0025others(4): Show | 7 | HG00323.hp1 HG01099.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.385-13519_385-1351 others(8): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42949354 | |||||
| chr4:42949373
|
AAAAC | A | 6 | a0001c0001t0001g0099a0001c0001t0001g0105a0001c0001t0003g0194others(3): Show | 6 | HG04115.hp2 NA18941.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.385-13516_385-1351 others(8): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42949373 | |||||
| chr4:42949375
|
AAC | A | 47 | a0001c0001t0001g0034a0001c0001t0001g0111a0001c0001t0002g0021others(44): Show | 47 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.385-13515_385-1351 others(6): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42949375 | |||||
| chr4:42949376
|
AC | A | 3 | a0001c0001t0002g0083a0001c0001t0002g0102a0001c0001t0004g0170 | 3 | HG01978.hp1 HG02055.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.385-13515delC | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42949376 | ||||||
| chr4:42949377
|
C | A | 82 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(79): Show | 82 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.385-13515C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42949377 | ||||||
| chr4:42949611
|
G | A | 2 | a0001c0001t0001g0075a0001c0001t0002g0076 | 2 | HG01993.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.385-13281G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42949611 | ||||||
| chr4:42949611
|
G | C | 103 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(100): Show | 103 | HG00323.hp1 HG00733.hp2 HG01099.hp1 others(100): Show |
intron_variant | MODIFIER | c.385-13281G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42949611 | ||||||
| chr4:42949642
|
C | T | 2 | a0001c0001t0002g0126a0001c0001t0002g0127 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.385-13250C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42949642 | ||||||
| chr4:42949692
|
T | C | 28 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0056others(25): Show | 28 | HG00140.hp1 HG00438.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.385-13200T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42949692 | ||||||
| chr4:42949716
|
G | A | 1 | a0002c0002t0001g0267 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.385-13176G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42949716 | ||||||
| chr4:42949748
|
T | C | 2 | a0001c0001t0004g0142a0003c0003t0002g0302 | 2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.385-13144T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42949748 | ||||||
| chr4:42949827
|
G | A | 99 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(96): Show | 99 | HG00323.hp1 HG00733.hp2 HG01099.hp1 others(96): Show |
intron_variant | MODIFIER | c.385-13065G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42949827 | ||||||
| chr4:42949906
|
C | T | 1 | a0002c0002t0001g0248 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.385-12986C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42949906 | ||||||
| chr4:42950018
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.385-12874C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42950018 | ||||||
| chr4:42950029
|
T | A | 2 | a0001c0001t0002g0030a0001c0001t0002g0031 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.385-12863T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42950029 | ||||||
| chr4:42950093
|
C | A | 9 | a0001c0001t0002g0014a0001c0001t0002g0126a0001c0001t0002g0127others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.385-12799C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42950093 | ||||||
| chr4:42950225
|
C | G | 1 | a0001c0001t0001g0095 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.385-12667C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42950225 | ||||||
| chr4:42950282
|
C | T | 166 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(163): Show | 166 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.385-12610C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42950282 | ||||||
| chr4:42950296
|
T | A | 8 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0281others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.385-12596T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42950296 | ||||||
| chr4:42950306
|
T | C | 1 | a0001c0001t0002g0094 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.385-12586T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42950306 | ||||||
| chr4:42950362
|
G | A | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.385-12530G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42950362 | ||||||
| chr4:42950387
|
G | A | 1 | a0002c0002t0001g0257 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.385-12505G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42950387 | ||||||
| chr4:42950396
|
T | G | 10 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0258others(7): Show | 10 | HG02015.hp2 NA18944.hp2 NA18955.hp2 others(7): Show |
intron_variant | MODIFIER | c.385-12496T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42950396 | ||||||
| chr4:42950430
|
G | T | 119 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(116): Show | 119 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.385-12462G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42950430 | ||||||
| chr4:42950535
|
C | G | 307 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(304): Show | 307 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.385-12357C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42950535 | ||||||
| chr4:42950573
|
G | A | 2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.385-12319G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42950573 | ||||||
| chr4:42950656
|
G | A | 1 | a0003c0003t0002g0336 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.385-12236G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42950656 | ||||||
| chr4:42950671
|
A | G | 21 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(18): Show | 21 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.385-12221A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42950671 | ||||||
| chr4:42950811
|
T | A | 1 | a0001c0001t0002g0081 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.385-12081T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42950811 | ||||||
| chr4:42950839
|
C | T | 120 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 120 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.385-12053C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42950839 | ||||||
| chr4:42950869
|
T | C | 1 | a0003c0003t0001g0317 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.385-12023T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42950869 | ||||||
| chr4:42950870
|
A | G | 1 | a0002c0002t0001g0248 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.385-12022A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42950870 | ||||||
| chr4:42951014
|
C | G | 11 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(8): Show | 11 | HG00140.hp2 NA18942.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.385-11878C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42951014 | ||||||
| chr4:42951041
|
A | T | 1 | a0002c0002t0002g0215 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.385-11851A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42951041 | ||||||
| chr4:42951143
|
G | T | 1 | a0003c0003t0001g0316 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.385-11749G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42951143 | ||||||
| chr4:42951278
|
C | T | 8 | a0001c0001t0002g0080a0001c0001t0003g0132a0001c0001t0003g0134others(5): Show | 8 | HG02074.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.385-11614C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42951278 | ||||||
| chr4:42951297
|
T | A | 2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.385-11595T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42951297 | ||||||
| chr4:42951420
|
G | T | 1 | a0001c0001t0004g0166 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.385-11472G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42951420 | ||||||
| chr4:42951440
|
T | C | 10 | a0001c0001t0001g0012a0001c0001t0002g0014a0001c0001t0002g0126others(7): Show | 10 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.385-11452T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42951440 | ||||||
| chr4:42951520
|
C | T | 8 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0281others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.385-11372C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42951520 | ||||||
| chr4:42951571
|
A | G | 9 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0281others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.385-11321A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42951571 | ||||||
| chr4:42951579
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.385-11313A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42951579 | ||||||
| chr4:42951631
|
C | T | 73 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0045others(70): Show | 73 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.385-11261C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42951631 | ||||||
| chr4:42951669
|
T | C | 1 | a0001c0001t0005g0157 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.385-11223T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42951669 | ||||||
| chr4:42951674
|
G | C | 1 | a0001c0001t0005g0211 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.385-11218G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42951674 | ||||||
| chr4:42951747
|
A | G | 1 | a0002c0002t0001g0258 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.385-11145A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42951747 | ||||||
| chr4:42952094
|
A | T | 19 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(16): Show | 19 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.385-10798A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42952094 | ||||||
| chr4:42952131
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.385-10761T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42952131 | ||||||
| chr4:42952222
|
A | C | 72 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0045others(69): Show | 72 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.385-10670A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42952222 | ||||||
| chr4:42952397
|
T | A | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.385-10495T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42952397 | ||||||
| chr4:42952397
|
T | C | 2 | a0001c0001t0002g0086a0003c0003t0002g0327 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.385-10495T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42952397 | ||||||
| chr4:42952399
|
G | A | 1 | a0002c0002t0001g0280 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.385-10493G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42952399 | ||||||
| chr4:42952508
|
T | C | 120 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 120 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.385-10384T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42952508 | ||||||
| chr4:42952543
|
G | A | 19 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(16): Show | 19 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.385-10349G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42952543 | ||||||
| chr4:42952754
|
T | G | 2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.385-10138T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42952754 | ||||||
| chr4:42952985
|
C | T | 1 | a0001c0001t0002g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.385-9907C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42952985 | ||||||
| chr4:42953055
|
C | A | 120 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 120 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.385-9837C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42953055 | ||||||
| chr4:42953217
|
C | T | 2 | a0001c0001t0002g0278a0001c0001t0005g0157 | 2 | HG01884.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.385-9675C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42953217 | ||||||
| chr4:42953237
|
G | C | 1 | a0001c0001t0005g0211 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.385-9655G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42953237 | ||||||
| chr4:42953540
|
C | T | 19 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(16): Show | 19 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.385-9352C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42953540 | ||||||
| chr4:42953547
|
G | T | 1 | a0001c0001t0003g0167 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.385-9345G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42953547 | ||||||
| chr4:42953904
|
C | A | 120 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 120 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.385-8988C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42953904 | ||||||
| chr4:42953913
|
A | T | 1 | a0001c0001t0003g0200 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.385-8979A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42953913 | ||||||
| chr4:42953961
|
G | A | 44 | a0001c0001t0001g0012a0001c0001t0001g0039a0001c0001t0001g0046others(41): Show | 44 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(41): Show |
intron_variant | MODIFIER | c.385-8931G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42953961 | ||||||
| chr4:42954003
|
C | T | 2 | a0002c0002t0001g0246a0002c0002t0001g0254 | 2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.385-8889C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42954003 | ||||||
| chr4:42954004
|
G | A | 120 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 120 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.385-8888G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42954004 | ||||||
| chr4:42954071
|
C | A | 1 | a0001c0001t0001g0115 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.385-8821C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42954071 | ||||||
| chr4:42954290
|
A | C | 1 | a0001c0001t0001g0095 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.385-8602A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42954290 | ||||||
| chr4:42954394
|
T | G | 1 | a0003c0003t0002g0300 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.385-8498T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42954394 | ||||||
| chr4:42954717
|
G | T | 8 | a0001c0001t0002g0013a0001c0001t0002g0044a0001c0001t0003g0209others(5): Show | 8 | HG00639.hp2 HG02109.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.385-8175G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42954717 | ||||||
| chr4:42954772
|
C | A | 1 | a0001c0001t0002g0092 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.385-8120C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42954772 | ||||||
| chr4:42954776
|
ATAGAGAG others(6): Show |
A | 1 | a0001c0001t0002g0104 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.385-8111_385-8099d others(15): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42954776 | |||||
| chr4:42955020
|
G | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | NA18981.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.385-7872G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42955020 | ||||||
| chr4:42955126
|
C | T | 1 | a0003c0003t0001g0333 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.385-7766C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42955126 | ||||||
| chr4:42955145
|
T | C | 2 | a0001c0001t0002g0013a0003c0003t0002g0329 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.385-7747T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42955145 | ||||||
| chr4:42955175
|
G | A | 167 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(164): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.385-7717G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42955175 | ||||||
| chr4:42955193
|
C | T | 1 | a0001c0001t0002g0036 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.385-7699C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42955193 | ||||||
| chr4:42955257
|
G | T | 120 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 120 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.385-7635G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42955257 | ||||||
| chr4:42955300
|
G | A | 19 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(16): Show | 19 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.385-7592G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42955300 | ||||||
| chr4:42955309
|
G | A | 2 | a0001c0001t0002g0020a0001c0001t0002g0022 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.385-7583G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42955309 | ||||||
| chr4:42955338
|
T | G | 2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.385-7554T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42955338 | ||||||
| chr4:42955414
|
A | C | 1 | a0002c0002t0001g0280 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.385-7478A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42955414 | ||||||
| chr4:42955439
|
G | A | 8 | a0001c0001t0002g0013a0001c0001t0002g0044a0001c0001t0003g0209others(5): Show | 8 | HG00639.hp2 HG02109.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.385-7453G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42955439 | ||||||
| chr4:42955514
|
A | T | 167 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(164): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.385-7378A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42955514 | ||||||
| chr4:42955658
|
A | G | 2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.385-7234A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42955658 | ||||||
| chr4:42955689
|
T | C | 19 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(16): Show | 19 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.385-7203T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42955689 | ||||||
| chr4:42955905
|
G | T | 1 | a0003c0003t0002g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.385-6987G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42955905 | ||||||
| chr4:42956088
|
G | C | 23 | a0001c0001t0001g0012a0001c0001t0001g0075a0001c0001t0002g0014others(20): Show | 23 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.385-6804G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42956088 | ||||||
| chr4:42956234
|
A | T | 1 | a0001c0001t0001g0011 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.385-6658A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42956234 | ||||||
| chr4:42956397
|
A | T | 1 | a0003c0003t0002g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.385-6495A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42956397 | ||||||
| chr4:42956452
|
A | AT | 14 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0058others(11): Show | 14 | HG02074.hp2 HG02145.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.385-6426dupT | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42956452 | |||||
| chr4:42956644
|
T | C | 1 | a0001c0001t0004g0170 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.385-6248T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42956644 | ||||||
| chr4:42956822
|
C | T | 3 | a0001c0001t0001g0075a0001c0001t0002g0076a0001c0001t0004g0141 | 3 | HG01993.hp2 HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.385-6070C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42956822 | ||||||
| chr4:42956851
|
C | T | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.385-6041C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42956851 | ||||||
| chr4:42956868
|
G | A | 1 | a0001c0001t0002g0278 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.385-6024G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42956868 | ||||||
| chr4:42956969
|
A | G | 20 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(17): Show | 20 | HG00140.hp2 HG00609.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.385-5923A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42956969 | ||||||
| chr4:42957081
|
A | G | 11 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(8): Show | 11 | HG00140.hp2 NA18942.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.385-5811A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42957081 | ||||||
| chr4:42957149
|
T | C | 2 | a0001c0001t0006g0003a0001c0001t0006g0016 | 2 | HG02572.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.385-5743T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42957149 | ||||||
| chr4:42957189
|
C | A | 1 | a0001c0001t0002g0081 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.385-5703C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42957189 | ||||||
| chr4:42957364
|
A | C | 19 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(16): Show | 19 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.385-5528A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42957364 | ||||||
| chr4:42957376
|
G | A | 23 | a0001c0001t0001g0012a0001c0001t0001g0075a0001c0001t0002g0014others(20): Show | 23 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.385-5516G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42957376 | ||||||
| chr4:42957383
|
A | C | 2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.385-5509A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42957383 | ||||||
| chr4:42957442
|
G | T | 8 | a0001c0001t0002g0013a0001c0001t0002g0044a0001c0001t0003g0209others(5): Show | 8 | HG00639.hp2 HG02109.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.385-5450G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42957442 | ||||||
| chr4:42957482
|
C | A | 23 | a0001c0001t0001g0012a0001c0001t0001g0075a0001c0001t0002g0014others(20): Show | 23 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.385-5410C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42957482 | ||||||
| chr4:42957682
|
C | T | 8 | a0001c0001t0002g0080a0001c0001t0003g0132a0001c0001t0003g0134others(5): Show | 8 | HG02074.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.385-5210C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42957682 | ||||||
| chr4:42957721
|
G | A | 23 | a0001c0001t0001g0012a0001c0001t0001g0075a0001c0001t0002g0014others(20): Show | 23 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.385-5171G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42957721 | ||||||
| chr4:42957797
|
C | T | 11 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(8): Show | 11 | HG00140.hp2 NA18942.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.385-5095C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42957797 | ||||||
| chr4:42958008
|
T | A | 2 | a0001c0001t0002g0107a0001c0001t0002g0108 | 2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.385-4884T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42958008 | ||||||
| chr4:42958170
|
C | G | 1 | a0001c0001t0002g0059 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.385-4722C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42958170 | ||||||
| chr4:42958313
|
A | T | 1 | a0001c0001t0002g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.385-4579A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42958313 | ||||||
| chr4:42958469
|
T | G | 44 | a0001c0001t0001g0012a0001c0001t0001g0039a0001c0001t0001g0046others(41): Show | 44 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(41): Show |
intron_variant | MODIFIER | c.385-4423T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42958469 | ||||||
| chr4:42958593
|
A | G | 2 | a0001c0001t0002g0278a0001c0001t0005g0157 | 2 | HG01884.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.385-4299A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42958593 | ||||||
| chr4:42958651
|
G | A | 51 | a0001c0001t0001g0034a0001c0001t0001g0111a0001c0001t0002g0021others(48): Show | 51 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.385-4241G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42958651 | ||||||
| chr4:42958776
|
G | A | 1 | a0001c0001t0001g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.385-4116G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42958776 | ||||||
| chr4:42958777
|
A | G | 2 | a0001c0001t0002g0104a0001c0001t0008g0106 | 2 | HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.385-4115A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42958777 | ||||||
| chr4:42958787
|
A | T | 2 | a0001c0001t0002g0086a0003c0003t0002g0327 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.385-4105A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42958787 | ||||||
| chr4:42958806
|
A | T | 8 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0281others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.385-4086A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42958806 | ||||||
| chr4:42958874
|
T | A | 2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.385-4018T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42958874 | ||||||
| chr4:42958930
|
G | A | 1 | a0001c0001t0002g0036 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.385-3962G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42958930 | ||||||
| chr4:42958979
|
G | T | 8 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0281others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.385-3913G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42958979 | ||||||
| chr4:42959195
|
T | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0113a0001c0001t0001g0116 | 3 | HG03654.hp2 HG03704.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.385-3697T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42959195 | ||||||
| chr4:42959227
|
A | G | 2 | a0001c0001t0002g0020a0001c0001t0002g0022 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.385-3665A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42959227 | ||||||
| chr4:42959231
|
C | G | 3 | a0001c0001t0001g0075a0001c0001t0002g0076a0001c0001t0004g0141 | 3 | HG01993.hp2 HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.385-3661C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42959231 | ||||||
| chr4:42959274
|
A | G | 1 | a0001c0001t0002g0081 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.385-3618A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42959274 | ||||||
| chr4:42959329
|
A | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.385-3563A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42959329 | ||||||
| chr4:42959340
|
G | A | 2 | a0001c0001t0002g0086a0003c0003t0002g0327 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.385-3552G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42959340 | ||||||
| chr4:42959348
|
G | A | 307 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(304): Show | 307 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.385-3544G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42959348 | ||||||
| chr4:42959535
|
G | A | 1 | a0001c0001t0004g0142 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.385-3357G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42959535 | ||||||
| chr4:42959553
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.385-3339C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42959553 | ||||||
| chr4:42959554
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.385-3338G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42959554 | ||||||
| chr4:42959616
|
ACT | A | 11 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(8): Show | 11 | HG00140.hp2 NA18942.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.385-3273_385-3272d others(4): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 42959616 | |||||
| chr4:42959644
|
C | T | 42 | a0001c0001t0001g0012a0001c0001t0001g0039a0001c0001t0001g0046others(39): Show | 42 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(39): Show |
intron_variant | MODIFIER | c.385-3248C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42959644 | ||||||
| chr4:42959880
|
G | T | 1 | a0003c0003t0002g0297 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.385-3012G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42959880 | ||||||
| chr4:42960024
|
G | A | 7 | a0001c0001t0002g0013a0001c0001t0002g0044a0001c0001t0003g0209others(4): Show | 7 | HG00639.hp2 HG02109.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.385-2868G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42960024 | ||||||
| chr4:42960207
|
T | C | 11 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(8): Show | 11 | HG00140.hp2 NA18942.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.385-2685T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42960207 | ||||||
| chr4:42960280
|
G | C | 2 | a0001c0001t0002g0104a0001c0001t0008g0106 | 2 | HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.385-2612G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42960280 | ||||||
| chr4:42960287
|
T | C | 1 | a0001c0001t0001g0122 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.385-2605T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42960287 | ||||||
| chr4:42960290
|
T | A | 2 | a0001c0001t0002g0278a0001c0001t0005g0157 | 2 | HG01884.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.385-2602T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42960290 | ||||||
| chr4:42960976
|
A | G | 23 | a0001c0001t0001g0012a0001c0001t0001g0075a0001c0001t0002g0014others(20): Show | 23 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.385-1916A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42960976 | ||||||
| chr4:42961164
|
T | C | 1 | a0001c0001t0009g0040 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.385-1728T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42961164 | ||||||
| chr4:42961187
|
T | C | 1 | a0002c0002t0001g0243 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.385-1705T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42961187 | ||||||
| chr4:42961241
|
G | A | 3 | a0001c0001t0001g0075a0001c0001t0002g0076a0001c0001t0004g0141 | 3 | HG01993.hp2 HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.385-1651G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42961241 | ||||||
| chr4:42961254
|
C | T | 21 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(18): Show | 21 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.385-1638C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42961254 | ||||||
| chr4:42961317
|
T | C | 1 | a0001c0001t0002g0281 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.385-1575T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42961317 | ||||||
| chr4:42961460
|
G | A | 1 | a0003c0003t0001g0317 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.385-1432G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42961460 | ||||||
| chr4:42961520
|
T | G | 307 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(304): Show | 307 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.385-1372T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42961520 | ||||||
| chr4:42961538
|
A | G | 3 | a0001c0001t0001g0082a0001c0001t0002g0081a0001c0001t0003g0144 | 3 | HG01891.hp2 HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.385-1354A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42961538 | ||||||
| chr4:42961633
|
G | A | 2 | a0001c0004t0002g0088a0001c0004t0002g0091 | 2 | HG02809.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.385-1259G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42961633 | ||||||
| chr4:42961819
|
G | T | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.385-1073G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42961819 | ||||||
| chr4:42961918
|
G | T | 19 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(16): Show | 19 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.385-974G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42961918 | ||||||
| chr4:42961989
|
G | T | 8 | a0001c0001t0002g0080a0001c0001t0003g0132a0001c0001t0003g0134others(5): Show | 8 | HG02074.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.385-903G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42961989 | ||||||
| chr4:42962044
|
T | C | 9 | a0001c0001t0002g0014a0001c0001t0002g0126a0001c0001t0002g0127others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.385-848T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42962044 | ||||||
| chr4:42962066
|
G | T | 1 | a0001c0001t0003g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.385-826G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42962066 | ||||||
| chr4:42962144
|
A | G | 4 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0183others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.385-748A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42962144 | ||||||
| chr4:42962159
|
G | A | 1 | a0002c0002t0002g0270 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.385-733G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42962159 | ||||||
| chr4:42962163
|
A | T | 1 | a0001c0001t0002g0026 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.385-729A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42962163 | ||||||
| chr4:42962436
|
G | A | 51 | a0001c0001t0001g0034a0001c0001t0001g0111a0001c0001t0002g0021others(48): Show | 51 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.385-456G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42962436 | ||||||
| chr4:42962553
|
C | T | 2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.385-339C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42962553 | ||||||
| chr4:42962554
|
G | A | 1 | a0003c0005t0002g0332 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.385-338G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42962554 | ||||||
| chr4:42962616
|
T | C | 2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.385-276T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42962616 | ||||||
| chr4:42962813
|
C | G | 1 | a0001c0001t0002g0054 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.385-79C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 1/3 | chr4 | 42962813 | ||||||
| chr4:42963142
|
A | C | 307 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(304): Show | 307 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
splice_region_variant&intron_variant | LOW | c.627+8A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42963142 | ||||||
| chr4:42963240
|
GT | G | 8 | a0001c0001t0002g0013a0001c0001t0002g0044a0001c0001t0003g0209others(5): Show | 8 | HG00639.hp2 HG02109.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+113delT | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42963240 | |||||
| chr4:42963282
|
C | G | 1 | a0001c0001t0002g0078 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.627+148C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42963282 | ||||||
| chr4:42963309
|
G | A | 19 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(16): Show | 19 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.627+175G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42963309 | ||||||
| chr4:42963338
|
A | T | 2 | a0001c0001t0002g0278a0001c0001t0005g0157 | 2 | HG01884.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.627+204A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42963338 | ||||||
| chr4:42963431
|
T | A | 5 | a0001c0001t0001g0099a0001c0001t0001g0105a0001c0001t0003g0194others(2): Show | 5 | NA18941.hp1 NA18957.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.627+297T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42963431 | ||||||
| chr4:42963738
|
T | C | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.627+604T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42963738 | ||||||
| chr4:42963773
|
A | G | 1 | a0002c0002t0001g0269 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.627+639A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42963773 | ||||||
| chr4:42963792
|
A | G | 1 | a0001c0001t0004g0147 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.627+658A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42963792 | ||||||
| chr4:42963973
|
A | G | 11 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(8): Show | 11 | HG00140.hp2 NA18942.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.627+839A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42963973 | ||||||
| chr4:42963985
|
A | G | 1 | a0001c0001t0009g0040 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.627+851A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42963985 | ||||||
| chr4:42964263
|
C | G | 8 | a0001c0001t0002g0080a0001c0001t0003g0132a0001c0001t0003g0134others(5): Show | 8 | HG02074.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+1129C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42964263 | ||||||
| chr4:42964641
|
A | C | 1 | a0001c0001t0001g0285 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.627+1507A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42964641 | ||||||
| chr4:42964742
|
AG | A | 3 | a0001c0001t0002g0018a0001c0001t0002g0089a0003c0003t0002g0303 | 3 | HG02257.hp1 HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.627+1610delG | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42964742 | |||||
| chr4:42964745
|
T | G | 2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.627+1611T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42964745 | ||||||
| chr4:42964757
|
G | A | 1 | a0001c0001t0002g0081 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.627+1623G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42964757 | ||||||
| chr4:42964916
|
C | T | 2 | a0003c0003t0001g0296a0003c0003t0001g0325 | 2 | NA18980.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.627+1782C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42964916 | ||||||
| chr4:42965373
|
CT | C | 8 | a0001c0001t0002g0080a0001c0001t0003g0132a0001c0001t0003g0134others(5): Show | 8 | HG02074.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+2240delT | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42965373 | ||||||
| chr4:42965412
|
C | T | 1 | a0001c0001t0004g0192 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.627+2278C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42965412 | ||||||
| chr4:42965462
|
A | T | 1 | a0001c0001t0001g0019 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.627+2328A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42965462 | ||||||
| chr4:42965690
|
T | G | 1 | a0001c0001t0003g0161 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.627+2556T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42965690 | ||||||
| chr4:42965853
|
C | T | 11 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(8): Show | 11 | HG00140.hp2 NA18942.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.627+2719C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42965853 | ||||||
| chr4:42965866
|
G | C | 1 | a0001c0004t0002g0091 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.627+2732G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42965866 | ||||||
| chr4:42966046
|
G | GA | 24 | a0001c0001t0001g0012a0001c0001t0001g0075a0001c0001t0001g0212others(21): Show | 24 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.627+2921dupA | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42966046 | |||||
| chr4:42966319
|
A | G | 2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.627+3185A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42966319 | ||||||
| chr4:42966500
|
G | A | 2 | a0003c0003t0001g0293a0003c0003t0001g0294 | 2 | NA18965.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.627+3366G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42966500 | ||||||
| chr4:42966596
|
A | G | 2 | a0001c0001t0002g0086a0003c0003t0002g0327 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.627+3462A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42966596 | ||||||
| chr4:42966623
|
A | G | 1 | a0003c0003t0002g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.627+3489A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42966623 | ||||||
| chr4:42966626
|
G | C | 1 | a0002c0002t0002g0271 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.627+3492G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42966626 | ||||||
| chr4:42966646
|
A | G | 19 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(16): Show | 19 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.627+3512A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42966646 | ||||||
| chr4:42966728
|
G | A | 2 | a0001c0001t0002g0086a0003c0003t0002g0327 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.627+3594G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42966728 | ||||||
| chr4:42966819
|
T | C | 8 | a0001c0001t0002g0080a0001c0001t0003g0132a0001c0001t0003g0134others(5): Show | 8 | HG02074.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+3685T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42966819 | ||||||
| chr4:42966928
|
A | G | 2 | a0002c0002t0001g0247a0002c0002t0001g0255 | 2 | HG01346.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.627+3794A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42966928 | ||||||
| chr4:42966944
|
C | T | 1 | a0002c0002t0001g0252 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.627+3810C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42966944 | ||||||
| chr4:42967001
|
G | A | 3 | a0001c0001t0001g0006a0003c0003t0002g0297a0003c0003t0002g0334 | 3 | HG02300.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.627+3867G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42967001 | ||||||
| chr4:42967147
|
G | T | 1 | a0001c0001t0001g0113 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.627+4013G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42967147 | ||||||
| chr4:42967450
|
T | G | 3 | a0001c0001t0002g0078a0001c0001t0002g0084a0003c0003t0002g0336 | 3 | HG02647.hp2 HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.627+4316T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42967450 | ||||||
| chr4:42967477
|
CACTT | C | 27 | a0001c0001t0001g0012a0001c0001t0001g0039a0001c0001t0001g0046others(24): Show | 27 | HG00140.hp2 HG01243.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.627+4345_627+4348d others(6): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42967477 | |||||
| chr4:42967533
|
C | T | 9 | a0001c0001t0002g0014a0001c0001t0002g0126a0001c0001t0002g0127others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.627+4399C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42967533 | ||||||
| chr4:42967902
|
A | C | 2 | a0001c0001t0002g0278a0001c0001t0005g0157 | 2 | HG01884.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.627+4768A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42967902 | ||||||
| chr4:42968146
|
C | T | 8 | a0001c0001t0002g0080a0001c0001t0003g0132a0001c0001t0003g0134others(5): Show | 8 | HG02074.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+5012C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42968146 | ||||||
| chr4:42968213
|
G | A | 19 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(16): Show | 19 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.627+5079G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42968213 | ||||||
| chr4:42968251
|
C | T | 2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.627+5117C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42968251 | ||||||
| chr4:42968545
|
A | G | 19 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(16): Show | 19 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.627+5411A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42968545 | ||||||
| chr4:42968741
|
C | G | 1 | a0001c0001t0002g0282 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.627+5607C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42968741 | ||||||
| chr4:42968804
|
A | T | 3 | a0001c0001t0002g0078a0001c0001t0002g0084a0003c0003t0002g0336 | 3 | HG02647.hp2 HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.627+5670A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42968804 | ||||||
| chr4:42968830
|
C | G | 1 | a0003c0003t0002g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.627+5696C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42968830 | ||||||
| chr4:42968857
|
A | G | 1 | a0001c0001t0003g0154 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.627+5723A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42968857 | ||||||
| chr4:42968881
|
T | C | 9 | a0001c0001t0002g0047a0001c0001t0002g0065a0001c0001t0002g0083others(6): Show | 9 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.627+5747T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42968881 | ||||||
| chr4:42969335
|
C | G | 3 | a0001c0001t0003g0159a0001c0001t0003g0160a0001c0001t0003g0161 | 3 | HG02886.hp1 HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.627+6201C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42969335 | ||||||
| chr4:42969392
|
C | T | 3 | a0001c0001t0003g0194a0001c0001t0003g0195a0001c0001t0003g0196 | 3 | NA18941.hp1 NA18957.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.627+6258C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42969392 | ||||||
| chr4:42969552
|
G | A | 2 | a0001c0001t0002g0086a0003c0003t0002g0327 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.627+6418G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42969552 | ||||||
| chr4:42969604
|
A | C | 1 | a0001c0001t0002g0278 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.627+6470A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42969604 | ||||||
| chr4:42969639
|
A | G | 1 | a0001c0001t0002g0043 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.627+6505A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42969639 | ||||||
| chr4:42969647
|
G | A | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.627+6513G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42969647 | ||||||
| chr4:42969717
|
G | C | 7 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(4): Show | 7 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.627+6583G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42969717 | ||||||
| chr4:42969828
|
G | A | 1 | a0001c0001t0002g0047 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.627+6694G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42969828 | ||||||
| chr4:42969829
|
T | C | 1 | a0001c0001t0002g0104 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.627+6695T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42969829 | ||||||
| chr4:42969868
|
G | C | 1 | a0003c0003t0001g0318 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.627+6734G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42969868 | ||||||
| chr4:42969984
|
A | C | 1 | a0001c0001t0001g0019 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.627+6850A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42969984 | ||||||
| chr4:42970120
|
C | T | 8 | a0001c0001t0002g0080a0001c0001t0003g0132a0001c0001t0003g0134others(5): Show | 8 | HG02074.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+6986C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42970120 | ||||||
| chr4:42970290
|
T | G | 19 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(16): Show | 19 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.627+7156T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42970290 | ||||||
| chr4:42970429
|
G | A | 2 | a0001c0001t0002g0086a0003c0003t0002g0327 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.627+7295G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42970429 | ||||||
| chr4:42970455
|
G | C | 2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.627+7321G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42970455 | ||||||
| chr4:42970564
|
A | G | 8 | a0001c0001t0002g0080a0001c0001t0003g0132a0001c0001t0003g0134others(5): Show | 8 | HG02074.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+7430A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42970564 | ||||||
| chr4:42970614
|
G | C | 3 | a0001c0001t0004g0142a0003c0003t0002g0291a0003c0003t0002g0302 | 3 | HG02109.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.627+7480G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42970614 | ||||||
| chr4:42970719
|
T | C | 1 | a0002c0002t0002g0225 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.627+7585T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42970719 | ||||||
| chr4:42970809
|
C | G | 1 | a0001c0001t0002g0085 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.627+7675C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42970809 | ||||||
| chr4:42970828
|
G | C | 330 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(327): Show | 330 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.627+7694G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42970828 | ||||||
| chr4:42970835
|
A | T | 8 | a0001c0001t0002g0080a0001c0001t0003g0132a0001c0001t0003g0134others(5): Show | 8 | HG02074.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+7701A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42970835 | ||||||
| chr4:42970872
|
T | G | 330 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(327): Show | 330 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.627+7738T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42970872 | ||||||
| chr4:42970936
|
C | T | 2 | a0003c0003t0001g0292a0003c0003t0001g0309 | 2 | NA18973.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.627+7802C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42970936 | ||||||
| chr4:42970953
|
G | A | 1 | a0001c0001t0002g0066 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.627+7819G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42970953 | ||||||
| chr4:42971017
|
C | T | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.627+7883C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42971017 | ||||||
| chr4:42971074
|
G | A | 4 | a0001c0001t0001g0075a0001c0001t0001g0212a0001c0001t0002g0076others(1): Show | 4 | HG01993.hp2 HG02145.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.627+7940G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42971074 | ||||||
| chr4:42971094
|
T | C | 3 | a0001c0001t0002g0078a0001c0001t0002g0084a0003c0003t0002g0336 | 3 | HG02647.hp2 HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.627+7960T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42971094 | ||||||
| chr4:42971241
|
A | G | 8 | a0001c0001t0002g0080a0001c0001t0003g0132a0001c0001t0003g0134others(5): Show | 8 | HG02074.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+8107A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42971241 | ||||||
| chr4:42971330
|
G | C | 45 | a0001c0001t0001g0012a0001c0001t0001g0039a0001c0001t0001g0046others(42): Show | 45 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(42): Show |
intron_variant | MODIFIER | c.627+8196G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42971330 | ||||||
| chr4:42971342
|
G | T | 3 | a0003c0003t0002g0314a0003c0003t0002g0323a0003c0003t0002g0335 | 3 | HG01243.hp1 HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.627+8208G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42971342 | ||||||
| chr4:42971353
|
A | T | 4 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0183others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+8219A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42971353 | ||||||
| chr4:42971358
|
C | T | 1 | a0002c0002t0002g0265 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.627+8224C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42971358 | ||||||
| chr4:42971418
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.627+8284T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42971418 | ||||||
| chr4:42971447
|
C | G | 4 | a0001c0001t0002g0080a0001c0001t0004g0136a0001c0001t0006g0003others(1): Show | 4 | HG02145.hp1 HG02257.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.627+8313C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42971447 | ||||||
| chr4:42971528
|
G | A | 1 | a0002c0002t0001g0223 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.627+8394G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42971528 | ||||||
| chr4:42971564
|
AG | A | 10 | a0001c0001t0001g0012a0001c0001t0002g0014a0001c0001t0002g0126others(7): Show | 10 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.627+8431delG | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42971564 | ||||||
| chr4:42971791
|
CA | C | 6 | a0001c0001t0001g0109a0001c0001t0002g0013a0001c0001t0002g0044others(3): Show | 6 | HG00639.hp1 HG00639.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.627+8667delA | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42971791 | |||||
| chr4:42971912
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.627+8778T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42971912 | ||||||
| chr4:42971932
|
T | A | 2 | a0001c0001t0002g0278a0001c0001t0005g0157 | 2 | HG01884.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.627+8798T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42971932 | ||||||
| chr4:42972058
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.627+8924G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42972058 | ||||||
| chr4:42972059
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.627+8925G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42972059 | ||||||
| chr4:42972060
|
C | A | 1 | a0001c0001t0001g0017 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.627+8926C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42972060 | ||||||
| chr4:42972061
|
T | A | 1 | a0001c0001t0001g0017 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.627+8927T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42972061 | ||||||
| chr4:42972063
|
A | T | 1 | a0001c0001t0001g0017 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.627+8929A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42972063 | ||||||
| chr4:42972141
|
A | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0285a0003c0003t0001g0290others(1): Show | 4 | HG01192.hp2 HG01978.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+9007A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42972141 | ||||||
| chr4:42972181
|
T | C | 8 | a0001c0001t0002g0080a0001c0001t0003g0132a0001c0001t0003g0134others(5): Show | 8 | HG02074.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+9047T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42972181 | ||||||
| chr4:42972269
|
G | C | 1 | a0001c0001t0002g0083 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.627+9135G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42972269 | ||||||
| chr4:42972335
|
T | C | 1 | a0001c0001t0002g0059 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.627+9201T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42972335 | ||||||
| chr4:42972371
|
A | G | 1 | a0001c0001t0003g0178 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.627+9237A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42972371 | ||||||
| chr4:42972453
|
T | C | 8 | a0001c0001t0002g0080a0001c0001t0003g0132a0001c0001t0003g0134others(5): Show | 8 | HG02074.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+9319T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42972453 | ||||||
| chr4:42972473
|
C | G | 1 | a0001c0001t0002g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.627+9339C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42972473 | ||||||
| chr4:42972534
|
T | C | 1 | a0001c0001t0003g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.627+9400T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42972534 | ||||||
| chr4:42972879
|
C | A | 2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.627+9745C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42972879 | ||||||
| chr4:42972881
|
GAATTACT others(118): Show |
G | 1 | a0002c0002t0001g0274 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.627+9748_627+9872d others(2): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42972881 | ||||||
| chr4:42972998
|
C | T | 1 | a0001c0001t0002g0081 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.627+9864C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42972998 | ||||||
| chr4:42973204
|
T | A | 1 | a0001c0001t0004g0148 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.627+10070T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42973204 | ||||||
| chr4:42973312
|
C | T | 113 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(110): Show | 113 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.627+10178C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42973312 | ||||||
| chr4:42973315
|
A | G | 1 | a0002c0002t0001g0274 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.627+10181A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42973315 | ||||||
| chr4:42973400
|
G | T | 15 | a0001c0001t0001g0012a0001c0001t0002g0014a0001c0001t0002g0020others(12): Show | 15 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.627+10266G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42973400 | ||||||
| chr4:42973468
|
C | A | 21 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(18): Show | 21 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.627+10334C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42973468 | ||||||
| chr4:42973468
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.627+10334C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42973468 | ||||||
| chr4:42973469
|
G | A | 2 | a0003c0003t0001g0313a0003c0003t0001g0316 | 2 | HG02056.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.627+10335G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42973469 | ||||||
| chr4:42973586
|
T | G | 1 | a0001c0001t0004g0204 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.627+10452T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42973586 | ||||||
| chr4:42973776
|
G | C | 8 | a0001c0001t0002g0080a0001c0001t0003g0132a0001c0001t0003g0134others(5): Show | 8 | HG02074.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+10642G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42973776 | ||||||
| chr4:42973910
|
T | A | 111 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(108): Show | 111 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.627+10776T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42973910 | ||||||
| chr4:42973982
|
T | C | 2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.627+10848T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42973982 | ||||||
| chr4:42974072
|
G | A | 1 | a0001c0001t0003g0134 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.627+10938G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42974072 | ||||||
| chr4:42974088
|
G | T | 1 | a0003c0003t0001g0290 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.627+10954G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42974088 | ||||||
| chr4:42974235
|
G | T | 19 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(16): Show | 19 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.627+11101G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42974235 | ||||||
| chr4:42974365
|
A | G | 8 | a0001c0001t0002g0080a0001c0001t0003g0132a0001c0001t0003g0134others(5): Show | 8 | HG02074.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+11231A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42974365 | ||||||
| chr4:42974431
|
A | C | 11 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(8): Show | 11 | HG00140.hp2 NA18942.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.627+11297A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42974431 | ||||||
| chr4:42974524
|
C | T | 21 | a0001c0001t0001g0012a0001c0001t0001g0075a0001c0001t0001g0212others(18): Show | 21 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.627+11390C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42974524 | ||||||
| chr4:42974543
|
G | A | 1 | a0001c0001t0003g0188 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.627+11409G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42974543 | ||||||
| chr4:42974576
|
C | T | 4 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0068others(1): Show | 4 | HG00733.hp2 HG01109.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.627+11442C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42974576 | ||||||
| chr4:42974589
|
T | C | 2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.627+11455T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42974589 | ||||||
| chr4:42974674
|
C | T | 1 | a0002c0002t0001g0257 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.627+11540C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42974674 | ||||||
| chr4:42974721
|
C | T | 1 | a0001c0001t0003g0140 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.627+11587C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42974721 | ||||||
| chr4:42974728
|
G | T | 1 | a0003c0003t0002g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.627+11594G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42974728 | ||||||
| chr4:42974755
|
G | A | 50 | a0001c0001t0001g0034a0001c0001t0001g0111a0001c0001t0002g0021others(47): Show | 50 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.627+11621G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42974755 | ||||||
| chr4:42974799
|
G | A | 2 | a0001c0001t0002g0086a0003c0003t0002g0327 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.627+11665G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42974799 | ||||||
| chr4:42974844
|
A | C | 4 | a0001c0001t0001g0075a0001c0001t0001g0212a0001c0001t0002g0076others(1): Show | 4 | HG01993.hp2 HG02145.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.627+11710A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42974844 | ||||||
| chr4:42974958
|
C | T | 2 | a0001c0001t0002g0086a0003c0003t0002g0327 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.627+11824C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42974958 | ||||||
| chr4:42975012
|
G | T | 1 | a0001c0001t0002g0081 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.627+11878G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42975012 | ||||||
| chr4:42975129
|
G | C | 4 | a0001c0001t0001g0075a0001c0001t0001g0212a0001c0001t0002g0076others(1): Show | 4 | HG01993.hp2 HG02145.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.627+11995G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42975129 | ||||||
| chr4:42975146
|
A | G | 5 | a0002c0002t0001g0216a0002c0002t0001g0217a0002c0002t0001g0218others(2): Show | 5 | HG00423.hp1 HG00544.hp2 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.627+12012A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42975146 | ||||||
| chr4:42975189
|
C | T | 113 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(110): Show | 113 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.627+12055C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42975189 | ||||||
| chr4:42975232
|
T | A | 1 | a0001c0001t0003g0143 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.627+12098T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42975232 | ||||||
| chr4:42975250
|
C | T | 2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.627+12116C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42975250 | ||||||
| chr4:42975534
|
G | A | 1 | a0002c0002t0001g0214 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.627+12400G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42975534 | ||||||
| chr4:42975595
|
G | A | 1 | a0001c0001t0002g0081 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.627+12461G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42975595 | ||||||
| chr4:42975640
|
G | A | 43 | a0001c0001t0001g0012a0001c0001t0001g0039a0001c0001t0001g0046others(40): Show | 43 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(40): Show |
intron_variant | MODIFIER | c.627+12506G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42975640 | ||||||
| chr4:42975648
|
A | C | 1 | a0003c0003t0002g0308 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.627+12514A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42975648 | ||||||
| chr4:42975739
|
G | A | 1 | a0004c0007t0002g0114 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.627+12605G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42975739 | ||||||
| chr4:42975853
|
A | C | 11 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(8): Show | 11 | HG00140.hp2 NA18942.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.627+12719A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42975853 | ||||||
| chr4:42975964
|
C | A | 1 | a0002c0002t0002g0271 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.627+12830C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42975964 | ||||||
| chr4:42976026
|
G | T | 21 | a0001c0001t0001g0012a0001c0001t0001g0075a0001c0001t0001g0212others(18): Show | 21 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.627+12892G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42976026 | ||||||
| chr4:42976158
|
C | T | 2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.627+13024C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42976158 | ||||||
| chr4:42976211
|
G | A | 1 | a0002c0002t0001g0267 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.627+13077G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42976211 | ||||||
| chr4:42976301
|
T | A | 1 | a0001c0001t0005g0211 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.627+13167T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42976301 | ||||||
| chr4:42976315
|
C | T | 22 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(19): Show | 22 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.627+13181C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42976315 | ||||||
| chr4:42976404
|
T | C | 2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.627+13270T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42976404 | ||||||
| chr4:42976426
|
C | G | 23 | a0001c0001t0001g0012a0001c0001t0001g0075a0001c0001t0001g0082others(20): Show | 23 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.627+13292C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42976426 | ||||||
| chr4:42976513
|
T | C | 166 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(163): Show | 166 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.627+13379T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42976513 | ||||||
| chr4:42976733
|
T | A | 1 | a0002c0002t0002g0229 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.627+13599T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42976733 | ||||||
| chr4:42976754
|
C | T | 1 | a0002c0002t0001g0213 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.627+13620C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42976754 | ||||||
| chr4:42976789
|
T | C | 8 | a0001c0001t0002g0080a0001c0001t0003g0132a0001c0001t0003g0134others(5): Show | 8 | HG02074.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+13655T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42976789 | ||||||
| chr4:42976813
|
G | A | 1 | a0001c0001t0004g0176 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.627+13679G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42976813 | ||||||
| chr4:42976830
|
T | C | 2 | a0002c0002t0002g0215a0002c0002t0002g0219 | 2 | NA18942.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.627+13696T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42976830 | ||||||
| chr4:42976860
|
G | A | 166 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(163): Show | 166 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.627+13726G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42976860 | ||||||
| chr4:42977071
|
G | T | 11 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(8): Show | 11 | HG00140.hp2 NA18942.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.627+13937G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42977071 | ||||||
| chr4:42977125
|
T | C | 1 | a0002c0002t0001g0274 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.627+13991T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42977125 | ||||||
| chr4:42977208
|
C | A | 1 | a0001c0001t0002g0033 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.627+14074C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42977208 | ||||||
| chr4:42977513
|
T | TGAGGTGA others(314): Show |
2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.627+14392_627+1439 others(325): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42977513 | |||||
| chr4:42977541
|
T | A | 2 | a0001c0001t0006g0003a0001c0001t0006g0016 | 2 | HG02572.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.627+14407T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42977541 | ||||||
| chr4:42977683
|
T | A | 3 | a0001c0001t0003g0164a0003c0003t0001g0311a0003c0003t0001g0319 | 3 | NA18950.hp1 NA18964.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.627+14549T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42977683 | ||||||
| chr4:42977722
|
T | G | 3 | a0001c0001t0001g0075a0001c0001t0002g0076a0001c0001t0004g0141 | 3 | HG01993.hp2 HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.627+14588T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42977722 | ||||||
| chr4:42977774
|
T | C | 113 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(110): Show | 113 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.627+14640T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42977774 | ||||||
| chr4:42977940
|
T | A | 1 | a0002c0002t0001g0222 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.627+14806T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42977940 | ||||||
| chr4:42978095
|
A | C | 15 | a0001c0001t0001g0012a0001c0001t0002g0014a0001c0001t0002g0020others(12): Show | 15 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.627+14961A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42978095 | ||||||
| chr4:42978161
|
A | G | 2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.627+15027A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42978161 | ||||||
| chr4:42978162
|
T | C | 1 | a0001c0001t0005g0211 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.627+15028T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42978162 | ||||||
| chr4:42978259
|
T | C | 113 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(110): Show | 113 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.627+15125T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42978259 | ||||||
| chr4:42978316
|
T | C | 11 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(8): Show | 11 | HG00140.hp2 NA18942.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.627+15182T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42978316 | ||||||
| chr4:42978346
|
T | C | 19 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(16): Show | 19 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.627+15212T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42978346 | ||||||
| chr4:42978442
|
A | G | 1 | a0001c0001t0001g0064 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.627+15308A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42978442 | ||||||
| chr4:42978570
|
A | C | 8 | a0001c0001t0002g0080a0001c0001t0003g0132a0001c0001t0003g0134others(5): Show | 8 | HG02074.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+15436A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42978570 | ||||||
| chr4:42978599
|
T | C | 21 | a0001c0001t0001g0012a0001c0001t0001g0075a0001c0001t0001g0212others(18): Show | 21 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.627+15465T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42978599 | ||||||
| chr4:42978624
|
A | G | 1 | a0002c0002t0001g0238 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.627+15490A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42978624 | ||||||
| chr4:42978635
|
T | G | 2 | a0001c0001t0002g0086a0003c0003t0002g0327 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.627+15501T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42978635 | ||||||
| chr4:42978824
|
C | G | 2 | a0001c0001t0002g0104a0001c0001t0008g0106 | 2 | HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.627+15690C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42978824 | ||||||
| chr4:42978828
|
CT | C | 20 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(17): Show | 20 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.627+15695delT | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42978828 | ||||||
| chr4:42978879
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.627+15745C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42978879 | ||||||
| chr4:42978915
|
C | T | 1 | a0001c0001t0004g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.627+15781C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42978915 | ||||||
| chr4:42978916
|
G | A | 1 | a0001c0004t0002g0087 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.627+15782G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42978916 | ||||||
| chr4:42979066
|
C | T | 8 | a0001c0001t0002g0080a0001c0001t0003g0132a0001c0001t0003g0134others(5): Show | 8 | HG02074.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+15932C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42979066 | ||||||
| chr4:42979074
|
CCT | C | 30 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(27): Show | 30 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.627+15948_627+1594 others(6): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42979074 | |||||
| chr4:42979093
|
C | T | 4 | a0002c0002t0001g0248a0002c0002t0001g0256a0002c0002t0001g0268others(1): Show | 4 | HG01433.hp2 HG02273.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+15959C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42979093 | ||||||
| chr4:42979176
|
C | T | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.627+16042C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42979176 | ||||||
| chr4:42979209
|
T | A | 21 | a0001c0001t0001g0012a0001c0001t0001g0075a0001c0001t0001g0212others(18): Show | 21 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.627+16075T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42979209 | ||||||
| chr4:42979295
|
A | G | 113 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(110): Show | 113 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.627+16161A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42979295 | ||||||
| chr4:42979306
|
T | C | 8 | a0001c0001t0002g0080a0001c0001t0003g0132a0001c0001t0003g0134others(5): Show | 8 | HG02074.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+16172T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42979306 | ||||||
| chr4:42979368
|
A | T | 167 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(164): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.627+16234A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42979368 | ||||||
| chr4:42979494
|
A | T | 307 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(304): Show | 307 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.627+16360A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42979494 | ||||||
| chr4:42979738
|
A | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0105 | 2 | NA18990.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.627+16604A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42979738 | ||||||
| chr4:42979748
|
T | A | 2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.627+16614T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42979748 | ||||||
| chr4:42979912
|
A | G | 1 | a0003c0003t0002g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.627+16778A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42979912 | ||||||
| chr4:42979986
|
A | G | 2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.627+16852A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42979986 | ||||||
| chr4:42980027
|
A | T | 5 | a0001c0001t0001g0125a0003c0003t0001g0286a0003c0003t0001g0287others(2): Show | 5 | NA18944.hp1 NA18964.hp1 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.627+16893A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42980027 | ||||||
| chr4:42980054
|
TC | T | 20 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(17): Show | 20 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.627+16922delC | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42980054 | |||||
| chr4:42980056
|
C | A | 130 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(127): Show | 130 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.627+16922C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42980056 | ||||||
| chr4:42980077
|
T | G | 1 | a0001c0001t0004g0197 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.627+16943T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42980077 | ||||||
| chr4:42980078
|
T | G | 1 | a0002c0002t0001g0255 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.627+16944T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42980078 | ||||||
| chr4:42980085
|
A | C | 1 | a0001c0001t0001g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.627+16951A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42980085 | ||||||
| chr4:42980186
|
G | T | 8 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0281others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+17052G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42980186 | ||||||
| chr4:42980237
|
G | A | 1 | a0003c0003t0001g0330 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.627+17103G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42980237 | ||||||
| chr4:42980257
|
CT | C | 50 | a0001c0001t0001g0034a0001c0001t0001g0111a0001c0001t0002g0021others(47): Show | 50 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.627+17126delT | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42980257 | |||||
| chr4:42980371
|
A | G | 111 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(108): Show | 111 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.627+17237A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42980371 | ||||||
| chr4:42980399
|
G | A | 3 | a0003c0003t0001g0313a0003c0003t0002g0297a0003c0003t0002g0334 | 3 | HG02922.hp1 HG03098.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.627+17265G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42980399 | ||||||
| chr4:42980443
|
A | G | 1 | a0001c0001t0005g0157 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.627+17309A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42980443 | ||||||
| chr4:42980484
|
T | A | 1 | a0002c0002t0001g0275 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.627+17350T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42980484 | ||||||
| chr4:42980491
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.627+17357A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42980491 | ||||||
| chr4:42980566
|
C | G | 11 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(8): Show | 11 | HG00140.hp2 NA18942.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.627+17432C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42980566 | ||||||
| chr4:42980633
|
G | A | 1 | a0002c0002t0001g0241 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.627+17499G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42980633 | ||||||
| chr4:42980661
|
C | T | 3 | a0001c0001t0002g0078a0001c0001t0002g0084a0003c0003t0002g0336 | 3 | HG02647.hp2 HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.627+17527C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42980661 | ||||||
| chr4:42980662
|
G | A | 2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.627+17528G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42980662 | ||||||
| chr4:42980725
|
C | T | 1 | a0003c0003t0001g0318 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.627+17591C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42980725 | ||||||
| chr4:42980776
|
C | A | 1 | a0001c0001t0003g0167 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.627+17642C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42980776 | ||||||
| chr4:42980888
|
C | T | 4 | a0001c0001t0002g0013a0001c0001t0002g0044a0003c0003t0001g0317others(1): Show | 4 | HG00639.hp2 HG02717.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+17754C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42980888 | ||||||
| chr4:42980960
|
G | GT | 15 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(12): Show | 15 | HG00140.hp2 HG01993.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.627+17836dupT | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42980960 | |||||
| chr4:42980960
|
G | GTT | 7 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0004g0155others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.627+17835_627+1783 others(6): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42980960 | |||||
| chr4:42980960
|
G | T | 2 | a0001c0001t0002g0086a0003c0003t0002g0327 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.627+17826G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42980960 | ||||||
| chr4:42980971
|
G | T | 1 | a0003c0003t0001g0295 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.627+17837G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42980971 | ||||||
| chr4:42980974
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.627+17840T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42980974 | ||||||
| chr4:42981046
|
T | C | 2 | a0001c0001t0002g0278a0001c0001t0005g0157 | 2 | HG01884.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.627+17912T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42981046 | ||||||
| chr4:42981099
|
C | T | 2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.627+17965C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42981099 | ||||||
| chr4:42981153
|
AT | A | 160 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(157): Show | 160 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.627+18032delT | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42981153 | |||||
| chr4:42981206
|
A | G | 2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.627+18072A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42981206 | ||||||
| chr4:42981207
|
T | C | 2 | a0001c0001t0002g0126a0001c0001t0002g0127 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.627+18073T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42981207 | ||||||
| chr4:42981256
|
A | G | 2 | a0001c0001t0002g0101a0001c0001t0002g0102 | 2 | NA18997.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.627+18122A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42981256 | ||||||
| chr4:42981271
|
C | G | 2 | a0001c0001t0002g0086a0003c0003t0002g0327 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.627+18137C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42981271 | ||||||
| chr4:42981390
|
G | T | 3 | a0001c0001t0001g0075a0001c0001t0002g0076a0001c0001t0004g0141 | 3 | HG01993.hp2 HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.627+18256G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42981390 | ||||||
| chr4:42981454
|
A | G | 2 | a0002c0002t0002g0229a0002c0002t0002g0230 | 2 | HG03831.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.627+18320A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42981454 | ||||||
| chr4:42981458
|
A | G | 19 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(16): Show | 19 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.627+18324A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42981458 | ||||||
| chr4:42981479
|
C | T | 113 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(110): Show | 113 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.627+18345C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42981479 | ||||||
| chr4:42981480
|
C | T | 2 | a0001c0001t0002g0081a0002c0002t0002g0266 | 2 | HG00544.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.627+18346C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42981480 | ||||||
| chr4:42981484
|
A | G | 2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.627+18350A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42981484 | ||||||
| chr4:42981488
|
C | T | 2 | a0001c0001t0002g0014a0001c0001t0004g0158 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.627+18354C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42981488 | ||||||
| chr4:42981567
|
G | C | 1 | a0002c0002t0001g0258 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.627+18433G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42981567 | ||||||
| chr4:42981616
|
A | T | 1 | a0002c0002t0001g0227 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.627+18482A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42981616 | ||||||
| chr4:42981628
|
T | C | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.627+18494T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42981628 | ||||||
| chr4:42981732
|
C | A | 16 | a0001c0001t0001g0012a0001c0001t0002g0014a0001c0001t0002g0020others(13): Show | 16 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.627+18598C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42981732 | ||||||
| chr4:42981771
|
T | C | 8 | a0001c0001t0002g0080a0001c0001t0003g0132a0001c0001t0003g0134others(5): Show | 8 | HG02074.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+18637T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42981771 | ||||||
| chr4:42981877
|
G | T | 22 | a0001c0001t0001g0012a0001c0001t0001g0075a0001c0001t0001g0212others(19): Show | 22 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.627+18743G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42981877 | ||||||
| chr4:42981909
|
C | G | 1 | a0002c0002t0001g0220 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.627+18775C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42981909 | ||||||
| chr4:42981978
|
C | A | 2 | a0001c0001t0002g0086a0003c0003t0002g0327 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.627+18844C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42981978 | ||||||
| chr4:42982055
|
C | CT | 144 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(141): Show | 144 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.627+18933dupT | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42982055 | |||||
| chr4:42982144
|
C | T | 2 | a0001c0001t0002g0014a0001c0001t0004g0158 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.627+19010C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42982144 | ||||||
| chr4:42982199
|
T | C | 1 | a0002c0002t0001g0231 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.627+19065T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42982199 | ||||||
| chr4:42982302
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.627+19168G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42982302 | ||||||
| chr4:42982370
|
A | G | 2 | a0001c0001t0002g0086a0003c0003t0002g0327 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.627+19236A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42982370 | ||||||
| chr4:42982386
|
C | T | 2 | a0001c0001t0002g0086a0003c0003t0002g0327 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.627+19252C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42982386 | ||||||
| chr4:42982417
|
G | C | 2 | a0001c0001t0002g0086a0003c0003t0002g0327 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.627+19283G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42982417 | ||||||
| chr4:42982424
|
A | G | 1 | a0003c0003t0002g0301 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.627+19290A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42982424 | ||||||
| chr4:42982490
|
A | G | 2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.627+19356A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42982490 | ||||||
| chr4:42982517
|
C | G | 8 | a0001c0001t0002g0080a0001c0001t0003g0132a0001c0001t0003g0134others(5): Show | 8 | HG02074.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+19383C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42982517 | ||||||
| chr4:42982517
|
C | T | 1 | a0001c0001t0001g0034 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.627+19383C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42982517 | ||||||
| chr4:42982691
|
G | A | 16 | a0001c0001t0001g0019a0001c0001t0001g0056a0001c0001t0001g0071others(13): Show | 16 | HG00140.hp1 HG00438.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.627+19557G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42982691 | ||||||
| chr4:42982730
|
T | C | 2 | a0001c0001t0002g0014a0001c0001t0004g0158 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.627+19596T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42982730 | ||||||
| chr4:42982733
|
T | C | 1 | a0002c0002t0001g0237 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.627+19599T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42982733 | ||||||
| chr4:42982740
|
T | C | 2 | a0001c0001t0002g0278a0001c0001t0005g0157 | 2 | HG01884.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.627+19606T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42982740 | ||||||
| chr4:42982882
|
C | T | 12 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(9): Show | 12 | HG00140.hp2 NA18942.hp2 NA18946.hp1 others(9): Show |
intron_variant | MODIFIER | c.627+19748C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42982882 | ||||||
| chr4:42982922
|
T | A | 19 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(16): Show | 19 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.627+19788T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42982922 | ||||||
| chr4:42982996
|
T | G | 1 | a0003c0003t0001g0295 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.627+19862T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42982996 | ||||||
| chr4:42983051
|
T | G | 1 | a0002c0002t0001g0221 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.627+19917T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42983051 | ||||||
| chr4:42983072
|
T | C | 5 | a0001c0001t0001g0090a0001c0001t0001g0285a0003c0003t0001g0326others(2): Show | 5 | HG02895.hp1 HG03041.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.627+19938T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42983072 | ||||||
| chr4:42983073
|
G | A | 4 | a0001c0001t0001g0090a0001c0001t0001g0285a0003c0003t0001g0326others(1): Show | 4 | HG02895.hp1 HG03041.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+19939G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42983073 | ||||||
| chr4:42983077
|
A | T | 2 | a0003c0003t0001g0298a0003c0003t0001g0338 | 2 | NA18949.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.627+19943A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42983077 | ||||||
| chr4:42983132
|
T | C | 24 | a0001c0001t0001g0012a0001c0001t0001g0075a0001c0001t0001g0082others(21): Show | 24 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.627+19998T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42983132 | ||||||
| chr4:42983152
|
A | T | 74 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0045others(71): Show | 74 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.627+20018A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42983152 | ||||||
| chr4:42983156
|
C | T | 2 | a0002c0002t0001g0245a0002c0002t0002g0270 | 2 | NA19004.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.627+20022C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42983156 | ||||||
| chr4:42983182
|
G | T | 111 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(108): Show | 111 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.627+20048G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42983182 | ||||||
| chr4:42983199
|
G | T | 3 | a0001c0001t0001g0082a0001c0001t0002g0081a0001c0001t0003g0144 | 3 | HG01891.hp2 HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.627+20065G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42983199 | ||||||
| chr4:42983240
|
T | A | 1 | a0001c0001t0004g0166 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.627+20106T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42983240 | ||||||
| chr4:42983331
|
G | C | 8 | a0001c0001t0001g0082a0001c0001t0002g0020a0001c0001t0002g0022others(5): Show | 8 | HG01891.hp2 HG02615.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.627+20197G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42983331 | ||||||
| chr4:42983367
|
G | T | 8 | a0001c0001t0001g0082a0001c0001t0002g0020a0001c0001t0002g0022others(5): Show | 8 | HG01891.hp2 HG02615.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.627+20233G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42983367 | ||||||
| chr4:42983372
|
G | A | 1 | a0001c0001t0002g0282 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.627+20238G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42983372 | ||||||
| chr4:42983373
|
C | T | 2 | a0001c0001t0002g0278a0001c0001t0005g0157 | 2 | HG01884.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.627+20239C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42983373 | ||||||
| chr4:42983435
|
A | G | 2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.627+20301A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42983435 | ||||||
| chr4:42983521
|
A | G | 1 | a0002c0002t0002g0271 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.627+20387A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42983521 | ||||||
| chr4:42983599
|
A | T | 1 | a0003c0003t0002g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.627+20465A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42983599 | ||||||
| chr4:42983646
|
C | A | 1 | a0002c0002t0001g0247 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.627+20512C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42983646 | ||||||
| chr4:42983741
|
T | C | 1 | a0002c0002t0002g0270 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.627+20607T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42983741 | ||||||
| chr4:42983776
|
C | A | 2 | a0001c0001t0004g0179a0001c0001t0004g0180 | 2 | HG00609.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.627+20642C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42983776 | ||||||
| chr4:42983784
|
T | C | 1 | a0001c0001t0004g0206 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.627+20650T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42983784 | ||||||
| chr4:42983787
|
T | C | 1 | a0001c0001t0004g0206 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.627+20653T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42983787 | ||||||
| chr4:42983788
|
C | T | 1 | a0001c0001t0004g0206 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.627+20654C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42983788 | ||||||
| chr4:42983838
|
C | CT | 7 | a0001c0001t0001g0075a0001c0001t0001g0116a0001c0001t0001g0146others(4): Show | 7 | HG01993.hp2 HG02145.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.627+20719dupT | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42983838 | |||||
| chr4:42983838
|
C | CTT | 20 | a0001c0001t0001g0012a0001c0001t0001g0082a0001c0001t0002g0014others(17): Show | 20 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.627+20718_627+2071 others(6): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42983838 | |||||
| chr4:42983838
|
CT | C | 83 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(80): Show | 83 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.627+20719delT | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42983838 | |||||
| chr4:42983872
|
G | A | 1 | a0001c0001t0006g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.627+20738G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42983872 | ||||||
| chr4:42983956
|
T | C | 167 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(164): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.627+20822T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42983956 | ||||||
| chr4:42983962
|
G | A | 1 | a0001c0001t0002g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.627+20828G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42983962 | ||||||
| chr4:42984052
|
T | C | 2 | a0001c0001t0002g0086a0003c0003t0002g0327 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.627+20918T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42984052 | ||||||
| chr4:42984056
|
G | A | 1 | a0003c0003t0001g0320 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.627+20922G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42984056 | ||||||
| chr4:42984106
|
G | C | 16 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0003g0208others(13): Show | 16 | HG02027.hp1 HG02056.hp1 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.627+20972G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42984106 | ||||||
| chr4:42984130
|
C | T | 6 | a0001c0001t0004g0168a0001c0001t0004g0169a0001c0001t0004g0170others(3): Show | 6 | HG00323.hp2 HG01978.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.627+20996C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42984130 | ||||||
| chr4:42984185
|
G | A | 1 | a0002c0002t0002g0225 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.627+21051G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42984185 | ||||||
| chr4:42984220
|
C | T | 1 | a0002c0002t0002g0225 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.627+21086C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42984220 | ||||||
| chr4:42984236
|
T | C | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.627+21102T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42984236 | ||||||
| chr4:42984260
|
T | A | 121 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(118): Show | 121 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.627+21126T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42984260 | ||||||
| chr4:42984649
|
C | T | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.627+21515C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42984649 | ||||||
| chr4:42984848
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.627+21714C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42984848 | ||||||
| chr4:42984897
|
C | T | 2 | a0001c0001t0004g0165a0003c0003t0002g0322 | 2 | HG00733.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.627+21763C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42984897 | ||||||
| chr4:42984902
|
C | T | 111 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(108): Show | 111 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.627+21768C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42984902 | ||||||
| chr4:42985193
|
G | A | 80 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(77): Show | 80 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.627+22059G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42985193 | ||||||
| chr4:42985204
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.627+22070C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42985204 | ||||||
| chr4:42985213
|
C | T | 1 | a0001c0001t0001g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.627+22079C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42985213 | ||||||
| chr4:42985270
|
C | T | 2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.627+22136C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42985270 | ||||||
| chr4:42985294
|
G | A | 1 | a0001c0001t0002g0037 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.627+22160G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42985294 | ||||||
| chr4:42985635
|
A | T | 4 | a0001c0001t0002g0013a0001c0001t0002g0044a0003c0003t0001g0317others(1): Show | 4 | HG00639.hp2 HG02717.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+22501A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42985635 | ||||||
| chr4:42985676
|
T | C | 1 | a0003c0003t0002g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.627+22542T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42985676 | ||||||
| chr4:42985873
|
T | C | 1 | a0001c0001t0002g0043 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.627+22739T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42985873 | ||||||
| chr4:42986014
|
C | A | 1 | a0001c0001t0002g0107 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.627+22880C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42986014 | ||||||
| chr4:42986228
|
T | C | 3 | a0001c0001t0004g0142a0003c0003t0002g0291a0003c0003t0002g0302 | 3 | HG02109.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.627+23094T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42986228 | ||||||
| chr4:42986275
|
A | C | 8 | a0001c0001t0002g0080a0001c0001t0003g0132a0001c0001t0003g0134others(5): Show | 8 | HG02074.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+23141A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42986275 | ||||||
| chr4:42986318
|
C | G | 2 | a0001c0001t0004g0155a0001c0001t0004g0156 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.627+23184C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42986318 | ||||||
| chr4:42986324
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.627+23190G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42986324 | ||||||
| chr4:42986357
|
T | A | 167 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(164): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.627+23223T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42986357 | ||||||
| chr4:42986393
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.627+23259G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42986393 | ||||||
| chr4:42986410
|
C | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0069 | 2 | HG00735.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.627+23276C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42986410 | ||||||
| chr4:42986474
|
C | A | 111 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(108): Show | 111 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.627+23340C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42986474 | ||||||
| chr4:42986542
|
C | T | 1 | a0001c0001t0004g0147 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.627+23408C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42986542 | ||||||
| chr4:42986768
|
A | C | 30 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(27): Show | 30 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.627+23634A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42986768 | ||||||
| chr4:42987002
|
A | ATG | 20 | a0001c0001t0001g0017a0001c0001t0001g0095a0001c0001t0001g0100others(17): Show | 20 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.627+23898_627+2389 others(6): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42987002 | |||||
| chr4:42987002
|
A | ATGTG | 67 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(64): Show | 67 | HG00140.hp1 HG00438.hp1 HG01106.hp2 others(64): Show |
intron_variant | MODIFIER | c.627+23896_627+2389 others(8): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42987002 | |||||
| chr4:42987002
|
A | ATGTGTG | 36 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(33): Show | 36 | HG00323.hp1 HG00733.hp2 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.627+23894_627+2389 others(10): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42987002 | |||||
| chr4:42987002
|
A | ATGTGTGT others(1): Show |
23 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(20): Show | 23 | HG00140.hp2 HG02027.hp1 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.627+23892_627+2389 others(12): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42987002 | |||||
| chr4:42987002
|
A | ATGTGTGT others(3): Show |
2 | a0001c0001t0001g0064a0003c0003t0002g0300 | 2 | NA19006.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.627+23890_627+2389 others(14): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42987002 | |||||
| chr4:42987002
|
A | G | 3 | a0001c0001t0004g0142a0003c0003t0002g0291a0003c0003t0002g0302 | 3 | HG02109.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.627+23868A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987002 | ||||||
| chr4:42987002
|
ATG | A | 6 | a0001c0001t0001g0075a0001c0001t0001g0212a0001c0001t0002g0076others(3): Show | 6 | HG01981.hp1 HG01993.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.627+23898_627+2389 others(6): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42987002 | |||||
| chr4:42987002
|
ATGTG | A | 6 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0044others(3): Show | 6 | HG00639.hp2 HG02615.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.627+23896_627+2389 others(8): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42987002 | |||||
| chr4:42987002
|
ATGTGTG | A | 21 | a0001c0001t0001g0012a0001c0001t0001g0082a0001c0001t0002g0020others(18): Show | 21 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.627+23894_627+2389 others(10): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42987002 | |||||
| chr4:42987036
|
A | T | 2 | a0001c0001t0002g0086a0003c0003t0002g0327 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.627+23902A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987036 | ||||||
| chr4:42987069
|
G | A | 22 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(19): Show | 22 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.627+23935G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987069 | ||||||
| chr4:42987201
|
C | A | 24 | a0001c0001t0001g0012a0001c0001t0001g0075a0001c0001t0001g0082others(21): Show | 24 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.627+24067C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987201 | ||||||
| chr4:42987211
|
TTATATAT others(35): Show |
T | 110 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(107): Show | 110 | HG00323.hp1 HG00438.hp1 HG00733.hp2 others(107): Show |
intron_variant | MODIFIER | c.627+24086_627+2412 others(46): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42987211 | |||||
| chr4:42987217
|
ATATAT | A | 7 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0281others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.627+24089_627+2409 others(9): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42987217 | |||||
| chr4:42987219
|
ATATTATA others(32): Show |
A | 9 | a0001c0001t0001g0056a0001c0001t0001g0121a0001c0001t0003g0135others(6): Show | 9 | HG00140.hp1 HG01346.hp1 HG04228.hp2 others(6): Show |
intron_variant | MODIFIER | c.627+24086_627+2412 others(43): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987219 | ||||||
| chr4:42987222
|
T | TATATATA others(9): Show |
1 | a0002c0002t0001g0272 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.627+24088_627+2408 others(20): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987222 | ||||||
| chr4:42987222
|
T | TATATTAT others(3): Show |
2 | a0001c0001t0001g0012a0001c0001t0002g0278 | 2 | HG01884.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.627+24088_627+2408 others(14): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987222 | ||||||
| chr4:42987222
|
T | TATTATAT others(8): Show |
13 | a0001c0001t0001g0111a0001c0001t0002g0001a0001c0001t0002g0002others(10): Show | 13 | HG01167.hp2 HG02027.hp2 HG02273.hp1 others(10): Show |
intron_variant | MODIFIER | c.627+24088_627+2408 others(19): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987222 | ||||||
| chr4:42987222
|
T | TATTATAT others(10): Show |
65 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0067others(62): Show | 65 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.627+24088_627+2408 others(21): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987222 | ||||||
| chr4:42987222
|
T | TATTATAT others(41): Show |
1 | a0002c0002t0001g0221 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.627+24088_627+2408 others(52): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987222 | ||||||
| chr4:42987222
|
T | TTATATAT others(4): Show |
17 | a0001c0001t0001g0082a0001c0001t0002g0014a0001c0001t0002g0020others(14): Show | 17 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.627+24096_627+2410 others(15): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42987222 | |||||
| chr4:42987222
|
T | TTATATAT others(6): Show |
29 | a0001c0001t0001g0058a0001c0001t0002g0013a0001c0001t0002g0033others(26): Show | 29 | HG00621.hp2 HG00639.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.627+24095_627+2410 others(17): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42987222 | |||||
| chr4:42987222
|
T | TTATATAT others(8): Show |
46 | a0001c0001t0001g0034a0001c0001t0001g0045a0001c0001t0002g0021others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.627+24093_627+2410 others(19): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42987222 | |||||
| chr4:42987222
|
T | TTATATAT others(48): Show |
1 | a0004c0007t0002g0114 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.627+24107_627+2410 others(59): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42987222 | |||||
| chr4:42987222
|
T | TTATATAT others(6): Show |
3 | a0001c0001t0001g0075a0001c0001t0002g0076a0001c0001t0004g0141 | 3 | HG01993.hp2 HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.627+24096_627+2409 others(17): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42987222 | |||||
| chr4:42987229
|
T | A | 1 | a0002c0002t0002g0225 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.627+24095T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987229 | ||||||
| chr4:42987229
|
TTATATAT others(15): Show |
T | 11 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(8): Show | 11 | HG00140.hp2 NA18942.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.627+24106_627+2412 others(26): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42987229 | |||||
| chr4:42987230
|
T | A | 1 | a0002c0002t0001g0221 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.627+24096T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987230 | ||||||
| chr4:42987231
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0004g0162 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.627+24107_627+2410 others(17): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42987231 | |||||
| chr4:42987231
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.627+24097A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987231 | ||||||
| chr4:42987236
|
TATATAAT others(6): Show |
T | 6 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0281others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.627+24103_627+2411 others(17): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987236 | ||||||
| chr4:42987236
|
TATATAAT others(8): Show |
T | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.627+24103_627+2411 others(19): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987236 | ||||||
| chr4:42987239
|
A | T | 2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.627+24105A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987239 | ||||||
| chr4:42987240
|
T | A | 2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.627+24106T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987240 | ||||||
| chr4:42987240
|
T | C | 3 | a0001c0001t0001g0075a0001c0001t0002g0076a0001c0001t0004g0141 | 3 | HG01993.hp2 HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.627+24106T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987240 | ||||||
| chr4:42987241
|
A | AATATATA others(35): Show |
1 | a0001c0001t0002g0078 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.627+24114_627+2411 others(46): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42987241 | |||||
| chr4:42987241
|
A | AATATATA others(37): Show |
2 | a0001c0001t0002g0084a0003c0003t0002g0336 | 2 | HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.627+24114_627+2411 others(48): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42987241 | |||||
| chr4:42987241
|
A | T | 4 | a0001c0001t0002g0050a0001c0001t0002g0062a0003c0003t0002g0297others(1): Show | 4 | HG01243.hp2 HG01361.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.627+24107A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987241 | ||||||
| chr4:42987242
|
A | T | 3 | a0001c0001t0001g0212a0001c0001t0004g0155a0001c0001t0004g0156 | 3 | HG02145.hp2 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.627+24108A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987242 | ||||||
| chr4:42987248
|
A | ATATACAA others(3): Show |
1 | a0001c0001t0001g0212 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.627+24114_627+2411 others(14): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987248 | ||||||
| chr4:42987248
|
A | T | 4 | a0001c0001t0002g0086a0003c0003t0002g0297a0003c0003t0002g0327others(1): Show | 4 | HG02559.hp1 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.627+24114A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987248 | ||||||
| chr4:42987249
|
A | T | 2 | a0001c0001t0004g0155a0001c0001t0004g0156 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.627+24115A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987249 | ||||||
| chr4:42987260
|
T | A | 4 | a0001c0001t0001g0075a0001c0001t0002g0076a0001c0001t0004g0141others(1): Show | 4 | HG01993.hp2 HG02630.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.627+24126T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987260 | ||||||
| chr4:42987260
|
TA | T | 9 | a0001c0001t0001g0056a0001c0001t0001g0121a0001c0001t0003g0135others(6): Show | 9 | HG00140.hp1 HG01346.hp1 HG04228.hp2 others(6): Show |
intron_variant | MODIFIER | c.627+24128delA | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42987260 | |||||
| chr4:42987261
|
A | AAT | 26 | a0001c0001t0001g0111a0001c0001t0002g0021a0001c0001t0002g0026others(23): Show | 26 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.627+24143_627+2414 others(6): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42987261 | |||||
| chr4:42987261
|
A | T | 12 | a0001c0001t0001g0075a0001c0001t0002g0030a0001c0001t0002g0031others(9): Show | 12 | HG01167.hp1 HG01169.hp2 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.627+24127A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987261 | ||||||
| chr4:42987262
|
A | T | 2 | a0001c0001t0002g0054a0001c0001t0010g0284 | 2 | HG03669.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.627+24128A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987262 | ||||||
| chr4:42987273
|
T | G | 1 | a0003c0005t0002g0332 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.627+24139T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987273 | ||||||
| chr4:42987275
|
T | G | 15 | a0001c0001t0001g0039a0001c0001t0001g0061a0001c0001t0001g0067others(12): Show | 15 | HG00673.hp1 HG01070.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.627+24141T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987275 | ||||||
| chr4:42987275
|
T | TAG | 8 | a0001c0001t0001g0034a0001c0001t0002g0042a0001c0001t0003g0153others(5): Show | 8 | HG02273.hp1 NA18941.hp2 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.627+24142_627+2414 others(6): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42987275 | |||||
| chr4:42987275
|
T | TAGAGAGA others(5): Show |
1 | a0002c0002t0002g0225 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.627+24142_627+2414 others(16): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42987275 | |||||
| chr4:42987277
|
T | G | 100 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0023others(97): Show | 100 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.627+24143T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987277 | ||||||
| chr4:42987277
|
T | TAG | 21 | a0001c0001t0001g0015a0001c0001t0002g0041a0001c0001t0002g0057others(18): Show | 21 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(18): Show |
intron_variant | MODIFIER | c.627+24165_627+2416 others(6): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42987277 | |||||
| chr4:42987279
|
G | T | 95 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0017others(92): Show | 95 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.627+24145G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987279 | ||||||
| chr4:42987281
|
G | T | 8 | a0001c0001t0001g0123a0001c0001t0002g0054a0001c0001t0002g0081others(5): Show | 8 | HG02572.hp1 HG02717.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+24147G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987281 | ||||||
| chr4:42987283
|
G | T | 1 | a0003c0003t0001g0317 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.627+24149G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987283 | ||||||
| chr4:42987360
|
G | A | 3 | a0001c0001t0002g0078a0001c0001t0002g0084a0003c0003t0002g0336 | 3 | HG02647.hp2 HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.627+24226G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987360 | ||||||
| chr4:42987471
|
G | A | 5 | a0001c0001t0001g0015a0001c0001t0002g0001a0001c0001t0002g0002others(2): Show | 5 | HG01167.hp2 HG03041.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.627+24337G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987471 | ||||||
| chr4:42987474
|
G | C | 9 | a0001c0001t0002g0014a0001c0001t0002g0126a0001c0001t0002g0127others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.627+24340G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987474 | ||||||
| chr4:42987804
|
A | G | 7 | a0001c0001t0002g0013a0001c0001t0002g0044a0001c0001t0004g0142others(4): Show | 7 | HG00639.hp2 HG02109.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.627+24670A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987804 | ||||||
| chr4:42987819
|
T | C | 8 | a0001c0001t0002g0080a0001c0001t0003g0132a0001c0001t0003g0134others(5): Show | 8 | HG02074.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+24685T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987819 | ||||||
| chr4:42987828
|
C | T | 2 | a0003c0003t0002g0297a0003c0003t0002g0334 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.627+24694C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987828 | ||||||
| chr4:42987866
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.627+24732T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987866 | ||||||
| chr4:42987918
|
C | T | 3 | a0001c0001t0004g0142a0003c0003t0002g0291a0003c0003t0002g0302 | 3 | HG02109.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.627+24784C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42987918 | ||||||
| chr4:42988365
|
A | C | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.627+25231A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42988365 | ||||||
| chr4:42988392
|
G | C | 2 | a0001c0001t0002g0078a0003c0003t0002g0336 | 2 | HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.627+25258G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42988392 | ||||||
| chr4:42988530
|
C | T | 1 | a0003c0003t0001g0317 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.627+25396C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42988530 | ||||||
| chr4:42988602
|
G | T | 120 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 120 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.627+25468G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42988602 | ||||||
| chr4:42988615
|
A | G | 8 | a0001c0001t0002g0080a0001c0001t0003g0132a0001c0001t0003g0134others(5): Show | 8 | HG02074.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+25481A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42988615 | ||||||
| chr4:42988733
|
A | G | 17 | a0001c0001t0001g0012a0001c0001t0001g0075a0001c0001t0001g0082others(14): Show | 17 | HG01884.hp1 HG01891.hp2 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.627+25599A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42988733 | ||||||
| chr4:42989086
|
G | A | 2 | a0001c0001t0004g0155a0001c0001t0004g0156 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.627+25952G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42989086 | ||||||
| chr4:42989149
|
G | A | 9 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.627+26015G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42989149 | ||||||
| chr4:42989417
|
T | A | 17 | a0001c0001t0001g0012a0001c0001t0001g0075a0001c0001t0001g0082others(14): Show | 17 | HG01884.hp1 HG01891.hp2 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.627+26283T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42989417 | ||||||
| chr4:42989437
|
G | A | 8 | a0002c0002t0001g0243a0002c0002t0001g0248a0002c0002t0001g0252others(5): Show | 8 | HG00673.hp2 HG01433.hp2 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.627+26303G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42989437 | ||||||
| chr4:42989523
|
C | T | 50 | a0001c0001t0001g0034a0001c0001t0001g0111a0001c0001t0002g0021others(47): Show | 50 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.627+26389C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42989523 | ||||||
| chr4:42989605
|
G | A | 7 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(4): Show | 7 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.627+26471G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42989605 | ||||||
| chr4:42989987
|
T | C | 9 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.627+26853T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42989987 | ||||||
| chr4:42990012
|
T | C | 9 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.627+26878T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42990012 | ||||||
| chr4:42990082
|
A | G | 1 | a0003c0003t0001g0318 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.627+26948A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42990082 | ||||||
| chr4:42990132
|
T | C | 1 | a0001c0001t0002g0054 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.627+26998T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42990132 | ||||||
| chr4:42990139
|
T | G | 1 | a0001c0001t0002g0126 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.627+27005T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42990139 | ||||||
| chr4:42990142
|
T | A | 2 | a0001c0001t0002g0086a0003c0003t0002g0327 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.627+27008T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42990142 | ||||||
| chr4:42990170
|
G | GTTATTTT others(3): Show |
1 | a0003c0003t0001g0299 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.627+27038_627+2703 others(14): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42990170 | |||||
| chr4:42990173
|
C | CT | 14 | a0001c0001t0001g0058a0001c0001t0002g0007a0001c0001t0002g0038others(11): Show | 14 | HG00423.hp2 HG00733.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.627+27075dupT | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42990173 | |||||
| chr4:42990173
|
C | CTT | 12 | a0001c0001t0002g0031a0001c0001t0002g0033a0001c0001t0002g0036others(9): Show | 12 | HG00438.hp2 HG00621.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.627+27074_627+2707 others(6): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42990173 | |||||
| chr4:42990173
|
C | CTTTT | 6 | a0001c0001t0004g0142a0001c0001t0004g0155a0001c0001t0004g0156others(3): Show | 6 | HG02572.hp2 HG03130.hp2 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.627+27072_627+2707 others(8): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42990173 | |||||
| chr4:42990173
|
C | CTTTTTTT others(3): Show |
5 | a0001c0001t0001g0109a0002c0002t0001g0236a0002c0002t0001g0237others(2): Show | 5 | HG00639.hp1 NA18997.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.627+27066_627+2707 others(14): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42990173 | |||||
| chr4:42990173
|
C | CTTTTTTT others(4): Show |
10 | a0001c0001t0001g0067a0001c0001t0002g0084a0002c0002t0001g0221others(7): Show | 10 | HG01255.hp2 HG01346.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.627+27065_627+2707 others(15): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42990173 | |||||
| chr4:42990173
|
C | CTTTTTTT others(5): Show |
16 | a0001c0001t0001g0124a0001c0001t0002g0001a0001c0001t0002g0021others(13): Show | 16 | HG00673.hp2 HG01071.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.627+27064_627+2707 others(16): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42990173 | |||||
| chr4:42990173
|
C | CTTTTTTT others(6): Show |
15 | a0001c0001t0002g0028a0001c0001t0002g0042a0001c0001t0002g0057others(12): Show | 15 | HG00323.hp2 HG00673.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.627+27063_627+2707 others(17): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42990173 | |||||
| chr4:42990173
|
C | CTTTTTTT others(7): Show |
8 | a0001c0001t0002g0002a0001c0001t0004g0131a0001c0001t0004g0162others(5): Show | 8 | HG01975.hp2 HG01978.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+27062_627+2707 others(18): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42990173 | |||||
| chr4:42990173
|
C | CTTTTTTT others(8): Show |
9 | a0001c0001t0001g0034a0001c0001t0002g0041a0001c0001t0002g0078others(6): Show | 9 | HG00544.hp1 HG00609.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.627+27061_627+2707 others(19): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42990173 | |||||
| chr4:42990173
|
C | CTTTTTTT others(9): Show |
3 | a0001c0001t0004g0171a0001c0001t0004g0207a0001c0001t0004g0210 | 3 | NA18984.hp1 NA19009.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.627+27060_627+2707 others(20): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42990173 | |||||
| chr4:42990173
|
C | CTTTTTTT others(10): Show |
6 | a0001c0001t0002g0026a0001c0001t0003g0151a0001c0001t0004g0179others(3): Show | 6 | HG00609.hp2 HG02015.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.627+27059_627+2707 others(21): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42990173 | |||||
| chr4:42990173
|
C | CTTTTTTT others(11): Show |
3 | a0002c0002t0001g0213a0002c0002t0001g0216a0002c0002t0001g0250 | 3 | HG02083.hp1 NA18943.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.627+27058_627+2707 others(22): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42990173 | |||||
| chr4:42990173
|
C | CTTTTTTT others(12): Show |
5 | a0001c0001t0003g0149a0002c0002t0001g0218a0002c0002t0001g0224others(2): Show | 5 | HG00621.hp1 HG03688.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.627+27057_627+2707 others(23): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42990173 | |||||
| chr4:42990173
|
C | CTTTTTTT others(13): Show |
4 | a0001c0001t0001g0015a0001c0001t0003g0185a0002c0002t0001g0220others(1): Show | 4 | HG00423.hp1 HG02523.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+27056_627+2707 others(24): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42990173 | |||||
| chr4:42990173
|
C | CTTTTTTT others(14): Show |
1 | a0002c0002t0001g0217 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.627+27055_627+2707 others(25): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42990173 | |||||
| chr4:42990173
|
C | CTTTTTTT others(15): Show |
2 | a0001c0001t0004g0147a0001c0001t0004g0152 | 2 | NA18941.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.627+27054_627+2707 others(26): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42990173 | |||||
| chr4:42990173
|
C | CTTTTTTT others(17): Show |
1 | a0001c0001t0004g0204 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.627+27052_627+2707 others(28): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42990173 | |||||
| chr4:42990173
|
C | T | 1 | a0003c0003t0001g0299 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.627+27039C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42990173 | ||||||
| chr4:42990173
|
CT | C | 11 | a0001c0001t0001g0039a0001c0001t0001g0061a0001c0001t0001g0064others(8): Show | 11 | HG00140.hp2 NA18942.hp2 NA18948.hp1 others(8): Show |
intron_variant | MODIFIER | c.627+27075delT | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42990173 | |||||
| chr4:42990173
|
CTT | C | 6 | a0001c0001t0002g0101a0001c0001t0002g0102a0001c0001t0003g0202others(3): Show | 6 | HG02717.hp2 NA18977.hp2 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.627+27074_627+2707 others(6): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42990173 | |||||
| chr4:42990173
|
CTTTT | C | 8 | a0001c0001t0002g0083a0002c0002t0001g0228a0002c0002t0001g0259others(5): Show | 8 | HG01243.hp1 HG01891.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.627+27072_627+2707 others(8): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42990173 | |||||
| chr4:42990173
|
CTTTTT | C | 12 | a0001c0001t0002g0047a0001c0001t0002g0065a0001c0001t0002g0126others(9): Show | 12 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.627+27071_627+2707 others(9): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42990173 | |||||
| chr4:42990173
|
CTTTTTTT others(2): Show |
C | 7 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0003g0132others(4): Show | 7 | HG02074.hp1 HG02572.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.627+27067_627+2707 others(13): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42990173 | |||||
| chr4:42990173
|
CTTTTTTT others(3): Show |
C | 24 | a0001c0001t0001g0045a0001c0001t0001g0069a0001c0001t0001g0071others(21): Show | 24 | HG00438.hp1 HG00735.hp1 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.627+27066_627+2707 others(14): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42990173 | |||||
| chr4:42990173
|
CTTTTTTT others(4): Show |
C | 87 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(84): Show | 87 | HG00140.hp1 HG01109.hp2 HG01192.hp2 others(84): Show |
intron_variant | MODIFIER | c.627+27065_627+2707 others(15): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42990173 | |||||
| chr4:42990173
|
CTTTTTTT others(5): Show |
C | 13 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(10): Show | 13 | HG00323.hp1 HG00733.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.627+27064_627+2707 others(16): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42990173 | |||||
| chr4:42990173
|
CTTTTTTT others(6): Show |
C | 6 | a0001c0001t0001g0075a0001c0001t0001g0212a0001c0001t0002g0076others(3): Show | 6 | HG01993.hp2 HG02145.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.627+27063_627+2707 others(17): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42990173 | |||||
| chr4:42990173
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0003g0182 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.627+27062_627+2707 others(18): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42990173 | |||||
| chr4:42990173
|
CTTTTTTT others(8): Show |
C | 1 | a0002c0002t0001g0257 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.627+27061_627+2707 others(19): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42990173 | |||||
| chr4:42990173
|
CTTTTTTT others(15): Show |
C | 1 | a0002c0002t0001g0276 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.627+27054_627+2707 others(26): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42990173 | |||||
| chr4:42990249
|
T | C | 1 | a0001c0001t0002g0108 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.627+27115T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42990249 | ||||||
| chr4:42990278
|
G | A | 17 | a0001c0001t0001g0012a0001c0001t0001g0075a0001c0001t0001g0082others(14): Show | 17 | HG01884.hp1 HG01891.hp2 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.627+27144G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42990278 | ||||||
| chr4:42990340
|
C | T | 3 | a0003c0003t0001g0313a0003c0003t0001g0315a0003c0003t0001g0316 | 3 | HG02056.hp1 HG02165.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.627+27206C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42990340 | ||||||
| chr4:42990341
|
G | A | 1 | a0001c0001t0005g0157 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.627+27207G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42990341 | ||||||
| chr4:42990412
|
C | G | 1 | a0001c0001t0002g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.627+27278C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42990412 | ||||||
| chr4:42990443
|
G | A | 20 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(17): Show | 20 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.627+27309G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42990443 | ||||||
| chr4:42990658
|
T | C | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.627+27524T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42990658 | ||||||
| chr4:42990715
|
AC | A | 5 | a0001c0001t0001g0067a0002c0002t0001g0222a0002c0002t0001g0223others(2): Show | 5 | HG01070.hp2 HG01255.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.627+27584delC | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42990715 | |||||
| chr4:42990794
|
A | G | 1 | a0003c0003t0001g0299 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.627+27660A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42990794 | ||||||
| chr4:42990799
|
T | C | 1 | a0002c0002t0001g0273 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.627+27665T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42990799 | ||||||
| chr4:42990850
|
C | T | 1 | a0003c0003t0002g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.627+27716C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42990850 | ||||||
| chr4:42990864
|
A | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0069 | 2 | HG00735.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.627+27730A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42990864 | ||||||
| chr4:42990907
|
C | A | 119 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(116): Show | 119 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.627+27773C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42990907 | ||||||
| chr4:42990982
|
A | G | 9 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.627+27848A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42990982 | ||||||
| chr4:42991236
|
C | T | 167 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(164): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.627+28102C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42991236 | ||||||
| chr4:42991281
|
C | T | 1 | a0001c0001t0006g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.627+28147C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42991281 | ||||||
| chr4:42991331
|
A | G | 19 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(16): Show | 19 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.627+28197A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42991331 | ||||||
| chr4:42991344
|
A | C | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.627+28210A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42991344 | ||||||
| chr4:42991352
|
T | C | 1 | a0003c0003t0002g0297 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.627+28218T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42991352 | ||||||
| chr4:42991473
|
C | CAT | 54 | a0001c0001t0001g0034a0001c0001t0001g0111a0001c0001t0002g0021others(51): Show | 54 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.627+28356_627+2835 others(6): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 42991473 | |||||
| chr4:42991514
|
T | G | 4 | a0001c0001t0001g0071a0001c0001t0001g0112a0001c0001t0001g0123others(1): Show | 4 | HG00438.hp1 NA18981.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.627+28380T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42991514 | ||||||
| chr4:42991556
|
A | C | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.627+28422A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42991556 | ||||||
| chr4:42991556
|
A | G | 19 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(16): Show | 19 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.627+28422A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42991556 | ||||||
| chr4:42991603
|
A | G | 3 | a0001c0001t0002g0038a0001c0001t0002g0050a0001c0001t0002g0062 | 3 | HG01243.hp2 HG01361.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.627+28469A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42991603 | ||||||
| chr4:42991626
|
A | G | 2 | a0001c0001t0002g0278a0001c0001t0005g0157 | 2 | HG01884.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.627+28492A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42991626 | ||||||
| chr4:42991769
|
T | C | 9 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.628-28585T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42991769 | ||||||
| chr4:42991825
|
A | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0032 | 2 | HG03654.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.628-28529A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42991825 | ||||||
| chr4:42991839
|
A | G | 2 | a0001c0001t0002g0041a0001c0001t0002g0057 | 2 | NA18981.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.628-28515A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42991839 | ||||||
| chr4:42991871
|
G | A | 48 | a0001c0001t0001g0034a0001c0001t0001g0111a0001c0001t0002g0021others(45): Show | 48 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.628-28483G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42991871 | ||||||
| chr4:42992066
|
A | T | 9 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.628-28288A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42992066 | ||||||
| chr4:42992094
|
C | T | 1 | a0001c0001t0005g0211 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.628-28260C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42992094 | ||||||
| chr4:42992151
|
C | A | 1 | a0001c0001t0002g0108 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.628-28203C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42992151 | ||||||
| chr4:42992257
|
C | A | 19 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(16): Show | 19 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.628-28097C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42992257 | ||||||
| chr4:42992282
|
A | G | 1 | a0001c0001t0002g0094 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.628-28072A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42992282 | ||||||
| chr4:42992494
|
G | C | 307 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(304): Show | 307 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.628-27860G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42992494 | ||||||
| chr4:42992530
|
G | A | 167 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(164): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.628-27824G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42992530 | ||||||
| chr4:42992626
|
G | A | 2 | a0002c0002t0001g0247a0002c0002t0001g0255 | 2 | HG01346.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.628-27728G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42992626 | ||||||
| chr4:42992686
|
C | T | 9 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.628-27668C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42992686 | ||||||
| chr4:42992726
|
C | A | 1 | a0003c0003t0002g0297 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.628-27628C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42992726 | ||||||
| chr4:42992882
|
A | G | 1 | a0003c0003t0002g0300 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.628-27472A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42992882 | ||||||
| chr4:42993088
|
G | A | 4 | a0001c0001t0001g0075a0001c0001t0001g0119a0001c0001t0002g0076others(1): Show | 4 | HG01993.hp2 HG02630.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-27266G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42993088 | ||||||
| chr4:42993194
|
G | A | 8 | a0001c0001t0001g0082a0001c0001t0002g0020a0001c0001t0002g0022others(5): Show | 8 | HG01891.hp2 HG02615.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.628-27160G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42993194 | ||||||
| chr4:42993201
|
G | A | 167 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(164): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.628-27153G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42993201 | ||||||
| chr4:42993214
|
C | T | 2 | a0001c0001t0002g0030a0001c0001t0002g0031 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.628-27140C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42993214 | ||||||
| chr4:42993244
|
T | C | 9 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.628-27110T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42993244 | ||||||
| chr4:42993256
|
C | T | 8 | a0001c0001t0002g0080a0001c0001t0003g0132a0001c0001t0003g0134others(5): Show | 8 | HG02074.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.628-27098C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42993256 | ||||||
| chr4:42993462
|
C | T | 3 | a0001c0001t0003g0134a0001c0001t0004g0133a0003c0003t0001g0312 | 3 | HG02027.hp1 HG02735.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.628-26892C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42993462 | ||||||
| chr4:42993463
|
G | A | 17 | a0001c0001t0001g0012a0001c0001t0001g0075a0001c0001t0001g0082others(14): Show | 17 | HG01884.hp1 HG01891.hp2 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.628-26891G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42993463 | ||||||
| chr4:42993587
|
C | T | 5 | a0002c0002t0001g0240a0002c0002t0001g0241a0002c0002t0001g0242others(2): Show | 5 | HG01358.hp2 HG01496.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.628-26767C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42993587 | ||||||
| chr4:42993686
|
C | T | 130 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(127): Show | 130 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.628-26668C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42993686 | ||||||
| chr4:42993702
|
T | A | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.628-26652T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42993702 | ||||||
| chr4:42993772
|
C | A | 9 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.628-26582C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42993772 | ||||||
| chr4:42993926
|
C | T | 2 | a0001c0001t0002g0013a0003c0003t0002g0329 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.628-26428C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42993926 | ||||||
| chr4:42993943
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.628-26411C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42993943 | ||||||
| chr4:42993949
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.628-26405A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42993949 | ||||||
| chr4:42993983
|
C | T | 11 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(8): Show | 11 | HG00140.hp2 NA18942.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.628-26371C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42993983 | ||||||
| chr4:42994056
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.628-26298G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42994056 | ||||||
| chr4:42994112
|
T | G | 9 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.628-26242T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42994112 | ||||||
| chr4:42994124
|
A | G | 1 | a0001c0001t0002g0033 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.628-26230A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42994124 | ||||||
| chr4:42994159
|
T | C | 1 | a0001c0001t0005g0211 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.628-26195T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42994159 | ||||||
| chr4:42994541
|
C | G | 6 | a0001c0001t0002g0013a0001c0001t0004g0142a0003c0003t0001g0317others(3): Show | 6 | HG02109.hp1 HG02717.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.628-25813C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42994541 | ||||||
| chr4:42994581
|
A | G | 130 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(127): Show | 130 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.628-25773A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42994581 | ||||||
| chr4:42994668
|
G | A | 1 | a0001c0001t0002g0127 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.628-25686G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42994668 | ||||||
| chr4:42994808
|
T | C | 9 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.628-25546T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42994808 | ||||||
| chr4:42995123
|
G | A | 167 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(164): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.628-25231G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42995123 | ||||||
| chr4:42995192
|
G | A | 1 | a0003c0003t0001g0321 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.628-25162G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42995192 | ||||||
| chr4:42995198
|
G | A | 1 | a0002c0002t0001g0243 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.628-25156G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42995198 | ||||||
| chr4:42995231
|
T | C | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.628-25123T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42995231 | ||||||
| chr4:42995269
|
T | G | 1 | a0001c0001t0004g0170 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.628-25085T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42995269 | ||||||
| chr4:42995342
|
C | A | 2 | a0001c0001t0002g0030a0001c0001t0002g0031 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.628-25012C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42995342 | ||||||
| chr4:42995573
|
A | G | 5 | a0002c0002t0001g0216a0002c0002t0001g0217a0002c0002t0001g0218others(2): Show | 5 | HG00423.hp1 HG00544.hp2 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.628-24781A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42995573 | ||||||
| chr4:42995583
|
G | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.628-24771G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42995583 | ||||||
| chr4:42995633
|
T | G | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.628-24721T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42995633 | ||||||
| chr4:42995715
|
G | C | 1 | a0001c0001t0001g0125 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.628-24639G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42995715 | ||||||
| chr4:42995763
|
C | T | 2 | a0001c0001t0002g0086a0003c0003t0002g0327 | 2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.628-24591C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42995763 | ||||||
| chr4:42995776
|
C | T | 6 | a0001c0001t0001g0015a0001c0001t0002g0001a0001c0001t0002g0002others(3): Show | 6 | HG01167.hp2 HG03041.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.628-24578C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42995776 | ||||||
| chr4:42995960
|
C | T | 1 | a0001c0001t0003g0202 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.628-24394C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42995960 | ||||||
| chr4:42996027
|
C | T | 9 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.628-24327C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42996027 | ||||||
| chr4:42996251
|
A | C | 111 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(108): Show | 111 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.628-24103A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42996251 | ||||||
| chr4:42996397
|
C | G | 1 | a0003c0003t0002g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.628-23957C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42996397 | ||||||
| chr4:42996431
|
T | A | 4 | a0001c0001t0002g0013a0001c0001t0002g0044a0003c0003t0001g0317others(1): Show | 4 | HG00639.hp2 HG02717.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-23923T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42996431 | ||||||
| chr4:42996456
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.628-23898T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42996456 | ||||||
| chr4:42996491
|
C | G | 4 | a0001c0001t0002g0013a0001c0001t0002g0044a0003c0003t0001g0317others(1): Show | 4 | HG00639.hp2 HG02717.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-23863C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42996491 | ||||||
| chr4:42996594
|
G | T | 9 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.628-23760G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42996594 | ||||||
| chr4:42996633
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.628-23721T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42996633 | ||||||
| chr4:42996847
|
A | G | 5 | a0001c0001t0004g0169a0001c0001t0004g0170a0001c0001t0004g0171others(2): Show | 5 | HG01978.hp1 HG01981.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.628-23507A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42996847 | ||||||
| chr4:42996848
|
C | T | 1 | a0003c0003t0001g0293 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.628-23506C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42996848 | ||||||
| chr4:42996888
|
C | T | 1 | a0001c0001t0003g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.628-23466C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42996888 | ||||||
| chr4:42996911
|
T | C | 1 | a0001c0001t0002g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.628-23443T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42996911 | ||||||
| chr4:42997055
|
A | G | 20 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(17): Show | 20 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.628-23299A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42997055 | ||||||
| chr4:42997096
|
A | G | 1 | a0003c0003t0002g0291 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.628-23258A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42997096 | ||||||
| chr4:42997177
|
T | C | 1 | a0002c0002t0001g0233 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.628-23177T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42997177 | ||||||
| chr4:42997434
|
A | G | 1 | a0001c0001t0003g0161 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.628-22920A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42997434 | ||||||
| chr4:42997478
|
C | A | 119 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(116): Show | 119 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.628-22876C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42997478 | ||||||
| chr4:42997820
|
C | T | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.628-22534C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42997820 | ||||||
| chr4:42997877
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.628-22477C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42997877 | ||||||
| chr4:42998009
|
T | G | 17 | a0001c0001t0001g0012a0001c0001t0001g0075a0001c0001t0001g0082others(14): Show | 17 | HG01884.hp1 HG01891.hp2 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.628-22345T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42998009 | ||||||
| chr4:42998039
|
G | A | 3 | a0001c0001t0001g0075a0001c0001t0002g0076a0001c0001t0004g0141 | 3 | HG01993.hp2 HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.628-22315G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42998039 | ||||||
| chr4:42998246
|
A | G | 3 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0027 | 3 | HG00323.hp1 HG01099.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.628-22108A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42998246 | ||||||
| chr4:42998338
|
C | A | 1 | a0002c0002t0001g0228 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.628-22016C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42998338 | ||||||
| chr4:42998393
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.628-21961T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42998393 | ||||||
| chr4:42998488
|
T | G | 8 | a0001c0001t0002g0080a0001c0001t0003g0132a0001c0001t0003g0134others(5): Show | 8 | HG02074.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.628-21866T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42998488 | ||||||
| chr4:42998876
|
A | C | 1 | a0001c0001t0002g0038 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.628-21478A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42998876 | ||||||
| chr4:42999277
|
T | C | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.628-21077T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42999277 | ||||||
| chr4:42999336
|
C | T | 19 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(16): Show | 19 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.628-21018C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42999336 | ||||||
| chr4:42999678
|
T | G | 30 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(27): Show | 30 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.628-20676T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42999678 | ||||||
| chr4:42999770
|
A | G | 10 | a0001c0001t0001g0012a0001c0001t0001g0082a0001c0001t0002g0014others(7): Show | 10 | HG02615.hp1 HG02615.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.628-20584A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42999770 | ||||||
| chr4:42999934
|
C | T | 1 | a0001c0001t0002g0007 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.628-20420C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42999934 | ||||||
| chr4:42999935
|
G | A | 2 | a0001c0001t0004g0204a0001c0001t0004g0205 | 2 | NA18952.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.628-20419G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42999935 | ||||||
| chr4:42999981
|
G | A | 1 | a0001c0001t0003g0144 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.628-20373G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 42999981 | ||||||
| chr4:43000112
|
C | T | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.628-20242C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43000112 | ||||||
| chr4:43000226
|
T | A | 1 | a0001c0001t0002g0044 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.628-20128T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43000226 | ||||||
| chr4:43000432
|
C | T | 4 | a0001c0001t0002g0013a0001c0001t0002g0044a0003c0003t0001g0317others(1): Show | 4 | HG00639.hp2 HG02717.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-19922C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43000432 | ||||||
| chr4:43000461
|
C | A | 1 | a0001c0001t0002g0037 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.628-19893C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43000461 | ||||||
| chr4:43000461
|
C | T | 11 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(8): Show | 11 | HG00140.hp2 NA18942.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.628-19893C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43000461 | ||||||
| chr4:43000462
|
G | A | 17 | a0001c0001t0001g0019a0001c0001t0001g0056a0001c0001t0001g0071others(14): Show | 17 | HG00140.hp1 HG00438.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.628-19892G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43000462 | ||||||
| chr4:43000468
|
C | A | 94 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(91): Show | 94 | HG00140.hp1 HG00438.hp1 HG01192.hp2 others(91): Show |
intron_variant | MODIFIER | c.628-19886C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43000468 | ||||||
| chr4:43000474
|
TA | T | 235 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(232): Show | 235 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.628-19857delA | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 43000474 | |||||
| chr4:43000474
|
TAA | T | 60 | a0001c0001t0001g0012a0001c0001t0001g0023a0001c0001t0001g0024others(57): Show | 60 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.628-19858_628-1985 others(6): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 43000474 | |||||
| chr4:43000474
|
TAAA | T | 10 | a0001c0001t0002g0020a0001c0001t0002g0126a0001c0001t0002g0127others(7): Show | 10 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.628-19859_628-1985 others(7): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 43000474 | |||||
| chr4:43000495
|
A | G | 49 | a0001c0001t0001g0111a0001c0001t0002g0021a0001c0001t0002g0026others(46): Show | 49 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.628-19859A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43000495 | ||||||
| chr4:43000502
|
G | A | 8 | a0001c0001t0002g0080a0001c0001t0003g0132a0001c0001t0003g0134others(5): Show | 8 | HG02074.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.628-19852G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43000502 | ||||||
| chr4:43000540
|
G | C | 1 | a0001c0001t0003g0132 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.628-19814G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43000540 | ||||||
| chr4:43000583
|
G | T | 10 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(7): Show | 10 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.628-19771G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43000583 | ||||||
| chr4:43000669
|
G | GTA | 98 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(95): Show | 98 | HG00140.hp1 HG00438.hp1 HG01167.hp2 others(95): Show |
intron_variant | MODIFIER | c.628-19672_628-1967 others(6): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 43000669 | |||||
| chr4:43000669
|
G | GTATATA | 9 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.628-19676_628-1967 others(10): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 43000669 | |||||
| chr4:43000868
|
C | T | 4 | a0001c0001t0001g0075a0001c0001t0001g0212a0001c0001t0002g0076others(1): Show | 4 | HG01993.hp2 HG02145.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-19486C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43000868 | ||||||
| chr4:43000895
|
A | G | 10 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(7): Show | 10 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.628-19459A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43000895 | ||||||
| chr4:43000995
|
C | T | 26 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(23): Show | 26 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.628-19359C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43000995 | ||||||
| chr4:43001044
|
A | T | 103 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(100): Show | 103 | HG00140.hp1 HG00438.hp1 HG01167.hp2 others(100): Show |
intron_variant | MODIFIER | c.628-19310A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43001044 | ||||||
| chr4:43001101
|
AT | A | 9 | a0001c0001t0002g0026a0001c0001t0002g0126a0001c0001t0002g0127others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.628-19239delT | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 43001101 | |||||
| chr4:43001142
|
C | A | 1 | a0001c0001t0001g0024 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.628-19212C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43001142 | ||||||
| chr4:43001143
|
T | C | 2 | a0003c0003t0002g0291a0003c0003t0002g0297 | 2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.628-19211T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43001143 | ||||||
| chr4:43001198
|
G | C | 1 | a0003c0003t0001g0299 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.628-19156G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43001198 | ||||||
| chr4:43001199
|
G | T | 1 | a0003c0003t0002g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.628-19155G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43001199 | ||||||
| chr4:43001213
|
G | A | 10 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(7): Show | 10 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.628-19141G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43001213 | ||||||
| chr4:43001310
|
A | T | 1 | a0001c0001t0003g0178 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.628-19044A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43001310 | ||||||
| chr4:43001320
|
A | G | 37 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0061others(34): Show | 37 | HG00140.hp2 HG00673.hp1 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.628-19034A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43001320 | ||||||
| chr4:43001562
|
C | T | 2 | a0001c0001t0002g0013a0003c0003t0001g0317 | 2 | HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.628-18792C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43001562 | ||||||
| chr4:43001602
|
T | C | 23 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(20): Show | 23 | HG00323.hp1 HG00733.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.628-18752T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43001602 | ||||||
| chr4:43001649
|
G | T | 4 | a0001c0001t0002g0014a0001c0001t0004g0155a0001c0001t0004g0156others(1): Show | 4 | HG02615.hp1 HG02886.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-18705G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43001649 | ||||||
| chr4:43001664
|
C | T | 3 | a0001c0001t0002g0030a0001c0001t0002g0031a0005c0006t0011g0283 | 3 | HG01167.hp1 HG01169.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.628-18690C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43001664 | ||||||
| chr4:43001667
|
G | A | 13 | a0001c0001t0002g0078a0001c0001t0002g0084a0001c0001t0002g0126others(10): Show | 13 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.628-18687G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43001667 | ||||||
| chr4:43001774
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0285a0003c0003t0001g0290others(1): Show | 4 | HG01192.hp2 HG01978.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-18580G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43001774 | ||||||
| chr4:43001827
|
T | C | 1 | a0002c0002t0001g0275 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.628-18527T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43001827 | ||||||
| chr4:43001854
|
A | AGAAG | 307 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(304): Show | 307 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.628-18498_628-1849 others(8): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 43001854 | |||||
| chr4:43001906
|
T | G | 1 | a0001c0001t0001g0212 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.628-18448T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43001906 | ||||||
| chr4:43001936
|
G | T | 149 | a0001c0001t0001g0034a0001c0001t0001g0039a0001c0001t0001g0045others(146): Show | 149 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.628-18418G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43001936 | ||||||
| chr4:43001951
|
T | C | 253 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(250): Show | 253 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.628-18403T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43001951 | ||||||
| chr4:43001998
|
C | T | 1 | a0001c0001t0002g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.628-18356C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43001998 | ||||||
| chr4:43002040
|
C | T | 1 | a0002c0002t0002g0225 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.628-18314C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43002040 | ||||||
| chr4:43002055
|
G | T | 1 | a0001c0001t0003g0178 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.628-18299G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43002055 | ||||||
| chr4:43002057
|
C | T | 89 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(86): Show | 89 | HG00140.hp1 HG00438.hp1 HG01192.hp2 others(86): Show |
intron_variant | MODIFIER | c.628-18297C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43002057 | ||||||
| chr4:43002075
|
A | G | 94 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0061others(91): Show | 94 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.628-18279A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43002075 | ||||||
| chr4:43002080
|
C | T | 180 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(177): Show | 180 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.628-18274C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43002080 | ||||||
| chr4:43002081
|
G | A | 3 | a0001c0004t0002g0087a0001c0004t0002g0088a0001c0004t0002g0091 | 3 | HG02809.hp2 HG03130.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.628-18273G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43002081 | ||||||
| chr4:43002162
|
A | G | 10 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(7): Show | 10 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.628-18192A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43002162 | ||||||
| chr4:43002171
|
G | A | 1 | a0001c0001t0003g0186 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.628-18183G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43002171 | ||||||
| chr4:43002220
|
C | T | 2 | a0001c0001t0002g0063a0001c0001t0002g0085 | 2 | HG00621.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.628-18134C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43002220 | ||||||
| chr4:43002236
|
C | T | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.628-18118C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43002236 | ||||||
| chr4:43002339
|
A | T | 2 | a0001c0001t0002g0092a0001c0001t0002g0093 | 2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.628-18015A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43002339 | ||||||
| chr4:43002378
|
C | T | 1 | a0001c0001t0002g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.628-17976C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43002378 | ||||||
| chr4:43002379
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0100 | 2 | HG03688.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.628-17975G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43002379 | ||||||
| chr4:43002410
|
C | T | 1 | a0001c0001t0002g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.628-17944C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43002410 | ||||||
| chr4:43002465
|
T | C | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.628-17889T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43002465 | ||||||
| chr4:43002769
|
G | T | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.628-17585G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43002769 | ||||||
| chr4:43002901
|
C | T | 1 | a0001c0001t0002g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.628-17453C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43002901 | ||||||
| chr4:43002923
|
T | A | 7 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0281others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-17431T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43002923 | ||||||
| chr4:43002974
|
A | T | 91 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(88): Show | 91 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.628-17380A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43002974 | ||||||
| chr4:43002995
|
G | GATAGTGA others(13): Show |
1 | a0003c0003t0001g0321 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.628-17358_628-1735 others(24): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 43002995 | |||||
| chr4:43003079
|
C | T | 1 | a0001c0001t0002g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.628-17275C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43003079 | ||||||
| chr4:43003249
|
C | T | 18 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0055others(15): Show | 18 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.628-17105C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43003249 | ||||||
| chr4:43003303
|
T | A | 7 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0281others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-17051T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43003303 | ||||||
| chr4:43003311
|
A | C | 1 | a0001c0001t0004g0171 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.628-17043A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43003311 | ||||||
| chr4:43003382
|
A | T | 1 | a0003c0003t0002g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.628-16972A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43003382 | ||||||
| chr4:43003443
|
G | T | 2 | a0001c0001t0005g0157a0001c0001t0005g0211 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.628-16911G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43003443 | ||||||
| chr4:43003750
|
C | A | 17 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0055others(14): Show | 17 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.628-16604C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43003750 | ||||||
| chr4:43003772
|
A | G | 1 | a0001c0001t0002g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.628-16582A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43003772 | ||||||
| chr4:43003853
|
A | G | 2 | a0001c0001t0002g0020a0001c0001t0002g0022 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.628-16501A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43003853 | ||||||
| chr4:43003915
|
G | A | 1 | a0003c0003t0001g0307 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.628-16439G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43003915 | ||||||
| chr4:43003952
|
G | A | 4 | a0001c0001t0002g0014a0001c0001t0004g0155a0001c0001t0004g0156others(1): Show | 4 | HG02615.hp1 HG02886.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-16402G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43003952 | ||||||
| chr4:43004190
|
C | G | 22 | a0001c0001t0002g0021a0001c0001t0002g0026a0001c0001t0002g0028others(19): Show | 22 | HG00544.hp1 HG00735.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.628-16164C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43004190 | ||||||
| chr4:43004242
|
T | A | 1 | a0002c0002t0001g0252 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.628-16112T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43004242 | ||||||
| chr4:43004357
|
G | A | 10 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(7): Show | 10 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.628-15997G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43004357 | ||||||
| chr4:43004441
|
A | G | 28 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0030others(25): Show | 28 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.628-15913A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43004441 | ||||||
| chr4:43004508
|
A | T | 18 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0055others(15): Show | 18 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.628-15846A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43004508 | ||||||
| chr4:43004523
|
A | G | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.628-15831A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43004523 | ||||||
| chr4:43004596
|
T | C | 2 | a0001c0001t0002g0101a0001c0001t0002g0102 | 2 | NA18997.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.628-15758T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43004596 | ||||||
| chr4:43004629
|
A | C | 198 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(195): Show | 198 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.628-15725A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43004629 | ||||||
| chr4:43004901
|
T | C | 1 | a0003c0003t0002g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.628-15453T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43004901 | ||||||
| chr4:43005028
|
G | A | 51 | a0001c0001t0002g0013a0001c0001t0002g0021a0001c0001t0002g0026others(48): Show | 51 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.628-15326G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43005028 | ||||||
| chr4:43005072
|
C | T | 1 | a0003c0003t0001g0299 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.628-15282C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43005072 | ||||||
| chr4:43005083
|
C | A | 2 | a0001c0001t0002g0076a0001c0001t0004g0141 | 2 | HG01993.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.628-15271C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43005083 | ||||||
| chr4:43005138
|
C | A | 1 | a0002c0002t0001g0258 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.628-15216C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43005138 | ||||||
| chr4:43005570
|
C | T | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG03704.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.628-14784C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43005570 | ||||||
| chr4:43005571
|
G | A | 1 | a0001c0001t0002g0281 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.628-14783G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43005571 | ||||||
| chr4:43005610
|
C | T | 54 | a0001c0001t0002g0013a0001c0001t0002g0021a0001c0001t0002g0026others(51): Show | 54 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.628-14744C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43005610 | ||||||
| chr4:43005653
|
T | C | 3 | a0003c0003t0002g0314a0003c0003t0002g0323a0003c0003t0002g0335 | 3 | HG01243.hp1 HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.628-14701T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43005653 | ||||||
| chr4:43005686
|
C | A | 17 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0055others(14): Show | 17 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.628-14668C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43005686 | ||||||
| chr4:43005722
|
G | A | 7 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0281others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-14632G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43005722 | ||||||
| chr4:43005820
|
G | A | 5 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0092others(2): Show | 5 | HG01167.hp2 HG02809.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.628-14534G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43005820 | ||||||
| chr4:43005844
|
G | A | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.628-14510G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43005844 | ||||||
| chr4:43005872
|
C | T | 1 | a0001c0001t0004g0204 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.628-14482C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43005872 | ||||||
| chr4:43005925
|
C | T | 3 | a0001c0001t0001g0056a0001c0001t0002g0145a0003c0003t0002g0329 | 3 | HG00140.hp1 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.628-14429C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43005925 | ||||||
| chr4:43006027
|
C | T | 1 | a0001c0001t0002g0104 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.628-14327C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43006027 | ||||||
| chr4:43006031
|
T | C | 52 | a0001c0001t0002g0013a0001c0001t0002g0021a0001c0001t0002g0026others(49): Show | 52 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.628-14323T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43006031 | ||||||
| chr4:43006032
|
A | G | 7 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0281others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-14322A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43006032 | ||||||
| chr4:43006060
|
A | G | 1 | a0001c0001t0002g0038 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.628-14294A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43006060 | ||||||
| chr4:43006097
|
T | C | 1 | a0001c0001t0002g0104 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.628-14257T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43006097 | ||||||
| chr4:43006158
|
A | G | 11 | a0001c0001t0002g0104a0001c0001t0002g0126a0001c0001t0002g0127others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.628-14196A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43006158 | ||||||
| chr4:43006185
|
C | T | 2 | a0001c0001t0005g0157a0001c0001t0005g0211 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.628-14169C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43006185 | ||||||
| chr4:43006257
|
G | A | 17 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0055others(14): Show | 17 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.628-14097G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43006257 | ||||||
| chr4:43006260
|
G | C | 1 | a0003c0003t0001g0330 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.628-14094G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43006260 | ||||||
| chr4:43006261
|
G | T | 1 | a0003c0003t0001g0330 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.628-14093G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43006261 | ||||||
| chr4:43006264
|
C | A | 1 | a0003c0003t0001g0330 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.628-14090C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43006264 | ||||||
| chr4:43006265
|
C | T | 1 | a0003c0003t0001g0330 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.628-14089C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43006265 | ||||||
| chr4:43006266
|
TTGAAAAA others(7): Show |
T | 1 | a0003c0003t0001g0330 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.628-14087_628-1407 others(18): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43006266 | ||||||
| chr4:43006281
|
G | C | 1 | a0003c0003t0001g0330 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.628-14073G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43006281 | ||||||
| chr4:43006300
|
G | A | 8 | a0001c0001t0001g0082a0001c0001t0002g0018a0001c0001t0002g0020others(5): Show | 8 | HG02257.hp1 HG02615.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.628-14054G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43006300 | ||||||
| chr4:43006572
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.628-13782C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43006572 | ||||||
| chr4:43006612
|
G | T | 1 | a0001c0001t0001g0073 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.628-13742G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43006612 | ||||||
| chr4:43006614
|
C | T | 1 | a0001c0001t0002g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.628-13740C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43006614 | ||||||
| chr4:43006648
|
C | T | 1 | a0004c0007t0002g0114 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.628-13706C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43006648 | ||||||
| chr4:43006681
|
A | G | 28 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0030others(25): Show | 28 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.628-13673A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43006681 | ||||||
| chr4:43006754
|
G | A | 7 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(4): Show | 7 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.628-13600G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43006754 | ||||||
| chr4:43006797
|
A | G | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.628-13557A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43006797 | ||||||
| chr4:43006837
|
G | A | 2 | a0001c0001t0002g0076a0001c0001t0004g0141 | 2 | HG01993.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.628-13517G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43006837 | ||||||
| chr4:43006872
|
C | T | 2 | a0003c0003t0001g0326a0003c0003t0001g0331 | 2 | HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.628-13482C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43006872 | ||||||
| chr4:43006987
|
G | A | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.628-13367G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43006987 | ||||||
| chr4:43007337
|
A | G | 3 | a0001c0001t0002g0033a0001c0001t0004g0165a0003c0003t0002g0322 | 3 | HG00733.hp1 HG01123.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.628-13017A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43007337 | ||||||
| chr4:43007391
|
T | C | 1 | a0001c0001t0001g0111 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.628-12963T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43007391 | ||||||
| chr4:43007473
|
G | C | 1 | a0002c0002t0001g0227 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.628-12881G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43007473 | ||||||
| chr4:43007607
|
A | C | 1 | a0001c0001t0001g0212 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.628-12747A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43007607 | ||||||
| chr4:43007687
|
A | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0009 | 2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.628-12667A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43007687 | ||||||
| chr4:43007917
|
C | T | 1 | a0001c0001t0004g0165 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.628-12437C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43007917 | ||||||
| chr4:43007918
|
G | A | 1 | a0001c0001t0002g0076 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.628-12436G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43007918 | ||||||
| chr4:43007932
|
G | A | 1 | a0003c0003t0001g0296 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.628-12422G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43007932 | ||||||
| chr4:43008000
|
T | C | 18 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0055others(15): Show | 18 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.628-12354T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43008000 | ||||||
| chr4:43008180
|
T | C | 7 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0281others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-12174T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43008180 | ||||||
| chr4:43008286
|
C | T | 1 | a0001c0001t0002g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.628-12068C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43008286 | ||||||
| chr4:43008372
|
A | G | 3 | a0001c0001t0002g0030a0001c0001t0002g0031a0005c0006t0011g0283 | 3 | HG01167.hp1 HG01169.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.628-11982A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43008372 | ||||||
| chr4:43008421
|
T | C | 1 | a0001c0001t0002g0107 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.628-11933T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43008421 | ||||||
| chr4:43008464
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.628-11890G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43008464 | ||||||
| chr4:43008533
|
C | G | 24 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0056others(21): Show | 24 | HG00140.hp1 HG00438.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.628-11821C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43008533 | ||||||
| chr4:43008576
|
G | C | 1 | a0001c0001t0005g0211 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.628-11778G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43008576 | ||||||
| chr4:43008615
|
G | A | 3 | a0003c0003t0001g0295a0003c0003t0001g0306a0003c0003t0001g0330 | 3 | HG02109.hp2 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.628-11739G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43008615 | ||||||
| chr4:43008616
|
G | A | 53 | a0001c0001t0002g0013a0001c0001t0002g0021a0001c0001t0002g0026others(50): Show | 53 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.628-11738G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43008616 | ||||||
| chr4:43008832
|
A | G | 1 | a0002c0002t0001g0258 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.628-11522A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43008832 | ||||||
| chr4:43008833
|
T | C | 2 | a0001c0001t0002g0076a0001c0001t0004g0141 | 2 | HG01993.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.628-11521T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43008833 | ||||||
| chr4:43008905
|
G | C | 10 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0281others(7): Show | 10 | HG01167.hp1 HG01169.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.628-11449G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43008905 | ||||||
| chr4:43008986
|
A | G | 7 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(4): Show | 7 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.628-11368A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43008986 | ||||||
| chr4:43009072
|
A | G | 2 | a0001c0001t0002g0076a0001c0001t0004g0141 | 2 | HG01993.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.628-11282A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43009072 | ||||||
| chr4:43009162
|
C | T | 1 | a0001c0001t0004g0137 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.628-11192C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43009162 | ||||||
| chr4:43009192
|
A | G | 103 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(100): Show | 103 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.628-11162A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43009192 | ||||||
| chr4:43009263
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.628-11091G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43009263 | ||||||
| chr4:43009295
|
G | C | 4 | a0001c0001t0002g0080a0001c0001t0004g0136a0001c0001t0006g0003others(1): Show | 4 | HG02145.hp1 HG02257.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-11059G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43009295 | ||||||
| chr4:43009343
|
T | C | 1 | a0002c0002t0002g0265 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.628-11011T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43009343 | ||||||
| chr4:43009372
|
A | G | 2 | a0001c0001t0005g0157a0001c0001t0005g0211 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.628-10982A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43009372 | ||||||
| chr4:43009446
|
T | C | 12 | a0001c0001t0001g0082a0001c0001t0002g0018a0001c0001t0002g0020others(9): Show | 12 | HG02257.hp1 HG02615.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.628-10908T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43009446 | ||||||
| chr4:43009491
|
A | G | 2 | a0003c0003t0001g0310a0003c0003t0001g0312 | 2 | HG02027.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.628-10863A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43009491 | ||||||
| chr4:43009675
|
C | T | 1 | a0002c0002t0001g0247 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.628-10679C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43009675 | ||||||
| chr4:43009709
|
A | G | 3 | a0001c0004t0002g0087a0001c0004t0002g0088a0001c0004t0002g0091 | 3 | HG02809.hp2 HG03130.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.628-10645A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43009709 | ||||||
| chr4:43009729
|
C | T | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.628-10625C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43009729 | ||||||
| chr4:43009750
|
A | AC | 14 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0076others(11): Show | 14 | HG01167.hp1 HG01169.hp2 HG01993.hp2 others(11): Show |
intron_variant | MODIFIER | c.628-10597dupC | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 43009750 | |||||
| chr4:43009830
|
T | G | 81 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(78): Show | 81 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.628-10524T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43009830 | ||||||
| chr4:43009852
|
A | C | 3 | a0001c0001t0002g0086a0001c0001t0004g0137a0003c0003t0002g0327 | 3 | HG02559.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.628-10502A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43009852 | ||||||
| chr4:43009891
|
C | T | 1 | a0003c0003t0002g0308 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.628-10463C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43009891 | ||||||
| chr4:43009973
|
G | A | 1 | a0001c0001t0003g0135 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.628-10381G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43009973 | ||||||
| chr4:43010049
|
C | G | 51 | a0001c0001t0002g0013a0001c0001t0002g0021a0001c0001t0002g0026others(48): Show | 51 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.628-10305C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43010049 | ||||||
| chr4:43010135
|
A | G | 1 | a0001c0001t0002g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.628-10219A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43010135 | ||||||
| chr4:43010171
|
A | G | 28 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0030others(25): Show | 28 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.628-10183A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43010171 | ||||||
| chr4:43010403
|
C | CA | 34 | a0001c0001t0001g0090a0001c0001t0002g0001a0001c0001t0002g0002others(31): Show | 34 | HG01167.hp2 HG01884.hp1 HG01993.hp2 others(31): Show |
intron_variant | MODIFIER | c.628-9936dupA | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 43010403 | |||||
| chr4:43010403
|
CA | C | 8 | a0001c0001t0001g0019a0001c0001t0001g0098a0002c0002t0001g0222others(5): Show | 8 | HG01070.hp2 HG02895.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.628-9936delA | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 43010403 | |||||
| chr4:43010505
|
G | A | 53 | a0001c0001t0002g0013a0001c0001t0002g0021a0001c0001t0002g0026others(50): Show | 53 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.628-9849G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43010505 | ||||||
| chr4:43010543
|
C | T | 1 | a0003c0003t0001g0306 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.628-9811C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43010543 | ||||||
| chr4:43010558
|
G | A | 1 | a0001c0001t0002g0108 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.628-9796G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43010558 | ||||||
| chr4:43010579
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.628-9775G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43010579 | ||||||
| chr4:43010613
|
A | C | 54 | a0001c0001t0002g0013a0001c0001t0002g0021a0001c0001t0002g0026others(51): Show | 54 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.628-9741A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43010613 | ||||||
| chr4:43010651
|
G | C | 1 | a0001c0001t0001g0212 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.628-9703G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43010651 | ||||||
| chr4:43010689
|
A | AT | 28 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0030others(25): Show | 28 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.628-9660dupT | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 43010689 | |||||
| chr4:43010733
|
G | T | 16 | a0001c0001t0001g0082a0001c0001t0002g0014a0001c0001t0002g0018others(13): Show | 16 | HG02257.hp1 HG02615.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.628-9621G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43010733 | ||||||
| chr4:43010739
|
A | AAAAAGAT others(4): Show |
1 | a0002c0002t0001g0221 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.628-9609_628-9608i others(13): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 43010739 | |||||
| chr4:43010801
|
A | G | 2 | a0002c0002t0001g0246a0002c0002t0001g0275 | 2 | HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.628-9553A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43010801 | ||||||
| chr4:43010805
|
G | C | 1 | a0003c0003t0001g0321 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.628-9549G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43010805 | ||||||
| chr4:43010860
|
G | A | 1 | a0001c0001t0002g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.628-9494G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43010860 | ||||||
| chr4:43010873
|
T | C | 1 | a0001c0001t0002g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.628-9481T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43010873 | ||||||
| chr4:43010897
|
A | T | 1 | a0001c0001t0001g0046 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.628-9457A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43010897 | ||||||
| chr4:43011027
|
G | A | 91 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(88): Show | 91 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.628-9327G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43011027 | ||||||
| chr4:43011274
|
A | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0125 | 2 | HG02132.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.628-9080A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43011274 | ||||||
| chr4:43011315
|
G | A | 8 | a0001c0001t0001g0082a0001c0001t0002g0018a0001c0001t0002g0020others(5): Show | 8 | HG02257.hp1 HG02615.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.628-9039G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43011315 | ||||||
| chr4:43011480
|
C | T | 2 | a0001c0001t0004g0138a0001c0001t0010g0284 | 2 | HG02647.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.628-8874C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43011480 | ||||||
| chr4:43011536
|
A | T | 1 | a0002c0002t0001g0240 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.628-8818A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43011536 | ||||||
| chr4:43011671
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.628-8683C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43011671 | ||||||
| chr4:43011672
|
G | T | 1 | a0003c0003t0001g0306 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.628-8682G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43011672 | ||||||
| chr4:43011970
|
A | G | 1 | a0003c0003t0001g0318 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.628-8384A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43011970 | ||||||
| chr4:43011993
|
C | T | 5 | a0001c0001t0002g0080a0001c0001t0004g0136a0001c0001t0005g0157others(2): Show | 5 | HG02145.hp1 HG02257.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.628-8361C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43011993 | ||||||
| chr4:43012081
|
C | T | 2 | a0001c0001t0003g0150a0002c0002t0001g0269 | 2 | NA18959.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.628-8273C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43012081 | ||||||
| chr4:43012238
|
T | G | 2 | a0001c0001t0002g0030a0001c0001t0002g0031 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.628-8116T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43012238 | ||||||
| chr4:43012284
|
C | T | 2 | a0003c0003t0001g0313a0003c0003t0001g0316 | 2 | HG02056.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.628-8070C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43012284 | ||||||
| chr4:43012436
|
T | A | 1 | a0001c0001t0002g0108 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.628-7918T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43012436 | ||||||
| chr4:43012514
|
G | T | 49 | a0001c0001t0002g0013a0001c0001t0002g0021a0001c0001t0002g0026others(46): Show | 49 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.628-7840G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43012514 | ||||||
| chr4:43012539
|
G | A | 11 | a0001c0001t0001g0082a0001c0001t0002g0018a0001c0001t0002g0020others(8): Show | 11 | HG02257.hp1 HG02615.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.628-7815G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43012539 | ||||||
| chr4:43012590
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.628-7764G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43012590 | ||||||
| chr4:43012591
|
A | G | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.628-7763A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43012591 | ||||||
| chr4:43012821
|
G | A | 7 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(4): Show | 7 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.628-7533G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43012821 | ||||||
| chr4:43012883
|
G | A | 1 | a0001c0001t0005g0211 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.628-7471G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43012883 | ||||||
| chr4:43012919
|
G | A | 28 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0030others(25): Show | 28 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.628-7435G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43012919 | ||||||
| chr4:43012924
|
C | A | 1 | a0001c0001t0001g0011 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.628-7430C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43012924 | ||||||
| chr4:43012927
|
A | C | 18 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0055others(15): Show | 18 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.628-7427A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43012927 | ||||||
| chr4:43012940
|
A | G | 1 | a0001c0001t0004g0180 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.628-7414A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43012940 | ||||||
| chr4:43013012
|
C | A | 1 | a0001c0001t0002g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.628-7342C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43013012 | ||||||
| chr4:43013169
|
G | A | 1 | a0001c0001t0002g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.628-7185G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43013169 | ||||||
| chr4:43013348
|
A | G | 21 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0126others(18): Show | 21 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.628-7006A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43013348 | ||||||
| chr4:43013355
|
T | C | 13 | a0001c0001t0001g0121a0001c0001t0001g0122a0002c0002t0001g0221others(10): Show | 13 | HG01928.hp1 HG02056.hp1 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.628-6999T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43013355 | ||||||
| chr4:43013414
|
A | T | 2 | a0001c0001t0005g0157a0001c0001t0005g0211 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.628-6940A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43013414 | ||||||
| chr4:43013445
|
A | G | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.628-6909A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43013445 | ||||||
| chr4:43013486
|
G | C | 19 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0055others(16): Show | 19 | HG01167.hp2 HG01884.hp1 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.628-6868G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43013486 | ||||||
| chr4:43013521
|
T | C | 1 | a0001c0001t0002g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.628-6833T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43013521 | ||||||
| chr4:43013560
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.628-6794A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43013560 | ||||||
| chr4:43013588
|
T | A | 220 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(217): Show | 220 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.628-6766T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43013588 | ||||||
| chr4:43013589
|
A | T | 220 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(217): Show | 220 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.628-6765A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43013589 | ||||||
| chr4:43013675
|
A | T | 1 | a0001c0001t0002g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.628-6679A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43013675 | ||||||
| chr4:43013753
|
A | C | 228 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(225): Show | 228 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.628-6601A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43013753 | ||||||
| chr4:43013801
|
T | C | 7 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(4): Show | 7 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.628-6553T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43013801 | ||||||
| chr4:43013826
|
G | A | 2 | a0001c0001t0002g0076a0001c0001t0004g0141 | 2 | HG01993.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.628-6528G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43013826 | ||||||
| chr4:43013855
|
T | C | 28 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0055others(25): Show | 28 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.628-6499T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43013855 | ||||||
| chr4:43013880
|
C | T | 3 | a0001c0004t0002g0087a0001c0004t0002g0088a0001c0004t0002g0091 | 3 | HG02809.hp2 HG03130.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.628-6474C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43013880 | ||||||
| chr4:43013883
|
A | T | 37 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0030others(34): Show | 37 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.628-6471A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43013883 | ||||||
| chr4:43013887
|
C | A | 3 | a0001c0004t0002g0087a0001c0004t0002g0088a0001c0004t0002g0091 | 3 | HG02809.hp2 HG03130.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.628-6467C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43013887 | ||||||
| chr4:43013927
|
G | T | 7 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0281others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-6427G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43013927 | ||||||
| chr4:43013944
|
G | A | 7 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0281others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-6410G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43013944 | ||||||
| chr4:43013951
|
A | G | 10 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(7): Show | 10 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.628-6403A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43013951 | ||||||
| chr4:43014054
|
C | CA | 26 | a0001c0001t0001g0024a0001c0001t0001g0124a0001c0001t0002g0001others(23): Show | 26 | HG01167.hp2 HG02109.hp1 HG02615.hp1 others(23): Show |
intron_variant | MODIFIER | c.628-6283dupA | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 43014054 | |||||
| chr4:43014054
|
CA | C | 163 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(160): Show | 163 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.628-6283delA | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 43014054 | |||||
| chr4:43014131
|
C | T | 1 | a0001c0001t0002g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.628-6223C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43014131 | ||||||
| chr4:43014132
|
G | T | 43 | a0001c0001t0002g0021a0001c0001t0002g0026a0001c0001t0002g0028others(40): Show | 43 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.628-6222G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43014132 | ||||||
| chr4:43014142
|
A | T | 1 | a0001c0001t0001g0103 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.628-6212A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43014142 | ||||||
| chr4:43014170
|
C | A | 2 | a0001c0001t0004g0155a0001c0001t0004g0156 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.628-6184C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43014170 | ||||||
| chr4:43014220
|
C | T | 37 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0030others(34): Show | 37 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.628-6134C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43014220 | ||||||
| chr4:43014226
|
C | G | 5 | a0001c0001t0001g0099a0001c0001t0001g0105a0001c0001t0003g0194others(2): Show | 5 | NA18941.hp1 NA18957.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.628-6128C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43014226 | ||||||
| chr4:43014301
|
T | C | 37 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0030others(34): Show | 37 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.628-6053T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43014301 | ||||||
| chr4:43014462
|
C | T | 7 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0281others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-5892C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43014462 | ||||||
| chr4:43014526
|
G | A | 2 | a0001c0001t0005g0157a0001c0001t0005g0211 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.628-5828G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43014526 | ||||||
| chr4:43014628
|
T | G | 1 | a0002c0002t0001g0251 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.628-5726T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43014628 | ||||||
| chr4:43014646
|
A | C | 37 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0030others(34): Show | 37 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.628-5708A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43014646 | ||||||
| chr4:43014685
|
A | G | 4 | a0001c0001t0002g0014a0001c0001t0004g0155a0001c0001t0004g0156others(1): Show | 4 | HG02615.hp1 HG02886.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-5669A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43014685 | ||||||
| chr4:43014733
|
T | G | 4 | a0001c0001t0002g0014a0001c0001t0004g0155a0001c0001t0004g0156others(1): Show | 4 | HG02615.hp1 HG02886.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-5621T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43014733 | ||||||
| chr4:43014793
|
G | A | 1 | a0001c0001t0002g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.628-5561G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43014793 | ||||||
| chr4:43014803
|
C | G | 2 | a0001c0001t0005g0157a0001c0001t0005g0211 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.628-5551C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43014803 | ||||||
| chr4:43014881
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.628-5473G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43014881 | ||||||
| chr4:43015040
|
C | G | 27 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0030others(24): Show | 27 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.628-5314C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43015040 | ||||||
| chr4:43015061
|
G | A | 1 | a0001c0001t0002g0042 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.628-5293G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43015061 | ||||||
| chr4:43015062
|
A | C | 37 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0030others(34): Show | 37 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.628-5292A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43015062 | ||||||
| chr4:43015170
|
G | C | 2 | a0001c0001t0005g0157a0001c0001t0005g0211 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.628-5184G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43015170 | ||||||
| chr4:43015193
|
G | A | 18 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0055others(15): Show | 18 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.628-5161G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43015193 | ||||||
| chr4:43015283
|
C | T | 8 | a0001c0001t0001g0012a0001c0001t0001g0075a0001c0001t0001g0096others(5): Show | 8 | HG02055.hp1 HG02723.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.628-5071C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43015283 | ||||||
| chr4:43015312
|
A | G | 9 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0281others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.628-5042A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43015312 | ||||||
| chr4:43015349
|
G | A | 29 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0055others(26): Show | 29 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.628-5005G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43015349 | ||||||
| chr4:43015486
|
G | C | 9 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0281others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.628-4868G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43015486 | ||||||
| chr4:43015494
|
A | T | 1 | a0001c0001t0001g0124 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.628-4860A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43015494 | ||||||
| chr4:43015534
|
A | G | 9 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0281others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.628-4820A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43015534 | ||||||
| chr4:43015614
|
C | T | 1 | a0001c0001t0001g0046 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.628-4740C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43015614 | ||||||
| chr4:43015779
|
T | C | 13 | a0001c0001t0001g0082a0001c0001t0002g0018a0001c0001t0002g0020others(10): Show | 13 | HG02257.hp1 HG02615.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.628-4575T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43015779 | ||||||
| chr4:43015947
|
C | G | 38 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(35): Show | 38 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(35): Show |
intron_variant | MODIFIER | c.628-4407C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43015947 | ||||||
| chr4:43015958
|
C | T | 93 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(90): Show | 93 | HG00140.hp1 HG00438.hp1 HG01192.hp2 others(90): Show |
intron_variant | MODIFIER | c.628-4396C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43015958 | ||||||
| chr4:43016088
|
C | G | 4 | a0002c0002t0001g0233a0003c0003t0001g0313a0003c0003t0001g0315others(1): Show | 4 | HG01928.hp1 HG02056.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-4266C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43016088 | ||||||
| chr4:43016185
|
C | T | 1 | a0001c0001t0002g0021 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.628-4169C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43016185 | ||||||
| chr4:43016213
|
A | G | 7 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0281others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-4141A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43016213 | ||||||
| chr4:43016431
|
C | G | 1 | a0003c0003t0001g0306 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.628-3923C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43016431 | ||||||
| chr4:43016487
|
C | T | 11 | a0001c0001t0002g0013a0001c0001t0002g0030a0001c0001t0002g0031others(8): Show | 11 | HG01167.hp1 HG01169.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.628-3867C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43016487 | ||||||
| chr4:43016575
|
T | C | 2 | a0001c0001t0005g0157a0001c0001t0005g0211 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.628-3779T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43016575 | ||||||
| chr4:43016624
|
G | A | 11 | a0001c0001t0002g0013a0001c0001t0002g0030a0001c0001t0002g0031others(8): Show | 11 | HG01167.hp1 HG01169.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.628-3730G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43016624 | ||||||
| chr4:43016633
|
TTG | T | 298 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(295): Show | 298 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.628-3698_628-3697d others(4): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 43016633 | |||||
| chr4:43016729
|
A | C | 6 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0092others(3): Show | 6 | HG01167.hp2 HG01884.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.628-3625A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43016729 | ||||||
| chr4:43016791
|
G | T | 27 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0055others(24): Show | 27 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.628-3563G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43016791 | ||||||
| chr4:43016863
|
C | T | 1 | a0003c0003t0002g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.628-3491C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43016863 | ||||||
| chr4:43016867
|
G | A | 43 | a0001c0001t0002g0021a0001c0001t0002g0026a0001c0001t0002g0028others(40): Show | 43 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.628-3487G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43016867 | ||||||
| chr4:43016932
|
G | A | 11 | a0001c0001t0002g0013a0001c0001t0002g0030a0001c0001t0002g0031others(8): Show | 11 | HG01167.hp1 HG01169.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.628-3422G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43016932 | ||||||
| chr4:43017066
|
A | G | 11 | a0001c0001t0002g0013a0001c0001t0002g0030a0001c0001t0002g0031others(8): Show | 11 | HG01167.hp1 HG01169.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.628-3288A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43017066 | ||||||
| chr4:43017207
|
T | C | 2 | a0003c0003t0002g0291a0003c0003t0002g0297 | 2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.628-3147T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43017207 | ||||||
| chr4:43017263
|
T | C | 9 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0281others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.628-3091T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43017263 | ||||||
| chr4:43017272
|
G | A | 26 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0055others(23): Show | 26 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.628-3082G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43017272 | ||||||
| chr4:43017318
|
A | C | 4 | a0001c0001t0003g0149a0001c0001t0004g0147a0001c0001t0004g0148others(1): Show | 4 | NA18941.hp2 NA18945.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-3036A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43017318 | ||||||
| chr4:43017337
|
G | T | 2 | a0001c0001t0002g0013a0001c0001t0002g0104 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.628-3017G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43017337 | ||||||
| chr4:43017357
|
T | C | 1 | a0002c0002t0001g0276 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.628-2997T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43017357 | ||||||
| chr4:43017359
|
T | C | 7 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0281others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-2995T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43017359 | ||||||
| chr4:43017492
|
T | G | 1 | a0003c0003t0001g0306 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.628-2862T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43017492 | ||||||
| chr4:43017560
|
A | G | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.628-2794A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43017560 | ||||||
| chr4:43017652
|
C | T | 194 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(191): Show | 194 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.628-2702C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43017652 | ||||||
| chr4:43017737
|
C | G | 4 | a0001c0001t0002g0013a0001c0001t0002g0104a0001c0001t0005g0157others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-2617C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43017737 | ||||||
| chr4:43017797
|
T | C | 9 | a0001c0001t0002g0080a0001c0001t0002g0086a0001c0001t0004g0136others(6): Show | 9 | HG02145.hp1 HG02257.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.628-2557T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43017797 | ||||||
| chr4:43017952
|
C | T | 3 | a0001c0001t0002g0086a0001c0001t0004g0137a0003c0003t0002g0327 | 3 | HG02559.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.628-2402C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43017952 | ||||||
| chr4:43017953
|
G | A | 2 | a0001c0001t0004g0142a0003c0003t0002g0302 | 2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.628-2401G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43017953 | ||||||
| chr4:43017959
|
T | G | 4 | a0001c0001t0002g0013a0001c0001t0002g0104a0001c0001t0005g0157others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-2395T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43017959 | ||||||
| chr4:43017969
|
C | T | 2 | a0001c0001t0004g0174a0001c0001t0004g0199 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.628-2385C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43017969 | ||||||
| chr4:43018052
|
G | C | 4 | a0001c0001t0002g0013a0001c0001t0002g0104a0001c0001t0005g0157others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-2302G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43018052 | ||||||
| chr4:43018133
|
G | T | 4 | a0001c0001t0002g0013a0001c0001t0002g0104a0001c0001t0005g0157others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-2221G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43018133 | ||||||
| chr4:43018148
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.628-2206A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43018148 | ||||||
| chr4:43018187
|
A | C | 2 | a0001c0001t0002g0013a0001c0001t0002g0104 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.628-2167A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43018187 | ||||||
| chr4:43018230
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.628-2124G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43018230 | ||||||
| chr4:43018299
|
A | C | 7 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(4): Show | 7 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.628-2055A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43018299 | ||||||
| chr4:43018426
|
C | T | 1 | a0003c0003t0002g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.628-1928C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43018426 | ||||||
| chr4:43018436
|
C | T | 18 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0055others(15): Show | 18 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.628-1918C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43018436 | ||||||
| chr4:43018447
|
C | T | 7 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0281others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-1907C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43018447 | ||||||
| chr4:43018481
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0003g0193 | 2 | HG00639.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.628-1873G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43018481 | ||||||
| chr4:43018500
|
A | G | 2 | a0001c0001t0002g0076a0001c0001t0004g0141 | 2 | HG01993.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.628-1854A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43018500 | ||||||
| chr4:43018537
|
C | T | 9 | a0001c0001t0002g0080a0001c0001t0002g0086a0001c0001t0004g0136others(6): Show | 9 | HG02145.hp1 HG02257.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.628-1817C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43018537 | ||||||
| chr4:43018617
|
A | C | 2 | a0001c0001t0002g0076a0001c0001t0004g0141 | 2 | HG01993.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.628-1737A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43018617 | ||||||
| chr4:43018821
|
G | C | 5 | a0002c0002t0001g0233a0003c0003t0001g0304a0003c0003t0001g0313others(2): Show | 5 | HG01928.hp1 HG02056.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.628-1533G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43018821 | ||||||
| chr4:43018878
|
C | T | 2 | a0001c0001t0004g0205a0001c0001t0010g0284 | 2 | HG04115.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.628-1476C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43018878 | ||||||
| chr4:43018905
|
T | C | 34 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(31): Show | 34 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.628-1449T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43018905 | ||||||
| chr4:43018910
|
G | A | 34 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(31): Show | 34 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.628-1444G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43018910 | ||||||
| chr4:43018936
|
C | G | 9 | a0001c0001t0002g0080a0001c0001t0002g0086a0001c0001t0004g0136others(6): Show | 9 | HG02145.hp1 HG02257.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.628-1418C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43018936 | ||||||
| chr4:43018953
|
A | C | 2 | a0001c0001t0002g0076a0001c0001t0004g0141 | 2 | HG01993.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.628-1401A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43018953 | ||||||
| chr4:43018974
|
T | C | 4 | a0001c0001t0002g0013a0001c0001t0002g0104a0001c0001t0005g0157others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-1380T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43018974 | ||||||
| chr4:43019018
|
A | G | 4 | a0001c0001t0002g0013a0001c0001t0002g0104a0001c0001t0005g0157others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-1336A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43019018 | ||||||
| chr4:43019021
|
A | G | 2 | a0001c0001t0002g0013a0001c0001t0002g0104 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.628-1333A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43019021 | ||||||
| chr4:43019089
|
T | C | 2 | a0001c0001t0002g0013a0001c0001t0002g0104 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.628-1265T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43019089 | ||||||
| chr4:43019097
|
C | T | 7 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0281others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-1257C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43019097 | ||||||
| chr4:43019151
|
C | G | 1 | a0002c0002t0001g0232 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.628-1203C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43019151 | ||||||
| chr4:43019211
|
A | G | 7 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0281others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-1143A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43019211 | ||||||
| chr4:43019339
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0212 | 2 | HG02145.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.628-1015G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43019339 | ||||||
| chr4:43019368
|
G | T | 11 | a0001c0001t0002g0018a0001c0001t0002g0020a0001c0001t0002g0022others(8): Show | 11 | HG02257.hp1 HG02615.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.628-986G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43019368 | ||||||
| chr4:43019497
|
C | G | 44 | a0001c0001t0002g0021a0001c0001t0002g0026a0001c0001t0002g0028others(41): Show | 44 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.628-857C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43019497 | ||||||
| chr4:43019574
|
A | T | 4 | a0001c0001t0002g0013a0001c0001t0002g0104a0001c0001t0005g0157others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-780A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43019574 | ||||||
| chr4:43019644
|
C | T | 4 | a0001c0001t0002g0013a0001c0001t0002g0104a0001c0001t0005g0157others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-710C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43019644 | ||||||
| chr4:43019645
|
G | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-709G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43019645 | ||||||
| chr4:43019855
|
C | T | 4 | a0001c0004t0002g0087a0001c0004t0002g0088a0001c0004t0002g0091others(1): Show | 4 | HG02572.hp2 HG02809.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-499C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43019855 | ||||||
| chr4:43019878
|
G | T | 1 | a0001c0001t0004g0136 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.628-476G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43019878 | ||||||
| chr4:43019969
|
G | A | 3 | a0001c0001t0002g0018a0001c0001t0002g0089a0003c0003t0002g0303 | 3 | HG02257.hp1 HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.628-385G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43019969 | ||||||
| chr4:43019970
|
T | G | 4 | a0001c0001t0002g0078a0001c0001t0002g0084a0001c0001t0004g0139others(1): Show | 4 | HG02647.hp2 HG02723.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-384T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43019970 | ||||||
| chr4:43019976
|
A | C | 1 | a0003c0003t0002g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.628-378A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43019976 | ||||||
| chr4:43020183
|
G | T | 6 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0281others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.628-171G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43020183 | ||||||
| chr4:43020205
|
T | C | 33 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(30): Show | 33 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.628-149T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 2/3 | chr4 | 43020205 | ||||||
| chr4:43020460
|
A | G | 4 | a0001c0001t0002g0013a0001c0001t0002g0104a0001c0001t0005g0157others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+41A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43020460 | ||||||
| chr4:43020507
|
C | A | 1 | a0001c0001t0002g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.693+88C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43020507 | ||||||
| chr4:43020541
|
A | G | 3 | a0003c0003t0002g0314a0003c0003t0002g0323a0003c0003t0002g0335 | 3 | HG01243.hp1 HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.693+122A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43020541 | ||||||
| chr4:43020591
|
G | T | 1 | a0001c0001t0003g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.693+172G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43020591 | ||||||
| chr4:43020609
|
C | T | 4 | a0001c0004t0002g0087a0001c0004t0002g0088a0001c0004t0002g0091others(1): Show | 4 | HG02572.hp2 HG02809.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+190C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43020609 | ||||||
| chr4:43020626
|
C | T | 4 | a0001c0001t0002g0013a0001c0001t0002g0104a0001c0001t0005g0157others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+207C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43020626 | ||||||
| chr4:43020751
|
A | G | 4 | a0001c0001t0002g0013a0001c0001t0002g0104a0001c0001t0005g0157others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+332A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43020751 | ||||||
| chr4:43020834
|
G | C | 27 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0055others(24): Show | 27 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.693+415G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43020834 | ||||||
| chr4:43020919
|
G | A | 2 | a0001c0001t0002g0076a0001c0001t0004g0141 | 2 | HG01993.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.693+500G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43020919 | ||||||
| chr4:43020920
|
G | A | 9 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.693+501G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43020920 | ||||||
| chr4:43020931
|
T | A | 27 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0055others(24): Show | 27 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.693+512T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43020931 | ||||||
| chr4:43021024
|
A | G | 6 | a0001c0001t0002g0013a0001c0001t0002g0076a0001c0001t0002g0104others(3): Show | 6 | HG01993.hp2 HG02630.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.693+605A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43021024 | ||||||
| chr4:43021118
|
C | A | 2 | a0001c0001t0005g0157a0001c0001t0005g0211 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.693+699C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43021118 | ||||||
| chr4:43021122
|
A | G | 1 | a0001c0001t0002g0278 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.693+703A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43021122 | ||||||
| chr4:43021167
|
T | C | 2 | a0001c0001t0002g0076a0001c0001t0004g0141 | 2 | HG01993.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.693+748T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43021167 | ||||||
| chr4:43021505
|
GA | G | 27 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0055others(24): Show | 27 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.693+1088delA | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 43021505 | |||||
| chr4:43021537
|
A | T | 3 | a0001c0001t0002g0281a0001c0001t0004g0138a0003c0003t0002g0329 | 3 | HG02647.hp1 HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.693+1118A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43021537 | ||||||
| chr4:43021539
|
A | T | 1 | a0001c0001t0002g0037 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.693+1120A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43021539 | ||||||
| chr4:43021605
|
T | C | 1 | a0001c0001t0005g0157 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.693+1186T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43021605 | ||||||
| chr4:43021652
|
C | T | 2 | a0001c0001t0005g0157a0001c0001t0005g0211 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.693+1233C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43021652 | ||||||
| chr4:43021697
|
G | A | 1 | a0001c0001t0002g0094 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.693+1278G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43021697 | ||||||
| chr4:43021727
|
G | A | 4 | a0001c0001t0002g0013a0001c0001t0002g0104a0001c0001t0005g0157others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+1308G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43021727 | ||||||
| chr4:43021749
|
A | G | 2 | a0002c0002t0001g0243a0002c0002t0001g0252 | 2 | HG00673.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.693+1330A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43021749 | ||||||
| chr4:43021752
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG02630.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.693+1333A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43021752 | ||||||
| chr4:43021862
|
T | C | 1 | a0001c0001t0002g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.693+1443T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43021862 | ||||||
| chr4:43022057
|
C | A | 1 | a0002c0002t0001g0213 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.693+1638C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43022057 | ||||||
| chr4:43022138
|
T | C | 4 | a0001c0001t0002g0013a0001c0001t0002g0104a0001c0001t0005g0157others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+1719T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43022138 | ||||||
| chr4:43022347
|
C | A | 27 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0055others(24): Show | 27 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.693+1928C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43022347 | ||||||
| chr4:43022351
|
T | C | 9 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.693+1932T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43022351 | ||||||
| chr4:43022352
|
G | A | 8 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(5): Show | 8 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.693+1933G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43022352 | ||||||
| chr4:43022378
|
C | T | 4 | a0001c0004t0002g0087a0001c0004t0002g0088a0001c0004t0002g0091others(1): Show | 4 | HG02572.hp2 HG02809.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+1959C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43022378 | ||||||
| chr4:43022397
|
G | A | 15 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(12): Show | 15 | HG00323.hp1 HG00733.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.693+1978G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43022397 | ||||||
| chr4:43022412
|
C | G | 1 | a0001c0001t0001g0077 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.693+1993C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43022412 | ||||||
| chr4:43022468
|
G | A | 101 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(98): Show | 101 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.693+2049G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43022468 | ||||||
| chr4:43022745
|
C | T | 4 | a0001c0004t0002g0087a0001c0004t0002g0088a0001c0004t0002g0091others(1): Show | 4 | HG02572.hp2 HG02809.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+2326C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43022745 | ||||||
| chr4:43022917
|
C | A | 3 | a0001c0001t0002g0086a0001c0001t0004g0137a0003c0003t0002g0327 | 3 | HG02559.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.693+2498C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43022917 | ||||||
| chr4:43023129
|
G | A | 27 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0055others(24): Show | 27 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.693+2710G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43023129 | ||||||
| chr4:43023238
|
C | A | 53 | a0001c0001t0002g0021a0001c0001t0002g0026a0001c0001t0002g0028others(50): Show | 53 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.693+2819C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43023238 | ||||||
| chr4:43023375
|
A | T | 4 | a0001c0001t0002g0013a0001c0001t0002g0104a0001c0001t0005g0157others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+2956A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43023375 | ||||||
| chr4:43023404
|
A | G | 44 | a0001c0001t0002g0021a0001c0001t0002g0026a0001c0001t0002g0028others(41): Show | 44 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.693+2985A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43023404 | ||||||
| chr4:43023412
|
G | T | 2 | a0002c0002t0001g0231a0002c0002t0001g0232 | 2 | NA19083.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.693+2993G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43023412 | ||||||
| chr4:43023439
|
C | T | 1 | a0001c0001t0010g0284 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.693+3020C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43023439 | ||||||
| chr4:43023675
|
T | C | 1 | a0001c0001t0004g0136 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.693+3256T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43023675 | ||||||
| chr4:43023701
|
A | G | 27 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0055others(24): Show | 27 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.693+3282A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43023701 | ||||||
| chr4:43023722
|
G | T | 52 | a0001c0001t0002g0021a0001c0001t0002g0026a0001c0001t0002g0028others(49): Show | 52 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.693+3303G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43023722 | ||||||
| chr4:43023816
|
G | A | 2 | a0001c0001t0002g0076a0001c0001t0004g0141 | 2 | HG01993.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.693+3397G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43023816 | ||||||
| chr4:43023856
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.693+3437T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43023856 | ||||||
| chr4:43023945
|
G | A | 6 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0281others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.693+3526G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43023945 | ||||||
| chr4:43024005
|
T | A | 1 | a0001c0001t0001g0068 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.693+3586T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43024005 | ||||||
| chr4:43024007
|
C | A | 1 | a0001c0001t0001g0068 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.693+3588C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43024007 | ||||||
| chr4:43024022
|
A | C | 2 | a0001c0001t0001g0082a0001c0001t0001g0212 | 2 | HG02145.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.693+3603A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43024022 | ||||||
| chr4:43024030
|
G | C | 2 | a0001c0001t0002g0013a0001c0001t0002g0104 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.693+3611G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43024030 | ||||||
| chr4:43024113
|
G | T | 1 | a0001c0001t0002g0007 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.693+3694G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43024113 | ||||||
| chr4:43024197
|
C | CTTTTTT | 18 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0103others(15): Show | 18 | HG00323.hp1 HG00639.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.693+3789_693+3794d others(8): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 43024197 | |||||
| chr4:43024197
|
C | CTTTTTTT | 195 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(192): Show | 195 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.693+3788_693+3794d others(9): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 43024197 | |||||
| chr4:43024197
|
C | CTTTTTTT others(1): Show |
61 | a0001c0001t0001g0006a0001c0001t0001g0061a0001c0001t0001g0068others(58): Show | 61 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.693+3787_693+3794d others(10): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 43024197 | |||||
| chr4:43024197
|
C | CTTTTTTT others(2): Show |
14 | a0001c0001t0001g0118a0001c0001t0002g0026a0001c0001t0002g0101others(11): Show | 14 | HG02572.hp1 HG02896.hp1 HG02897.hp1 others(11): Show |
intron_variant | MODIFIER | c.693+3786_693+3794d others(11): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 43024197 | |||||
| chr4:43024197
|
C | CTTTTTTT others(3): Show |
13 | a0001c0001t0002g0055a0001c0001t0002g0107a0001c0001t0002g0282others(10): Show | 13 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.693+3785_693+3794d others(12): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 43024197 | |||||
| chr4:43024197
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0002g0108a0001c0001t0004g0166 | 2 | NA19043.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.693+3784_693+3794d others(13): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 43024197 | |||||
| chr4:43024225
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.693+3806T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43024225 | ||||||
| chr4:43024259
|
G | T | 286 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(283): Show | 286 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.693+3840G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43024259 | ||||||
| chr4:43024288
|
C | G | 256 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(253): Show | 256 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.693+3869C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43024288 | ||||||
| chr4:43024373
|
C | A | 4 | a0001c0001t0002g0013a0001c0001t0002g0104a0001c0001t0005g0157others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+3954C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43024373 | ||||||
| chr4:43024511
|
T | TC | 307 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(304): Show | 307 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.693+4092_693+4093i others(3): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43024511 | ||||||
| chr4:43024541
|
G | A | 5 | a0002c0002t0001g0233a0003c0003t0001g0304a0003c0003t0001g0313others(2): Show | 5 | HG01928.hp1 HG02056.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.693+4122G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43024541 | ||||||
| chr4:43024585
|
A | G | 4 | a0001c0001t0002g0013a0001c0001t0002g0104a0001c0001t0005g0157others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+4166A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43024585 | ||||||
| chr4:43024615
|
G | A | 44 | a0001c0001t0002g0021a0001c0001t0002g0026a0001c0001t0002g0028others(41): Show | 44 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.693+4196G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43024615 | ||||||
| chr4:43024620
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.693+4201A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43024620 | ||||||
| chr4:43024715
|
A | T | 27 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0055others(24): Show | 27 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.693+4296A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43024715 | ||||||
| chr4:43025117
|
A | C | 1 | a0001c0001t0002g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.693+4698A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43025117 | ||||||
| chr4:43025124
|
A | G | 307 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(304): Show | 307 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.693+4705A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43025124 | ||||||
| chr4:43025125
|
A | T | 307 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(304): Show | 307 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.693+4706A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43025125 | ||||||
| chr4:43025126
|
C | T | 307 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(304): Show | 307 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.693+4707C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43025126 | ||||||
| chr4:43025309
|
A | G | 2 | a0001c0001t0001g0082a0001c0001t0001g0212 | 2 | HG02145.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.693+4890A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43025309 | ||||||
| chr4:43025372
|
C | T | 2 | a0001c0001t0002g0013a0001c0001t0002g0104 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.693+4953C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43025372 | ||||||
| chr4:43025443
|
CTT | C | 4 | a0001c0001t0002g0013a0001c0001t0002g0104a0001c0001t0005g0157others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-4915_694-4914d others(4): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 43025443 | |||||
| chr4:43025714
|
C | T | 1 | a0001c0001t0004g0162 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.694-4647C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43025714 | ||||||
| chr4:43025751
|
C | A | 4 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.694-4610C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43025751 | ||||||
| chr4:43025818
|
T | C | 9 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.694-4543T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43025818 | ||||||
| chr4:43025912
|
C | T | 4 | a0001c0001t0002g0013a0001c0001t0002g0104a0001c0001t0005g0157others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-4449C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43025912 | ||||||
| chr4:43025949
|
C | T | 4 | a0001c0001t0002g0013a0001c0001t0002g0104a0001c0001t0005g0157others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-4412C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43025949 | ||||||
| chr4:43025961
|
G | A | 9 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0128others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.694-4400G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43025961 | ||||||
| chr4:43025963
|
G | C | 1 | a0001c0001t0002g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.694-4398G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43025963 | ||||||
| chr4:43025971
|
G | A | 1 | a0001c0001t0003g0150 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.694-4390G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43025971 | ||||||
| chr4:43025975
|
C | CA | 84 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0061others(81): Show | 84 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.694-4369dupA | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 43025975 | |||||
| chr4:43025975
|
C | CAA | 6 | a0001c0001t0001g0109a0001c0001t0002g0080a0001c0001t0002g0281others(3): Show | 6 | HG00639.hp1 HG01978.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.694-4370_694-4369d others(4): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 43025975 | |||||
| chr4:43025975
|
CA | C | 30 | a0001c0001t0001g0004a0001c0001t0002g0001a0001c0001t0002g0002others(27): Show | 30 | HG01167.hp2 HG01168.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.694-4369delA | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 43025975 | |||||
| chr4:43026054
|
T | TA | 92 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(89): Show | 92 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.694-4307_694-4306i others(3): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43026054 | ||||||
| chr4:43026151
|
C | T | 27 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0055others(24): Show | 27 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.694-4210C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43026151 | ||||||
| chr4:43026263
|
C | G | 18 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0055others(15): Show | 18 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.694-4098C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43026263 | ||||||
| chr4:43026298
|
A | G | 1 | a0003c0003t0001g0287 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.694-4063A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43026298 | ||||||
| chr4:43026344
|
T | G | 1 | a0001c0001t0002g0049 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.694-4017T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43026344 | ||||||
| chr4:43026440
|
GCACTGGG others(53): Show |
G | 27 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0055others(24): Show | 27 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.694-3894_694-3835d others(62): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 43026440 | |||||
| chr4:43026630
|
C | T | 1 | a0001c0001t0004g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.694-3731C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43026630 | ||||||
| chr4:43026677
|
A | G | 92 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(89): Show | 92 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.694-3684A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43026677 | ||||||
| chr4:43026716
|
T | C | 4 | a0001c0001t0002g0013a0001c0001t0002g0104a0001c0001t0005g0157others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-3645T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43026716 | ||||||
| chr4:43026853
|
C | A | 1 | a0003c0003t0001g0325 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.694-3508C>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43026853 | ||||||
| chr4:43026869
|
G | A | 4 | a0001c0001t0002g0013a0001c0001t0002g0104a0001c0001t0005g0157others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-3492G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43026869 | ||||||
| chr4:43026904
|
G | A | 1 | a0003c0003t0001g0288 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.694-3457G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43026904 | ||||||
| chr4:43026914
|
C | T | 4 | a0001c0001t0002g0013a0001c0001t0002g0104a0001c0001t0005g0157others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-3447C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43026914 | ||||||
| chr4:43026966
|
G | A | 1 | a0001c0001t0002g0007 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.694-3395G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43026966 | ||||||
| chr4:43027268
|
A | T | 2 | a0001c0001t0002g0076a0001c0001t0004g0141 | 2 | HG01993.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.694-3093A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43027268 | ||||||
| chr4:43027432
|
C | G | 4 | a0001c0001t0003g0151a0001c0001t0003g0153a0001c0001t0003g0154others(1): Show | 4 | NA18942.hp1 NA18948.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.694-2929C>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43027432 | ||||||
| chr4:43027457
|
G | A | 5 | a0001c0001t0001g0099a0001c0001t0001g0105a0001c0001t0003g0194others(2): Show | 5 | NA18941.hp1 NA18957.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.694-2904G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43027457 | ||||||
| chr4:43027475
|
A | G | 1 | a0003c0003t0001g0307 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.694-2886A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43027475 | ||||||
| chr4:43027514
|
A | G | 1 | a0001c0001t0004g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.694-2847A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43027514 | ||||||
| chr4:43027569
|
G | T | 1 | a0002c0002t0001g0257 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.694-2792G>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43027569 | ||||||
| chr4:43027996
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.694-2365C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43027996 | ||||||
| chr4:43028066
|
C | T | 4 | a0001c0001t0002g0013a0001c0001t0002g0104a0001c0001t0005g0157others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-2295C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43028066 | ||||||
| chr4:43028129
|
T | A | 1 | a0001c0001t0001g0025 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.694-2232T>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43028129 | ||||||
| chr4:43028130
|
G | A | 33 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(30): Show | 33 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.694-2231G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43028130 | ||||||
| chr4:43028165
|
G | A | 18 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0055others(15): Show | 18 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.694-2196G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43028165 | ||||||
| chr4:43028171
|
G | C | 1 | a0001c0001t0002g0042 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.694-2190G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43028171 | ||||||
| chr4:43028242
|
C | T | 13 | a0001c0001t0001g0121a0001c0001t0001g0122a0002c0002t0001g0221others(10): Show | 13 | HG01928.hp1 HG02056.hp1 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.694-2119C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43028242 | ||||||
| chr4:43028486
|
G | A | 1 | a0005c0006t0011g0283 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.694-1875G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43028486 | ||||||
| chr4:43028591
|
G | A | 1 | a0001c0001t0004g0198 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.694-1770G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43028591 | ||||||
| chr4:43028637
|
C | T | 4 | a0001c0001t0002g0013a0001c0001t0002g0104a0001c0001t0005g0157others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-1724C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43028637 | ||||||
| chr4:43028671
|
G | A | 3 | a0001c0001t0003g0194a0001c0001t0003g0195a0001c0001t0003g0196 | 3 | NA18941.hp1 NA18957.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.694-1690G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43028671 | ||||||
| chr4:43028794
|
G | C | 4 | a0001c0001t0002g0013a0001c0001t0002g0104a0001c0001t0005g0157others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-1567G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43028794 | ||||||
| chr4:43028947
|
C | T | 31 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(28): Show | 31 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.694-1414C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43028947 | ||||||
| chr4:43029023
|
A | G | 3 | a0002c0002t0001g0257a0003c0003t0001g0298a0003c0003t0001g0338 | 3 | HG02155.hp1 NA18949.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.694-1338A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43029023 | ||||||
| chr4:43029433
|
C | T | 2 | a0001c0001t0002g0030a0001c0001t0002g0031 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.694-928C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43029433 | ||||||
| chr4:43029441
|
T | G | 4 | a0001c0001t0002g0014a0001c0001t0004g0155a0001c0001t0004g0156others(1): Show | 4 | HG02615.hp1 HG02886.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-920T>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43029441 | ||||||
| chr4:43029444
|
T | C | 27 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0055others(24): Show | 27 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.694-917T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43029444 | ||||||
| chr4:43029480
|
T | C | 2 | a0001c0001t0002g0013a0001c0001t0002g0104 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.694-881T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43029480 | ||||||
| chr4:43029488
|
C | T | 1 | a0003c0003t0002g0324 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.694-873C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43029488 | ||||||
| chr4:43029606
|
C | T | 2 | a0001c0001t0006g0003a0001c0001t0006g0016 | 2 | HG02572.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.694-755C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43029606 | ||||||
| chr4:43029739
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.694-622A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43029739 | ||||||
| chr4:43029757
|
G | C | 1 | a0001c0001t0002g0033 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.694-604G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43029757 | ||||||
| chr4:43029764
|
G | A | 1 | a0001c0001t0002g0081 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.694-597G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43029764 | ||||||
| chr4:43029817
|
C | T | 2 | a0001c0001t0005g0157a0001c0001t0005g0211 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.694-544C>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43029817 | ||||||
| chr4:43029851
|
A | T | 6 | a0001c0001t0002g0030a0001c0001t0002g0031a0001c0001t0002g0281others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.694-510A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43029851 | ||||||
| chr4:43029972
|
C | CAA | 33 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0013others(30): Show | 33 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.694-388_694-387ins others(2): Show |
GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 43029972 | |||||
| chr4:43029980
|
A | G | 1 | a0002c0002t0001g0273 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.694-381A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43029980 | ||||||
| chr4:43029993
|
A | T | 1 | a0002c0002t0001g0235 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.694-368A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43029993 | ||||||
| chr4:43030025
|
A | G | 1 | a0001c0001t0002g0044 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.694-336A>G | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43030025 | ||||||
| chr4:43030035
|
G | A | 7 | a0001c0001t0002g0018a0001c0001t0002g0020a0001c0001t0002g0022others(4): Show | 7 | HG02257.hp1 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.694-326G>A | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43030035 | ||||||
| chr4:43030035
|
G | C | 2 | a0003c0003t0002g0291a0003c0003t0002g0297 | 2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.694-326G>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43030035 | ||||||
| chr4:43030213
|
A | T | 1 | a0003c0003t0002g0327 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.694-148A>T | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43030213 | ||||||
| chr4:43030229
|
T | C | 1 | a0003c0003t0002g0329 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.694-132T>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43030229 | ||||||
| chr4:43030275
|
A | C | 1 | a0001c0001t0002g0052 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.694-86A>C | GRXCR1 | ENSG00000215203.3 | transcript | ENST00000399770.3 | protein_coding | 3/3 | chr4 | 43030275 |