| geneid | 23151 |
|---|---|
| ensemblid | ENSG00000075240.17 |
| hgncid | 29113 |
| symbol | GRAMD4 |
| name | GRAM domain containing 4 |
| refseq_nuc | NM_015124.5 |
| refseq_prot | NP_055939.1 |
| ensembl_nuc | ENST00000406902.6 |
| ensembl_prot | ENSP00000385689.1 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 46620386 |
| end | 46679785 |
| strand | + |
| ver | v1.2 |
| region | chr22:46620386-46679785 |
| region5000 | chr22:46615386-46684785 |
| regionname0 | GRAMD4_chr22_46620386_46679785 |
| regionname5000 | GRAMD4_chr22_46615386_46684785 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 578 | 326 | 82 | 70 | 120 | 14 | 38 | 84 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0002 | 0/0 | 578 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1737 | 297 | 69 | 63 | 116 | 14 | 34 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| c0002 | 0/0 | 1737 | 20 | 9 | 6 | 2 | 0 | 3 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| c0003 | 0/0 | 1737 | 2 | 2 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| c0004 | 1/0 | 1737 | 2 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| c0005 | 0/0 | 1737 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| c0006 | 0/0 | 1737 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| c0007 | 0/0 | 1737 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| c0008 | 0/0 | 1737 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| c0009 | 0/0 | 1737 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| c0010 | 0/0 | 1737 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| c0011 | 0/0 | 1737 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| 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 | 2764 | 78 | 0 | 14 | 56 | 0 | 8 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0002 | 0/0 | 2764 | 52 | 1 | 16 | 25 | 6 | 4 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0003 | 0/1 | 2764 | 43 | 13 | 12 | 4 | 5 | 8 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0004 | 0/0 | 2764 | 25 | 15 | 5 | 2 | 0 | 3 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0005 | 0/0 | 2764 | 16 | 6 | 2 | 0 | 1 | 7 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0006 | 0/0 | 2764 | 14 | 0 | 0 | 14 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0007 | 0/0 | 2763 | 9 | 7 | 2 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0008 | 0/0 | 2765 | 9 | 9 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0009 | 0/0 | 2764 | 6 | 1 | 3 | 0 | 0 | 2 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0010 | 0/0 | 2764 | 4 | 4 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0011 | 0/0 | 2765 | 3 | 3 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0012 | 0/0 | 2763 | 3 | 0 | 0 | 2 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0013 | 0/0 | 2763 | 2 | 1 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0014 | 0/0 | 2764 | 2 | 1 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0015 | 0/0 | 2764 | 2 | 2 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0016 | 1/0 | 2764 | 2 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0017 | 0/0 | 2764 | 2 | 1 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0018 | 0/0 | 2763 | 2 | 1 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0019 | 0/0 | 2763 | 2 | 2 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0020 | 0/0 | 2764 | 2 | 1 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0021 | 0/0 | 2764 | 2 | 0 | 0 | 2 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0022 | 0/0 | 2764 | 2 | 0 | 0 | 2 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0023 | 0/0 | 2764 | 2 | 0 | 2 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0024 | 0/0 | 2764 | 2 | 0 | 2 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0025 | 0/0 | 2764 | 2 | 1 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0026 | 0/0 | 2764 | 2 | 0 | 0 | 2 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0027 | 0/0 | 2764 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0028 | 0/0 | 2764 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0029 | 0/0 | 2764 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0030 | 0/0 | 2765 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0031 | 0/0 | 2764 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0032 | 0/0 | 2764 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0033 | 0/0 | 2763 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0034 | 0/0 | 2763 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0035 | 0/0 | 2763 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0036 | 0/0 | 2763 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0037 | 0/0 | 2764 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0038 | 0/0 | 2764 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0039 | 0/0 | 2764 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0040 | 0/0 | 2764 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0041 | 0/0 | 2765 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0042 | 0/0 | 2764 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0043 | 0/0 | 2764 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0044 | 0/0 | 2764 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0045 | 0/0 | 2764 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0046 | 0/0 | 2764 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0047 | 0/0 | 2764 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0048 | 0/0 | 2764 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0049 | 0/0 | 2764 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0050 | 0/0 | 2764 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0051 | 0/0 | 2764 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0052 | 0/0 | 2764 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0053 | 0/0 | 2764 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0054 | 0/0 | 2764 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0055 | 0/0 | 2765 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0056 | 0/0 | 2764 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0057 | 0/0 | 2764 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0058 | 0/0 | 2764 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0059 | 0/0 | 2764 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0060 | 0/0 | 2764 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0061 | 0/0 | 2764 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0062 | 0/0 | 2764 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0063 | 0/0 | 2764 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| t0064 | 0/0 | 2764 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0051 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0223 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1737 | 297 | 69 | 63 | 116 | 14 | 34 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0002 | 0/0 | 1737 | 20 | 9 | 6 | 2 | 0 | 3 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0003 | 0/0 | 1737 | 2 | 2 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0004 | 1/0 | 1737 | 2 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0005 | 0/0 | 1737 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0006 | 0/0 | 1737 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0007 | 0/0 | 1737 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0008 | 0/0 | 1737 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0009 | 0/0 | 1737 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0002c0010 | 0/0 | 1737 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0002c0011 | 0/0 | 1737 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4500 | 77 | 0 | 14 | 55 | 0 | 8 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0002 | 0/0 | 4500 | 50 | 1 | 16 | 25 | 6 | 2 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0003 | 0/1 | 4500 | 41 | 11 | 12 | 4 | 5 | 8 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0004 | 0/0 | 4500 | 7 | 6 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0005 | 0/0 | 4500 | 16 | 6 | 2 | 0 | 1 | 7 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0006 | 0/0 | 4500 | 14 | 0 | 0 | 14 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0007 | 0/0 | 4499 | 9 | 7 | 2 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0008 | 0/0 | 4501 | 9 | 9 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0009 | 0/0 | 4500 | 6 | 1 | 3 | 0 | 0 | 2 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0010 | 0/0 | 4500 | 4 | 4 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0011 | 0/0 | 4501 | 3 | 3 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0012 | 0/0 | 4499 | 3 | 0 | 0 | 2 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0013 | 0/0 | 4499 | 2 | 1 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0014 | 0/0 | 4500 | 2 | 1 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0015 | 0/0 | 4500 | 2 | 2 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0016 | 0/0 | 4500 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0017 | 0/0 | 4500 | 2 | 1 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0018 | 0/0 | 4499 | 2 | 1 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0019 | 0/0 | 4499 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0020 | 0/0 | 4500 | 2 | 1 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0021 | 0/0 | 4500 | 2 | 0 | 0 | 2 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0022 | 0/0 | 4500 | 2 | 0 | 0 | 2 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0023 | 0/0 | 4500 | 2 | 0 | 2 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0024 | 0/0 | 4500 | 2 | 0 | 2 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0025 | 0/0 | 4500 | 2 | 1 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0026 | 0/0 | 4500 | 2 | 0 | 0 | 2 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0027 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0028 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0029 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0030 | 0/0 | 4501 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0031 | 0/0 | 4500 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0032 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0033 | 0/0 | 4499 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0034 | 0/0 | 4499 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0035 | 0/0 | 4499 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0036 | 0/0 | 4499 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0037 | 0/0 | 4500 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0038 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0039 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0040 | 0/0 | 4500 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0041 | 0/0 | 4501 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0043 | 0/0 | 4500 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0044 | 0/0 | 4500 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0045 | 0/0 | 4500 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0048 | 0/0 | 4500 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0049 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0050 | 0/0 | 4500 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0051 | 0/0 | 4500 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0052 | 0/0 | 4500 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0054 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0056 | 0/0 | 4500 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0057 | 0/0 | 4500 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0058 | 0/0 | 4500 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0059 | 0/0 | 4500 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0060 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0061 | 0/0 | 4500 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0063 | 0/0 | 4500 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0001t0064 | 0/0 | 4500 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0002t0002 | 0/0 | 4500 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0002t0004 | 0/0 | 4500 | 18 | 9 | 5 | 2 | 0 | 2 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0002t0046 | 0/0 | 4500 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0003t0003 | 0/0 | 4500 | 2 | 2 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0004t0001 | 0/0 | 4500 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0004t0016 | 1/0 | 4500 | 1 | 0 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0005t0002 | 0/0 | 4500 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0006t0042 | 0/0 | 4500 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0007t0019 | 0/0 | 4499 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0008t0055 | 0/0 | 4501 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0001c0009t0062 | 0/0 | 4500 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0002c0010t0047 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| a0002c0011t0053 | 0/0 | 4500 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | copy fasta | chr22 | 46615386 | 46684785 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0223 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0005g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0005g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0005g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0005g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0005g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0005g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0005g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0005g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0006g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0006g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0006g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0006g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0006g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0006g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0006g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0006g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0006g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0006g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0006g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0006g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0006g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0006g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0007g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0007g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0007g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0007g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0007g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0007g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0008g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0008g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0008g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0008g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0008g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0008g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0008g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0008g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0008g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0009g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0009g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0009g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0009g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0009g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0009g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0010g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0010g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0010g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0010g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0011g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0011g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0011g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0012g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0012g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0012g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0013g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0013g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0014g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0014g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0015g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0015g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0016g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0017g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0017g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0018g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0018g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0019g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0020g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0020g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0021g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0021g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0022g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0022g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0023g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0023g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0024g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0025g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0025g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0026g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0026g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0027g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0028g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0029g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0030g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0031g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0032g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0033g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0034g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0035g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0036g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0037g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0038g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0039g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0040g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0041g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0043g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0044g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0045g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0048g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0049g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0050g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0051g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0052g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0054g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0056g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0057g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0058g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0059g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0060g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0061g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0063g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0001t0064g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0002t0004g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0002t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0002t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0002t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0002t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0002t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0002t0004g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0002t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0002t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0002t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0002t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0002t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0002t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0002t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0002t0004g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0002t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0002t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0002t0046g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0003t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0003t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0004t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0004t0016g0051 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0005t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0006t0042g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0007t0019g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0008t0055g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0001c0009t0062g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0002c0010t0047g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| a0002c0011t0053g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0297 | EUR | GBR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0208 | EUR | GBR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0248 | EUR | GBR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0269 | EUR | GBR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0319 | EUR | FIN | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG00323 | hp2 | a0001 | c0001 | t0005 | g0145 | EUR | FIN | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | CHS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG00438 | hp2 | a0001 | c0001 | t0006 | g0192 | EAS | CHS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG00597 | hp1 | a0001 | c0006 | t0042 | g0318 | EAS | CHS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | CHS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0281 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0312 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG00642 | hp2 | a0001 | c0001 | t0007 | g0027 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG00673 | hp2 | a0001 | c0001 | t0021 | g0156 | EAS | CHS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0245 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG00733 | hp2 | a0001 | c0001 | t0025 | g0265 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0266 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG00735 | hp2 | a0001 | c0001 | t0056 | g0313 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0315 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0258 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0206 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG00741 | hp2 | a0001 | c0001 | t0064 | g0306 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01069 | hp1 | a0001 | c0001 | t0024 | g0004 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0305 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0104 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01070 | hp2 | a0001 | c0001 | t0013 | g0020 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0169 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01071 | hp2 | a0001 | c0001 | t0024 | g0004 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0214 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01106 | hp1 | a0001 | c0001 | t0009 | g0047 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01106 | hp2 | a0001 | c0009 | t0062 | g0303 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01109 | hp1 | a0001 | c0002 | t0004 | g0095 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0307 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01168 | hp1 | a0001 | c0001 | t0009 | g0050 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01168 | hp2 | a0001 | c0001 | t0005 | g0142 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0259 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0225 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01243 | hp1 | a0001 | c0001 | t0007 | g0033 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0085 | AMR | PUR | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0310 | AMR | CLM | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0226 | AMR | CLM | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0212 | AMR | CLM | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0314 | AMR | CLM | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0240 | AMR | CLM | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01361 | hp1 | a0001 | c0001 | t0063 | g0227 | AMR | CLM | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01361 | hp2 | a0001 | c0002 | t0046 | g0089 | AMR | CLM | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01433 | hp1 | a0001 | c0001 | t0048 | g0191 | AMR | CLM | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0205 | AMR | CLM | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01496 | hp1 | a0001 | c0001 | t0014 | g0058 | AMR | CLM | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01496 | hp2 | a0001 | c0002 | t0004 | g0002 | AMR | CLM | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01515 | hp1 | a0001 | c0001 | t0018 | g0247 | EUR | IBS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0279 | EUR | IBS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0283 | EUR | IBS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0241 | EUR | IBS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0007 | EUR | IBS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0224 | EUR | IBS | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0061 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01884 | hp2 | a0001 | c0001 | t0010 | g0185 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0243 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01891 | hp2 | a0001 | c0002 | t0004 | g0092 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01934 | hp2 | a0001 | c0002 | t0004 | g0117 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01943 | hp2 | a0001 | c0001 | t0020 | g0231 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01952 | hp1 | a0001 | c0001 | t0023 | g0122 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01952 | hp2 | a0001 | c0001 | t0017 | g0045 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01975 | hp1 | a0001 | c0002 | t0004 | g0118 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0296 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01978 | hp1 | a0001 | c0001 | t0009 | g0056 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01981 | hp2 | a0001 | c0001 | t0043 | g0311 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG01993 | hp2 | a0001 | c0002 | t0004 | g0086 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02015 | hp1 | a0001 | c0001 | t0006 | g0194 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02027 | hp2 | a0001 | c0001 | t0040 | g0246 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02040 | hp2 | a0001 | c0001 | t0036 | g0173 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02071 | hp1 | a0001 | c0001 | t0006 | g0102 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02071 | hp2 | a0001 | c0001 | t0022 | g0138 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02135 | hp2 | a0001 | c0001 | t0006 | g0164 | EAS | KHV | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02145 | hp1 | a0001 | c0001 | t0027 | g0038 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02145 | hp2 | a0001 | c0001 | t0009 | g0049 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0293 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | CDX | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CDX | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02257 | hp1 | a0001 | c0001 | t0029 | g0053 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02257 | hp2 | a0001 | c0001 | t0017 | g0043 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02258 | hp1 | a0001 | c0001 | t0032 | g0046 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0298 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0299 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02293 | hp2 | a0001 | c0001 | t0023 | g0121 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0221 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02451 | hp1 | a0001 | c0002 | t0004 | g0096 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0025 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02572 | hp2 | a0002 | c0011 | t0053 | g0019 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02615 | hp1 | a0001 | c0001 | t0007 | g0028 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0001 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02622 | hp1 | a0001 | c0002 | t0004 | g0091 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0036 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0024 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0084 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02647 | hp1 | a0001 | c0002 | t0004 | g0069 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02647 | hp2 | a0001 | c0001 | t0054 | g0251 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02683 | hp1 | a0001 | c0001 | t0009 | g0048 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0228 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0250 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02698 | hp2 | a0001 | c0001 | t0035 | g0263 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0083 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0233 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02723 | hp1 | a0001 | c0001 | t0008 | g0011 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02723 | hp2 | a0001 | c0001 | t0011 | g0183 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02735 | hp1 | a0001 | c0001 | t0050 | g0147 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02735 | hp2 | a0001 | c0001 | t0005 | g0213 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02738 | hp1 | a0001 | c0001 | t0016 | g0018 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02738 | hp2 | a0001 | c0001 | t0009 | g0054 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02809 | hp1 | a0001 | c0001 | t0008 | g0010 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02809 | hp2 | a0001 | c0001 | t0018 | g0230 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02818 | hp1 | a0001 | c0001 | t0008 | g0009 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0001 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02886 | hp1 | a0002 | c0010 | t0047 | g0064 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02886 | hp2 | a0001 | c0002 | t0004 | g0097 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02896 | hp1 | a0001 | c0001 | t0019 | g0062 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0039 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0188 | AFR | ESN | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0035 | AFR | ESN | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02965 | hp1 | a0001 | c0002 | t0004 | g0032 | AFR | ESN | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02965 | hp2 | a0001 | c0001 | t0030 | g0044 | AFR | ESN | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02970 | hp1 | a0001 | c0002 | t0004 | g0094 | AFR | ESN | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02970 | hp2 | a0001 | c0007 | t0019 | g0182 | AFR | ESN | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0014 | AFR | ESN | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02976 | hp2 | a0001 | c0001 | t0033 | g0037 | AFR | ESN | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0216 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0237 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03041 | hp1 | a0001 | c0001 | t0028 | g0060 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03041 | hp2 | a0001 | c0001 | t0049 | g0042 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03098 | hp1 | a0001 | c0002 | t0004 | g0093 | AFR | MSL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0040 | AFR | MSL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03130 | hp1 | a0001 | c0001 | t0015 | g0190 | AFR | ESN | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | ESN | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0218 | AFR | ESN | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03195 | hp2 | a0001 | c0001 | t0020 | g0232 | AFR | ESN | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0023 | AFR | MSL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03225 | hp2 | a0001 | c0001 | t0008 | g0015 | AFR | MSL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0063 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0234 | AFR | MSL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03486 | hp2 | a0001 | c0001 | t0060 | g0280 | AFR | MSL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0207 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03491 | hp2 | a0001 | c0001 | t0012 | g0005 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03492 | hp2 | a0001 | c0001 | t0031 | g0059 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03516 | hp1 | a0001 | c0001 | t0008 | g0012 | AFR | ESN | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0013 | AFR | ESN | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0041 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0029 | AFR | GWD | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03579 | hp1 | a0001 | c0001 | t0038 | g0180 | AFR | MSL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03579 | hp2 | a0001 | c0001 | t0039 | g0077 | AFR | MSL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0105 | SAS | PJL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03688 | hp1 | a0001 | c0002 | t0004 | g0099 | SAS | STU | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03688 | hp2 | a0001 | c0001 | t0005 | g0143 | SAS | STU | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | BEB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0244 | SAS | BEB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0215 | SAS | BEB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0111 | SAS | BEB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03927 | hp1 | a0001 | c0002 | t0004 | g0090 | SAS | BEB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0222 | SAS | BEB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0144 | SAS | BEB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0274 | SAS | BEB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG04115 | hp1 | a0001 | c0005 | t0002 | g0294 | SAS | STU | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0071 | SAS | STU | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG04199 | hp1 | a0001 | c0001 | t0045 | g0140 | SAS | STU | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG04199 | hp2 | a0001 | c0001 | t0005 | g0211 | SAS | STU | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | STU | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | STU | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0278 | SAS | STU | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | STU | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18522 | hp1 | a0001 | c0001 | t0015 | g0189 | AFR | YRI | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | YRI | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | CHB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CHB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18906 | hp1 | a0001 | c0001 | t0008 | g0016 | AFR | YRI | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0008 | AFR | YRI | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18946 | hp2 | a0001 | c0001 | t0006 | g0195 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18948 | hp1 | a0001 | c0001 | t0006 | g0170 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18951 | hp1 | a0001 | c0001 | t0012 | g0079 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18959 | hp2 | a0001 | c0001 | t0006 | g0199 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18964 | hp1 | a0001 | c0001 | t0012 | g0078 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18969 | hp2 | a0001 | c0001 | t0006 | g0198 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18970 | hp1 | a0001 | c0001 | t0059 | g0284 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18971 | hp2 | a0001 | c0001 | t0037 | g0065 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18975 | hp1 | a0001 | c0002 | t0004 | g0088 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18975 | hp2 | a0001 | c0001 | t0026 | g0082 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18980 | hp2 | a0001 | c0001 | t0052 | g0136 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18985 | hp2 | a0001 | c0004 | t0001 | g0321 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18991 | hp2 | a0001 | c0002 | t0004 | g0070 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18994 | hp2 | a0001 | c0001 | t0006 | g0076 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18995 | hp2 | a0001 | c0001 | t0044 | g0316 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18998 | hp1 | a0001 | c0001 | t0006 | g0200 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19002 | hp1 | a0001 | c0001 | t0022 | g0176 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19030 | hp1 | a0001 | c0008 | t0055 | g0067 | AFR | LWK | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0242 | AFR | LWK | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19043 | hp1 | a0001 | c0001 | t0011 | g0057 | AFR | LWK | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19043 | hp2 | a0001 | c0001 | t0041 | g0006 | AFR | LWK | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19056 | hp1 | a0001 | c0001 | t0034 | g0201 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19057 | hp1 | a0001 | c0001 | t0061 | g0289 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19064 | hp1 | a0001 | c0001 | t0021 | g0155 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19065 | hp1 | a0001 | c0001 | t0058 | g0277 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19067 | hp1 | a0001 | c0001 | t0026 | g0292 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19068 | hp2 | a0001 | c0001 | t0051 | g0162 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19074 | hp2 | a0001 | c0001 | t0006 | g0202 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19081 | hp2 | a0001 | c0001 | t0006 | g0174 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19085 | hp2 | a0001 | c0001 | t0006 | g0302 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19090 | hp1 | a0001 | c0001 | t0006 | g0193 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19240 | hp1 | a0001 | c0001 | t0010 | g0034 | AFR | YRI | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA19240 | hp2 | a0001 | c0001 | t0010 | g0187 | AFR | YRI | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA20752 | hp1 | a0001 | c0001 | t0057 | g0304 | EUR | TSI | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0268 | EUR | TSI | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | GIH | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0295 | SAS | GIH | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02109 | hp1 | a0001 | c0001 | t0025 | g0256 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02109 | hp2 | a0001 | c0003 | t0003 | g0235 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02486 | hp1 | a0001 | c0001 | t0014 | g0052 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02486 | hp2 | a0001 | c0001 | t0013 | g0055 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0026 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03471 | hp1 | a0001 | c0001 | t0007 | g0022 | AFR | MSL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG03471 | hp2 | a0001 | c0001 | t0010 | g0186 | AFR | MSL | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0267 | AFR | USA | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | USA | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA20300 | hp1 | a0001 | c0001 | t0011 | g0184 | AFR | USA | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA20300 | hp2 | a0001 | c0002 | t0004 | g0002 | AFR | USA | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA21309 | hp1 | a0001 | c0003 | t0003 | g0236 | AFR | LWK | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0229 | AFR | LWK | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0223 | REF | REF | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| homoSapiens_grch38 | hp1 | a0001 | c0004 | t0016 | g0051 | REF | REF | GRAMD4_chr22_46615386_46684785 | GRAMD4 | chr22 | 46615386 | 46684785 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:46626917
|
G | T | 1 | a0002 | 2 | HG02572.hp2 HG02886.hp1 |
missense_variant | MODERATE | c.118G>T | p.Val40Leu | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/19 | 347/4500 | 118/1737 | 40/578 | chr22 | 46626917 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:46663095
|
T | C | 10 | a0001c0001a0001c0002a0001c0003others(7): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
synonymous_variant | LOW | c.522T>C | p.Phe174Phe | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 6/19 | 751/4500 | 522/1737 | 174/578 | chr22 | 46663095 | ||
| chr22:46663104
|
C | T | 1 | a0001c0009 | 1 | HG01106.hp2 | synonymous_variant | LOW | c.531C>T | p.Tyr177Tyr | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 6/19 | 760/4500 | 531/1737 | 177/578 | chr22 | 46663104 | ||
| chr22:46664030
|
C | T | 1 | a0001c0008 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.630C>T | p.Arg210Arg | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/19 | 859/4500 | 630/1737 | 210/578 | chr22 | 46664030 | ||
| chr22:46664042
|
G | A | 2 | a0001c0002a0002c0010 | 21 | HG01109.hp1 HG01361.hp2 HG01496.hp2 others(18): Show |
synonymous_variant | LOW | c.642G>A | p.Pro214Pro | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/19 | 871/4500 | 642/1737 | 214/578 | chr22 | 46664042 | ||
| chr22:46668155
|
C | T | 1 | a0001c0003 | 2 | HG02109.hp2 NA21309.hp1 |
synonymous_variant | LOW | c.918C>T | p.Ala306Ala | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 11/19 | 1147/4500 | 918/1737 | 306/578 | chr22 | 46668155 | ||
| chr22:46674727
|
C | T | 1 | a0001c0007 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.1455C>T | p.Asn485Asn | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 16/19 | 1684/4500 | 1455/1737 | 485/578 | chr22 | 46674727 | ||
| chr22:46674745
|
G | A | 1 | a0001c0005 | 1 | HG04115.hp1 | synonymous_variant | LOW | c.1473G>A | p.Thr491Thr | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 16/19 | 1702/4500 | 1473/1737 | 491/578 | chr22 | 46674745 | ||
| chr22:46675507
|
G | A | 1 | a0001c0006 | 1 | HG00597.hp1 | synonymous_variant | LOW | c.1518G>A | p.Lys506Lys | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 17/19 | 1747/4500 | 1518/1737 | 506/578 | chr22 | 46675507 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:46620455
|
C | T | 57 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(54): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
5_prime_UTR_variant | MODIFIER | c.-160C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/19 | 6345 | chr22 | 46620455 | |||||
| chr22:46620456
|
G | A | 1 | a0001c0001t0027 | 1 | HG02145.hp1 | 5_prime_UTR_variant | MODIFIER | c.-159G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/19 | 6344 | chr22 | 46620456 | |||||
| chr22:46677302
|
CT | C | 11 | a0001c0001t0007a0001c0001t0012a0001c0001t0013others(8): Show | 23 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*64delT | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 64 | INFO_REALIGN_3_PRIME | chr22 | 46677302 | ||||
| chr22:46677357
|
T | C | 3 | a0001c0001t0007a0001c0001t0013a0001c0001t0029 | 12 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*106T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 106 | chr22 | 46677357 | |||||
| chr22:46677525
|
G | A | 1 | a0001c0001t0037 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*274G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 274 | chr22 | 46677525 | |||||
| chr22:46677560
|
C | G | 1 | a0001c0001t0064 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*309C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 309 | chr22 | 46677560 | |||||
| chr22:46677631
|
C | T | 1 | a0001c0001t0032 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*380C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 380 | chr22 | 46677631 | |||||
| chr22:46677670
|
A | G | 1 | a0001c0001t0063 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*419A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 419 | chr22 | 46677670 | |||||
| chr22:46677824
|
C | T | 18 | a0001c0001t0002a0001c0001t0006a0001c0001t0017others(15): Show | 83 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*573C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 573 | chr22 | 46677824 | |||||
| chr22:46677831
|
C | T | 1 | a0001c0009t0062 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*580C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 580 | chr22 | 46677831 | |||||
| chr22:46677836
|
G | A | 1 | a0001c0001t0038 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*585G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 585 | chr22 | 46677836 | |||||
| chr22:46677879
|
A | G | 10 | a0001c0001t0007a0001c0001t0011a0001c0001t0013others(7): Show | 21 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*628A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 628 | chr22 | 46677879 | |||||
| chr22:46677904
|
G | A | 9 | a0001c0001t0003a0001c0001t0014a0001c0001t0018others(6): Show | 53 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*653G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 653 | chr22 | 46677904 | |||||
| chr22:46677961
|
C | G | 1 | a0001c0001t0031 | 1 | HG03492.hp2 | 3_prime_UTR_variant | MODIFIER | c.*710C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 710 | chr22 | 46677961 | |||||
| chr22:46677964
|
C | T | 9 | a0001c0001t0003a0001c0001t0014a0001c0001t0018others(6): Show | 53 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*713C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 713 | chr22 | 46677964 | |||||
| chr22:46677978
|
T | C | 44 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(41): Show | 172 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*727T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 727 | chr22 | 46677978 | |||||
| chr22:46678047
|
G | A | 1 | a0001c0001t0039 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*796G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 796 | chr22 | 46678047 | |||||
| chr22:46678212
|
C | G | 4 | a0001c0001t0005a0001c0001t0009a0001c0001t0049others(1): Show | 24 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*961C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 961 | chr22 | 46678212 | |||||
| chr22:46678240
|
C | T | 1 | a0001c0001t0061 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*989C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 989 | chr22 | 46678240 | |||||
| chr22:46678300
|
C | T | 2 | a0001c0001t0038a0001c0001t0048 | 2 | HG01433.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1049C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 1049 | chr22 | 46678300 | |||||
| chr22:46678360
|
C | G | 1 | a0001c0001t0060 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1109C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 1109 | chr22 | 46678360 | |||||
| chr22:46678361
|
G | A | 19 | a0001c0001t0002a0001c0001t0006a0001c0001t0017others(16): Show | 84 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*1110G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 1110 | chr22 | 46678361 | |||||
| chr22:46678365
|
G | A | 1 | a0002c0011t0053 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1114G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 1114 | chr22 | 46678365 | |||||
| chr22:46678373
|
G | C | 5 | a0001c0001t0006a0001c0001t0034a0001c0001t0036others(2): Show | 18 | HG00438.hp2 HG00597.hp1 HG02015.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1122G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 1122 | chr22 | 46678373 | |||||
| chr22:46678384
|
G | A | 20 | a0001c0001t0002a0001c0001t0006a0001c0001t0017others(17): Show | 85 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*1133G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 1133 | chr22 | 46678384 | |||||
| chr22:46678584
|
C | T | 1 | a0002c0010t0047 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1333C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 1333 | chr22 | 46678584 | |||||
| chr22:46678621
|
C | T | 1 | a0001c0001t0052 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1370C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 1370 | chr22 | 46678621 | |||||
| chr22:46678944
|
C | T | 1 | a0001c0001t0024 | 2 | HG01069.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1693C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 1693 | chr22 | 46678944 | |||||
| chr22:46679040
|
T | C | 45 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(42): Show | 177 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*1789T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 1789 | chr22 | 46679040 | |||||
| chr22:46679146
|
T | C | 1 | a0001c0001t0054 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1895T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 1895 | chr22 | 46679146 | |||||
| chr22:46679168
|
A | C | 1 | a0001c0001t0020 | 2 | HG01943.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1917A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 1917 | chr22 | 46679168 | |||||
| chr22:46679352
|
G | GC | 6 | a0001c0001t0008a0001c0001t0011a0001c0001t0028others(3): Show | 16 | HG02723.hp1 HG02723.hp2 HG02809.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2106dupC | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 2107 | INFO_REALIGN_3_PRIME | chr22 | 46679352 | ||||
| chr22:46679381
|
G | A | 1 | a0001c0001t0056 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2130G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 2130 | chr22 | 46679381 | |||||
| chr22:46679385
|
G | T | 2 | a0001c0001t0019a0001c0007t0019 | 2 | HG02896.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2134G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 2134 | chr22 | 46679385 | |||||
| chr22:46679565
|
C | T | 47 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(44): Show | 179 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*2314C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 2314 | chr22 | 46679565 | |||||
| chr22:46679696
|
A | T | 1 | a0001c0001t0025 | 2 | HG00733.hp2 HG02109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2445A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 19/19 | 2445 | chr22 | 46679696 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:46620567
|
T | TAGGGGGC | 133 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0204others(130): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.-50+23_-50+29dupCA others(5): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46620567 | |||||
| chr22:46620645
|
A | C | 3 | a0001c0001t0015g0189a0001c0001t0015g0190a0001c0001t0048g0191 | 3 | HG01433.hp1 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-50+80A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46620645 | ||||||
| chr22:46620729
|
G | A | 3 | a0001c0001t0015g0189a0001c0001t0015g0190a0001c0001t0048g0191 | 3 | HG01433.hp1 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-50+164G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46620729 | ||||||
| chr22:46620762
|
G | A | 3 | a0001c0001t0015g0189a0001c0001t0015g0190a0001c0001t0048g0191 | 3 | HG01433.hp1 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-50+197G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46620762 | ||||||
| chr22:46620985
|
A | G | 7 | a0001c0001t0005g0188a0001c0001t0010g0185a0001c0001t0010g0186others(4): Show | 7 | HG01884.hp2 HG02723.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50+420A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46620985 | ||||||
| chr22:46621033
|
G | A | 1 | a0001c0007t0019g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-50+468G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621033 | ||||||
| chr22:46621074
|
C | T | 2 | a0001c0001t0001g0181a0001c0001t0038g0180 | 2 | HG03579.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-50+509C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621074 | ||||||
| chr22:46621086
|
G | A | 10 | a0001c0001t0004g0017a0001c0001t0008g0008a0001c0001t0008g0009others(7): Show | 10 | HG02572.hp1 HG02723.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-50+521G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621086 | ||||||
| chr22:46621139
|
C | T | 122 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(119): Show | 125 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.-50+574C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621139 | ||||||
| chr22:46621153
|
A | G | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-50+588A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621153 | ||||||
| chr22:46621158
|
G | T | 5 | a0001c0001t0005g0188a0001c0001t0010g0185a0001c0001t0010g0186others(2): Show | 5 | HG01884.hp2 HG02922.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-50+593G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621158 | ||||||
| chr22:46621388
|
T | C | 1 | a0001c0001t0016g0018 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-50+823T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621388 | ||||||
| chr22:46621441
|
TGGAGGGC others(65): Show |
T | 2 | a0001c0001t0013g0020a0001c0001t0048g0191 | 2 | HG01070.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.-50+1011_-50+1082d others(74): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46621441 | |||||
| chr22:46621441
|
TGGAGGGC others(137): Show |
T | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-50+939_-50+1082de others(1): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46621441 | |||||
| chr22:46621504
|
GGTGTGTC others(137): Show |
G | 14 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0204others(11): Show | 14 | HG00438.hp2 HG00621.hp2 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.-50+976_-50+1119de others(1): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46621504 | |||||
| chr22:46621514
|
G | A | 1 | a0001c0001t0037g0065 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-50+949G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621514 | ||||||
| chr22:46621528
|
CCCCGGTG others(64): Show |
C | 1 | a0001c0001t0001g0066 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-50+967_-50+1037de others(72): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46621528 | |||||
| chr22:46621541
|
GCAGGCTG others(137): Show |
G | 1 | a0001c0001t0005g0063 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-50+1002_-50+1145d others(2): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46621541 | |||||
| chr22:46621551
|
GGCGTAGC others(209): Show |
G | 1 | a0002c0010t0047g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-50+988_-50+1203de others(1): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46621551 | |||||
| chr22:46621567
|
A | G | 1 | a0001c0001t0002g0320 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-50+1002A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621567 | ||||||
| chr22:46621576
|
G | A | 2 | a0001c0001t0015g0189a0001c0001t0015g0190 | 2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-50+1011G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621576 | ||||||
| chr22:46621576
|
GGTGTGTC others(65): Show |
G | 277 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0068others(274): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.-50+1048_-50+1119d others(74): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46621576 | |||||
| chr22:46621586
|
G | A | 2 | a0001c0001t0015g0189a0001c0001t0015g0190 | 2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-50+1021G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621586 | ||||||
| chr22:46621613
|
G | A | 2 | a0001c0001t0015g0189a0001c0001t0015g0190 | 2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-50+1048G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621613 | ||||||
| chr22:46621613
|
GCAGGCTG others(65): Show |
G | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-50+1074_-50+1145d others(74): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46621613 | |||||
| chr22:46621639
|
A | G | 2 | a0001c0001t0015g0189a0001c0001t0015g0190 | 2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-50+1074A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621639 | ||||||
| chr22:46621648
|
A | G | 5 | a0001c0001t0001g0066a0001c0001t0004g0061a0001c0001t0015g0189others(2): Show | 5 | HG01884.hp1 HG02896.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+1083A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621648 | ||||||
| chr22:46621649
|
G | C | 2 | a0001c0001t0015g0189a0001c0001t0015g0190 | 2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-50+1084G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621649 | ||||||
| chr22:46621680
|
C | T | 1 | a0001c0001t0028g0060 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-50+1115C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621680 | ||||||
| chr22:46621685
|
A | G | 3 | a0001c0001t0015g0189a0001c0001t0015g0190a0001c0001t0048g0191 | 3 | HG01433.hp1 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-50+1120A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621685 | ||||||
| chr22:46621727
|
C | T | 2 | a0001c0001t0011g0183a0001c0001t0011g0184 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-50+1162C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621727 | ||||||
| chr22:46621814
|
C | T | 3 | a0001c0001t0015g0189a0001c0001t0015g0190a0001c0001t0038g0180 | 3 | HG03130.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-50+1249C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46621814 | ||||||
| chr22:46622051
|
C | T | 1 | a0001c0001t0004g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-50+1486C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622051 | ||||||
| chr22:46622060
|
G | A | 1 | a0001c0008t0055g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-50+1495G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622060 | ||||||
| chr22:46622269
|
C | T | 80 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0204others(77): Show | 81 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.-50+1704C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622269 | ||||||
| chr22:46622334
|
C | T | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-50+1769C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622334 | ||||||
| chr22:46622370
|
C | T | 7 | a0001c0001t0005g0001a0001c0001t0005g0039a0001c0001t0005g0040others(4): Show | 8 | HG02572.hp2 HG02615.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-50+1805C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622370 | ||||||
| chr22:46622445
|
G | C | 1 | a0001c0001t0004g0021 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-50+1880G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622445 | ||||||
| chr22:46622674
|
G | A | 1 | a0001c0001t0017g0043 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-50+2109G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622674 | ||||||
| chr22:46622799
|
C | T | 3 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254 | 3 | HG01256.hp2 HG01258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-50+2234C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622799 | ||||||
| chr22:46622867
|
A | G | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0022g0176 | 3 | NA19002.hp1 NA19066.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.-50+2302A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622867 | ||||||
| chr22:46622868
|
C | T | 2 | a0001c0001t0004g0061a0001c0001t0019g0062 | 2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-50+2303C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622868 | ||||||
| chr22:46622869
|
G | A | 4 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0255others(1): Show | 4 | NA18939.hp2 NA19002.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+2304G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622869 | ||||||
| chr22:46622885
|
C | T | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-50+2320C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622885 | ||||||
| chr22:46622890
|
C | T | 147 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(144): Show | 150 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.-50+2325C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622890 | ||||||
| chr22:46622899
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-50+2334A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622899 | ||||||
| chr22:46622912
|
T | TA | 16 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(13): Show | 16 | HG00741.hp1 HG01192.hp2 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.-50+2366dupA | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46622912 | |||||
| chr22:46622912
|
TA | T | 78 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0204others(75): Show | 79 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.-50+2366delA | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46622912 | |||||
| chr22:46622913
|
A | T | 2 | a0001c0001t0002g0319a0002c0011t0053g0019 | 2 | HG00323.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-50+2348A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622913 | ||||||
| chr22:46622922
|
A | G | 1 | a0001c0001t0002g0319 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-50+2357A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622922 | ||||||
| chr22:46622971
|
C | T | 2 | a0002c0010t0047g0064a0002c0011t0053g0019 | 2 | HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-50+2406C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622971 | ||||||
| chr22:46622993
|
A | G | 1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-50+2428A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46622993 | ||||||
| chr22:46623044
|
C | T | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-50+2479C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623044 | ||||||
| chr22:46623045
|
G | A | 1 | a0001c0001t0039g0077 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-50+2480G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623045 | ||||||
| chr22:46623068
|
G | A | 2 | a0001c0001t0002g0259a0001c0001t0005g0258 | 2 | HG00738.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-50+2503G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623068 | ||||||
| chr22:46623090
|
G | A | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-50+2525G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623090 | ||||||
| chr22:46623091
|
A | G | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-50+2526A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623091 | ||||||
| chr22:46623102
|
G | A | 5 | a0001c0001t0001g0080a0001c0001t0002g0081a0001c0001t0012g0078others(2): Show | 5 | HG02074.hp2 NA18951.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+2537G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623102 | ||||||
| chr22:46623199
|
C | T | 142 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(139): Show | 145 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.-50+2634C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623199 | ||||||
| chr22:46623227
|
G | C | 1 | a0001c0001t0048g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-50+2662G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623227 | ||||||
| chr22:46623361
|
C | T | 7 | a0001c0001t0003g0083a0001c0001t0003g0084a0001c0001t0003g0085others(4): Show | 7 | HG01243.hp1 HG01243.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50+2796C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623361 | ||||||
| chr22:46623362
|
G | A | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-50+2797G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623362 | ||||||
| chr22:46623525
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-50+2960C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623525 | ||||||
| chr22:46623529
|
T | G | 2 | a0001c0001t0004g0017a0001c0001t0007g0022 | 2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-50+2964T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623529 | ||||||
| chr22:46623563
|
C | T | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-50+2998C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623563 | ||||||
| chr22:46623597
|
C | T | 81 | a0001c0001t0001g0197a0001c0001t0001g0204a0001c0001t0001g0255others(78): Show | 82 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.-50+3032C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623597 | ||||||
| chr22:46623639
|
G | A | 31 | a0001c0001t0001g0087a0001c0001t0001g0098a0001c0001t0001g0177others(28): Show | 32 | HG00438.hp2 HG01109.hp1 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.-50+3074G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623639 | ||||||
| chr22:46623784
|
CT | C | 6 | a0001c0001t0001g0103a0001c0001t0003g0104a0001c0001t0003g0207others(3): Show | 6 | HG00099.hp2 HG01070.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49-2951delT | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46623784 | |||||
| chr22:46623816
|
C | T | 4 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0010g0034others(1): Show | 4 | HG02622.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-2935C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623816 | ||||||
| chr22:46623835
|
G | A | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-49-2916G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623835 | ||||||
| chr22:46623860
|
C | T | 3 | a0001c0001t0006g0102a0001c0001t0036g0173a0001c0006t0042g0318 | 3 | HG00597.hp1 HG02040.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.-49-2891C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623860 | ||||||
| chr22:46623874
|
C | T | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-49-2877C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623874 | ||||||
| chr22:46623891
|
C | G | 3 | a0001c0001t0005g0188a0001c0001t0011g0057a0001c0001t0013g0055 | 3 | HG02486.hp2 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-49-2860C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623891 | ||||||
| chr22:46623926
|
C | T | 1 | a0001c0001t0001g0178 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-49-2825C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623926 | ||||||
| chr22:46623970
|
T | C | 158 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(155): Show | 162 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.-49-2781T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623970 | ||||||
| chr22:46623973
|
A | G | 4 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0010g0034others(1): Show | 4 | HG02622.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-2778A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623973 | ||||||
| chr22:46623998
|
T | A | 2 | a0002c0010t0047g0064a0002c0011t0053g0019 | 2 | HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-49-2753T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46623998 | ||||||
| chr22:46624003
|
G | A | 101 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0204others(98): Show | 102 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.-49-2748G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46624003 | ||||||
| chr22:46624039
|
C | A | 102 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(99): Show | 105 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.-49-2712C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46624039 | ||||||
| chr22:46624083
|
A | G | 2 | a0001c0001t0003g0030a0001c0001t0003g0031 | 2 | HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-49-2668A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46624083 | ||||||
| chr22:46624158
|
G | T | 3 | a0001c0001t0015g0189a0001c0001t0015g0190a0001c0001t0048g0191 | 3 | HG01433.hp1 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-49-2593G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46624158 | ||||||
| chr22:46624243
|
C | CT | 12 | a0001c0001t0001g0254a0001c0001t0004g0017a0001c0001t0008g0008others(9): Show | 12 | HG01256.hp2 HG01515.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-49-2497dupT | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46624243 | |||||
| chr22:46624243
|
CT | C | 7 | a0001c0001t0003g0210a0001c0001t0011g0183a0001c0001t0011g0184others(4): Show | 7 | HG02572.hp2 HG02723.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-49-2497delT | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46624243 | |||||
| chr22:46624274
|
C | T | 1 | a0002c0010t0047g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-49-2477C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46624274 | ||||||
| chr22:46624291
|
C | G | 7 | a0001c0001t0001g0177a0001c0001t0001g0181a0001c0001t0002g0100others(4): Show | 7 | NA18955.hp1 NA18962.hp2 NA18985.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49-2460C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46624291 | ||||||
| chr22:46624316
|
C | T | 148 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(145): Show | 152 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.-49-2435C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46624316 | ||||||
| chr22:46624324
|
C | CT | 19 | a0001c0001t0001g0309a0001c0001t0002g0203a0001c0001t0002g0310others(16): Show | 19 | HG00621.hp2 HG00642.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.-49-2402dupT | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46624324 | |||||
| chr22:46624324
|
C | CTT | 6 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0010g0034others(3): Show | 6 | HG02622.hp2 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49-2403_-49-2402d others(4): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46624324 | |||||
| chr22:46624324
|
C | CTTT | 14 | a0001c0001t0001g0066a0001c0001t0001g0109a0001c0001t0001g0110others(11): Show | 14 | HG00438.hp1 HG02145.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.-49-2404_-49-2402d others(5): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46624324 | |||||
| chr22:46624324
|
C | CTTTT | 91 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0068others(88): Show | 94 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.-49-2405_-49-2402d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46624324 | |||||
| chr22:46624324
|
C | CTTTTT | 20 | a0001c0001t0001g0098a0001c0001t0001g0163a0001c0001t0001g0165others(17): Show | 20 | HG00597.hp2 HG02135.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.-49-2406_-49-2402d others(7): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46624324 | |||||
| chr22:46624349
|
T | TTTC | 10 | a0001c0001t0003g0248a0001c0001t0004g0021a0001c0001t0005g0063others(7): Show | 10 | HG00140.hp1 HG00642.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.-49-2402_-49-2401i others(5): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46624349 | ||||||
| chr22:46624448
|
T | C | 4 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0027g0038others(1): Show | 4 | HG02145.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-2303T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46624448 | ||||||
| chr22:46624548
|
G | A | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-49-2203G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46624548 | ||||||
| chr22:46624687
|
A | G | 60 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0252others(57): Show | 60 | HG00099.hp2 HG00733.hp1 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.-49-2064A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46624687 | ||||||
| chr22:46624783
|
C | T | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-49-1968C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46624783 | ||||||
| chr22:46624858
|
A | AT | 18 | a0001c0001t0001g0204a0001c0001t0001g0255a0001c0001t0001g0308others(15): Show | 18 | HG01175.hp1 HG01261.hp2 HG01516.hp2 others(15): Show |
intron_variant | MODIFIER | c.-49-1873dupT | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46624858 | |||||
| chr22:46624858
|
AT | A | 148 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0068others(145): Show | 152 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.-49-1873delT | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46624858 | |||||
| chr22:46624883
|
C | G | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-49-1868C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46624883 | ||||||
| chr22:46624892
|
G | C | 1 | a0001c0001t0002g0264 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-49-1859G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46624892 | ||||||
| chr22:46625006
|
G | A | 2 | a0001c0001t0004g0061a0001c0001t0019g0062 | 2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-49-1745G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625006 | ||||||
| chr22:46625077
|
G | T | 1 | a0001c0001t0002g0307 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-49-1674G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625077 | ||||||
| chr22:46625082
|
A | G | 1 | a0001c0001t0003g0245 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-49-1669A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625082 | ||||||
| chr22:46625095
|
T | C | 1 | a0001c0001t0003g0245 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-49-1656T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625095 | ||||||
| chr22:46625116
|
T | C | 9 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0010others(6): Show | 9 | HG02723.hp1 HG02809.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.-49-1635T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625116 | ||||||
| chr22:46625139
|
C | T | 1 | a0001c0001t0003g0210 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-49-1612C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625139 | ||||||
| chr22:46625162
|
C | T | 3 | a0001c0001t0005g0188a0001c0001t0011g0057a0001c0001t0013g0055 | 3 | HG02486.hp2 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-49-1589C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625162 | ||||||
| chr22:46625297
|
G | A | 1 | a0001c0001t0025g0256 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-49-1454G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625297 | ||||||
| chr22:46625306
|
T | G | 147 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(144): Show | 151 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.-49-1445T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625306 | ||||||
| chr22:46625327
|
C | T | 1 | a0001c0002t0004g0099 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-49-1424C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625327 | ||||||
| chr22:46625329
|
A | G | 93 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0204others(90): Show | 94 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.-49-1422A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625329 | ||||||
| chr22:46625401
|
C | T | 7 | a0001c0001t0002g0305a0001c0001t0002g0314a0001c0001t0002g0315others(4): Show | 7 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49-1350C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625401 | ||||||
| chr22:46625460
|
G | A | 3 | a0001c0001t0006g0102a0001c0001t0036g0173a0001c0006t0042g0318 | 3 | HG00597.hp1 HG02040.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.-49-1291G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625460 | ||||||
| chr22:46625546
|
C | T | 2 | a0001c0001t0015g0189a0001c0001t0015g0190 | 2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-49-1205C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625546 | ||||||
| chr22:46625725
|
G | A | 1 | a0001c0001t0032g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-49-1026G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625725 | ||||||
| chr22:46625732
|
G | A | 1 | a0001c0001t0013g0020 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-49-1019G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625732 | ||||||
| chr22:46625820
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-49-931C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46625820 | ||||||
| chr22:46626099
|
G | T | 147 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(144): Show | 151 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.-49-652G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46626099 | ||||||
| chr22:46626219
|
A | G | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-49-532A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46626219 | ||||||
| chr22:46626348
|
G | C | 10 | a0001c0001t0004g0017a0001c0001t0008g0008a0001c0001t0008g0009others(7): Show | 10 | HG02572.hp1 HG02723.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-49-403G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46626348 | ||||||
| chr22:46626360
|
T | A | 2 | a0001c0001t0004g0061a0001c0001t0019g0062 | 2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-49-391T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46626360 | ||||||
| chr22:46626466
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-49-285C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46626466 | ||||||
| chr22:46626565
|
C | T | 34 | a0001c0001t0001g0098a0001c0001t0004g0017a0001c0001t0004g0035others(31): Show | 35 | HG01109.hp1 HG01361.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.-49-186C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46626565 | ||||||
| chr22:46626565
|
CGTGCCCT others(102): Show |
C | 8 | a0001c0001t0003g0234a0001c0001t0004g0233a0001c0001t0020g0231others(5): Show | 8 | HG01943.hp2 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-49-177_-49-69del | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 46626565 | |||||
| chr22:46626607
|
T | A | 1 | a0001c0001t0003g0207 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-49-144T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46626607 | ||||||
| chr22:46626620
|
C | T | 4 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0010g0034others(1): Show | 4 | HG02622.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-131C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46626620 | ||||||
| chr22:46626667
|
G | T | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-49-84G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 1/18 | chr22 | 46626667 | ||||||
| chr22:46626992
|
G | T | 2 | a0001c0001t0004g0061a0001c0001t0019g0062 | 2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.162+31G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46626992 | ||||||
| chr22:46627132
|
C | T | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.162+171C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46627132 | ||||||
| chr22:46627135
|
G | C | 2 | a0001c0001t0007g0033a0001c0002t0004g0032 | 2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.162+174G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46627135 | ||||||
| chr22:46627189
|
G | C | 5 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0010g0034others(2): Show | 5 | HG02622.hp2 HG02922.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.162+228G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46627189 | ||||||
| chr22:46627232
|
G | A | 18 | a0001c0001t0002g0209a0001c0001t0002g0259a0001c0001t0002g0266others(15): Show | 18 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.162+271G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46627232 | ||||||
| chr22:46627237
|
T | C | 1 | a0001c0001t0007g0026 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.162+276T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46627237 | ||||||
| chr22:46627271
|
G | A | 2 | a0001c0001t0004g0061a0001c0001t0019g0062 | 2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.162+310G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46627271 | ||||||
| chr22:46627353
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.162+392G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46627353 | ||||||
| chr22:46627564
|
T | C | 312 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(309): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.162+603T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46627564 | ||||||
| chr22:46627576
|
C | T | 4 | a0001c0001t0003g0234a0001c0001t0004g0233a0001c0003t0003g0235others(1): Show | 4 | HG02109.hp2 HG02717.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+615C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46627576 | ||||||
| chr22:46627628
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.162+667C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46627628 | ||||||
| chr22:46627642
|
C | T | 1 | a0001c0001t0028g0060 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.162+681C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46627642 | ||||||
| chr22:46627819
|
G | A | 2 | a0002c0010t0047g0064a0002c0011t0053g0019 | 2 | HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.162+858G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46627819 | ||||||
| chr22:46627832
|
C | T | 4 | a0001c0001t0003g0229a0001c0001t0003g0245a0001c0001t0014g0052others(1): Show | 4 | HG00733.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+871C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46627832 | ||||||
| chr22:46627876
|
G | A | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.162+915G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46627876 | ||||||
| chr22:46627979
|
T | C | 1 | a0001c0001t0001g0114 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.162+1018T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46627979 | ||||||
| chr22:46628090
|
C | A | 1 | a0001c0001t0002g0270 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.162+1129C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628090 | ||||||
| chr22:46628280
|
C | T | 31 | a0001c0001t0001g0098a0001c0001t0004g0017a0001c0001t0004g0035others(28): Show | 32 | HG01109.hp1 HG01361.hp2 HG01496.hp2 others(29): Show |
intron_variant | MODIFIER | c.162+1319C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628280 | ||||||
| chr22:46628295
|
G | C | 1 | a0001c0001t0001g0181 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.162+1334G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628295 | ||||||
| chr22:46628336
|
G | A | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.162+1375G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628336 | ||||||
| chr22:46628453
|
TGTGCGTT others(25): Show |
T | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.162+1528_162+1559d others(34): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46628453 | |||||
| chr22:46628454
|
G | T | 5 | a0001c0001t0006g0102a0001c0001t0006g0174a0001c0001t0006g0302others(2): Show | 5 | HG00597.hp1 HG02040.hp2 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+1493G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628454 | ||||||
| chr22:46628475
|
GGGTGGAC others(95): Show |
G | 13 | a0001c0001t0003g0248a0001c0001t0005g0063a0001c0001t0007g0022others(10): Show | 13 | HG00140.hp1 HG00642.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.162+1528_162+1629d others(2): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46628475 | |||||
| chr22:46628489
|
C | T | 140 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(137): Show | 143 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.162+1528C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628489 | ||||||
| chr22:46628491
|
T | TGCG | 138 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(135): Show | 141 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.162+1530_162+1531i others(5): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628491 | ||||||
| chr22:46628491
|
T | TGCGTGGT others(67): Show |
1 | a0001c0001t0008g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.162+1530_162+1531i others(76): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628491 | ||||||
| chr22:46628507
|
G | GGGTGGAC others(29): Show |
18 | a0001c0001t0001g0098a0001c0002t0002g0071a0001c0002t0004g0002others(15): Show | 19 | HG01109.hp1 HG01361.hp2 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.162+1566_162+1567i others(38): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46628507 | |||||
| chr22:46628507
|
G | GGGTGGAC others(64): Show |
7 | a0001c0001t0004g0017a0001c0001t0008g0008a0001c0001t0008g0009others(4): Show | 7 | HG02572.hp1 HG02723.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.162+1566_162+1567i others(73): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46628507 | |||||
| chr22:46628507
|
GGGTGGAC others(28): Show |
G | 101 | a0001c0001t0001g0115a0001c0001t0001g0196a0001c0001t0001g0197others(98): Show | 103 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.162+1616_162+1650d others(37): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46628507 | |||||
| chr22:46628521
|
T | C | 2 | a0001c0001t0002g0301a0001c0001t0002g0317 | 2 | NA18995.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.162+1560T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628521 | ||||||
| chr22:46628526
|
G | GT | 108 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(105): Show | 110 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.162+1566dupT | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46628526 | |||||
| chr22:46628526
|
G | GTTGGTGT others(206): Show |
4 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0010g0034others(1): Show | 4 | HG02622.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+1566_162+1567i others(215): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46628526 | |||||
| chr22:46628542
|
A | G | 6 | a0001c0001t0002g0301a0001c0001t0002g0317a0001c0001t0008g0013others(3): Show | 6 | HG03516.hp2 HG03579.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+1581A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628542 | ||||||
| chr22:46628577
|
A | G | 8 | a0001c0001t0001g0166a0001c0001t0004g0017a0001c0001t0008g0008others(5): Show | 8 | HG00597.hp2 HG02572.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.162+1616A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628577 | ||||||
| chr22:46628596
|
G | T | 1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.162+1635G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628596 | ||||||
| chr22:46628612
|
G | A | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.162+1651G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628612 | ||||||
| chr22:46628630
|
C | T | 1 | a0001c0001t0003g0244 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.162+1669C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628630 | ||||||
| chr22:46628646
|
G | A | 3 | a0001c0001t0009g0047a0001c0001t0009g0048a0001c0001t0009g0054 | 3 | HG01106.hp1 HG02683.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.162+1685G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628646 | ||||||
| chr22:46628730
|
A | G | 3 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0033g0037 | 3 | HG02622.hp2 HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.162+1769A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628730 | ||||||
| chr22:46628801
|
T | C | 6 | a0001c0001t0011g0183a0001c0001t0011g0184a0001c0001t0015g0189others(3): Show | 6 | HG02723.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+1840T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628801 | ||||||
| chr22:46628901
|
G | A | 2 | a0001c0001t0009g0056a0001c0001t0017g0043 | 2 | HG01978.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.162+1940G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628901 | ||||||
| chr22:46628921
|
C | T | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.162+1960C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46628921 | ||||||
| chr22:46629099
|
G | A | 1 | a0001c0001t0013g0055 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.162+2138G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629099 | ||||||
| chr22:46629117
|
C | G | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.162+2156C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629117 | ||||||
| chr22:46629156
|
G | T | 1 | a0001c0001t0001g0157 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.162+2195G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629156 | ||||||
| chr22:46629173
|
G | A | 1 | a0002c0010t0047g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.162+2212G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629173 | ||||||
| chr22:46629196
|
G | A | 1 | a0001c0001t0008g0008 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.162+2235G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629196 | ||||||
| chr22:46629204
|
T | G | 3 | a0001c0001t0008g0013a0001c0001t0008g0014a0001c0001t0008g0016 | 3 | HG02976.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.162+2243T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629204 | ||||||
| chr22:46629247
|
G | A | 5 | a0001c0001t0003g0083a0001c0001t0003g0084a0001c0001t0003g0085others(2): Show | 5 | HG01243.hp2 HG01496.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.162+2286G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629247 | ||||||
| chr22:46629260
|
C | T | 1 | a0001c0001t0002g0300 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.162+2299C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629260 | ||||||
| chr22:46629296
|
C | T | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.162+2335C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629296 | ||||||
| chr22:46629373
|
G | A | 1 | a0001c0001t0003g0242 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.162+2412G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629373 | ||||||
| chr22:46629427
|
G | A | 1 | a0001c0001t0002g0314 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.162+2466G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629427 | ||||||
| chr22:46629449
|
G | C | 1 | a0001c0001t0006g0198 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.162+2488G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629449 | ||||||
| chr22:46629453
|
C | T | 1 | a0001c0001t0003g0228 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.162+2492C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629453 | ||||||
| chr22:46629769
|
T | C | 1 | a0001c0001t0004g0021 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.162+2808T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629769 | ||||||
| chr22:46629787
|
C | T | 1 | a0001c0001t0004g0021 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.162+2826C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629787 | ||||||
| chr22:46629931
|
G | A | 2 | a0001c0001t0004g0061a0001c0001t0019g0062 | 2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.162+2970G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629931 | ||||||
| chr22:46629932
|
C | T | 6 | a0001c0001t0011g0183a0001c0001t0011g0184a0001c0001t0015g0189others(3): Show | 6 | HG02723.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+2971C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629932 | ||||||
| chr22:46629971
|
G | A | 1 | a0001c0002t0046g0089 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.162+3010G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46629971 | ||||||
| chr22:46630029
|
T | C | 2 | a0001c0001t0004g0061a0001c0001t0019g0062 | 2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.162+3068T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630029 | ||||||
| chr22:46630185
|
C | T | 1 | a0001c0001t0056g0313 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.162+3224C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630185 | ||||||
| chr22:46630210
|
G | A | 1 | a0001c0001t0013g0020 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.162+3249G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630210 | ||||||
| chr22:46630254
|
G | C | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.162+3293G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630254 | ||||||
| chr22:46630256
|
G | A | 4 | a0001c0001t0011g0183a0001c0001t0011g0184a0001c0001t0028g0060others(1): Show | 4 | HG02723.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+3295G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630256 | ||||||
| chr22:46630356
|
C | T | 92 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(89): Show | 95 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.162+3395C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630356 | ||||||
| chr22:46630414
|
T | G | 1 | a0001c0001t0003g0212 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.162+3453T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630414 | ||||||
| chr22:46630464
|
C | T | 2 | a0001c0001t0021g0155a0001c0001t0021g0156 | 2 | HG00673.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.162+3503C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630464 | ||||||
| chr22:46630545
|
T | C | 1 | a0001c0001t0048g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.162+3584T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630545 | ||||||
| chr22:46630570
|
C | A | 150 | a0001c0001t0001g0003a0001c0001t0001g0066a0001c0001t0001g0068others(147): Show | 153 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.162+3609C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630570 | ||||||
| chr22:46630638
|
G | A | 2 | a0001c0001t0003g0030a0001c0001t0003g0031 | 2 | HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.162+3677G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630638 | ||||||
| chr22:46630638
|
G | T | 1 | a0001c0001t0004g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.162+3677G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630638 | ||||||
| chr22:46630694
|
G | A | 7 | a0001c0001t0004g0233a0001c0001t0011g0183a0001c0001t0011g0184others(4): Show | 7 | HG02486.hp1 HG02717.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.162+3733G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630694 | ||||||
| chr22:46630824
|
T | G | 2 | a0001c0001t0004g0061a0001c0001t0019g0062 | 2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.162+3863T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630824 | ||||||
| chr22:46630848
|
C | T | 1 | a0001c0001t0048g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.162+3887C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630848 | ||||||
| chr22:46630849
|
GGTGTGCC others(46): Show |
G | 102 | a0001c0001t0001g0115a0001c0001t0001g0151a0001c0001t0001g0152others(99): Show | 103 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.162+3905_162+3957d others(55): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46630849 | |||||
| chr22:46630869
|
C | T | 1 | a0001c0001t0004g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.162+3908C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630869 | ||||||
| chr22:46630871
|
G | A | 4 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0010g0034others(1): Show | 4 | HG02622.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+3910G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630871 | ||||||
| chr22:46630899
|
C | T | 1 | a0001c0001t0004g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.162+3938C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630899 | ||||||
| chr22:46630900
|
G | T | 1 | a0002c0010t0047g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.162+3939G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630900 | ||||||
| chr22:46630931
|
C | T | 39 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0003g0006others(36): Show | 39 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.162+3970C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630931 | ||||||
| chr22:46630946
|
C | T | 8 | a0001c0001t0001g0308a0001c0001t0002g0296a0001c0001t0002g0297others(5): Show | 8 | HG00099.hp1 HG00642.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.162+3985C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630946 | ||||||
| chr22:46630947
|
G | A | 4 | a0001c0001t0011g0183a0001c0001t0011g0184a0001c0001t0028g0060others(1): Show | 4 | HG02723.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+3986G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630947 | ||||||
| chr22:46630955
|
C | T | 93 | a0001c0001t0001g0005a0001c0001t0001g0066a0001c0001t0001g0068others(90): Show | 95 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.162+3994C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46630955 | ||||||
| chr22:46631035
|
C | T | 1 | a0001c0002t0004g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.162+4074C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46631035 | ||||||
| chr22:46631120
|
T | C | 121 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(118): Show | 124 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.162+4159T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46631120 | ||||||
| chr22:46631126
|
C | T | 1 | a0001c0001t0032g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.162+4165C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46631126 | ||||||
| chr22:46631175
|
C | T | 1 | a0001c0001t0004g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.162+4214C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46631175 | ||||||
| chr22:46631202
|
A | G | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.162+4241A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46631202 | ||||||
| chr22:46631218
|
G | A | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.162+4257G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46631218 | ||||||
| chr22:46631389
|
A | ACTCCTGG others(140): Show |
1 | a0001c0001t0005g0188 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.162+4455_162+4456i others(149): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631389 | |||||
| chr22:46631389
|
A | ACTCCTGG others(42): Show |
1 | a0001c0002t0004g0090 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.162+4460_162+4461i others(51): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631389 | |||||
| chr22:46631389
|
A | ACTCCTGG others(91): Show |
1 | a0001c0001t0003g0226 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.162+4460_162+4461i others(100): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631389 | |||||
| chr22:46631389
|
ACTCCTGG others(91): Show |
A | 10 | a0001c0001t0001g0098a0001c0002t0002g0071a0001c0002t0004g0002others(7): Show | 11 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.162+4461_162+4558d others(100): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631389 | |||||
| chr22:46631389
|
ACTCCTGG others(140): Show |
A | 11 | a0001c0001t0028g0060a0001c0001t0030g0044a0001c0002t0004g0032others(8): Show | 11 | HG01109.hp1 HG01891.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.162+4461_162+4607d others(2): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631389 | |||||
| chr22:46631389
|
ACTCCTGG others(189): Show |
A | 2 | a0001c0001t0011g0183a0001c0001t0011g0184 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.162+4461_162+4656d others(2): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631389 | |||||
| chr22:46631389
|
ACTCCTGG others(238): Show |
A | 2 | a0001c0001t0013g0055a0001c0001t0054g0251 | 2 | HG02486.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.162+4461_162+4705d others(2): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631389 | |||||
| chr22:46631422
|
A | AGCCTGTG others(287): Show |
1 | a0001c0001t0001g0196 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.162+4509_162+4510i others(296): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631422 | |||||
| chr22:46631422
|
A | AGCCTGTG others(42): Show |
11 | a0001c0001t0001g0103a0001c0001t0001g0109a0001c0001t0003g0030others(8): Show | 11 | HG01070.hp1 HG01071.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.162+4993_162+5041d others(51): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631422 | |||||
| chr22:46631422
|
A | AGCCTGTG others(238): Show |
1 | a0001c0001t0006g0198 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.162+4558_162+4559i others(247): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631422 | |||||
| chr22:46631422
|
A | AGCCTGTG others(91): Show |
49 | a0001c0001t0003g0006a0001c0001t0003g0083a0001c0001t0003g0084others(46): Show | 49 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.162+4944_162+5041d others(100): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631422 | |||||
| chr22:46631422
|
A | AGCCTGTG others(140): Show |
3 | a0001c0001t0002g0270a0001c0005t0002g0294a0001c0008t0055g0067 | 3 | HG00423.hp2 HG04115.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.162+4895_162+5041d others(149): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631422 | |||||
| chr22:46631422
|
A | AGCCTGTG others(189): Show |
20 | a0001c0001t0002g0172a0001c0001t0002g0209a0001c0001t0002g0269others(17): Show | 20 | HG00140.hp2 HG00738.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.162+4846_162+5041d others(198): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631422 | |||||
| chr22:46631422
|
A | AGCCTGTG others(238): Show |
64 | a0001c0001t0001g0115a0001c0001t0001g0197a0001c0001t0001g0255others(61): Show | 65 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.162+4797_162+5041d others(247): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631422 | |||||
| chr22:46631422
|
A | AGCCTGTG others(287): Show |
9 | a0001c0001t0001g0271a0001c0001t0001g0309a0001c0001t0002g0249others(6): Show | 10 | HG00733.hp2 HG02015.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.162+4748_162+5041d others(296): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631422 | |||||
| chr22:46631422
|
A | AGCCTGTG others(532): Show |
2 | a0001c0001t0015g0189a0001c0001t0015g0190 | 2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.162+4503_162+5041d others(541): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631422 | |||||
| chr22:46631422
|
A | G | 4 | a0001c0001t0001g0112a0001c0001t0003g0226a0001c0001t0005g0188others(1): Show | 4 | HG00438.hp1 HG01255.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+4461A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46631422 | ||||||
| chr22:46631422
|
AGCCTGTG others(42): Show |
A | 13 | a0001c0001t0001g0146a0001c0001t0001g0252a0001c0001t0001g0254others(10): Show | 13 | HG00741.hp1 HG01175.hp2 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.162+4993_162+5041d others(51): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631422 | |||||
| chr22:46631422
|
AGCCTGTG others(91): Show |
A | 1 | a0001c0004t0001g0321 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.162+4944_162+5041d others(100): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631422 | |||||
| chr22:46631422
|
AGCCTGTG others(140): Show |
A | 3 | a0001c0001t0004g0036a0001c0001t0010g0034a0001c0001t0033g0037 | 3 | HG02622.hp2 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.162+4895_162+5041d others(2): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631422 | |||||
| chr22:46631422
|
AGCCTGTG others(189): Show |
A | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.162+4846_162+5041d others(2): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631422 | |||||
| chr22:46631422
|
AGCCTGTG others(238): Show |
A | 1 | a0001c0001t0004g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.162+4797_162+5041d others(2): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631422 | |||||
| chr22:46631422
|
AGCCTGTG others(287): Show |
A | 6 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0010others(3): Show | 6 | HG02723.hp1 HG02809.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+4748_162+5041d others(2): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631422 | |||||
| chr22:46631422
|
AGCCTGTG others(336): Show |
A | 13 | a0001c0001t0003g0248a0001c0001t0004g0021a0001c0001t0005g0063others(10): Show | 13 | HG00140.hp1 HG00642.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.162+4699_162+5041d others(2): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631422 | |||||
| chr22:46631437
|
G | GTCTCCTG others(287): Show |
1 | a0001c0001t0048g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.162+4769_162+4770i others(296): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631437 | |||||
| chr22:46631520
|
G | A | 1 | a0001c0001t0003g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.162+4559G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46631520 | ||||||
| chr22:46631616
|
A | ACGGCCTG others(42): Show |
1 | a0002c0010t0047g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.162+4703_162+4704i others(51): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631616 | |||||
| chr22:46631647
|
G | GGGGATGG others(285): Show |
1 | a0001c0001t0002g0260 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.162+4968_162+4969i others(294): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631647 | |||||
| chr22:46631661
|
C | T | 6 | a0001c0001t0001g0080a0001c0001t0001g0148a0001c0001t0001g0149others(3): Show | 6 | HG00673.hp1 HG02074.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+4700C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46631661 | ||||||
| chr22:46631714
|
A | G | 1 | a0002c0010t0047g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.162+4753A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46631714 | ||||||
| chr22:46631759
|
C | CCTCACGG others(91): Show |
1 | a0001c0001t0040g0246 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.162+4895_162+4896i others(100): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631759 | |||||
| chr22:46631763
|
A | G | 1 | a0002c0010t0047g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.162+4802A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46631763 | ||||||
| chr22:46631765
|
G | A | 1 | a0001c0001t0013g0055 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.162+4804G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46631765 | ||||||
| chr22:46631813
|
C | CGGCCTGT others(91): Show |
1 | a0001c0001t0001g0220 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.162+4949_162+4950i others(100): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46631813 | |||||
| chr22:46631901
|
T | A | 1 | a0001c0002t0004g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.162+4940T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46631901 | ||||||
| chr22:46632009
|
C | T | 1 | a0001c0001t0005g0041 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.162+5048C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46632009 | ||||||
| chr22:46632010
|
G | A | 154 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(151): Show | 157 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.162+5049G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46632010 | ||||||
| chr22:46632033
|
C | T | 14 | a0001c0001t0003g0248a0001c0001t0004g0021a0001c0001t0005g0063others(11): Show | 14 | HG00140.hp1 HG00642.hp2 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.162+5072C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46632033 | ||||||
| chr22:46632093
|
T | C | 100 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(97): Show | 102 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.162+5132T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46632093 | ||||||
| chr22:46632137
|
C | T | 1 | a0001c0001t0004g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.162+5176C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46632137 | ||||||
| chr22:46632141
|
G | C | 1 | a0001c0001t0001g0123 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.162+5180G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46632141 | ||||||
| chr22:46632311
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.162+5350G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46632311 | ||||||
| chr22:46632317
|
G | A | 2 | a0001c0001t0004g0061a0001c0001t0019g0062 | 2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.162+5356G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46632317 | ||||||
| chr22:46632417
|
A | T | 100 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(97): Show | 102 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.163-5423A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46632417 | ||||||
| chr22:46632436
|
T | G | 7 | a0001c0001t0004g0017a0001c0001t0008g0008a0001c0001t0008g0009others(4): Show | 7 | HG02572.hp1 HG02723.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.163-5404T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46632436 | ||||||
| chr22:46632728
|
C | G | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.163-5112C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46632728 | ||||||
| chr22:46632850
|
G | A | 1 | a0001c0001t0048g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.163-4990G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46632850 | ||||||
| chr22:46633058
|
C | T | 1 | a0001c0001t0002g0293 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.163-4782C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46633058 | ||||||
| chr22:46633145
|
T | C | 1 | a0001c0001t0004g0021 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.163-4695T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46633145 | ||||||
| chr22:46633289
|
T | C | 1 | a0001c0002t0004g0090 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.163-4551T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46633289 | ||||||
| chr22:46633319
|
C | T | 2 | a0001c0001t0003g0218a0001c0001t0003g0242 | 2 | HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.163-4521C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46633319 | ||||||
| chr22:46633354
|
C | T | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.163-4486C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46633354 | ||||||
| chr22:46633557
|
G | T | 7 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0010g0034others(4): Show | 7 | HG02622.hp2 HG02723.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.163-4283G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46633557 | ||||||
| chr22:46633583
|
G | A | 18 | a0001c0001t0004g0017a0001c0001t0004g0035a0001c0001t0004g0036others(15): Show | 18 | HG01884.hp1 HG02572.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.163-4257G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46633583 | ||||||
| chr22:46633586
|
G | C | 92 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(89): Show | 94 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.163-4254G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46633586 | ||||||
| chr22:46633596
|
C | G | 1 | a0001c0002t0002g0071 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.163-4244C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46633596 | ||||||
| chr22:46633657
|
G | T | 3 | a0001c0001t0004g0036a0001c0001t0010g0034a0001c0001t0033g0037 | 3 | HG02622.hp2 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.163-4183G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46633657 | ||||||
| chr22:46633680
|
A | T | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.163-4160A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46633680 | ||||||
| chr22:46633691
|
G | A | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.163-4149G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46633691 | ||||||
| chr22:46633740
|
G | C | 3 | a0001c0001t0011g0183a0001c0001t0011g0184a0001c0001t0028g0060 | 3 | HG02723.hp2 HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.163-4100G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46633740 | ||||||
| chr22:46633821
|
C | T | 3 | a0001c0001t0008g0013a0001c0001t0008g0014a0001c0001t0008g0016 | 3 | HG02976.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.163-4019C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46633821 | ||||||
| chr22:46633996
|
C | T | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.163-3844C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46633996 | ||||||
| chr22:46633999
|
A | G | 4 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0010g0034others(1): Show | 4 | HG02622.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-3841A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46633999 | ||||||
| chr22:46634076
|
G | A | 11 | a0001c0001t0004g0017a0001c0001t0004g0035a0001c0001t0004g0036others(8): Show | 11 | HG01884.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-3764G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46634076 | ||||||
| chr22:46634079
|
C | T | 13 | a0001c0001t0004g0021a0001c0001t0005g0063a0001c0001t0007g0022others(10): Show | 13 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.163-3761C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46634079 | ||||||
| chr22:46634153
|
G | C | 1 | a0001c0001t0040g0246 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.163-3687G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46634153 | ||||||
| chr22:46634179
|
G | T | 6 | a0001c0001t0002g0285a0001c0001t0002g0291a0001c0001t0002g0320others(3): Show | 6 | NA18970.hp1 NA18980.hp1 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-3661G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46634179 | ||||||
| chr22:46634180
|
G | T | 1 | a0001c0001t0004g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.163-3660G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46634180 | ||||||
| chr22:46634190
|
A | G | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.163-3650A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46634190 | ||||||
| chr22:46634254
|
G | C | 8 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0010g0034others(5): Show | 8 | HG02622.hp2 HG02723.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.163-3586G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46634254 | ||||||
| chr22:46634304
|
G | A | 3 | a0001c0001t0008g0013a0001c0001t0008g0014a0001c0001t0008g0016 | 3 | HG02976.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.163-3536G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46634304 | ||||||
| chr22:46634343
|
A | C | 146 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(143): Show | 149 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.163-3497A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46634343 | ||||||
| chr22:46634547
|
C | T | 1 | a0001c0001t0037g0065 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.163-3293C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46634547 | ||||||
| chr22:46634711
|
C | T | 93 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(90): Show | 95 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.163-3129C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46634711 | ||||||
| chr22:46634829
|
G | A | 1 | a0001c0001t0006g0194 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.163-3011G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46634829 | ||||||
| chr22:46634892
|
G | A | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.163-2948G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46634892 | ||||||
| chr22:46634901
|
T | G | 1 | a0001c0001t0030g0044 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.163-2939T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46634901 | ||||||
| chr22:46634945
|
CA | C | 12 | a0001c0001t0003g0212a0001c0001t0004g0017a0001c0001t0005g0039others(9): Show | 12 | HG01257.hp2 HG02572.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.163-2881delA | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46634945 | |||||
| chr22:46634951
|
A | T | 1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.163-2889A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46634951 | ||||||
| chr22:46634958
|
A | C | 1 | a0001c0001t0001g0177 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.163-2882A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46634958 | ||||||
| chr22:46635013
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.163-2827C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635013 | ||||||
| chr22:46635058
|
A | ACCACCCC others(39): Show |
20 | a0001c0001t0001g0220a0001c0001t0003g0006a0001c0001t0003g0205others(17): Show | 20 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.163-2761_163-2760i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635058 | |||||
| chr22:46635066
|
T | TGGCCACT others(593): Show |
1 | a0001c0001t0033g0037 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.163-2761_163-2760i others(602): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635066 | |||||
| chr22:46635066
|
T | TGGCCACT others(223): Show |
1 | a0001c0002t0002g0071 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.163-2761_163-2760i others(232): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635066 | |||||
| chr22:46635066
|
T | TGGCCACT others(39): Show |
2 | a0001c0001t0003g0104a0001c0001t0003g0169 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.163-2761_163-2760i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635066 | |||||
| chr22:46635067
|
GGCCACTC others(39): Show |
G | 1 | a0001c0001t0010g0034 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.163-2760_163-2715d others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635067 | |||||
| chr22:46635080
|
T | C | 52 | a0001c0001t0001g0098a0001c0001t0001g0220a0001c0001t0003g0006others(49): Show | 53 | HG00140.hp1 HG00741.hp1 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.163-2760T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635080 | ||||||
| chr22:46635086
|
A | G | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.163-2754A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635086 | ||||||
| chr22:46635087
|
G | A | 51 | a0001c0001t0001g0098a0001c0001t0001g0220a0001c0001t0003g0006others(48): Show | 52 | HG00140.hp1 HG00741.hp1 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.163-2753G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635087 | ||||||
| chr22:46635104
|
C | T | 3 | a0001c0001t0003g0210a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | NA18946.hp1 NA18952.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.163-2736C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635104 | ||||||
| chr22:46635107
|
G | A | 10 | a0001c0001t0003g0210a0001c0001t0003g0238a0001c0001t0003g0239others(7): Show | 10 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.163-2733G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635107 | ||||||
| chr22:46635107
|
G | GACCCCGG others(131): Show |
1 | a0001c0001t0002g0317 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.163-2733_163-2732i others(140): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635107 | ||||||
| chr22:46635107
|
G | GACCCCGG others(177): Show |
2 | a0001c0001t0030g0044a0001c0001t0048g0191 | 2 | HG01433.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.163-2733_163-2732i others(186): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635107 | ||||||
| chr22:46635107
|
G | GCCCCCGG others(39): Show |
1 | a0001c0001t0005g0213 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.163-2728_163-2727i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635107 | |||||
| chr22:46635108
|
C | A | 17 | a0001c0001t0001g0098a0001c0001t0001g0166a0001c0001t0003g0234others(14): Show | 18 | HG00597.hp2 HG01109.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.163-2732C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635108 | ||||||
| chr22:46635112
|
C | CGGCCACT others(315): Show |
1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.163-2728_163-2727i others(324): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635112 | ||||||
| chr22:46635112
|
C | T | 12 | a0001c0001t0003g0210a0001c0001t0003g0238a0001c0001t0003g0239others(9): Show | 12 | HG01433.hp1 HG01891.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-2728C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635112 | ||||||
| chr22:46635113
|
A | AGCCACTC others(269): Show |
1 | a0001c0001t0002g0312 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.163-2691_163-2690i others(278): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635113 | |||||
| chr22:46635113
|
A | AGCCACTC others(775): Show |
1 | a0001c0001t0043g0311 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.163-2691_163-2690i others(784): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635113 | |||||
| chr22:46635113
|
A | AGCCACTC others(407): Show |
1 | a0001c0001t0002g0264 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.163-2691_163-2690i others(416): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635113 | |||||
| chr22:46635113
|
A | AGCCACTC others(315): Show |
17 | a0001c0001t0002g0209a0001c0001t0002g0259a0001c0001t0002g0266others(14): Show | 17 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.163-2691_163-2690i others(324): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635113 | |||||
| chr22:46635113
|
A | AGCCACTC others(915): Show |
1 | a0001c0001t0011g0183 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.163-2709_163-2708i others(924): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635113 | |||||
| chr22:46635113
|
A | AGCCACTC others(961): Show |
1 | a0001c0001t0011g0184 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.163-2709_163-2708i others(970): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635113 | |||||
| chr22:46635113
|
A | AGCCACTC others(1329): Show |
1 | a0001c0001t0028g0060 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.163-2709_163-2708i others(1338): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635113 | |||||
| chr22:46635113
|
A | G | 38 | a0001c0001t0001g0220a0001c0001t0003g0006a0001c0001t0003g0104others(35): Show | 38 | HG00140.hp1 HG00741.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.163-2727A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635113 | ||||||
| chr22:46635126
|
C | CTGGGGAA others(178): Show |
1 | a0001c0001t0005g0039 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.163-2691_163-2690i others(187): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635126 | |||||
| chr22:46635131
|
G | A | 1 | a0001c0002t0002g0071 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.163-2709G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635131 | ||||||
| chr22:46635132
|
A | AACCGTGT others(177): Show |
1 | a0001c0001t0004g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.163-2691_163-2690i others(186): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635132 | |||||
| chr22:46635132
|
A | G | 28 | a0001c0001t0001g0220a0001c0001t0003g0006a0001c0001t0003g0104others(25): Show | 28 | HG00140.hp1 HG00741.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.163-2708A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635132 | ||||||
| chr22:46635133
|
A | ACCGTGTC others(1695): Show |
1 | a0001c0001t0002g0310 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.163-2691_163-2690i others(1704): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635133 | |||||
| chr22:46635133
|
A | G | 2 | a0001c0001t0033g0037a0001c0002t0002g0071 | 2 | HG02976.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.163-2707A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635133 | ||||||
| chr22:46635135
|
C | CGTGTCCT others(912): Show |
1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.163-2691_163-2690i others(921): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635135 | |||||
| chr22:46635141
|
C | T | 5 | a0001c0002t0004g0032a0001c0002t0004g0069a0001c0002t0004g0092others(2): Show | 5 | HG01891.hp2 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-2699C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635141 | ||||||
| chr22:46635150
|
T | C | 144 | a0001c0001t0001g0003a0001c0001t0001g0098a0001c0001t0001g0106others(141): Show | 148 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.163-2690T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635150 | ||||||
| chr22:46635150
|
T | TCCACCCC others(39): Show |
1 | a0001c0001t0015g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.163-2683_163-2682i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635150 | |||||
| chr22:46635152
|
C | CG | 46 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0002g0007others(43): Show | 48 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.163-2688_163-2687i others(3): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635152 | ||||||
| chr22:46635152
|
C | CGACCCCG others(455): Show |
1 | a0001c0001t0006g0076 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.163-2688_163-2687i others(464): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635152 | ||||||
| chr22:46635153
|
A | G | 47 | a0001c0001t0001g0003a0001c0001t0001g0106a0001c0001t0001g0113others(44): Show | 48 | HG00099.hp1 HG00741.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.163-2687A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635153 | ||||||
| chr22:46635154
|
C | A | 33 | a0001c0001t0001g0219a0001c0001t0001g0308a0001c0001t0002g0171others(30): Show | 33 | HG00099.hp1 HG00741.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.163-2686C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635154 | ||||||
| chr22:46635154
|
C | CCCCCAGC others(85): Show |
1 | a0001c0001t0015g0189 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.163-2683_163-2682i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635154 | |||||
| chr22:46635158
|
T | C | 73 | a0001c0001t0001g0003a0001c0001t0001g0106a0001c0001t0001g0113others(70): Show | 74 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.163-2682T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635158 | ||||||
| chr22:46635158
|
T | G | 46 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0002g0007others(43): Show | 48 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.163-2682T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635158 | ||||||
| chr22:46635158
|
T | TGGCCACT others(39): Show |
2 | a0001c0001t0010g0186a0001c0001t0010g0187 | 2 | HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.163-2662_163-2617d others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635158 | |||||
| chr22:46635158
|
T | TGGCCACT others(39): Show |
1 | a0001c0001t0010g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.163-2663_163-2662i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635158 | |||||
| chr22:46635158
|
T | TGGCCACT others(223): Show |
1 | a0001c0002t0004g0070 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.163-2663_163-2662i others(232): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635158 | |||||
| chr22:46635159
|
G | GCCACTCC others(130): Show |
5 | a0001c0001t0006g0193a0001c0001t0006g0199a0001c0001t0006g0200others(2): Show | 5 | NA18959.hp2 NA18998.hp1 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-2681_163-2680i others(139): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635159 | ||||||
| chr22:46635159
|
G | GCCACTCC others(176): Show |
1 | a0001c0001t0005g0188 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.163-2681_163-2680i others(185): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635159 | ||||||
| chr22:46635159
|
G | GCCACTCC others(176): Show |
34 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0002g0007others(31): Show | 36 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.163-2681_163-2680i others(185): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635159 | ||||||
| chr22:46635159
|
G | GCCACTCC others(406): Show |
1 | a0001c0001t0006g0170 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.163-2681_163-2680i others(415): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635159 | ||||||
| chr22:46635159
|
G | GCCACTCC others(130): Show |
1 | a0001c0001t0002g0281 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.163-2681_163-2680i others(139): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635159 | ||||||
| chr22:46635159
|
G | GCCACTCC others(130): Show |
3 | a0001c0001t0006g0192a0001c0001t0006g0194a0001c0001t0006g0195 | 3 | HG00438.hp2 HG02015.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.163-2681_163-2680i others(139): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635159 | ||||||
| chr22:46635159
|
G | GCCACTCC others(314): Show |
1 | a0001c0001t0002g0282 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.163-2681_163-2680i others(323): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635159 | ||||||
| chr22:46635159
|
G | GGCCACTC others(223): Show |
1 | a0001c0001t0026g0292 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.163-2641_163-2640i others(232): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635159 | |||||
| chr22:46635159
|
G | GGCCACTC others(39): Show |
1 | a0001c0001t0002g0317 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.163-2669_163-2668i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635159 | |||||
| chr22:46635178
|
A | G | 68 | a0001c0001t0001g0098a0001c0001t0001g0220a0001c0001t0002g0209others(65): Show | 69 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.163-2662A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635178 | ||||||
| chr22:46635179
|
A | ACCGTGTC others(223): Show |
2 | a0001c0002t0004g0090a0001c0002t0004g0095 | 2 | HG01109.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.163-2654_163-2653i others(232): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635179 | |||||
| chr22:46635187
|
C | CTCCCTGC others(39): Show |
1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.163-2642_163-2641i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635187 | |||||
| chr22:46635187
|
C | CTCCCTGC others(775): Show |
3 | a0001c0001t0008g0013a0001c0001t0008g0014a0001c0001t0008g0016 | 3 | HG02976.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.163-2641_163-2640i others(784): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635187 | |||||
| chr22:46635187
|
C | T | 16 | a0001c0001t0001g0098a0001c0002t0004g0002a0001c0002t0004g0032others(13): Show | 17 | HG01361.hp2 HG01496.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.163-2653C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635187 | ||||||
| chr22:46635194
|
C | CCCCCACC others(959): Show |
1 | a0001c0001t0004g0295 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.163-2642_163-2641i others(968): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635194 | |||||
| chr22:46635194
|
C | CCCCCACC others(821): Show |
1 | a0001c0001t0001g0308 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.163-2642_163-2641i others(830): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635194 | |||||
| chr22:46635194
|
C | CCCCCACC others(1097): Show |
1 | a0001c0001t0002g0296 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.163-2642_163-2641i others(1106): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635194 | |||||
| chr22:46635194
|
C | CCCCCACC others(913): Show |
3 | a0001c0001t0002g0297a0001c0001t0002g0298a0001c0001t0002g0299 | 3 | HG00099.hp1 HG02273.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.163-2642_163-2641i others(922): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635194 | |||||
| chr22:46635194
|
C | CCCCCACC others(453): Show |
4 | a0001c0001t0002g0274a0001c0001t0002g0278a0001c0001t0017g0045others(1): Show | 4 | HG01952.hp2 HG03942.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-2642_163-2641i others(462): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635194 | |||||
| chr22:46635194
|
C | CCCCCGAC others(38): Show |
1 | a0001c0001t0005g0063 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.163-2641_163-2640i others(47): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635194 | |||||
| chr22:46635194
|
C | CCCCCGAC others(499): Show |
1 | a0001c0001t0001g0255 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.163-2641_163-2640i others(508): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635194 | |||||
| chr22:46635196
|
C | T | 10 | a0001c0001t0001g0072a0001c0001t0001g0116a0001c0001t0001g0168others(7): Show | 10 | HG00741.hp2 HG01433.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.163-2644C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635196 | ||||||
| chr22:46635199
|
G | A | 21 | a0001c0001t0001g0072a0001c0001t0001g0116a0001c0001t0001g0168others(18): Show | 21 | HG00642.hp1 HG00741.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.163-2641G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635199 | ||||||
| chr22:46635199
|
G | GACCCCGG others(681): Show |
1 | a0001c0001t0007g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.163-2641_163-2640i others(690): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635199 | ||||||
| chr22:46635199
|
G | GACCCCGG others(544): Show |
1 | a0001c0001t0004g0021 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.163-2641_163-2640i others(553): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635199 | ||||||
| chr22:46635199
|
G | GACCCCGG others(681): Show |
1 | a0001c0001t0007g0027 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.163-2641_163-2640i others(690): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635199 | ||||||
| chr22:46635199
|
G | GACCCCGG others(727): Show |
6 | a0001c0001t0007g0024a0001c0001t0007g0025a0001c0001t0007g0026others(3): Show | 6 | HG02451.hp2 HG02486.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-2641_163-2640i others(736): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635199 | ||||||
| chr22:46635200
|
C | A | 122 | a0001c0001t0001g0003a0001c0001t0001g0098a0001c0001t0001g0106others(119): Show | 126 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.163-2640C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635200 | ||||||
| chr22:46635200
|
C | CCCCCGGC others(39): Show |
7 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0154others(4): Show | 8 | HG01069.hp1 HG01071.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.163-2617_163-2616i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635200 | |||||
| chr22:46635200
|
C | CCCCCGGC others(269): Show |
1 | a0001c0001t0001g0073 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.163-2617_163-2616i others(278): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635200 | |||||
| chr22:46635200
|
C | CCCCCGGC others(39): Show |
1 | a0001c0001t0001g0075 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.163-2617_163-2616i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635200 | |||||
| chr22:46635204
|
C | CGGCCACT others(177): Show |
1 | a0001c0001t0001g0139 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.163-2617_163-2616i others(186): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635204 | |||||
| chr22:46635204
|
C | CGGCCACT others(39): Show |
1 | a0001c0001t0003g0212 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.163-2595_163-2550d others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635204 | |||||
| chr22:46635204
|
C | T | 18 | a0001c0001t0001g0072a0001c0001t0001g0116a0001c0001t0001g0168others(15): Show | 18 | HG00642.hp1 HG00741.hp2 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.163-2636C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635204 | ||||||
| chr22:46635204
|
CGGCCACT others(39): Show |
C | 1 | a0001c0001t0031g0059 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.163-2595_163-2550d others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635204 | |||||
| chr22:46635205
|
G | A | 1 | a0001c0001t0005g0039 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.163-2635G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635205 | ||||||
| chr22:46635223
|
G | A | 16 | a0001c0001t0001g0255a0001c0001t0001g0308a0001c0001t0002g0274others(13): Show | 16 | HG00099.hp1 HG01952.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.163-2617G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635223 | ||||||
| chr22:46635223
|
G | GAACCGTG others(499): Show |
4 | a0001c0001t0002g0172a0001c0001t0002g0290a0001c0001t0002g0293others(1): Show | 4 | HG01943.hp1 HG02148.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-2617_163-2616i others(508): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635223 | ||||||
| chr22:46635224
|
G | A | 192 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(189): Show | 196 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.163-2616G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635224 | ||||||
| chr22:46635225
|
A | ACCGTGTC others(269): Show |
1 | a0001c0001t0004g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.163-2596_163-2595i others(278): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635225 | |||||
| chr22:46635225
|
A | G | 21 | a0001c0001t0001g0112a0001c0001t0001g0255a0001c0001t0001g0308others(18): Show | 21 | HG00099.hp1 HG00438.hp1 HG01943.hp1 others(18): Show |
intron_variant | MODIFIER | c.163-2615A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635225 | ||||||
| chr22:46635227
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.163-2613C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635227 | ||||||
| chr22:46635230
|
G | GTCCTCCC others(177): Show |
4 | a0001c0001t0001g0005a0001c0001t0001g0252a0001c0001t0001g0254others(1): Show | 4 | HG01256.hp2 HG01258.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-2596_163-2595i others(186): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635230 | |||||
| chr22:46635230
|
G | GTCCTCCC others(39): Show |
6 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0010others(3): Show | 6 | HG02723.hp1 HG02809.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-2596_163-2595i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635230 | |||||
| chr22:46635233
|
C | T | 27 | a0001c0001t0001g0098a0001c0001t0004g0061a0001c0001t0007g0024others(24): Show | 28 | HG00642.hp2 HG01243.hp1 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.163-2607C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635233 | ||||||
| chr22:46635235
|
C | G | 1 | a0001c0001t0015g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.163-2605C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635235 | ||||||
| chr22:46635242
|
C | CCCACCCC others(223): Show |
1 | a0001c0001t0063g0227 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.163-2591_163-2590i others(232): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635242 | |||||
| chr22:46635242
|
C | CCCGACCC others(545): Show |
1 | a0001c0001t0001g0153 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.163-2596_163-2595i others(554): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635242 | |||||
| chr22:46635242
|
C | T | 66 | a0001c0001t0001g0125a0001c0001t0001g0160a0001c0001t0001g0177others(63): Show | 68 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.163-2598C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635242 | ||||||
| chr22:46635244
|
C | CG | 3 | a0001c0001t0011g0183a0001c0001t0011g0184a0001c0001t0028g0060 | 3 | HG02723.hp2 HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.163-2596_163-2595i others(3): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635244 | ||||||
| chr22:46635244
|
C | CGACCCCG others(223): Show |
3 | a0001c0001t0007g0022a0001c0001t0007g0023a0001c0001t0013g0020 | 3 | HG01070.hp2 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.163-2596_163-2595i others(232): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635244 | ||||||
| chr22:46635244
|
C | CGACCCCG others(86): Show |
1 | a0001c0001t0001g0074 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.163-2596_163-2595i others(95): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635244 | ||||||
| chr22:46635245
|
A | ACCCCCAG others(85): Show |
2 | a0001c0001t0002g0171a0001c0001t0002g0257 | 2 | NA18982.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.163-2591_163-2590i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635245 | |||||
| chr22:46635245
|
A | G | 83 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0072others(80): Show | 84 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.163-2595A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635245 | ||||||
| chr22:46635246
|
C | A | 70 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0072others(67): Show | 71 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.163-2594C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635246 | ||||||
| chr22:46635249
|
CT | C | 4 | a0001c0001t0001g0074a0001c0001t0007g0022a0001c0001t0007g0023others(1): Show | 4 | HG01070.hp2 HG03225.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-2590delT | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635249 | ||||||
| chr22:46635250
|
T | C | 106 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0072others(103): Show | 107 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.163-2590T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635250 | ||||||
| chr22:46635250
|
T | TGGCCACT others(39): Show |
2 | a0001c0001t0002g0317a0001c0001t0005g0039 | 2 | HG02896.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.163-2571_163-2570i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635250 | |||||
| chr22:46635251
|
G | A | 3 | a0001c0001t0001g0112a0001c0001t0002g0171a0001c0001t0002g0257 | 3 | HG00438.hp1 NA18982.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.163-2589G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635251 | ||||||
| chr22:46635251
|
G | GGCCACTC others(269): Show |
1 | a0001c0001t0002g0312 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.163-2571_163-2570i others(278): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635251 | |||||
| chr22:46635268
|
G | GGAACCGT others(224): Show |
1 | a0001c0001t0023g0121 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.163-2571_163-2570i others(233): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635268 | |||||
| chr22:46635269
|
G | A | 7 | a0001c0001t0001g0005a0001c0001t0001g0252a0001c0001t0001g0254others(4): Show | 7 | HG01109.hp1 HG01256.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.163-2571G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635269 | ||||||
| chr22:46635270
|
G | A | 168 | a0001c0001t0001g0003a0001c0001t0001g0066a0001c0001t0001g0068others(165): Show | 172 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.163-2570G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635270 | ||||||
| chr22:46635271
|
A | ACCGTGTC others(1099): Show |
1 | a0001c0001t0004g0035 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.163-2549_163-2548i others(1108): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635271 | |||||
| chr22:46635271
|
A | ACCGTGTC others(131): Show |
10 | a0001c0001t0001g0098a0001c0002t0004g0002a0001c0002t0004g0086others(7): Show | 11 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-2562_163-2561i others(140): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635271 | |||||
| chr22:46635271
|
A | G | 8 | a0001c0001t0001g0005a0001c0001t0001g0252a0001c0001t0001g0254others(5): Show | 8 | HG01109.hp1 HG01256.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.163-2569A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635271 | ||||||
| chr22:46635273
|
C | T | 1 | a0001c0001t0002g0317 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.163-2567C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635273 | ||||||
| chr22:46635274
|
G | C | 2 | a0001c0001t0001g0252a0001c0001t0001g0254 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.163-2566G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635274 | ||||||
| chr22:46635276
|
G | A | 2 | a0001c0001t0001g0252a0001c0001t0001g0254 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.163-2564G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635276 | ||||||
| chr22:46635276
|
G | GTCCTCCC others(269): Show |
1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.163-2553_163-2552i others(278): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635276 | |||||
| chr22:46635279
|
C | CTCCCTGC others(131): Show |
1 | a0001c0001t0005g0063 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.163-2549_163-2548i others(140): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635279 | |||||
| chr22:46635279
|
C | T | 34 | a0001c0001t0002g0209a0001c0001t0002g0259a0001c0001t0002g0264others(31): Show | 34 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.163-2561C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635279 | ||||||
| chr22:46635281
|
C | G | 3 | a0001c0001t0005g0213a0001c0001t0030g0044a0001c0001t0048g0191 | 3 | HG01433.hp1 HG02735.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.163-2559C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635281 | ||||||
| chr22:46635285
|
GC | G | 6 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0010others(3): Show | 6 | HG02723.hp1 HG02809.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-2550delC | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635285 | |||||
| chr22:46635286
|
C | CCCCCACC others(361): Show |
1 | a0001c0007t0019g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.163-2550_163-2549i others(370): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635286 | |||||
| chr22:46635286
|
C | T | 3 | a0001c0001t0005g0213a0001c0001t0030g0044a0001c0001t0048g0191 | 3 | HG01433.hp1 HG02735.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.163-2554C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635286 | ||||||
| chr22:46635288
|
C | T | 52 | a0001c0001t0001g0112a0001c0001t0001g0160a0001c0001t0001g0196others(49): Show | 54 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.163-2552C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635288 | ||||||
| chr22:46635290
|
C | G | 1 | a0001c0001t0015g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.163-2550C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635290 | ||||||
| chr22:46635291
|
G | A | 129 | a0001c0001t0001g0005a0001c0001t0001g0066a0001c0001t0001g0068others(126): Show | 131 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.163-2549G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635291 | ||||||
| chr22:46635291
|
G | GACCCCGG others(454): Show |
1 | a0001c0001t0001g0115 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.163-2549_163-2548i others(463): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635291 | ||||||
| chr22:46635292
|
C | A | 93 | a0001c0001t0001g0003a0001c0001t0001g0075a0001c0001t0001g0098others(90): Show | 96 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.163-2548C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635292 | ||||||
| chr22:46635292
|
C | CCCCCGGC others(39): Show |
4 | a0001c0001t0001g0177a0001c0001t0002g0100a0001c0001t0002g0175others(1): Show | 4 | NA18955.hp1 NA18962.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-2525_163-2524i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635292 | |||||
| chr22:46635296
|
C | CAGCCACT others(315): Show |
1 | a0001c0001t0006g0198 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.163-2544_163-2543i others(324): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635296 | ||||||
| chr22:46635296
|
C | CAGCCACT others(453): Show |
1 | a0001c0001t0001g0273 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.163-2544_163-2543i others(462): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635296 | ||||||
| chr22:46635296
|
C | T | 70 | a0001c0001t0001g0005a0001c0001t0001g0066a0001c0001t0001g0068others(67): Show | 70 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.163-2544C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635296 | ||||||
| chr22:46635297
|
G | A | 3 | a0001c0001t0001g0261a0001c0001t0001g0271a0001c0001t0001g0309 | 3 | NA18612.hp1 NA18955.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.163-2543G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635297 | ||||||
| chr22:46635314
|
G | GA | 3 | a0001c0001t0001g0252a0001c0001t0001g0254a0001c0001t0002g0262 | 3 | HG01256.hp2 HG01258.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.163-2526_163-2525i others(3): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635314 | ||||||
| chr22:46635315
|
G | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0072a0001c0001t0001g0074others(14): Show | 17 | HG01255.hp1 HG01433.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.163-2525G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635315 | ||||||
| chr22:46635316
|
G | A | 135 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0073others(132): Show | 136 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.163-2524G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635316 | ||||||
| chr22:46635316
|
G | GACCGTGT others(85): Show |
1 | a0001c0001t0001g0148 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.163-2504_163-2503i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635316 | |||||
| chr22:46635316
|
G | GACCGTGT others(132): Show |
2 | a0001c0001t0004g0061a0001c0001t0019g0062 | 2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.163-2516_163-2515i others(141): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635316 | |||||
| chr22:46635316
|
G | GACCGTGT others(39): Show |
1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.163-2516_163-2515i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635316 | |||||
| chr22:46635317
|
A | G | 20 | a0001c0001t0001g0005a0001c0001t0001g0072a0001c0001t0001g0074others(17): Show | 20 | HG01255.hp1 HG01256.hp2 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.163-2523A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635317 | ||||||
| chr22:46635322
|
G | A | 7 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0116others(4): Show | 7 | HG03130.hp1 NA18952.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.163-2518G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635322 | ||||||
| chr22:46635322
|
G | GTCCTCCC others(85): Show |
1 | a0001c0001t0022g0138 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.163-2504_163-2503i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635322 | |||||
| chr22:46635322
|
G | GTCCTCCC others(223): Show |
1 | a0001c0001t0001g0146 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.163-2504_163-2503i others(232): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635322 | |||||
| chr22:46635325
|
C | T | 6 | a0001c0001t0001g0108a0001c0001t0001g0115a0001c0001t0003g0250others(3): Show | 6 | HG02293.hp2 HG02698.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-2515C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635325 | ||||||
| chr22:46635327
|
C | G | 19 | a0001c0001t0002g0209a0001c0001t0002g0259a0001c0001t0002g0264others(16): Show | 19 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.163-2513C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635327 | ||||||
| chr22:46635332
|
C | T | 19 | a0001c0001t0002g0209a0001c0001t0002g0259a0001c0001t0002g0264others(16): Show | 19 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.163-2508C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635332 | ||||||
| chr22:46635334
|
C | T | 25 | a0001c0001t0001g0157a0001c0001t0001g0255a0001c0001t0001g0261others(22): Show | 25 | HG00099.hp1 HG00642.hp1 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.163-2506C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635334 | ||||||
| chr22:46635337
|
A | C | 1 | a0001c0001t0003g0240 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.163-2503A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635337 | ||||||
| chr22:46635337
|
A | G | 183 | a0001c0001t0001g0003a0001c0001t0001g0066a0001c0001t0001g0068others(180): Show | 187 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.163-2503A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635337 | ||||||
| chr22:46635338
|
C | A | 100 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0073others(97): Show | 102 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.163-2502C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635338 | ||||||
| chr22:46635338
|
C | CCCCCGGC others(85): Show |
1 | a0001c0001t0001g0103 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.163-2499_163-2498i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635338 | |||||
| chr22:46635342
|
T | C | 199 | a0001c0001t0001g0003a0001c0001t0001g0066a0001c0001t0001g0068others(196): Show | 204 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.163-2498T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635342 | ||||||
| chr22:46635342
|
T | TGGCCACT others(85): Show |
1 | a0001c0001t0001g0157 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.163-2480_163-2479i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635342 | |||||
| chr22:46635342
|
T | TGGCCACT others(315): Show |
1 | a0001c0001t0003g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.163-2480_163-2479i others(324): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635342 | |||||
| chr22:46635342
|
T | TGGCCACT others(85): Show |
8 | a0001c0001t0003g0208a0001c0001t0003g0214a0001c0001t0003g0215others(5): Show | 8 | HG00099.hp2 HG00733.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.163-2480_163-2479i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635342 | |||||
| chr22:46635342
|
T | TGGCCACT others(315): Show |
1 | a0001c0001t0003g0283 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.163-2480_163-2479i others(324): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635342 | |||||
| chr22:46635342
|
T | TGGCCACT others(545): Show |
1 | a0001c0001t0001g0261 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.163-2485_163-2484i others(554): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635342 | |||||
| chr22:46635342
|
T | TGGCCACT others(361): Show |
2 | a0001c0001t0001g0271a0001c0001t0001g0309 | 2 | NA18955.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.163-2485_163-2484i others(370): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635342 | |||||
| chr22:46635343
|
G | A | 6 | a0001c0002t0004g0032a0001c0002t0004g0069a0001c0002t0004g0088others(3): Show | 6 | HG01891.hp2 HG02647.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-2497G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635343 | ||||||
| chr22:46635357
|
T | TGGGGAAC others(364): Show |
1 | a0001c0001t0004g0036 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.163-2480_163-2479i others(373): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635357 | |||||
| chr22:46635361
|
A | AGGCCGTA others(86): Show |
3 | a0001c0001t0001g0127a0001c0001t0006g0164a0001c0001t0024g0004 | 4 | HG01069.hp1 HG01071.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-2478_163-2477i others(95): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635361 | |||||
| chr22:46635361
|
A | AGGCCGTA others(362): Show |
1 | a0001c0001t0001g0126 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.163-2478_163-2477i others(371): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635361 | |||||
| chr22:46635361
|
A | AGGCCGTA others(269): Show |
3 | a0001c0001t0002g0278a0001c0001t0017g0045a0001c0005t0002g0294 | 3 | HG01952.hp2 HG04115.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.163-2478_163-2477i others(278): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635361 | |||||
| chr22:46635361
|
A | G | 232 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0073others(229): Show | 234 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.163-2479A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635361 | ||||||
| chr22:46635362
|
G | A | 91 | a0001c0001t0001g0073a0001c0001t0001g0108a0001c0001t0001g0112others(88): Show | 93 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.163-2478G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635362 | ||||||
| chr22:46635363
|
A | G | 87 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0072others(84): Show | 90 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.163-2477A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635363 | ||||||
| chr22:46635365
|
C | T | 3 | a0001c0001t0011g0183a0001c0001t0011g0184a0001c0001t0028g0060 | 3 | HG02723.hp2 HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.163-2475C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635365 | ||||||
| chr22:46635366
|
G | C | 6 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0116others(3): Show | 6 | HG02071.hp2 NA18952.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-2474G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635366 | ||||||
| chr22:46635368
|
G | A | 38 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0001g0074others(35): Show | 39 | HG00099.hp1 HG00642.hp1 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.163-2472G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635368 | ||||||
| chr22:46635368
|
G | GTCCTCCC others(39): Show |
1 | a0001c0002t0004g0090 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.163-2470_163-2469i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635368 | |||||
| chr22:46635371
|
A | C | 265 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(262): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.163-2469A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635371 | ||||||
| chr22:46635371
|
A | T | 57 | a0001c0001t0001g0115a0001c0001t0001g0252a0001c0001t0001g0254others(54): Show | 57 | HG00323.hp2 HG00738.hp2 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.163-2469A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635371 | ||||||
| chr22:46635373
|
C | G | 9 | a0001c0001t0007g0024a0001c0001t0007g0025a0001c0001t0007g0026others(6): Show | 9 | HG00642.hp2 HG01243.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.163-2467C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635373 | ||||||
| chr22:46635378
|
C | CCCCCGCC others(316): Show |
1 | a0001c0001t0009g0056 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.163-2434_163-2433i others(325): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635378 | |||||
| chr22:46635378
|
C | CCCCCGCC others(315): Show |
11 | a0001c0001t0005g0105a0001c0001t0005g0142a0001c0001t0005g0144others(8): Show | 11 | HG00738.hp2 HG01106.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.163-2434_163-2433i others(324): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635378 | |||||
| chr22:46635378
|
C | CCCCCGCC others(591): Show |
3 | a0001c0001t0005g0111a0001c0001t0005g0143a0001c0001t0050g0147 | 3 | HG02735.hp1 HG03688.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.163-2434_163-2433i others(600): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635378 | |||||
| chr22:46635378
|
C | CCCCCGCC others(361): Show |
1 | a0001c0001t0005g0211 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.163-2434_163-2433i others(370): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635378 | |||||
| chr22:46635383
|
G | A | 148 | a0001c0001t0001g0003a0001c0001t0001g0073a0001c0001t0001g0075others(145): Show | 153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.163-2457G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635383 | ||||||
| chr22:46635383
|
G | GACCCCGG others(85): Show |
2 | a0001c0001t0006g0302a0001c0001t0032g0046 | 2 | HG02258.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.163-2457_163-2456i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635383 | ||||||
| chr22:46635384
|
C | A | 32 | a0001c0001t0001g0112a0001c0001t0001g0139a0001c0001t0001g0146others(29): Show | 32 | HG00438.hp1 HG00673.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.163-2456C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635384 | ||||||
| chr22:46635384
|
C | CCCCCGGC others(269): Show |
2 | a0001c0003t0003g0235a0001c0003t0003g0236 | 2 | HG02109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.163-2434_163-2433i others(278): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635384 | |||||
| chr22:46635384
|
C | CCCCCGGC others(270): Show |
1 | a0001c0001t0014g0058 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.163-2434_163-2433i others(279): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635384 | |||||
| chr22:46635384
|
C | CCCCCGGC others(269): Show |
12 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0083others(9): Show | 12 | HG01243.hp2 HG01891.hp1 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-2434_163-2433i others(278): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635384 | |||||
| chr22:46635384
|
C | CCCCCGGC others(453): Show |
1 | a0001c0001t0003g0218 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.163-2434_163-2433i others(462): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635384 | |||||
| chr22:46635388
|
C | CGGCCACT others(39): Show |
1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.163-2434_163-2433i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635388 | |||||
| chr22:46635388
|
C | CGGCCACT others(39): Show |
2 | a0001c0001t0010g0185a0001c0001t0020g0232 | 2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.163-2424_163-2423i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635388 | |||||
| chr22:46635388
|
C | CGGCCACT others(406): Show |
1 | a0001c0001t0003g0212 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.163-2424_163-2423i others(415): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635388 | |||||
| chr22:46635388
|
C | T | 138 | a0001c0001t0001g0003a0001c0001t0001g0073a0001c0001t0001g0075others(135): Show | 141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.163-2452C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635388 | ||||||
| chr22:46635389
|
G | A | 1 | a0001c0002t0004g0099 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.163-2451G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635389 | ||||||
| chr22:46635405
|
G | GGAGGCCG others(451): Show |
1 | a0001c0001t0005g0145 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.163-2434_163-2433i others(460): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635405 | |||||
| chr22:46635406
|
G | GA | 6 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0116others(3): Show | 6 | HG02071.hp2 NA18952.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-2434_163-2433i others(3): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635406 | ||||||
| chr22:46635407
|
G | A | 70 | a0001c0001t0001g0003a0001c0001t0001g0066a0001c0001t0001g0068others(67): Show | 71 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.163-2433G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635407 | ||||||
| chr22:46635408
|
G | A | 54 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0103others(51): Show | 54 | HG00408.hp1 HG00741.hp2 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.163-2432G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635408 | ||||||
| chr22:46635409
|
A | G | 77 | a0001c0001t0001g0003a0001c0001t0001g0066a0001c0001t0001g0068others(74): Show | 78 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.163-2431A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635409 | ||||||
| chr22:46635412
|
G | C | 17 | a0001c0001t0001g0003a0001c0001t0001g0106a0001c0001t0001g0113others(14): Show | 18 | HG01993.hp1 HG02129.hp2 HG02165.hp2 others(15): Show |
intron_variant | MODIFIER | c.163-2428G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635412 | ||||||
| chr22:46635414
|
G | A | 67 | a0001c0001t0001g0003a0001c0001t0001g0066a0001c0001t0001g0068others(64): Show | 68 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.163-2426G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635414 | ||||||
| chr22:46635414
|
G | GTCCTCCC others(39): Show |
1 | a0001c0001t0030g0044 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.163-2424_163-2423i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635414 | |||||
| chr22:46635414
|
G | GTCCTCCC others(85): Show |
1 | a0001c0001t0048g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.163-2424_163-2423i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635414 | |||||
| chr22:46635414
|
G | GTCCTCCC others(177): Show |
1 | a0001c0001t0004g0035 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.163-2424_163-2423i others(186): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635414 | |||||
| chr22:46635417
|
T | C | 192 | a0001c0001t0001g0003a0001c0001t0001g0066a0001c0001t0001g0068others(189): Show | 194 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.163-2423T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635417 | ||||||
| chr22:46635417
|
T | TTCCCTGC others(131): Show |
1 | a0001c0001t0005g0041 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.163-2411_163-2410i others(140): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635417 | |||||
| chr22:46635417
|
T | TTCCCTGC others(223): Show |
7 | a0001c0001t0002g0286a0001c0001t0002g0287a0001c0001t0005g0001others(4): Show | 8 | HG02615.hp2 HG02818.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.163-2411_163-2410i others(232): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635417 | |||||
| chr22:46635417
|
T | TTCCCTGC others(269): Show |
3 | a0001c0001t0002g0007a0001c0001t0002g0279a0001c0001t0002g0281 | 4 | HG00639.hp1 HG01256.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-2411_163-2410i others(278): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635417 | |||||
| chr22:46635419
|
C | G | 19 | a0001c0001t0002g0317a0001c0001t0003g0030a0001c0001t0003g0031others(16): Show | 19 | HG00741.hp2 HG01243.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.163-2421C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635419 | ||||||
| chr22:46635423
|
GC | G | 8 | a0001c0001t0007g0024a0001c0001t0007g0025a0001c0001t0007g0026others(5): Show | 8 | HG00642.hp2 HG01243.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.163-2412delC | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635423 | |||||
| chr22:46635424
|
C | CCCCCACC others(498): Show |
3 | a0001c0001t0003g0210a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | NA18946.hp1 NA18952.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.163-2412_163-2411i others(507): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635424 | |||||
| chr22:46635424
|
C | T | 19 | a0001c0001t0002g0317a0001c0001t0003g0030a0001c0001t0003g0031others(16): Show | 19 | HG00741.hp2 HG01243.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.163-2416C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635424 | ||||||
| chr22:46635426
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.163-2414C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635426 | ||||||
| chr22:46635428
|
C | G | 1 | a0001c0001t0015g0189 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.163-2412C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635428 | ||||||
| chr22:46635429
|
G | A | 71 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0072others(68): Show | 71 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.163-2411G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635429 | ||||||
| chr22:46635429
|
G | GACCCCGG others(39): Show |
1 | a0001c0002t0046g0089 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.163-2411_163-2410i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635429 | ||||||
| chr22:46635429
|
G | GACCCCGG others(177): Show |
1 | a0001c0001t0060g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.163-2411_163-2410i others(186): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635429 | ||||||
| chr22:46635429
|
G | GACCCCGG others(269): Show |
37 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0002g0081others(34): Show | 37 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.163-2411_163-2410i others(278): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635429 | ||||||
| chr22:46635429
|
G | GACCCCGG others(362): Show |
1 | a0001c0001t0006g0195 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.163-2411_163-2410i others(371): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635429 | ||||||
| chr22:46635430
|
C | A | 21 | a0001c0001t0001g0098a0001c0001t0001g0103a0001c0001t0001g0126others(18): Show | 22 | HG00639.hp2 HG01257.hp2 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.163-2410C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635430 | ||||||
| chr22:46635434
|
C | CGGCCACT others(315): Show |
1 | a0001c0001t0004g0036 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.163-2388_163-2387i others(324): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635434 | |||||
| chr22:46635434
|
C | T | 111 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0080others(108): Show | 112 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.163-2406C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635434 | ||||||
| chr22:46635435
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.163-2405G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635435 | ||||||
| chr22:46635449
|
T | G | 8 | a0001c0001t0007g0024a0001c0001t0007g0025a0001c0001t0007g0026others(5): Show | 8 | HG00642.hp2 HG01243.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.163-2391T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635449 | ||||||
| chr22:46635453
|
A | AG | 11 | a0001c0001t0001g0003a0001c0001t0001g0106a0001c0001t0001g0113others(8): Show | 12 | HG01993.hp1 NA18612.hp2 NA18948.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-2385dupG | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635453 | |||||
| chr22:46635453
|
A | G | 60 | a0001c0001t0001g0072a0001c0001t0001g0098a0001c0001t0001g0116others(57): Show | 62 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.163-2387A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635453 | ||||||
| chr22:46635454
|
G | A | 40 | a0001c0001t0001g0098a0001c0001t0001g0261a0001c0001t0001g0271others(37): Show | 41 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.163-2386G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635454 | ||||||
| chr22:46635454
|
G | GACCGTGT others(360): Show |
1 | a0001c0001t0003g0244 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.163-2386_163-2385i others(369): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635454 | ||||||
| chr22:46635455
|
G | A | 58 | a0001c0001t0001g0072a0001c0001t0001g0098a0001c0001t0001g0116others(55): Show | 60 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.163-2385G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635455 | ||||||
| chr22:46635455
|
G | GCCGTGTC others(39): Show |
1 | a0001c0001t0005g0142 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.163-2361_163-2360i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635455 | |||||
| chr22:46635455
|
G | GCTGTATC others(130): Show |
1 | a0001c0002t0004g0090 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.163-2384_163-2383i others(139): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635455 | |||||
| chr22:46635457
|
C | T | 5 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0006g0164others(2): Show | 5 | HG00639.hp2 HG02135.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.163-2383C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635457 | ||||||
| chr22:46635458
|
G | C | 38 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0080others(35): Show | 38 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.163-2382G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635458 | ||||||
| chr22:46635460
|
G | A | 123 | a0001c0001t0001g0005a0001c0001t0001g0066a0001c0001t0001g0068others(120): Show | 124 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.163-2380G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635460 | ||||||
| chr22:46635463
|
C | T | 18 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0116others(15): Show | 19 | HG01069.hp1 HG01071.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.163-2377C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635463 | ||||||
| chr22:46635465
|
C | G | 1 | a0001c0001t0003g0212 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.163-2375C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635465 | ||||||
| chr22:46635470
|
C | T | 1 | a0001c0001t0003g0212 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.163-2370C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635470 | ||||||
| chr22:46635472
|
C | CCCACCCC others(85): Show |
1 | a0001c0001t0064g0306 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.163-2342_163-2341i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635472 | |||||
| chr22:46635472
|
C | T | 24 | a0001c0001t0001g0261a0001c0001t0001g0271a0001c0001t0001g0309others(21): Show | 24 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.163-2368C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635472 | ||||||
| chr22:46635474
|
C | CG | 3 | a0001c0001t0001g0158a0001c0001t0015g0190a0001c0001t0022g0138 | 3 | HG02071.hp2 HG03130.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.163-2366_163-2365i others(3): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635474 | ||||||
| chr22:46635475
|
A | ACCCCCGG others(315): Show |
1 | a0001c0002t0004g0088 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.163-2361_163-2360i others(324): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635475 | |||||
| chr22:46635475
|
A | C | 1 | a0001c0001t0001g0158 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.163-2365A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635475 | ||||||
| chr22:46635475
|
A | G | 60 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0072others(57): Show | 61 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.163-2365A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635475 | ||||||
| chr22:46635476
|
C | A | 3 | a0001c0001t0001g0074a0001c0002t0002g0071a0002c0010t0047g0064 | 3 | HG02886.hp1 HG04115.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.163-2364C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635476 | ||||||
| chr22:46635480
|
T | C | 164 | a0001c0001t0001g0003a0001c0001t0001g0066a0001c0001t0001g0068others(161): Show | 167 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.163-2360T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635480 | ||||||
| chr22:46635480
|
T | TGGCCACT others(544): Show |
6 | a0001c0001t0003g0206a0001c0001t0003g0224a0001c0001t0003g0225others(3): Show | 6 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-2286_163-2285i others(553): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635480 | |||||
| chr22:46635480
|
T | TGGCCACT others(39): Show |
5 | a0001c0001t0001g0098a0001c0002t0004g0002a0001c0002t0004g0086others(2): Show | 6 | HG01496.hp2 HG01934.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-2342_163-2341i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635480 | |||||
| chr22:46635499
|
A | AG | 34 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0080others(31): Show | 34 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.163-2339dupG | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635499 | |||||
| chr22:46635499
|
A | G | 127 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0001g0106others(124): Show | 130 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.163-2341A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635499 | ||||||
| chr22:46635500
|
G | A | 6 | a0001c0001t0004g0036a0001c0001t0011g0057a0001c0001t0033g0037others(3): Show | 6 | HG02622.hp2 HG02886.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-2340G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635500 | ||||||
| chr22:46635500
|
G | GACCGTGT others(85): Show |
1 | a0001c0001t0002g0317 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.163-2340_163-2339i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635500 | ||||||
| chr22:46635501
|
G | A | 125 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0001g0106others(122): Show | 128 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.163-2339G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635501 | ||||||
| chr22:46635503
|
C | T | 16 | a0001c0001t0001g0074a0001c0001t0001g0252a0001c0001t0001g0254others(13): Show | 16 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.163-2337C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635503 | ||||||
| chr22:46635504
|
C | G | 223 | a0001c0001t0001g0003a0001c0001t0001g0066a0001c0001t0001g0068others(220): Show | 227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.163-2336C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635504 | ||||||
| chr22:46635506
|
A | G | 176 | a0001c0001t0001g0003a0001c0001t0001g0066a0001c0001t0001g0068others(173): Show | 180 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.163-2334A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635506 | ||||||
| chr22:46635509
|
C | CTCCCTGC others(407): Show |
1 | a0001c0001t0015g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.163-2320_163-2319i others(416): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635509 | |||||
| chr22:46635509
|
C | CTCCCTGC others(85): Show |
2 | a0001c0001t0002g0286a0001c0001t0002g0287 | 2 | NA18964.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.163-2320_163-2319i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635509 | |||||
| chr22:46635509
|
C | CTCCCTGC others(85): Show |
1 | a0001c0001t0033g0037 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.163-2320_163-2319i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635509 | |||||
| chr22:46635509
|
C | CTCCCTGC others(177): Show |
5 | a0001c0002t0004g0032a0001c0002t0004g0069a0001c0002t0004g0092others(2): Show | 5 | HG01891.hp2 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-2319_163-2318i others(186): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635509 | |||||
| chr22:46635509
|
C | CTCCCTGC others(821): Show |
1 | a0001c0001t0015g0189 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.163-2319_163-2318i others(830): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635509 | |||||
| chr22:46635509
|
C | CTCCCTGC others(39): Show |
1 | a0001c0002t0004g0099 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.163-2296_163-2295i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635509 | |||||
| chr22:46635509
|
C | CTCCCTGC others(543): Show |
1 | a0001c0001t0003g0205 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.163-2321_163-2320i others(552): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635509 | |||||
| chr22:46635509
|
C | CTCCCTGC others(543): Show |
2 | a0001c0001t0003g0104a0001c0001t0003g0169 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.163-2321_163-2320i others(552): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635509 | |||||
| chr22:46635509
|
C | T | 108 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0001g0106others(105): Show | 111 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.163-2331C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635509 | ||||||
| chr22:46635515
|
GC | G | 8 | a0001c0001t0007g0024a0001c0001t0007g0025a0001c0001t0007g0026others(5): Show | 8 | HG00642.hp2 HG01243.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.163-2320delC | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635515 | |||||
| chr22:46635516
|
C | CCCCCACC others(177): Show |
1 | a0001c0001t0010g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.163-2320_163-2319i others(186): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635516 | |||||
| chr22:46635516
|
C | CCCCCACC others(131): Show |
2 | a0001c0001t0010g0186a0001c0001t0010g0187 | 2 | HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.163-2320_163-2319i others(140): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635516 | |||||
| chr22:46635516
|
C | CCCCCGCC others(774): Show |
1 | a0001c0001t0003g0214 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.163-2286_163-2285i others(783): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635516 | |||||
| chr22:46635516
|
C | CCCCCGCC others(774): Show |
2 | a0001c0001t0003g0208a0001c0001t0003g0215 | 2 | HG00099.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.163-2286_163-2285i others(783): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635516 | |||||
| chr22:46635521
|
G | A | 84 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0074others(81): Show | 85 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.163-2319G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635521 | ||||||
| chr22:46635522
|
C | A | 1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.163-2318C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635522 | ||||||
| chr22:46635523
|
C | T | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.163-2317C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635523 | ||||||
| chr22:46635526
|
C | CGGCCACT others(498): Show |
4 | a0001c0001t0003g0245a0001c0001t0014g0052a0001c0001t0018g0230others(1): Show | 4 | HG00733.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-2286_163-2285i others(507): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635526 | |||||
| chr22:46635526
|
C | CGGCCACT others(361): Show |
1 | a0001c0001t0005g0039 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.163-2296_163-2295i others(370): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635526 | |||||
| chr22:46635526
|
C | T | 43 | a0001c0001t0001g0123a0001c0001t0001g0154a0001c0001t0001g0252others(40): Show | 44 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.163-2314C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635526 | ||||||
| chr22:46635527
|
G | A | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.163-2313G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635527 | ||||||
| chr22:46635533
|
T | C | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.163-2307T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635533 | ||||||
| chr22:46635541
|
T | A | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.163-2299T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635541 | ||||||
| chr22:46635541
|
T | G | 8 | a0001c0001t0007g0024a0001c0001t0007g0025a0001c0001t0007g0026others(5): Show | 8 | HG00642.hp2 HG01243.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.163-2299T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635541 | ||||||
| chr22:46635545
|
A | AG | 32 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0075others(29): Show | 32 | HG00438.hp1 HG00673.hp1 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.163-2293dupG | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635545 | |||||
| chr22:46635545
|
A | G | 130 | a0001c0001t0001g0003a0001c0001t0001g0066a0001c0001t0001g0068others(127): Show | 134 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.163-2295A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635545 | ||||||
| chr22:46635546
|
G | A | 3 | a0001c0001t0011g0057a0001c0001t0054g0251a0002c0010t0047g0064 | 3 | HG02647.hp2 HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.163-2294G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635546 | ||||||
| chr22:46635547
|
G | A | 129 | a0001c0001t0001g0003a0001c0001t0001g0066a0001c0001t0001g0068others(126): Show | 133 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.163-2293G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635547 | ||||||
| chr22:46635547
|
G | GCCGTATC others(177): Show |
1 | a0001c0001t0043g0311 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.163-2289_163-2288i others(186): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635547 | |||||
| chr22:46635547
|
G | GCCGTATC others(131): Show |
2 | a0001c0001t0001g0261a0001c0001t0006g0302 | 2 | NA18612.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.163-2289_163-2288i others(140): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635547 | |||||
| chr22:46635547
|
G | GCTGTATC others(498): Show |
1 | a0001c0002t0004g0088 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.163-2292_163-2291i others(507): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635547 | |||||
| chr22:46635547
|
G | GGCCGTGT others(40): Show |
1 | a0001c0001t0023g0121 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.163-2293_163-2292i others(49): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635547 | ||||||
| chr22:46635549
|
C | CGTATCCT others(85): Show |
1 | a0001c0001t0009g0054 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.163-2289_163-2288i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635549 | |||||
| chr22:46635549
|
C | T | 34 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0083others(31): Show | 35 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.163-2291C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635549 | ||||||
| chr22:46635550
|
G | C | 10 | a0001c0001t0001g0074a0001c0001t0001g0123a0001c0001t0001g0154others(7): Show | 10 | HG00408.hp1 HG02451.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.163-2290G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635550 | ||||||
| chr22:46635552
|
G | A | 43 | a0001c0001t0001g0074a0001c0001t0001g0123a0001c0001t0001g0154others(40): Show | 44 | HG00408.hp1 HG00735.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.163-2288G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635552 | ||||||
| chr22:46635552
|
G | GTCCTCCC others(361): Show |
1 | a0001c0007t0019g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.163-2274_163-2273i others(370): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635552 | |||||
| chr22:46635552
|
G | GTCTTCCC others(590): Show |
1 | a0001c0001t0003g0221 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.163-2286_163-2285i others(599): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635552 | |||||
| chr22:46635552
|
G | GTCTTCCC others(498): Show |
12 | a0001c0001t0001g0220a0001c0001t0003g0006a0001c0001t0003g0207others(9): Show | 12 | HG01255.hp2 HG02027.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-2286_163-2285i others(507): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635552 | |||||
| chr22:46635552
|
G | GTCTTCCC others(589): Show |
1 | a0001c0001t0003g0244 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.163-2286_163-2285i others(598): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635552 | |||||
| chr22:46635552
|
G | GTCTTCCC others(681): Show |
1 | a0001c0001t0003g0283 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.163-2286_163-2285i others(690): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635552 | |||||
| chr22:46635555
|
C | CTCCCTGC others(178): Show |
1 | a0001c0001t0002g0274 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.163-2274_163-2273i others(187): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635555 | |||||
| chr22:46635555
|
C | CTCCCTGC others(85): Show |
2 | a0001c0001t0001g0271a0001c0001t0001g0273 | 2 | HG02027.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.163-2274_163-2273i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635555 | |||||
| chr22:46635555
|
C | CTCCCTGC others(85): Show |
1 | a0001c0001t0001g0309 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.163-2250_163-2249i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635555 | |||||
| chr22:46635555
|
C | T | 140 | a0001c0001t0001g0003a0001c0001t0001g0066a0001c0001t0001g0068others(137): Show | 144 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.163-2285C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635555 | ||||||
| chr22:46635557
|
C | G | 1 | a0001c0001t0005g0063 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.163-2283C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635557 | ||||||
| chr22:46635561
|
GC | G | 8 | a0001c0001t0001g0252a0001c0001t0001g0254a0001c0001t0008g0008others(5): Show | 8 | HG01256.hp2 HG01258.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.163-2274delC | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635561 | |||||
| chr22:46635562
|
C | CCCCCACC others(84): Show |
3 | a0001c0001t0007g0022a0001c0001t0007g0023a0001c0001t0013g0020 | 3 | HG01070.hp2 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.163-2274_163-2273i others(93): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635562 | |||||
| chr22:46635562
|
C | CCCCGCCC others(589): Show |
1 | a0001c0001t0003g0240 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.163-2275_163-2274i others(598): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635562 | |||||
| chr22:46635567
|
G | A | 137 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0075others(134): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.163-2273G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635567 | ||||||
| chr22:46635567
|
GCCCCCGG others(37): Show |
G | 1 | a0001c0001t0010g0034 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.163-2272_163-2229d others(46): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635567 | ||||||
| chr22:46635568
|
C | A | 1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.163-2272C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635568 | ||||||
| chr22:46635572
|
C | CCGGCCAC others(40): Show |
1 | a0001c0002t0004g0070 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.163-2268_163-2267i others(49): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635572 | ||||||
| chr22:46635572
|
C | CGGCCACT others(85): Show |
1 | a0001c0001t0009g0056 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.163-2240_163-2239i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635572 | |||||
| chr22:46635572
|
C | CGGCCACT others(39): Show |
18 | a0001c0001t0001g0098a0001c0001t0005g0105a0001c0001t0005g0111others(15): Show | 19 | HG01106.hp1 HG01168.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.163-2246_163-2245i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635572 | |||||
| chr22:46635572
|
C | CGGCCACT others(269): Show |
1 | a0001c0001t0017g0043 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.163-2246_163-2245i others(278): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635572 | |||||
| chr22:46635572
|
C | CGGCCACT others(315): Show |
2 | a0001c0001t0005g0213a0001c0001t0020g0232 | 2 | HG02735.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.163-2250_163-2249i others(324): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635572 | |||||
| chr22:46635572
|
C | CGGCCACT others(85): Show |
4 | a0001c0001t0003g0210a0001c0001t0003g0238a0001c0001t0003g0239others(1): Show | 4 | HG02965.hp2 NA18946.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-2250_163-2249i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635572 | |||||
| chr22:46635572
|
C | CGGCCACT others(177): Show |
1 | a0001c0001t0048g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.163-2250_163-2249i others(186): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635572 | |||||
| chr22:46635572
|
C | CGGCCACT others(177): Show |
1 | a0001c0001t0001g0115 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.163-2250_163-2249i others(186): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635572 | |||||
| chr22:46635572
|
C | CGGCCACT others(131): Show |
1 | a0001c0001t0001g0126 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.163-2250_163-2249i others(140): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635572 | |||||
| chr22:46635572
|
C | CGGCCACT others(177): Show |
3 | a0001c0001t0005g0001a0001c0001t0005g0040a0001c0001t0049g0042 | 4 | HG02615.hp2 HG02818.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-2250_163-2249i others(186): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635572 | |||||
| chr22:46635572
|
C | T | 61 | a0001c0001t0001g0072a0001c0001t0001g0116a0001c0001t0001g0179others(58): Show | 62 | HG00733.hp1 HG00735.hp2 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.163-2268C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635572 | ||||||
| chr22:46635575
|
C | G | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.163-2265C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635575 | ||||||
| chr22:46635587
|
T | G | 3 | a0001c0001t0007g0022a0001c0001t0007g0023a0001c0001t0013g0020 | 3 | HG01070.hp2 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.163-2253T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635587 | ||||||
| chr22:46635589
|
G | GGGAACCG others(267): Show |
1 | a0001c0001t0005g0041 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.163-2250_163-2249i others(276): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635589 | |||||
| chr22:46635591
|
A | G | 207 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(204): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.163-2249A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635591 | ||||||
| chr22:46635592
|
G | A | 4 | a0001c0001t0004g0021a0001c0001t0011g0057a0001c0001t0015g0189others(1): Show | 4 | HG02258.hp2 HG03130.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-2248G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635592 | ||||||
| chr22:46635593
|
G | A | 205 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(202): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.163-2247G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635593 | ||||||
| chr22:46635593
|
G | GCCGTATC others(131): Show |
3 | a0001c0001t0008g0013a0001c0001t0008g0014a0001c0001t0008g0016 | 3 | HG02976.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.163-2243_163-2242i others(140): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635593 | |||||
| chr22:46635595
|
C | T | 4 | a0001c0001t0001g0072a0001c0001t0001g0116a0001c0001t0001g0179others(1): Show | 4 | HG02572.hp2 NA18952.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-2245C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635595 | ||||||
| chr22:46635598
|
G | A | 4 | a0001c0001t0001g0072a0001c0001t0001g0116a0001c0001t0001g0179others(1): Show | 4 | HG02572.hp2 NA18952.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-2242G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635598 | ||||||
| chr22:46635601
|
T | C | 26 | a0001c0001t0001g0072a0001c0001t0001g0115a0001c0001t0001g0116others(23): Show | 27 | HG00408.hp1 HG00639.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.163-2239T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635601 | ||||||
| chr22:46635601
|
T | TTCCCTGC others(39): Show |
1 | a0001c0001t0004g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.163-2229_163-2228i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635601 | |||||
| chr22:46635603
|
C | G | 1 | a0001c0001t0004g0021 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.163-2237C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635603 | ||||||
| chr22:46635607
|
G | GC | 123 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(120): Show | 124 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.163-2229dupC | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635607 | |||||
| chr22:46635607
|
G | GCCCCCGA others(224): Show |
1 | a0001c0001t0001g0157 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.163-2229_163-2228i others(233): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635607 | |||||
| chr22:46635607
|
G | GCCCCCGA others(178): Show |
2 | a0001c0001t0001g0112a0001c0001t0001g0146 | 2 | HG00438.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.163-2229_163-2228i others(187): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635607 | |||||
| chr22:46635607
|
G | GCCCCCGA others(86): Show |
1 | a0001c0001t0004g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.163-2229_163-2228i others(95): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635607 | |||||
| chr22:46635612
|
G | A | 19 | a0001c0001t0001g0072a0001c0001t0001g0116a0001c0001t0001g0123others(16): Show | 19 | HG00408.hp1 HG00735.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.163-2228G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635612 | ||||||
| chr22:46635617
|
C | T | 22 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0001g0106others(19): Show | 24 | HG01993.hp1 HG02615.hp2 HG02818.hp2 others(21): Show |
intron_variant | MODIFIER | c.163-2223C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635617 | ||||||
| chr22:46635618
|
G | A | 9 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0010others(6): Show | 9 | HG01361.hp1 HG02647.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.163-2222G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635618 | ||||||
| chr22:46635618
|
G | GGCCACTC others(222): Show |
1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.163-2195_163-2194i others(231): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635618 | |||||
| chr22:46635624
|
T | C | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.163-2216T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635624 | ||||||
| chr22:46635632
|
T | G | 9 | a0001c0001t0005g0063a0001c0001t0007g0024a0001c0001t0007g0025others(6): Show | 9 | HG00642.hp2 HG01243.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.163-2208T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635632 | ||||||
| chr22:46635635
|
G | A | 9 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0010others(6): Show | 9 | HG02572.hp2 HG02647.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.163-2205G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635635 | ||||||
| chr22:46635635
|
G | GGGCCCGT others(85): Show |
1 | a0001c0002t0004g0086 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.163-2203_163-2202i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635635 | |||||
| chr22:46635636
|
G | A | 32 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0001g0106others(29): Show | 33 | HG00323.hp2 HG00642.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.163-2204G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635636 | ||||||
| chr22:46635637
|
G | A | 2 | a0001c0001t0011g0057a0002c0010t0047g0064 | 2 | HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.163-2203G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635637 | ||||||
| chr22:46635637
|
GACCGTGT others(39): Show |
G | 1 | a0001c0001t0031g0059 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.163-2202_163-2157d others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635637 | ||||||
| chr22:46635638
|
A | G | 31 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0001g0106others(28): Show | 32 | HG00323.hp2 HG00642.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.163-2202A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635638 | ||||||
| chr22:46635640
|
C | CGTGTCCT others(39): Show |
2 | a0001c0001t0004g0035a0001c0001t0010g0186 | 2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.163-2181_163-2180i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635640 | |||||
| chr22:46635640
|
C | CGTGTCCT others(85): Show |
1 | a0001c0002t0004g0117 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.163-2181_163-2180i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635640 | |||||
| chr22:46635640
|
C | CGTGTCCT others(85): Show |
8 | a0001c0001t0001g0098a0001c0002t0002g0071a0001c0002t0004g0002others(5): Show | 9 | HG01361.hp2 HG01496.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.163-2181_163-2180i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635640 | |||||
| chr22:46635640
|
C | CGTGTCCT others(268): Show |
1 | a0001c0001t0004g0021 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.163-2181_163-2180i others(277): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635640 | |||||
| chr22:46635640
|
C | CGTGTCCT others(40): Show |
2 | a0001c0001t0004g0036a0001c0001t0033g0037 | 2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.163-2183_163-2182i others(49): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635640 | |||||
| chr22:46635640
|
C | CGTGTCTT others(590): Show |
2 | a0001c0001t0004g0061a0001c0001t0019g0062 | 2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.163-2195_163-2194i others(599): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635640 | |||||
| chr22:46635640
|
C | CGTGTCTT others(130): Show |
1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.163-2195_163-2194i others(139): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635640 | |||||
| chr22:46635640
|
C | CT | 77 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0255others(74): Show | 79 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.163-2200_163-2199i others(3): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635640 | ||||||
| chr22:46635640
|
C | CTGTGTCC others(132): Show |
1 | a0001c0001t0005g0188 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.163-2200_163-2199i others(141): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635640 | ||||||
| chr22:46635640
|
C | T | 31 | a0001c0001t0001g0003a0001c0001t0001g0106a0001c0001t0001g0113others(28): Show | 33 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.163-2200C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635640 | ||||||
| chr22:46635643
|
G | A | 15 | a0001c0001t0001g0003a0001c0001t0001g0106a0001c0001t0001g0113others(12): Show | 16 | HG01993.hp1 HG02451.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.163-2197G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635643 | ||||||
| chr22:46635646
|
C | T | 96 | a0001c0001t0001g0005a0001c0001t0001g0066a0001c0001t0001g0068others(93): Show | 96 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.163-2194C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635646 | ||||||
| chr22:46635652
|
GC | G | 5 | a0001c0001t0001g0072a0001c0001t0001g0116a0001c0001t0001g0179others(2): Show | 5 | HG01109.hp1 HG02293.hp2 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.163-2183delC | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635652 | |||||
| chr22:46635655
|
C | T | 1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.163-2185C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635655 | ||||||
| chr22:46635658
|
A | G | 99 | a0001c0001t0001g0005a0001c0001t0001g0066a0001c0001t0001g0068others(96): Show | 99 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.163-2182A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635658 | ||||||
| chr22:46635660
|
T | C | 133 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(130): Show | 134 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.163-2180T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635660 | ||||||
| chr22:46635663
|
C | T | 62 | a0001c0001t0001g0003a0001c0001t0001g0066a0001c0001t0001g0068others(59): Show | 63 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.163-2177C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635663 | ||||||
| chr22:46635664
|
A | G | 127 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(124): Show | 128 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.163-2176A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635664 | ||||||
| chr22:46635670
|
C | T | 133 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(130): Show | 134 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.163-2170C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635670 | ||||||
| chr22:46635678
|
A | G | 1 | a0001c0001t0002g0264 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.163-2162A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635678 | ||||||
| chr22:46635678
|
A | T | 130 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(127): Show | 131 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.163-2162A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635678 | ||||||
| chr22:46635681
|
G | A | 1 | a0001c0001t0004g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.163-2159G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635681 | ||||||
| chr22:46635682
|
G | A | 64 | a0001c0001t0001g0003a0001c0001t0001g0066a0001c0001t0001g0068others(61): Show | 65 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.163-2158G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635682 | ||||||
| chr22:46635683
|
A | G | 117 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(114): Show | 118 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.163-2157A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635683 | ||||||
| chr22:46635684
|
G | A | 66 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0075others(63): Show | 66 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.163-2156G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635684 | ||||||
| chr22:46635684
|
G | C | 1 | a0001c0001t0002g0264 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.163-2156G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635684 | ||||||
| chr22:46635686
|
T | C | 79 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0073others(76): Show | 80 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.163-2154T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635686 | ||||||
| chr22:46635689
|
G | A | 50 | a0001c0001t0001g0005a0001c0001t0001g0066a0001c0001t0001g0068others(47): Show | 50 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.163-2151G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635689 | ||||||
| chr22:46635692
|
C | T | 47 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0103others(44): Show | 47 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.163-2148C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635692 | ||||||
| chr22:46635698
|
GCT | G | 34 | a0001c0001t0001g0003a0001c0001t0001g0106a0001c0001t0001g0113others(31): Show | 35 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.163-2140_163-2139d others(4): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635698 | |||||
| chr22:46635699
|
C | CCCCCGCC others(905): Show |
1 | a0001c0001t0005g0063 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.163-2141_163-2140i others(914): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635699 | ||||||
| chr22:46635699
|
C | CCCCCGCC others(676): Show |
1 | a0001c0001t0007g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.163-2141_163-2140i others(685): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635699 | ||||||
| chr22:46635699
|
C | CCCCCGCC others(905): Show |
1 | a0001c0001t0013g0020 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.163-2141_163-2140i others(914): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635699 | ||||||
| chr22:46635699
|
C | CCCCCGCC others(265): Show |
8 | a0001c0001t0007g0024a0001c0001t0007g0025a0001c0001t0007g0026others(5): Show | 8 | HG00642.hp2 HG01243.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.163-2141_163-2140i others(274): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635699 | ||||||
| chr22:46635699
|
C | CCCCCGCC others(38): Show |
1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.163-2141_163-2140i others(47): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635699 | ||||||
| chr22:46635699
|
CT | C | 92 | a0001c0001t0001g0005a0001c0001t0001g0066a0001c0001t0001g0068others(89): Show | 92 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.163-2140delT | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635699 | ||||||
| chr22:46635700
|
T | C | 2 | a0001c0001t0003g0226a0001c0001t0038g0180 | 2 | HG01255.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.163-2140T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635700 | ||||||
| chr22:46635700
|
T | G | 11 | a0001c0001t0005g0063a0001c0001t0007g0022a0001c0001t0007g0024others(8): Show | 11 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.163-2140T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635700 | ||||||
| chr22:46635702
|
C | T | 1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.163-2138C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635702 | ||||||
| chr22:46635705
|
A | G | 72 | a0001c0001t0001g0003a0001c0001t0001g0073a0001c0001t0001g0075others(69): Show | 73 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.163-2135A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635705 | ||||||
| chr22:46635707
|
C | T | 5 | a0001c0001t0001g0179a0001c0001t0002g0264a0001c0001t0004g0233others(2): Show | 5 | HG01109.hp1 HG02056.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.163-2133C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635707 | ||||||
| chr22:46635710
|
T | C | 51 | a0001c0001t0001g0003a0001c0001t0001g0106a0001c0001t0001g0113others(48): Show | 52 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.163-2130T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635710 | ||||||
| chr22:46635711
|
G | A | 10 | a0001c0001t0001g0179a0001c0001t0002g0264a0001c0001t0004g0233others(7): Show | 10 | HG01109.hp1 HG01891.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.163-2129G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635711 | ||||||
| chr22:46635712
|
A | G | 124 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(121): Show | 125 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.163-2128A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635712 | ||||||
| chr22:46635717
|
T | C | 5 | a0001c0001t0001g0179a0001c0001t0002g0264a0001c0001t0004g0233others(2): Show | 5 | HG01109.hp1 HG02056.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.163-2123T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635717 | ||||||
| chr22:46635725
|
T | A | 5 | a0001c0001t0001g0179a0001c0001t0002g0264a0001c0001t0004g0233others(2): Show | 5 | HG01109.hp1 HG02056.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.163-2115T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635725 | ||||||
| chr22:46635728
|
G | A | 5 | a0001c0002t0004g0032a0001c0002t0004g0069a0001c0002t0004g0092others(2): Show | 5 | HG01891.hp2 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-2112G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635728 | ||||||
| chr22:46635728
|
G | GA | 24 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0075others(21): Show | 24 | HG00673.hp1 HG01192.hp2 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.163-2112_163-2111i others(3): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635728 | ||||||
| chr22:46635729
|
G | A | 53 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0074others(50): Show | 53 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.163-2111G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635729 | ||||||
| chr22:46635730
|
G | A | 7 | a0001c0001t0001g0179a0001c0001t0002g0264a0001c0001t0004g0233others(4): Show | 7 | HG01109.hp1 HG02056.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.163-2110G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635730 | ||||||
| chr22:46635731
|
C | A | 40 | a0001c0001t0001g0003a0001c0001t0001g0106a0001c0001t0001g0113others(37): Show | 41 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.163-2109C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635731 | ||||||
| chr22:46635731
|
C | CTGTATCC others(313): Show |
1 | a0001c0001t0023g0122 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.163-2109_163-2108i others(322): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635731 | ||||||
| chr22:46635731
|
C | CTGTATCC others(129): Show |
1 | a0001c0001t0001g0149 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.163-2109_163-2108i others(138): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635731 | ||||||
| chr22:46635731
|
C | CTGTATCC others(130): Show |
1 | a0001c0001t0001g0073 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.163-2109_163-2108i others(139): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635731 | ||||||
| chr22:46635731
|
C | CTGTATCC others(129): Show |
16 | a0001c0001t0001g0075a0001c0001t0001g0103a0001c0001t0001g0148others(13): Show | 16 | HG00673.hp1 HG01361.hp1 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.163-2109_163-2108i others(138): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635731 | ||||||
| chr22:46635731
|
C | CTGTATCC others(358): Show |
1 | a0001c0001t0001g0150 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.163-2109_163-2108i others(367): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635731 | ||||||
| chr22:46635731
|
C | G | 60 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0074others(57): Show | 60 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.163-2109C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635731 | ||||||
| chr22:46635733
|
C | CGTGTCTT others(222): Show |
1 | a0001c0001t0001g0123 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.163-2102_163-2101i others(231): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635733 | |||||
| chr22:46635733
|
C | CGTGTCTT others(175): Show |
2 | a0001c0002t0004g0091a0001c0002t0004g0096 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.163-2102_163-2101i others(184): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635733 | |||||
| chr22:46635733
|
C | CGTGTCTT others(84): Show |
3 | a0001c0001t0008g0013a0001c0001t0008g0014a0001c0001t0008g0016 | 3 | HG02976.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.163-2102_163-2101i others(93): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635733 | |||||
| chr22:46635733
|
C | CGTGTCTT others(85): Show |
2 | a0001c0001t0056g0313a0001c0009t0062g0303 | 2 | HG00735.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.163-2102_163-2101i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635733 | |||||
| chr22:46635733
|
C | CGTGTCTT others(84): Show |
3 | a0001c0001t0011g0183a0001c0001t0011g0184a0001c0001t0028g0060 | 3 | HG02723.hp2 HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.163-2102_163-2101i others(93): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635733 | |||||
| chr22:46635733
|
C | CTATCCTC others(683): Show |
2 | a0001c0001t0001g0005a0001c0001t0012g0005 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.163-2107_163-2106i others(692): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635733 | ||||||
| chr22:46635733
|
C | CTGTGTCC others(40): Show |
16 | a0001c0001t0002g0209a0001c0001t0002g0259a0001c0001t0002g0266others(13): Show | 16 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.163-2107_163-2106i others(49): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635733 | ||||||
| chr22:46635733
|
C | T | 42 | a0001c0001t0001g0003a0001c0001t0001g0073a0001c0001t0001g0075others(39): Show | 43 | HG00673.hp1 HG01109.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.163-2107C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635733 | ||||||
| chr22:46635736
|
G | A | 1 | a0001c0001t0003g0250 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.163-2104G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635736 | ||||||
| chr22:46635739
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.163-2101C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635739 | ||||||
| chr22:46635746
|
C | CCCCCCGC others(39): Show |
1 | a0001c0001t0002g0282 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.163-2088_163-2043d others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635746 | |||||
| chr22:46635747
|
C | CCCCACTC others(590): Show |
1 | a0001c0001t0004g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.163-2090_163-2089i others(599): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635747 | |||||
| chr22:46635747
|
C | CCCCACTC others(39): Show |
18 | a0001c0001t0001g0003a0001c0001t0001g0106a0001c0001t0001g0113others(15): Show | 19 | HG01891.hp2 HG01993.hp1 HG02647.hp1 others(16): Show |
intron_variant | MODIFIER | c.163-2090_163-2089i others(48): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635747 | |||||
| chr22:46635747
|
C | CCCCCGCC others(642): Show |
1 | a0001c0001t0058g0277 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.163-2068_163-2067i others(651): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635747 | |||||
| chr22:46635747
|
C | CCCCGACC others(683): Show |
1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.163-2090_163-2089i others(692): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635747 | |||||
| chr22:46635747
|
C | CCCCGACC others(630): Show |
1 | a0001c0001t0007g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.163-2090_163-2089i others(639): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635747 | |||||
| chr22:46635747
|
C | CCCCGCCC others(683): Show |
1 | a0002c0010t0047g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.163-2090_163-2089i others(692): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635747 | |||||
| chr22:46635747
|
C | CCCCGCCC others(131): Show |
1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.163-2090_163-2089i others(140): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635747 | |||||
| chr22:46635747
|
C | CCCGCCCC others(85): Show |
8 | a0001c0001t0001g0087a0001c0001t0001g0129a0001c0001t0001g0130others(5): Show | 8 | HG01081.hp1 HG01257.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.163-2091_163-2090i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635747 | |||||
| chr22:46635747
|
C | CCCGCCCC others(84): Show |
34 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0074others(31): Show | 34 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.163-2091_163-2090i others(93): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635747 | |||||
| chr22:46635747
|
C | CCCGCCCC others(85): Show |
1 | a0001c0001t0001g0137 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.163-2091_163-2090i others(94): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635747 | |||||
| chr22:46635747
|
C | T | 52 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0075others(49): Show | 52 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.163-2093C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635747 | ||||||
| chr22:46635752
|
G | A | 119 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(116): Show | 120 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.163-2088G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635752 | ||||||
| chr22:46635752
|
GCCCCTGG others(40): Show |
G | 2 | a0001c0001t0001g0072a0001c0001t0001g0116 | 2 | NA18952.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.163-2083_163-2037d others(49): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635752 | |||||
| chr22:46635757
|
T | C | 1 | a0001c0001t0031g0059 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.163-2083T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635757 | ||||||
| chr22:46635759
|
G | A | 119 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(116): Show | 121 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.163-2081G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635759 | ||||||
| chr22:46635773
|
A | G | 121 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(118): Show | 123 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.163-2067A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635773 | ||||||
| chr22:46635776
|
T | A | 2 | a0001c0001t0001g0154a0001c0001t0003g0250 | 2 | HG02698.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.163-2064T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635776 | ||||||
| chr22:46635776
|
T | G | 119 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(116): Show | 121 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.163-2064T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635776 | ||||||
| chr22:46635778
|
G | C | 119 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(116): Show | 121 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.163-2062G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635778 | ||||||
| chr22:46635778
|
G | GCCGTGTC others(131): Show |
1 | a0001c0001t0003g0250 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.163-2044_163-2043i others(140): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635778 | |||||
| chr22:46635778
|
G | GCTGTATC others(177): Show |
1 | a0001c0001t0001g0154 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.163-2061_163-2060i others(186): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46635778 | |||||
| chr22:46635798
|
C | A | 1 | a0001c0001t0001g0253 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.163-2042C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635798 | ||||||
| chr22:46635798
|
C | CG | 7 | a0001c0001t0001g0075a0001c0001t0001g0115a0001c0001t0001g0127others(4): Show | 7 | HG02622.hp1 HG03831.hp1 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.163-2042_163-2041i others(3): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635798 | ||||||
| chr22:46635799
|
A | C | 8 | a0001c0001t0001g0075a0001c0001t0001g0115a0001c0001t0001g0127others(5): Show | 8 | HG02622.hp1 HG03831.hp1 HG04204.hp2 others(5): Show |
intron_variant | MODIFIER | c.163-2041A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635799 | ||||||
| chr22:46635799
|
A | G | 95 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(92): Show | 97 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.163-2041A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635799 | ||||||
| chr22:46635815
|
G | A | 12 | a0001c0001t0005g0063a0001c0001t0007g0022a0001c0001t0007g0023others(9): Show | 12 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.163-2025G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635815 | ||||||
| chr22:46635841
|
C | T | 1 | a0001c0001t0056g0313 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.163-1999C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635841 | ||||||
| chr22:46635922
|
G | A | 1 | a0001c0001t0002g0266 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.163-1918G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635922 | ||||||
| chr22:46635943
|
G | A | 1 | a0001c0001t0009g0056 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.163-1897G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635943 | ||||||
| chr22:46635962
|
C | T | 2 | a0001c0001t0008g0013a0001c0001t0008g0016 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.163-1878C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46635962 | ||||||
| chr22:46636070
|
C | T | 156 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0220others(153): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.163-1770C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46636070 | ||||||
| chr22:46636151
|
G | A | 3 | a0001c0001t0010g0185a0001c0001t0010g0186a0001c0001t0010g0187 | 3 | HG01884.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.163-1689G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46636151 | ||||||
| chr22:46636189
|
A | G | 304 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(301): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.163-1651A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46636189 | ||||||
| chr22:46636532
|
G | A | 92 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(89): Show | 94 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.163-1308G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46636532 | ||||||
| chr22:46636718
|
A | G | 4 | a0001c0001t0005g0001a0001c0001t0005g0039a0001c0001t0005g0040others(1): Show | 5 | HG02615.hp2 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.163-1122A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46636718 | ||||||
| chr22:46636750
|
G | T | 13 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0006g0076others(10): Show | 13 | HG00438.hp2 HG02015.hp1 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.163-1090G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46636750 | ||||||
| chr22:46637029
|
G | C | 3 | a0001c0001t0008g0013a0001c0001t0008g0014a0001c0001t0008g0016 | 3 | HG02976.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.163-811G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46637029 | ||||||
| chr22:46637062
|
G | A | 1 | a0001c0001t0004g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.163-778G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46637062 | ||||||
| chr22:46637068
|
A | G | 15 | a0001c0001t0004g0021a0001c0001t0005g0063a0001c0001t0007g0022others(12): Show | 15 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.163-772A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46637068 | ||||||
| chr22:46637120
|
G | C | 250 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(247): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.163-720G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46637120 | ||||||
| chr22:46637145
|
C | T | 7 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0010g0034others(4): Show | 7 | HG02622.hp2 HG02723.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.163-695C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46637145 | ||||||
| chr22:46637256
|
C | CT | 182 | a0001c0001t0001g0074a0001c0001t0001g0098a0001c0001t0001g0196others(179): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.163-570dupT | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46637256 | |||||
| chr22:46637256
|
C | CTT | 15 | a0001c0001t0002g0278a0001c0001t0004g0021a0001c0001t0005g0063others(12): Show | 15 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.163-571_163-570dup others(2): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46637256 | |||||
| chr22:46637313
|
C | T | 3 | a0001c0001t0008g0013a0001c0001t0008g0014a0001c0001t0008g0016 | 3 | HG02976.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.163-527C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46637313 | ||||||
| chr22:46637543
|
T | G | 3 | a0001c0001t0010g0185a0001c0001t0010g0186a0001c0001t0010g0187 | 3 | HG01884.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.163-297T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46637543 | ||||||
| chr22:46637554
|
T | C | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.163-286T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46637554 | ||||||
| chr22:46637637
|
G | A | 95 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(92): Show | 97 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.163-203G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46637637 | ||||||
| chr22:46637731
|
A | AT | 95 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(92): Show | 97 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.163-108dupT | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 46637731 | |||||
| chr22:46637796
|
G | A | 2 | a0001c0001t0015g0189a0001c0001t0015g0190 | 2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.163-44G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 2/18 | chr22 | 46637796 | ||||||
| chr22:46638085
|
C | T | 1 | a0001c0001t0001g0219 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.283+125C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46638085 | ||||||
| chr22:46638108
|
C | T | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.283+148C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46638108 | ||||||
| chr22:46638149
|
G | C | 4 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0010g0034others(1): Show | 4 | HG02622.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+189G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46638149 | ||||||
| chr22:46638245
|
A | G | 3 | a0001c0001t0038g0180a0001c0001t0054g0251a0002c0011t0053g0019 | 3 | HG02572.hp2 HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.283+285A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46638245 | ||||||
| chr22:46638522
|
G | A | 2 | a0001c0001t0004g0061a0001c0001t0019g0062 | 2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.283+562G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46638522 | ||||||
| chr22:46638825
|
C | T | 96 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0255others(93): Show | 98 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.283+865C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46638825 | ||||||
| chr22:46638830
|
G | A | 7 | a0001c0001t0011g0183a0001c0001t0011g0184a0001c0001t0028g0060others(4): Show | 7 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.283+870G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46638830 | ||||||
| chr22:46638932
|
G | A | 58 | a0001c0001t0001g0220a0001c0001t0003g0006a0001c0001t0003g0030others(55): Show | 58 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.283+972G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46638932 | ||||||
| chr22:46638941
|
T | C | 96 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0255others(93): Show | 98 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.283+981T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46638941 | ||||||
| chr22:46639026
|
C | A | 1 | a0001c0001t0011g0184 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.283+1066C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46639026 | ||||||
| chr22:46639031
|
A | G | 1 | a0001c0001t0004g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.283+1071A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46639031 | ||||||
| chr22:46639078
|
T | G | 1 | a0001c0001t0005g0143 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.283+1118T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46639078 | ||||||
| chr22:46639118
|
A | G | 6 | a0001c0001t0005g0001a0001c0001t0005g0039a0001c0001t0005g0040others(3): Show | 7 | HG02615.hp2 HG02818.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+1158A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46639118 | ||||||
| chr22:46639153
|
A | AGT | 24 | a0001c0001t0003g0208a0001c0001t0003g0214a0001c0001t0003g0215others(21): Show | 24 | HG00099.hp2 HG00733.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.283+1220_283+1221d others(4): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46639153 | |||||
| chr22:46639153
|
A | AGTGT | 74 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(71): Show | 76 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.283+1218_283+1221d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46639153 | |||||
| chr22:46639153
|
A | AGTGTGT | 4 | a0001c0001t0001g0179a0001c0001t0019g0062a0001c0001t0023g0121others(1): Show | 4 | HG01952.hp1 HG02293.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+1216_283+1221d others(8): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46639153 | |||||
| chr22:46639153
|
AGT | A | 124 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0255others(121): Show | 125 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.283+1220_283+1221d others(4): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46639153 | |||||
| chr22:46639153
|
AGTGT | A | 8 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(5): Show | 8 | HG01175.hp2 HG01433.hp1 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.283+1218_283+1221d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46639153 | |||||
| chr22:46639153
|
AGTGTGT | A | 4 | a0001c0001t0002g0007a0001c0001t0002g0279a0001c0001t0016g0018others(1): Show | 5 | HG01256.hp1 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.283+1216_283+1221d others(8): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46639153 | |||||
| chr22:46639153
|
AGTGTGTG others(5): Show |
A | 2 | a0001c0001t0015g0189a0001c0001t0015g0190 | 2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.283+1210_283+1221d others(14): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46639153 | |||||
| chr22:46639182
|
A | G | 3 | a0001c0001t0008g0013a0001c0001t0008g0014a0001c0001t0008g0016 | 3 | HG02976.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.283+1222A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46639182 | ||||||
| chr22:46639292
|
G | GCCTGTGT others(15): Show |
65 | a0001c0001t0001g0220a0001c0001t0003g0006a0001c0001t0003g0030others(62): Show | 65 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.283+1341_283+1362d others(24): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46639292 | |||||
| chr22:46639473
|
C | G | 3 | a0001c0001t0011g0183a0001c0001t0011g0184a0001c0001t0028g0060 | 3 | HG02723.hp2 HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.283+1513C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46639473 | ||||||
| chr22:46639480
|
G | A | 16 | a0001c0001t0001g0098a0001c0002t0002g0071a0001c0002t0004g0002others(13): Show | 17 | HG01361.hp2 HG01496.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.283+1520G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46639480 | ||||||
| chr22:46639614
|
G | C | 1 | a0001c0007t0019g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.283+1654G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46639614 | ||||||
| chr22:46639627
|
G | A | 5 | a0001c0001t0002g0262a0001c0001t0002g0264a0001c0001t0002g0270others(2): Show | 5 | HG00423.hp2 HG02056.hp2 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.283+1667G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46639627 | ||||||
| chr22:46639632
|
CTG | C | 16 | a0001c0001t0001g0098a0001c0002t0002g0071a0001c0002t0004g0002others(13): Show | 17 | HG01361.hp2 HG01496.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.283+1679_283+1680d others(4): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46639632 | |||||
| chr22:46639653
|
C | G | 1 | a0001c0001t0007g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.283+1693C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46639653 | ||||||
| chr22:46639717
|
G | T | 60 | a0001c0001t0001g0220a0001c0001t0003g0006a0001c0001t0003g0030others(57): Show | 60 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.283+1757G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46639717 | ||||||
| chr22:46639826
|
G | C | 1 | a0001c0001t0048g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.283+1866G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46639826 | ||||||
| chr22:46640043
|
G | A | 1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.283+2083G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46640043 | ||||||
| chr22:46640125
|
G | A | 1 | a0001c0005t0002g0294 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.283+2165G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46640125 | ||||||
| chr22:46640162
|
C | T | 16 | a0001c0001t0001g0098a0001c0002t0002g0071a0001c0002t0004g0002others(13): Show | 17 | HG01361.hp2 HG01496.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.283+2202C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46640162 | ||||||
| chr22:46640199
|
T | C | 65 | a0001c0001t0001g0220a0001c0001t0003g0006a0001c0001t0003g0030others(62): Show | 65 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.283+2239T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46640199 | ||||||
| chr22:46640214
|
G | A | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | HG02129.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.283+2254G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46640214 | ||||||
| chr22:46640281
|
C | G | 320 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(317): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.283+2321C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46640281 | ||||||
| chr22:46640398
|
T | C | 1 | a0001c0007t0019g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.283+2438T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46640398 | ||||||
| chr22:46640554
|
G | A | 61 | a0001c0001t0001g0220a0001c0001t0003g0006a0001c0001t0003g0030others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.283+2594G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46640554 | ||||||
| chr22:46640596
|
G | A | 1 | a0001c0001t0030g0044 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.283+2636G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46640596 | ||||||
| chr22:46640637
|
G | A | 1 | a0001c0001t0003g0205 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.283+2677G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46640637 | ||||||
| chr22:46640786
|
G | A | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.283+2826G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46640786 | ||||||
| chr22:46640787
|
A | G | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.283+2827A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46640787 | ||||||
| chr22:46640820
|
C | T | 104 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(101): Show | 107 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.283+2860C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46640820 | ||||||
| chr22:46640978
|
C | A | 1 | a0001c0002t0004g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.283+3018C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46640978 | ||||||
| chr22:46641025
|
C | T | 1 | a0002c0010t0047g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.283+3065C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46641025 | ||||||
| chr22:46641157
|
T | C | 187 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0220others(184): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.283+3197T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46641157 | ||||||
| chr22:46641176
|
G | A | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.283+3216G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46641176 | ||||||
| chr22:46641265
|
G | A | 1 | a0001c0001t0003g0221 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.283+3305G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46641265 | ||||||
| chr22:46641292
|
C | T | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.283+3332C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46641292 | ||||||
| chr22:46641392
|
TAAGG | T | 301 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(298): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.283+3459_283+3462d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46641392 | |||||
| chr22:46641424
|
C | G | 1 | a0001c0001t0004g0021 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.283+3464C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46641424 | ||||||
| chr22:46641466
|
C | T | 1 | a0001c0001t0009g0048 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.283+3506C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46641466 | ||||||
| chr22:46641471
|
T | G | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.283+3511T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46641471 | ||||||
| chr22:46641560
|
T | C | 2 | a0001c0001t0008g0013a0001c0001t0008g0016 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.283+3600T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46641560 | ||||||
| chr22:46641621
|
G | A | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.283+3661G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46641621 | ||||||
| chr22:46641810
|
G | A | 10 | a0001c0001t0007g0022a0001c0001t0007g0023a0001c0001t0007g0024others(7): Show | 10 | HG00642.hp2 HG01243.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.283+3850G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46641810 | ||||||
| chr22:46641871
|
G | A | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.283+3911G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46641871 | ||||||
| chr22:46641881
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.283+3921G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46641881 | ||||||
| chr22:46641929
|
C | T | 1 | a0001c0001t0002g0288 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.283+3969C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46641929 | ||||||
| chr22:46641952
|
A | T | 1 | a0001c0001t0001g0177 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.283+3992A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46641952 | ||||||
| chr22:46641962
|
G | A | 13 | a0001c0001t0004g0021a0001c0001t0005g0063a0001c0001t0007g0022others(10): Show | 13 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.283+4002G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46641962 | ||||||
| chr22:46642069
|
T | A | 1 | a0001c0001t0006g0199 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.283+4109T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46642069 | ||||||
| chr22:46642162
|
C | T | 1 | a0001c0001t0003g0208 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.283+4202C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46642162 | ||||||
| chr22:46642184
|
G | A | 57 | a0001c0001t0001g0220a0001c0001t0003g0006a0001c0001t0003g0030others(54): Show | 57 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.283+4224G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46642184 | ||||||
| chr22:46642210
|
G | A | 2 | a0001c0001t0003g0083a0001c0001t0003g0084 | 2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.283+4250G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46642210 | ||||||
| chr22:46642390
|
A | G | 5 | a0001c0001t0008g0008a0001c0001t0008g0010a0001c0001t0008g0011others(2): Show | 5 | HG02723.hp1 HG02809.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+4430A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46642390 | ||||||
| chr22:46642444
|
G | C | 3 | a0001c0001t0008g0013a0001c0001t0008g0014a0001c0001t0008g0016 | 3 | HG02976.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.283+4484G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46642444 | ||||||
| chr22:46642862
|
G | A | 1 | a0001c0001t0003g0085 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.283+4902G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46642862 | ||||||
| chr22:46642964
|
T | TATCC | 15 | a0001c0001t0002g0259a0001c0001t0002g0266a0001c0001t0002g0267others(12): Show | 15 | HG00733.hp2 HG00735.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.283+5031_283+5034d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46642964 | |||||
| chr22:46642973
|
A | T | 2 | a0001c0001t0006g0174a0001c0001t0006g0302 | 2 | NA19081.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.283+5013A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46642973 | ||||||
| chr22:46643084
|
T | TATCC | 150 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(147): Show | 153 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.283+5159_283+5162d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643084 | |||||
| chr22:46643084
|
T | TATCCATC others(1): Show |
17 | a0001c0001t0001g0110a0001c0001t0001g0158a0001c0001t0001g0219others(14): Show | 17 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.283+5155_283+5162d others(10): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643084 | |||||
| chr22:46643084
|
T | TATCCATC others(5): Show |
1 | a0001c0001t0007g0026 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.283+5151_283+5162d others(14): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643084 | |||||
| chr22:46643084
|
TATCCATC others(1): Show |
T | 8 | a0001c0001t0002g0257a0001c0001t0002g0264a0001c0001t0002g0278others(5): Show | 8 | HG01952.hp2 HG02056.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.283+5155_283+5162d others(10): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643084 | |||||
| chr22:46643088
|
C | CATCCATC others(505): Show |
1 | a0001c0001t0064g0306 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.283+5154_283+5155i others(514): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643088 | |||||
| chr22:46643092
|
C | CATCCATC others(505): Show |
1 | a0001c0001t0006g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.283+5154_283+5155i others(514): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643092 | |||||
| chr22:46643092
|
C | CATCCATC others(501): Show |
1 | a0001c0001t0002g0267 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.283+5154_283+5155i others(510): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643092 | |||||
| chr22:46643092
|
C | CATCCATC others(497): Show |
9 | a0001c0001t0001g0197a0001c0001t0001g0255a0001c0001t0002g0301others(6): Show | 9 | HG00438.hp2 HG02083.hp2 NA18939.hp2 others(6): Show |
intron_variant | MODIFIER | c.283+5154_283+5155i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643092 | |||||
| chr22:46643092
|
C | CATCCATC others(493): Show |
1 | a0001c0001t0006g0194 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.283+5154_283+5155i others(502): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643092 | |||||
| chr22:46643092
|
C | CATCCATC others(493): Show |
1 | a0001c0001t0002g0310 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.283+5154_283+5155i others(502): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643092 | |||||
| chr22:46643092
|
C | CATCCATC others(493): Show |
1 | a0001c0001t0004g0061 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.283+5150_283+5151i others(502): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643092 | |||||
| chr22:46643092
|
C | CATCCATC others(493): Show |
2 | a0001c0001t0008g0013a0001c0001t0008g0016 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.283+5150_283+5151i others(502): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643092 | |||||
| chr22:46643111
|
C | CCATG | 73 | a0001c0001t0001g0261a0001c0001t0001g0271a0001c0001t0001g0273others(70): Show | 75 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.283+5154_283+5155i others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643111 | |||||
| chr22:46643111
|
C | G | 3 | a0001c0001t0004g0233a0001c0001t0008g0014a0001c0001t0019g0062 | 3 | HG02717.hp2 HG02896.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.283+5151C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643111 | ||||||
| chr22:46643123
|
G | C | 17 | a0001c0001t0001g0197a0001c0001t0001g0255a0001c0001t0002g0267others(14): Show | 17 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.283+5163G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643123 | ||||||
| chr22:46643129
|
A | T | 76 | a0001c0001t0001g0261a0001c0001t0001g0271a0001c0001t0001g0273others(73): Show | 78 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.283+5169A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643129 | ||||||
| chr22:46643135
|
G | C | 77 | a0001c0001t0001g0261a0001c0001t0001g0271a0001c0001t0001g0273others(74): Show | 79 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.283+5175G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643135 | ||||||
| chr22:46643141
|
T | A | 94 | a0001c0001t0001g0197a0001c0001t0001g0255a0001c0001t0001g0261others(91): Show | 96 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.283+5181T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643141 | ||||||
| chr22:46643147
|
C | CCATCCAT others(509): Show |
1 | a0001c0001t0004g0035 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.283+5218_283+5219i others(518): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643147 | |||||
| chr22:46643147
|
C | CCATCCAT others(497): Show |
1 | a0001c0001t0019g0062 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.283+5214_283+5215i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643147 | |||||
| chr22:46643147
|
C | CCATCCAT others(493): Show |
1 | a0001c0001t0008g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.283+5214_283+5215i others(502): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643147 | |||||
| chr22:46643147
|
C | G | 17 | a0001c0001t0001g0197a0001c0001t0001g0255a0001c0001t0002g0267others(14): Show | 17 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.283+5187C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643147 | ||||||
| chr22:46643151
|
C | CCATCCAT others(505): Show |
1 | a0001c0001t0003g0222 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.283+5230_283+5231i others(514): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643151 | |||||
| chr22:46643151
|
C | CCATCCAT others(501): Show |
1 | a0001c0001t0003g0212 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.283+5226_283+5227i others(510): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643151 | |||||
| chr22:46643151
|
C | CCATCCAT others(497): Show |
1 | a0001c0001t0003g0239 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.283+5226_283+5227i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643151 | |||||
| chr22:46643151
|
C | CCATCCAT others(489): Show |
2 | a0001c0001t0003g0030a0001c0001t0003g0031 | 2 | HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.283+5222_283+5223i others(498): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643151 | |||||
| chr22:46643151
|
C | CCATCCAT others(517): Show |
1 | a0001c0001t0007g0026 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.283+5222_283+5223i others(526): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643151 | |||||
| chr22:46643151
|
C | CCATCCAT others(513): Show |
2 | a0001c0001t0004g0036a0001c0001t0033g0037 | 2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.283+5222_283+5223i others(522): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643151 | |||||
| chr22:46643151
|
C | CCATCCAT others(509): Show |
1 | a0001c0001t0010g0034 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.283+5222_283+5223i others(518): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643151 | |||||
| chr22:46643151
|
C | CCATCCAT others(501): Show |
1 | a0001c0001t0048g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.283+5218_283+5219i others(510): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643151 | |||||
| chr22:46643151
|
C | CCATCCAT others(509): Show |
1 | a0001c0001t0005g0063 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.283+5218_283+5219i others(518): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643151 | |||||
| chr22:46643151
|
C | CCATCCAT others(497): Show |
2 | a0001c0001t0006g0198a0001c0001t0034g0201 | 2 | NA18969.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.283+5214_283+5215i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643151 | |||||
| chr22:46643151
|
C | CCATCCAT others(513): Show |
1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.283+5214_283+5215i others(522): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643151 | |||||
| chr22:46643151
|
C | G | 17 | a0001c0001t0001g0197a0001c0001t0001g0255a0001c0001t0002g0267others(14): Show | 17 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.283+5191C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643151 | ||||||
| chr22:46643155
|
C | CCATCCAT others(501): Show |
1 | a0001c0001t0001g0220 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.283+5230_283+5231i others(510): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | |||||
| chr22:46643155
|
C | CCATCCAT others(497): Show |
1 | a0001c0001t0003g0238 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.283+5226_283+5227i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | |||||
| chr22:46643155
|
C | CCATCCAT others(509): Show |
1 | a0001c0001t0006g0202 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.283+5226_283+5227i others(518): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | |||||
| chr22:46643155
|
C | CCATCCAT others(501): Show |
1 | a0001c0008t0055g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.283+5226_283+5227i others(510): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | |||||
| chr22:46643155
|
C | CCATCCAT others(501): Show |
1 | a0001c0001t0003g0241 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.283+5226_283+5227i others(510): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | |||||
| chr22:46643155
|
C | CCATCCAT others(505): Show |
1 | a0001c0001t0018g0247 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.283+5226_283+5227i others(514): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | |||||
| chr22:46643155
|
C | CCATCCAT others(501): Show |
5 | a0001c0001t0003g0206a0001c0001t0003g0224a0001c0001t0003g0225others(2): Show | 5 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+5226_283+5227i others(510): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | |||||
| chr22:46643155
|
C | CCATCCAT others(497): Show |
3 | a0001c0001t0003g0207a0001c0001t0003g0228a0001c0001t0003g0229 | 3 | HG02683.hp2 HG03491.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.283+5226_283+5227i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | |||||
| chr22:46643155
|
C | CCATCCAT others(497): Show |
1 | a0001c0001t0003g0223 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.283+5226_283+5227i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | |||||
| chr22:46643155
|
C | CCATCCAT others(493): Show |
4 | a0001c0001t0003g0208a0001c0001t0003g0214a0001c0001t0003g0215others(1): Show | 4 | HG00099.hp2 HG01081.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+5226_283+5227i others(502): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | |||||
| chr22:46643155
|
C | CCATCCAT others(493): Show |
5 | a0001c0001t0003g0210a0001c0001t0003g0245a0001c0001t0014g0052others(2): Show | 5 | HG00733.hp1 HG02027.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.283+5226_283+5227i others(502): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | |||||
| chr22:46643155
|
C | CCATCCAT others(509): Show |
1 | a0001c0001t0003g0250 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.283+5226_283+5227i others(518): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | |||||
| chr22:46643155
|
C | CCATCCAT others(505): Show |
7 | a0001c0001t0001g0005a0001c0001t0001g0151a0001c0001t0002g0100others(4): Show | 7 | HG01952.hp1 HG02040.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+5226_283+5227i others(514): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | |||||
| chr22:46643155
|
C | CCATCCAT others(513): Show |
1 | a0001c0001t0015g0189 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.283+5222_283+5223i others(522): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | |||||
| chr22:46643155
|
C | CCATCCAT others(529): Show |
1 | a0001c0001t0028g0060 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.283+5222_283+5223i others(538): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | |||||
| chr22:46643155
|
C | CCATCCAT others(505): Show |
1 | a0001c0002t0004g0092 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.283+5222_283+5223i others(514): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | |||||
| chr22:46643155
|
C | CCATCCAT others(505): Show |
3 | a0001c0002t0004g0032a0001c0002t0004g0093a0001c0002t0004g0094 | 3 | HG02965.hp1 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.283+5222_283+5223i others(514): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | |||||
| chr22:46643155
|
C | CCATCCAT others(501): Show |
1 | a0001c0002t0004g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.283+5222_283+5223i others(510): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | |||||
| chr22:46643155
|
C | CCATCCAT others(525): Show |
1 | a0001c0001t0005g0105 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.283+5222_283+5223i others(534): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | |||||
| chr22:46643155
|
C | CCATCCAT others(497): Show |
1 | a0001c0001t0003g0218 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.283+5222_283+5223i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | |||||
| chr22:46643155
|
C | CCATCCAT others(493): Show |
3 | a0001c0001t0003g0217a0001c0001t0003g0242a0001c0001t0003g0243 | 3 | HG01891.hp1 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.283+5222_283+5223i others(502): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | |||||
| chr22:46643155
|
C | CCATCCAT others(517): Show |
2 | a0001c0002t0002g0071a0001c0002t0004g0070 | 2 | HG04115.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.283+5222_283+5223i others(526): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | |||||
| chr22:46643155
|
C | CCATCCAT others(513): Show |
8 | a0001c0001t0001g0098a0001c0002t0004g0002a0001c0002t0004g0086others(5): Show | 9 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.283+5222_283+5223i others(522): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | |||||
| chr22:46643155
|
C | CCATCCAT others(513): Show |
1 | a0001c0002t0004g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.283+5222_283+5223i others(522): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | |||||
| chr22:46643155
|
C | CCATCCAT others(497): Show |
1 | a0001c0001t0030g0044 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.283+5218_283+5219i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | |||||
| chr22:46643155
|
C | CCATCCAT others(505): Show |
1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.283+5218_283+5219i others(514): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | |||||
| chr22:46643155
|
C | CCATCCAT others(513): Show |
1 | a0001c0001t0004g0021 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.283+5218_283+5219i others(522): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | |||||
| chr22:46643155
|
C | CCATCCAT others(513): Show |
1 | a0001c0001t0007g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.283+5218_283+5219i others(522): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | |||||
| chr22:46643155
|
C | CCATCCAT others(509): Show |
9 | a0001c0001t0007g0022a0001c0001t0007g0023a0001c0001t0007g0024others(6): Show | 9 | HG00642.hp2 HG01070.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.283+5218_283+5219i others(518): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | |||||
| chr22:46643155
|
C | CCATCCAT others(501): Show |
1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.283+5218_283+5219i others(510): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | |||||
| chr22:46643155
|
C | CCATCCAT others(513): Show |
1 | a0001c0001t0004g0017 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.283+5218_283+5219i others(522): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | |||||
| chr22:46643155
|
C | CCATCCAT others(509): Show |
1 | a0001c0001t0032g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.283+5218_283+5219i others(518): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643155 | |||||
| chr22:46643155
|
C | G | 14 | a0001c0001t0001g0197a0001c0001t0001g0255a0001c0001t0002g0267others(11): Show | 14 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.283+5195C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643155 | ||||||
| chr22:46643159
|
C | CCATCCAT others(490): Show |
1 | a0001c0001t0001g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.283+5215_283+5216i others(499): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(529): Show |
1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.283+5230_283+5231i others(538): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(505): Show |
11 | a0001c0001t0001g0072a0001c0001t0001g0080a0001c0001t0001g0107others(8): Show | 12 | HG00423.hp1 HG00673.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.283+5230_283+5231i others(514): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(509): Show |
1 | a0001c0001t0001g0165 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.283+5230_283+5231i others(518): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(505): Show |
1 | a0001c0001t0010g0186 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.283+5226_283+5227i others(514): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(489): Show |
1 | a0001c0001t0020g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.283+5226_283+5227i others(498): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(505): Show |
3 | a0001c0001t0002g0264a0001c0001t0002g0278a0001c0005t0002g0294 | 3 | HG02056.hp2 HG04115.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.283+5226_283+5227i others(514): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(501): Show |
2 | a0001c0001t0002g0257a0001c0001t0002g0300 | 2 | HG02132.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.283+5226_283+5227i others(510): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(497): Show |
3 | a0001c0001t0003g0244a0001c0001t0003g0283a0001c0001t0058g0277 | 3 | HG01516.hp1 HG03831.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.283+5226_283+5227i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(493): Show |
7 | a0001c0001t0003g0006a0001c0001t0003g0104a0001c0001t0003g0169others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+5226_283+5227i others(502): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(497): Show |
1 | a0001c0001t0003g0226 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.283+5226_283+5227i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(497): Show |
1 | a0001c0001t0017g0045 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.283+5226_283+5227i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(505): Show |
4 | a0001c0001t0001g0115a0001c0001t0001g0119a0001c0001t0001g0120others(1): Show | 4 | HG00621.hp1 HG02083.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+5226_283+5227i others(514): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(505): Show |
1 | a0001c0001t0001g0163 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.283+5226_283+5227i others(514): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(509): Show |
1 | a0001c0001t0001g0178 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.283+5226_283+5227i others(518): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(505): Show |
2 | a0001c0001t0001g0134a0001c0001t0001g0154 | 2 | NA19065.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.283+5226_283+5227i others(514): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(501): Show |
50 | a0001c0001t0001g0003a0001c0001t0001g0066a0001c0001t0001g0068others(47): Show | 51 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.283+5226_283+5227i others(510): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(497): Show |
1 | a0001c0001t0001g0141 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.283+5226_283+5227i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(489): Show |
4 | a0001c0001t0001g0112a0001c0001t0001g0125a0001c0001t0001g0127others(1): Show | 4 | HG00438.hp1 HG02135.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+5226_283+5227i others(498): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(501): Show |
1 | a0001c0001t0001g0177 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.283+5226_283+5227i others(510): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(493): Show |
1 | a0001c0003t0003g0235 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.283+5226_283+5227i others(502): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(489): Show |
1 | a0001c0003t0003g0236 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.283+5226_283+5227i others(498): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(493): Show |
1 | a0001c0001t0063g0227 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.283+5226_283+5227i others(502): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(513): Show |
1 | a0001c0001t0015g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.283+5222_283+5223i others(522): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(501): Show |
1 | a0001c0001t0010g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.283+5222_283+5223i others(510): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(497): Show |
1 | a0001c0001t0010g0187 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.283+5222_283+5223i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(485): Show |
1 | a0001c0001t0020g0231 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.283+5222_283+5223i others(494): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(525): Show |
7 | a0001c0001t0005g0142a0001c0001t0005g0143a0001c0001t0005g0144others(4): Show | 7 | HG00323.hp2 HG01168.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.283+5222_283+5223i others(534): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(521): Show |
1 | a0001c0001t0005g0111 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.283+5222_283+5223i others(530): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(489): Show |
6 | a0001c0001t0003g0083a0001c0001t0003g0084a0001c0001t0003g0085others(3): Show | 6 | HG01243.hp2 HG01496.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+5222_283+5223i others(498): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(517): Show |
1 | a0001c0002t0004g0095 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.283+5222_283+5223i others(526): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(517): Show |
1 | a0001c0001t0011g0184 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.283+5222_283+5223i others(526): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(513): Show |
1 | a0001c0001t0011g0183 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.283+5222_283+5223i others(522): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(485): Show |
1 | a0001c0001t0003g0234 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.283+5222_283+5223i others(494): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(497): Show |
1 | a0001c0007t0019g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.283+5218_283+5219i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(493): Show |
2 | a0001c0001t0004g0233a0001c0001t0052g0136 | 2 | HG02717.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.283+5218_283+5219i others(502): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(505): Show |
6 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0010others(3): Show | 6 | HG02723.hp1 HG02809.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+5218_283+5219i others(514): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(501): Show |
1 | a0001c0001t0002g0270 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.283+5214_283+5215i others(510): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(493): Show |
1 | a0001c0001t0056g0313 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.283+5214_283+5215i others(502): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(497): Show |
1 | a0001c0001t0002g0282 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.283+5214_283+5215i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(497): Show |
1 | a0001c0001t0044g0316 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.283+5214_283+5215i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(497): Show |
1 | a0001c0001t0060g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.283+5214_283+5215i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(493): Show |
15 | a0001c0001t0002g0081a0001c0001t0002g0259a0001c0001t0002g0266others(12): Show | 15 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.283+5214_283+5215i others(502): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(489): Show |
4 | a0001c0001t0005g0001a0001c0001t0005g0039a0001c0001t0005g0040others(1): Show | 5 | HG02615.hp2 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+5214_283+5215i others(498): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(493): Show |
1 | a0001c0001t0001g0261 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.283+5214_283+5215i others(502): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(489): Show |
1 | a0001c0001t0002g0172 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.283+5214_283+5215i others(498): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(489): Show |
26 | a0001c0001t0001g0271a0001c0001t0001g0273a0001c0001t0001g0309others(23): Show | 26 | HG00597.hp1 HG00639.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.283+5214_283+5215i others(498): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(477): Show |
7 | a0001c0001t0002g0296a0001c0001t0002g0297a0001c0001t0002g0298others(4): Show | 7 | HG00099.hp1 HG00642.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+5214_283+5215i others(486): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(485): Show |
2 | a0001c0001t0005g0041a0001c0001t0005g0188 | 2 | HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.283+5214_283+5215i others(494): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(485): Show |
6 | a0001c0001t0002g0007a0001c0001t0002g0171a0001c0001t0002g0275others(3): Show | 7 | HG01109.hp2 HG01256.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+5214_283+5215i others(494): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(473): Show |
1 | a0001c0001t0001g0308 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.283+5214_283+5215i others(482): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(493): Show |
1 | a0001c0001t0002g0203 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.283+5214_283+5215i others(502): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643159
|
C | CCATCCAT others(489): Show |
1 | a0001c0001t0002g0274 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.283+5214_283+5215i others(498): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643159 | |||||
| chr22:46643163
|
C | CCATCCAT others(497): Show |
2 | a0001c0001t0001g0073a0001c0001t0023g0121 | 2 | HG01192.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.283+5226_283+5227i others(506): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643163 | |||||
| chr22:46643163
|
C | CCATCCAT others(525): Show |
1 | a0001c0001t0005g0213 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.283+5222_283+5223i others(534): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643163 | |||||
| chr22:46643163
|
C | CCATCCAT others(521): Show |
1 | a0001c0001t0009g0048 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.283+5222_283+5223i others(530): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643163 | |||||
| chr22:46643163
|
C | CCATCCAT others(521): Show |
4 | a0001c0001t0005g0258a0001c0001t0009g0047a0001c0001t0009g0054others(1): Show | 4 | HG00738.hp2 HG01106.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+5222_283+5223i others(530): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643163 | |||||
| chr22:46643163
|
C | CCATCCAT others(517): Show |
1 | a0001c0001t0009g0050 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.283+5222_283+5223i others(526): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643163 | |||||
| chr22:46643163
|
C | CCATCCAT others(517): Show |
1 | a0001c0001t0009g0056 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.283+5222_283+5223i others(526): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643163 | |||||
| chr22:46643163
|
C | CCATCCAT others(517): Show |
1 | a0001c0002t0004g0091 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.283+5222_283+5223i others(526): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643163 | |||||
| chr22:46643163
|
C | CCATCCAT others(513): Show |
1 | a0001c0001t0009g0049 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.283+5218_283+5219i others(522): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643163 | |||||
| chr22:46643163
|
C | CCATCCAT others(485): Show |
1 | a0002c0010t0047g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.283+5214_283+5215i others(494): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643163 | |||||
| chr22:46643167
|
C | CCATCCAT others(513): Show |
1 | a0001c0002t0004g0096 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.283+5222_283+5223i others(522): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643167 | |||||
| chr22:46643171
|
C | CCATCCAT others(477): Show |
1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.283+5218_283+5219i others(486): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643171 | |||||
| chr22:46643180
|
C | CATTTATC others(245): Show |
1 | a0001c0002t0004g0088 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.283+5222_283+5223i others(254): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643180 | |||||
| chr22:46643204
|
T | C | 5 | a0001c0001t0011g0057a0001c0002t0004g0088a0001c0002t0004g0091others(2): Show | 5 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.283+5244T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643204 | ||||||
| chr22:46643211
|
C | T | 1 | a0001c0002t0004g0088 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.283+5251C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643211 | ||||||
| chr22:46643237
|
A | ATCCCTGG others(326): Show |
1 | a0001c0002t0004g0088 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.283+5279_283+5280i others(335): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643237 | |||||
| chr22:46643249
|
A | T | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.283+5289A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643249 | ||||||
| chr22:46643327
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.283+5367G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643327 | ||||||
| chr22:46643327
|
G | C | 67 | a0001c0001t0001g0220a0001c0001t0002g0209a0001c0001t0003g0030others(64): Show | 67 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.283+5367G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643327 | ||||||
| chr22:46643331
|
C | CCATG | 3 | a0001c0001t0003g0104a0001c0001t0003g0169a0001c0001t0005g0063 | 3 | HG01070.hp1 HG01071.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.283+5371_283+5372i others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643331 | ||||||
| chr22:46643331
|
C | G | 64 | a0001c0001t0001g0220a0001c0001t0002g0209a0001c0001t0003g0030others(61): Show | 64 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.283+5371C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643331 | ||||||
| chr22:46643332
|
T | C | 67 | a0001c0001t0001g0220a0001c0001t0002g0209a0001c0001t0003g0030others(64): Show | 67 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.283+5372T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643332 | ||||||
| chr22:46643332
|
TATCC | T | 237 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(234): Show | 242 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.283+5392_283+5395d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46643332 | |||||
| chr22:46643336
|
C | T | 67 | a0001c0001t0001g0220a0001c0001t0002g0209a0001c0001t0003g0030others(64): Show | 67 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.283+5376C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643336 | ||||||
| chr22:46643394
|
T | C | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.283+5434T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643394 | ||||||
| chr22:46643869
|
G | A | 304 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(301): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.283+5909G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643869 | ||||||
| chr22:46643984
|
G | A | 3 | a0001c0001t0008g0013a0001c0001t0008g0014a0001c0001t0008g0016 | 3 | HG02976.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.283+6024G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46643984 | ||||||
| chr22:46644201
|
C | T | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.283+6241C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644201 | ||||||
| chr22:46644207
|
C | T | 3 | a0001c0001t0011g0183a0001c0001t0011g0184a0001c0001t0028g0060 | 3 | HG02723.hp2 HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.283+6247C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644207 | ||||||
| chr22:46644236
|
C | T | 1 | a0001c0001t0002g0317 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.283+6276C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644236 | ||||||
| chr22:46644303
|
G | A | 5 | a0001c0001t0004g0061a0001c0001t0008g0013a0001c0001t0008g0014others(2): Show | 5 | HG01884.hp1 HG02896.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.283+6343G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644303 | ||||||
| chr22:46644326
|
T | G | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.283+6366T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644326 | ||||||
| chr22:46644339
|
T | C | 304 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(301): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.283+6379T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644339 | ||||||
| chr22:46644444
|
C | A | 1 | a0001c0001t0002g0272 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.283+6484C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644444 | ||||||
| chr22:46644513
|
C | T | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.283+6553C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644513 | ||||||
| chr22:46644583
|
T | C | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.283+6623T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644583 | ||||||
| chr22:46644587
|
C | T | 2 | a0001c0001t0015g0189a0001c0001t0015g0190 | 2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.283+6627C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644587 | ||||||
| chr22:46644679
|
C | G | 20 | a0001c0001t0001g0098a0001c0002t0002g0071a0001c0002t0004g0002others(17): Show | 21 | HG01109.hp1 HG01361.hp2 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.283+6719C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644679 | ||||||
| chr22:46644697
|
G | GTT | 12 | a0001c0001t0005g0111a0001c0001t0005g0143a0001c0001t0005g0144others(9): Show | 13 | HG00323.hp2 HG01106.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.283+6773_283+6774d others(4): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | |||||
| chr22:46644697
|
G | GTTT | 6 | a0001c0001t0005g0213a0001c0001t0008g0014a0001c0001t0009g0048others(3): Show | 6 | HG01975.hp1 HG02683.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.283+6772_283+6774d others(5): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | |||||
| chr22:46644697
|
G | GTTTTTTT others(4): Show |
1 | a0001c0002t0004g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.283+6764_283+6774d others(13): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | |||||
| chr22:46644697
|
G | GTTTTTTT others(6): Show |
2 | a0001c0002t0004g0093a0001c0002t0004g0094 | 2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.283+6762_283+6774d others(15): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | |||||
| chr22:46644697
|
G | GTTTTTTT others(10): Show |
2 | a0001c0001t0001g0098a0001c0002t0004g0092 | 2 | HG01891.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.283+6758_283+6774d others(19): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | |||||
| chr22:46644697
|
G | GTTTTTTT others(16): Show |
1 | a0001c0002t0004g0090 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.283+6752_283+6774d others(25): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | |||||
| chr22:46644697
|
G | GTTTTTTT others(27): Show |
1 | a0001c0002t0004g0095 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.283+6741_283+6774d others(36): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | |||||
| chr22:46644697
|
GTTT | G | 11 | a0001c0001t0001g0080a0001c0001t0001g0158a0001c0001t0001g0253others(8): Show | 11 | HG00738.hp2 HG02074.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.283+6772_283+6774d others(5): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | |||||
| chr22:46644697
|
GTTTT | G | 43 | a0001c0001t0001g0005a0001c0001t0001g0066a0001c0001t0001g0072others(40): Show | 44 | HG00423.hp1 HG00597.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.283+6771_283+6774d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | |||||
| chr22:46644697
|
GTTTTT | G | 34 | a0001c0001t0001g0003a0001c0001t0001g0068a0001c0001t0001g0073others(31): Show | 35 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.283+6770_283+6774d others(7): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | |||||
| chr22:46644697
|
GTTTTTT | G | 15 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0134others(12): Show | 15 | HG00741.hp1 HG01175.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.283+6769_283+6774d others(8): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | |||||
| chr22:46644697
|
GTTTTTTT | G | 48 | a0001c0001t0001g0220a0001c0001t0003g0006a0001c0001t0003g0030others(45): Show | 48 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.283+6768_283+6774d others(9): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | |||||
| chr22:46644697
|
GTTTTTTT others(5): Show |
G | 3 | a0001c0001t0004g0061a0001c0001t0004g0233a0001c0001t0019g0062 | 3 | HG01884.hp1 HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.283+6763_283+6774d others(14): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | |||||
| chr22:46644697
|
GTTTTTTT others(6): Show |
G | 1 | a0001c0001t0015g0190 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.283+6762_283+6774d others(15): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | |||||
| chr22:46644697
|
GTTTTTTT others(7): Show |
G | 3 | a0001c0001t0011g0183a0001c0001t0011g0184a0001c0001t0015g0189 | 3 | HG02723.hp2 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.283+6761_283+6774d others(16): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | |||||
| chr22:46644697
|
GTTTTTTT others(8): Show |
G | 1 | a0001c0001t0013g0055 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.283+6760_283+6774d others(17): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | |||||
| chr22:46644697
|
GTTTTTTT others(9): Show |
G | 12 | a0001c0001t0004g0021a0001c0001t0005g0063a0001c0001t0007g0022others(9): Show | 12 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.283+6759_283+6774d others(18): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | |||||
| chr22:46644697
|
GTTTTTTT others(10): Show |
G | 1 | a0001c0001t0001g0125 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.283+6758_283+6774d others(19): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | |||||
| chr22:46644697
|
GTTTTTTT others(11): Show |
G | 11 | a0001c0001t0001g0103a0001c0001t0001g0109a0001c0001t0001g0112others(8): Show | 11 | HG00423.hp2 HG00438.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.283+6757_283+6774d others(20): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | |||||
| chr22:46644697
|
GTTTTTTT others(12): Show |
G | 91 | a0001c0001t0001g0197a0001c0001t0001g0255a0001c0001t0001g0261others(88): Show | 93 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.283+6756_283+6774d others(21): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | |||||
| chr22:46644697
|
GTTTTTTT others(13): Show |
G | 1 | a0001c0001t0002g0172 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.283+6755_283+6774d others(22): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644697 | |||||
| chr22:46644707
|
T | G | 1 | a0001c0001t0001g0253 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.283+6747T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644707 | ||||||
| chr22:46644710
|
T | G | 1 | a0001c0001t0003g0223 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.283+6750T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644710 | ||||||
| chr22:46644711
|
T | G | 6 | a0001c0001t0003g0206a0001c0001t0003g0210a0001c0001t0003g0225others(3): Show | 6 | HG00741.hp1 HG01175.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.283+6751T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644711 | ||||||
| chr22:46644712
|
T | G | 46 | a0001c0001t0001g0220a0001c0001t0003g0006a0001c0001t0003g0030others(43): Show | 46 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.283+6752T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644712 | ||||||
| chr22:46644713
|
T | G | 2 | a0001c0001t0003g0242a0001c0001t0040g0246 | 2 | HG02027.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.283+6753T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644713 | ||||||
| chr22:46644720
|
T | G | 5 | a0001c0001t0003g0208a0001c0001t0003g0214a0001c0001t0003g0215others(2): Show | 5 | HG00099.hp2 HG01081.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+6760T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644720 | ||||||
| chr22:46644721
|
T | G | 9 | a0001c0001t0007g0022a0001c0001t0007g0023a0001c0001t0007g0024others(6): Show | 9 | HG00642.hp2 HG01243.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.283+6761T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644721 | ||||||
| chr22:46644757
|
G | A | 2 | a0001c0001t0004g0061a0001c0001t0019g0062 | 2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.283+6797G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644757 | ||||||
| chr22:46644780
|
C | T | 13 | a0001c0001t0004g0021a0001c0001t0005g0063a0001c0001t0007g0022others(10): Show | 13 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.283+6820C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644780 | ||||||
| chr22:46644843
|
C | T | 1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.283+6883C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644843 | ||||||
| chr22:46644845
|
A | C | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.283+6885A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46644845 | ||||||
| chr22:46644897
|
C | CTT | 15 | a0001c0001t0002g0171a0001c0001t0002g0260a0001c0001t0002g0272others(12): Show | 16 | HG02015.hp2 HG02132.hp2 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.283+6969_283+6970d others(4): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644897 | |||||
| chr22:46644897
|
C | CTTT | 24 | a0001c0001t0002g0081a0001c0001t0002g0203a0001c0001t0002g0249others(21): Show | 24 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(21): Show |
intron_variant | MODIFIER | c.283+6968_283+6970d others(5): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644897 | |||||
| chr22:46644897
|
C | CTTTT | 30 | a0001c0001t0001g0197a0001c0001t0001g0308a0001c0001t0002g0007others(27): Show | 31 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.283+6967_283+6970d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644897 | |||||
| chr22:46644897
|
C | CTTTTT | 10 | a0001c0001t0002g0269a0001c0001t0002g0293a0001c0001t0002g0317others(7): Show | 10 | HG00140.hp2 HG01106.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.283+6966_283+6970d others(7): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644897 | |||||
| chr22:46644897
|
CT | C | 60 | a0001c0001t0001g0005a0001c0001t0001g0074a0001c0001t0001g0146others(57): Show | 61 | HG01070.hp1 HG01071.hp1 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.283+6970delT | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644897 | |||||
| chr22:46644897
|
CTT | C | 90 | a0001c0001t0001g0080a0001c0001t0001g0087a0001c0001t0001g0098others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.283+6969_283+6970d others(4): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644897 | |||||
| chr22:46644897
|
CTTT | C | 54 | a0001c0001t0001g0003a0001c0001t0001g0066a0001c0001t0001g0068others(51): Show | 56 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.283+6968_283+6970d others(5): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644897 | |||||
| chr22:46644897
|
CTTTTTTT others(11): Show |
C | 2 | a0001c0001t0002g0259a0001c0001t0002g0266 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.283+6953_283+6970d others(20): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644897 | |||||
| chr22:46644897
|
CTTTTTTT others(12): Show |
C | 6 | a0001c0001t0002g0267a0001c0001t0002g0268a0001c0001t0002g0307others(3): Show | 6 | HG00733.hp2 HG01109.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.283+6952_283+6970d others(21): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46644897 | |||||
| chr22:46645001
|
C | T | 156 | a0001c0001t0001g0197a0001c0001t0001g0220a0001c0001t0001g0255others(153): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.283+7041C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46645001 | ||||||
| chr22:46645018
|
T | A | 1 | a0001c0002t0004g0097 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.283+7058T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46645018 | ||||||
| chr22:46645169
|
A | C | 1 | a0001c0001t0028g0060 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.283+7209A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46645169 | ||||||
| chr22:46645231
|
G | T | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.283+7271G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46645231 | ||||||
| chr22:46645320
|
G | A | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.283+7360G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46645320 | ||||||
| chr22:46645366
|
G | A | 1 | a0001c0001t0002g0315 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.283+7406G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46645366 | ||||||
| chr22:46645402
|
A | G | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.283+7442A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46645402 | ||||||
| chr22:46645439
|
C | G | 1 | a0001c0001t0048g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.283+7479C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46645439 | ||||||
| chr22:46645595
|
A | C | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.283+7635A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46645595 | ||||||
| chr22:46645795
|
A | G | 4 | a0001c0001t0003g0208a0001c0001t0003g0214a0001c0001t0003g0215others(1): Show | 4 | HG00099.hp2 HG01081.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+7835A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46645795 | ||||||
| chr22:46645804
|
C | G | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.283+7844C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46645804 | ||||||
| chr22:46645805
|
G | C | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.283+7845G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46645805 | ||||||
| chr22:46645806
|
T | G | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.283+7846T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46645806 | ||||||
| chr22:46645902
|
G | A | 2 | a0001c0001t0015g0189a0001c0001t0015g0190 | 2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.283+7942G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46645902 | ||||||
| chr22:46645979
|
G | A | 2 | a0001c0001t0015g0189a0001c0001t0015g0190 | 2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.283+8019G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46645979 | ||||||
| chr22:46646049
|
C | T | 1 | a0001c0001t0020g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.283+8089C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46646049 | ||||||
| chr22:46646065
|
T | G | 1 | a0001c0001t0001g0134 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.283+8105T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46646065 | ||||||
| chr22:46646186
|
G | A | 1 | a0001c0001t0002g0081 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.283+8226G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46646186 | ||||||
| chr22:46646277
|
A | G | 1 | a0001c0001t0001g0066 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.283+8317A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46646277 | ||||||
| chr22:46646321
|
C | T | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.283+8361C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46646321 | ||||||
| chr22:46646324
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.283+8364T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46646324 | ||||||
| chr22:46646473
|
C | T | 3 | a0001c0001t0008g0013a0001c0001t0008g0014a0001c0001t0008g0016 | 3 | HG02976.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.283+8513C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46646473 | ||||||
| chr22:46646571
|
T | C | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.283+8611T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46646571 | ||||||
| chr22:46646657
|
G | T | 2 | a0001c0001t0008g0010a0001c0001t0008g0011 | 2 | HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.283+8697G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46646657 | ||||||
| chr22:46646742
|
C | A | 1 | a0001c0001t0005g0144 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.283+8782C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46646742 | ||||||
| chr22:46646769
|
G | A | 1 | a0001c0001t0005g0040 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.283+8809G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46646769 | ||||||
| chr22:46646798
|
C | T | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.283+8838C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46646798 | ||||||
| chr22:46646799
|
G | A | 1 | a0001c0001t0002g0281 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.283+8839G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46646799 | ||||||
| chr22:46646868
|
G | A | 11 | a0001c0001t0004g0021a0001c0001t0007g0022a0001c0001t0007g0023others(8): Show | 11 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.283+8908G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46646868 | ||||||
| chr22:46646897
|
A | AC | 4 | a0001c0001t0001g0112a0001c0001t0001g0125a0001c0001t0001g0127others(1): Show | 4 | HG00438.hp1 HG02135.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+8939dupC | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46646897 | |||||
| chr22:46646900
|
A | G | 4 | a0001c0001t0001g0112a0001c0001t0001g0125a0001c0001t0001g0127others(1): Show | 4 | HG00438.hp1 HG02135.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+8940A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46646900 | ||||||
| chr22:46646904
|
A | G | 4 | a0001c0001t0001g0112a0001c0001t0001g0125a0001c0001t0001g0127others(1): Show | 4 | HG00438.hp1 HG02135.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+8944A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46646904 | ||||||
| chr22:46647016
|
C | T | 1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.283+9056C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647016 | ||||||
| chr22:46647263
|
T | C | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.283+9303T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647263 | ||||||
| chr22:46647284
|
T | A | 1 | a0001c0001t0001g0074 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.283+9324T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647284 | ||||||
| chr22:46647285
|
G | T | 1 | a0001c0001t0001g0074 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.283+9325G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647285 | ||||||
| chr22:46647286
|
A | G | 1 | a0001c0001t0001g0074 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.283+9326A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647286 | ||||||
| chr22:46647293
|
C | A | 2 | a0001c0001t0011g0183a0001c0001t0011g0184 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.283+9333C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647293 | ||||||
| chr22:46647308
|
T | G | 2 | a0001c0001t0001g0114a0001c0001t0001g0135 | 2 | NA19088.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.283+9348T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647308 | ||||||
| chr22:46647313
|
A | G | 1 | a0001c0001t0001g0220 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.283+9353A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647313 | ||||||
| chr22:46647383
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.283+9423A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647383 | ||||||
| chr22:46647438
|
C | T | 1 | a0001c0001t0006g0193 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.283+9478C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647438 | ||||||
| chr22:46647439
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.283+9479G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647439 | ||||||
| chr22:46647503
|
TG | T | 10 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0061others(7): Show | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.283+9549delG | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46647503 | |||||
| chr22:46647578
|
G | C | 1 | a0001c0001t0058g0277 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.283+9618G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647578 | ||||||
| chr22:46647616
|
G | A | 3 | a0001c0003t0003g0235a0001c0003t0003g0236a0002c0011t0053g0019 | 3 | HG02109.hp2 HG02572.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.283+9656G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647616 | ||||||
| chr22:46647658
|
G | A | 1 | a0001c0001t0024g0004 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.283+9698G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647658 | ||||||
| chr22:46647669
|
G | A | 13 | a0001c0001t0004g0021a0001c0001t0005g0063a0001c0001t0007g0022others(10): Show | 13 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.283+9709G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647669 | ||||||
| chr22:46647707
|
A | G | 303 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(300): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.283+9747A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647707 | ||||||
| chr22:46647707
|
A | T | 2 | a0001c0001t0015g0189a0001c0001t0015g0190 | 2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.283+9747A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647707 | ||||||
| chr22:46647785
|
C | G | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.283+9825C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647785 | ||||||
| chr22:46647798
|
A | G | 3 | a0001c0002t0004g0091a0001c0002t0004g0095a0001c0002t0004g0096 | 3 | HG01109.hp1 HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.283+9838A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647798 | ||||||
| chr22:46647846
|
A | G | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.283+9886A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647846 | ||||||
| chr22:46647928
|
T | C | 11 | a0001c0001t0001g0073a0001c0001t0001g0087a0001c0001t0001g0119others(8): Show | 11 | HG00621.hp1 HG01081.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.283+9968T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647928 | ||||||
| chr22:46647966
|
A | G | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.283+10006A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647966 | ||||||
| chr22:46647967
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.283+10007G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46647967 | ||||||
| chr22:46648099
|
T | C | 2 | a0001c0001t0004g0017a0001c0001t0032g0046 | 2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.284-10088T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648099 | ||||||
| chr22:46648318
|
G | GTGGA | 40 | a0001c0001t0001g0068a0001c0001t0001g0087a0001c0001t0001g0115others(37): Show | 40 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.284-9830_284-9827d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648318 | |||||
| chr22:46648318
|
GTGGA | G | 49 | a0001c0001t0001g0137a0001c0001t0003g0006a0001c0001t0003g0221others(46): Show | 50 | HG00642.hp2 HG00738.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.284-9830_284-9827d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648318 | |||||
| chr22:46648318
|
GTGGATGG others(1): Show |
G | 6 | a0001c0001t0008g0013a0001c0001t0008g0014a0001c0001t0008g0016others(3): Show | 6 | HG02647.hp2 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-9834_284-9827d others(10): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648318 | |||||
| chr22:46648318
|
GTGGATGG others(5): Show |
G | 8 | a0001c0001t0001g0163a0001c0001t0010g0185a0001c0001t0010g0186others(5): Show | 8 | HG01433.hp1 HG01884.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.284-9838_284-9827d others(14): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648318 | |||||
| chr22:46648357
|
GATGA | G | 4 | a0001c0002t0004g0032a0001c0002t0004g0069a0001c0002t0004g0092others(1): Show | 4 | HG01891.hp2 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-9826_284-9823d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648357 | |||||
| chr22:46648361
|
A | G | 1 | a0001c0002t0004g0093 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.284-9826A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648361 | ||||||
| chr22:46648686
|
T | G | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.284-9501T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648686 | ||||||
| chr22:46648686
|
T | TGATGGAT others(21): Show |
2 | a0001c0001t0030g0044a0001c0001t0048g0191 | 2 | HG01433.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.284-9468_284-9441d others(30): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648686 | |||||
| chr22:46648699
|
C | CATGG | 12 | a0001c0001t0004g0021a0001c0001t0005g0063a0001c0001t0007g0022others(9): Show | 12 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.284-9464_284-9461d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648699 | |||||
| chr22:46648699
|
C | G | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.284-9488C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648699 | ||||||
| chr22:46648715
|
G | GATGGATG others(141): Show |
1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.284-9465_284-9464i others(150): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648715 | |||||
| chr22:46648727
|
C | CATGGATG others(1): Show |
4 | a0001c0001t0010g0185a0001c0001t0010g0186a0001c0001t0010g0187others(1): Show | 4 | HG01884.hp2 HG03471.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-9448_284-9441d others(10): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648727 | |||||
| chr22:46648727
|
C | G | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.284-9460C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648727 | ||||||
| chr22:46648767
|
C | CATGG | 15 | a0001c0001t0002g0259a0001c0001t0002g0266a0001c0001t0002g0267others(12): Show | 15 | HG00639.hp1 HG00733.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.284-9388_284-9385d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648767 | |||||
| chr22:46648767
|
C | G | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.284-9420C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648767 | ||||||
| chr22:46648767
|
CATGG | C | 18 | a0001c0001t0005g0105a0001c0001t0005g0111a0001c0001t0005g0142others(15): Show | 18 | HG00738.hp2 HG01106.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.284-9388_284-9385d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648767 | |||||
| chr22:46648767
|
CATGGATG others(53): Show |
C | 6 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0010others(3): Show | 6 | HG02723.hp1 HG02809.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-9400_284-9341d others(62): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648767 | |||||
| chr22:46648787
|
G | C | 4 | a0001c0001t0010g0185a0001c0001t0010g0186a0001c0001t0010g0187others(1): Show | 4 | HG01884.hp2 HG02572.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-9400G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648787 | ||||||
| chr22:46648795
|
G | GATGGATG others(5): Show |
1 | a0001c0001t0003g0223 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.284-9385_284-9384i others(14): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648795 | |||||
| chr22:46648799
|
G | C | 2 | a0001c0001t0004g0021a0001c0001t0027g0038 | 2 | HG02145.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.284-9388G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648799 | ||||||
| chr22:46648799
|
GATGC | G | 5 | a0001c0001t0002g0172a0001c0001t0002g0293a0001c0001t0030g0044others(2): Show | 5 | HG01433.hp1 HG01943.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.284-9384_284-9381d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648799 | |||||
| chr22:46648803
|
C | CATGG | 107 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0068others(104): Show | 109 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.284-9344_284-9341d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648803 | |||||
| chr22:46648803
|
C | CATGGATG others(1): Show |
6 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0003g0218others(3): Show | 6 | HG01255.hp2 HG02129.hp2 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.284-9348_284-9341d others(10): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648803 | |||||
| chr22:46648803
|
C | CATGGATG others(5): Show |
1 | a0001c0001t0001g0154 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.284-9352_284-9341d others(14): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648803 | |||||
| chr22:46648803
|
C | G | 86 | a0001c0001t0001g0197a0001c0001t0001g0255a0001c0001t0001g0261others(83): Show | 88 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.284-9384C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648803 | ||||||
| chr22:46648803
|
CATGG | C | 12 | a0001c0001t0002g0259a0001c0001t0002g0266a0001c0001t0002g0267others(9): Show | 12 | HG00733.hp2 HG00735.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.284-9344_284-9341d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648803 | |||||
| chr22:46648803
|
CATGGATG others(9): Show |
C | 1 | a0001c0001t0001g0080 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.284-9356_284-9341d others(18): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648803 | |||||
| chr22:46648807
|
G | C | 65 | a0001c0001t0001g0197a0001c0001t0001g0255a0001c0001t0001g0261others(62): Show | 67 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.284-9380G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648807 | ||||||
| chr22:46648807
|
G | GATGC | 9 | a0001c0001t0002g0203a0001c0001t0002g0288a0001c0001t0006g0102others(6): Show | 9 | HG00597.hp1 HG00621.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.284-9377_284-9376i others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648807 | |||||
| chr22:46648808
|
A | G | 1 | a0001c0001t0002g0270 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.284-9379A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648808 | ||||||
| chr22:46648811
|
G | C | 5 | a0001c0001t0002g0172a0001c0001t0002g0293a0001c0001t0030g0044others(2): Show | 5 | HG01433.hp1 HG01943.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.284-9376G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648811 | ||||||
| chr22:46648823
|
G | C | 1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.284-9364G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648823 | ||||||
| chr22:46648827
|
G | C | 3 | a0001c0001t0010g0185a0001c0001t0010g0186a0001c0001t0010g0187 | 3 | HG01884.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.284-9360G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648827 | ||||||
| chr22:46648831
|
G | C | 8 | a0001c0001t0005g0145a0001c0001t0008g0013a0001c0001t0008g0014others(5): Show | 8 | HG00323.hp2 HG02145.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.284-9356G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648831 | ||||||
| chr22:46648847
|
C | CATGGATG others(5): Show |
1 | a0001c0001t0011g0183 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.284-9336_284-9325d others(14): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648847 | |||||
| chr22:46648847
|
C | CATGGATG others(41): Show |
1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.284-9325_284-9324i others(50): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648847 | |||||
| chr22:46648847
|
C | G | 17 | a0001c0001t0005g0063a0001c0001t0007g0022a0001c0001t0007g0023others(14): Show | 17 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.284-9340C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648847 | ||||||
| chr22:46648851
|
G | C | 3 | a0001c0001t0007g0022a0001c0001t0007g0029a0001c0001t0013g0055 | 3 | HG02486.hp2 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.284-9336G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648851 | ||||||
| chr22:46648851
|
G | GATGC | 7 | a0001c0001t0005g0063a0001c0001t0007g0023a0001c0001t0007g0024others(4): Show | 7 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-9333_284-9332i others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648851 | |||||
| chr22:46648855
|
G | C | 2 | a0001c0001t0003g0215a0001c0001t0038g0180 | 2 | HG03579.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.284-9332G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648855 | ||||||
| chr22:46648859
|
G | GATGGATG others(29): Show |
3 | a0001c0001t0008g0013a0001c0001t0008g0014a0001c0001t0008g0016 | 3 | HG02976.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.284-9325_284-9324i others(38): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648859 | |||||
| chr22:46648863
|
C | CATGG | 4 | a0001c0001t0001g0219a0001c0001t0015g0190a0001c0003t0003g0235others(1): Show | 4 | HG02109.hp2 HG03130.hp1 NA20905.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-9292_284-9289d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648863 | |||||
| chr22:46648863
|
C | G | 22 | a0001c0001t0003g0215a0001c0001t0005g0063a0001c0001t0005g0145others(19): Show | 22 | HG00323.hp2 HG00642.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.284-9324C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648863 | ||||||
| chr22:46648867
|
G | C | 13 | a0001c0001t0005g0063a0001c0001t0007g0022a0001c0001t0007g0023others(10): Show | 13 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.284-9320G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648867 | ||||||
| chr22:46648867
|
G | GATGGATG others(5): Show |
1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.284-9309_284-9308i others(14): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648867 | |||||
| chr22:46648871
|
G | C | 1 | a0001c0001t0003g0215 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.284-9316G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648871 | ||||||
| chr22:46648871
|
G | GATGGATG others(5): Show |
1 | a0001c0001t0005g0145 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.284-9305_284-9304i others(14): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648871 | |||||
| chr22:46648875
|
G | C | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.284-9312G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648875 | ||||||
| chr22:46648875
|
G | GATGC | 3 | a0001c0001t0010g0185a0001c0001t0010g0186a0001c0001t0010g0187 | 3 | HG01884.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.284-9309_284-9308i others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648875 | |||||
| chr22:46648879
|
G | GATGGATG others(9): Show |
1 | a0001c0001t0006g0199 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.284-9293_284-9292i others(18): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648879 | |||||
| chr22:46648895
|
G | C | 2 | a0001c0001t0004g0021a0001c0001t0030g0044 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.284-9292G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648895 | ||||||
| chr22:46648899
|
C | CATGG | 6 | a0001c0001t0005g0211a0001c0001t0005g0258a0001c0001t0009g0047others(3): Show | 6 | HG00738.hp2 HG01106.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-9256_284-9253d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648899 | |||||
| chr22:46648899
|
C | G | 17 | a0001c0001t0001g0168a0001c0001t0003g0208a0001c0001t0003g0214others(14): Show | 17 | HG00099.hp2 HG00323.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.284-9288C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648899 | ||||||
| chr22:46648903
|
G | C | 6 | a0001c0001t0001g0168a0001c0001t0003g0208a0001c0001t0003g0214others(3): Show | 6 | HG00099.hp2 HG01081.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-9284G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648903 | ||||||
| chr22:46648907
|
G | C | 5 | a0001c0001t0010g0185a0001c0001t0010g0186a0001c0001t0010g0187others(2): Show | 5 | HG01884.hp2 HG03041.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-9280G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648907 | ||||||
| chr22:46648907
|
G | GATGGATG others(17): Show |
1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.284-9257_284-9256i others(26): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648907 | |||||
| chr22:46648907
|
G | GATGGATG others(161): Show |
1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.284-9257_284-9256i others(170): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648907 | |||||
| chr22:46648911
|
G | C | 2 | a0001c0001t0003g0215a0001c0001t0005g0145 | 2 | HG00323.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.284-9276G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648911 | ||||||
| chr22:46648911
|
G | GATGGATG others(21): Show |
9 | a0001c0001t0005g0105a0001c0001t0005g0111a0001c0001t0005g0142others(6): Show | 9 | HG01168.hp2 HG02257.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-9253_284-9252i others(30): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648911 | |||||
| chr22:46648911
|
G | GATGGATG others(25): Show |
1 | a0001c0001t0009g0049 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.284-9253_284-9252i others(34): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648911 | |||||
| chr22:46648915
|
G | C | 2 | a0001c0001t0006g0199a0001c0001t0027g0038 | 2 | HG02145.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.284-9272G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648915 | ||||||
| chr22:46648915
|
G | GATGGATG others(17): Show |
2 | a0001c0001t0002g0281a0001c0001t0002g0290 | 2 | HG00639.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.284-9253_284-9252i others(26): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648915 | |||||
| chr22:46648919
|
GATGGATG others(9): Show |
G | 1 | a0001c0001t0048g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.284-9252_284-9237d others(18): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648919 | |||||
| chr22:46648923
|
G | C | 1 | a0001c0001t0004g0021 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.284-9264G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648923 | ||||||
| chr22:46648931
|
GATGC | G | 5 | a0001c0002t0004g0032a0001c0002t0004g0069a0001c0002t0004g0092others(2): Show | 5 | HG01891.hp2 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.284-9252_284-9249d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648931 | |||||
| chr22:46648935
|
C | CATGG | 4 | a0001c0001t0001g0087a0001c0001t0001g0109a0001c0001t0018g0230others(1): Show | 4 | HG01981.hp1 HG02809.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-9205_284-9202d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648935 | |||||
| chr22:46648935
|
C | G | 35 | a0001c0001t0001g0168a0001c0001t0002g0281a0001c0001t0002g0290others(32): Show | 35 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.284-9252C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648935 | ||||||
| chr22:46648935
|
CATGG | C | 51 | a0001c0001t0001g0005a0001c0001t0001g0112a0001c0001t0001g0125others(48): Show | 52 | HG00140.hp1 HG00438.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.284-9205_284-9202d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648935 | |||||
| chr22:46648935
|
CATGGATG others(1): Show |
C | 17 | a0001c0001t0001g0098a0001c0001t0011g0183a0001c0002t0002g0071others(14): Show | 18 | HG01109.hp1 HG01361.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.284-9209_284-9202d others(10): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648935 | |||||
| chr22:46648935
|
CATGGATG others(5): Show |
C | 1 | a0001c0001t0003g0239 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.284-9213_284-9202d others(14): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648935 | |||||
| chr22:46648939
|
G | C | 7 | a0001c0001t0001g0168a0001c0001t0003g0208a0001c0001t0003g0214others(4): Show | 7 | HG00099.hp2 HG01081.hp2 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-9248G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648939 | ||||||
| chr22:46648943
|
G | C | 12 | a0001c0001t0008g0013a0001c0001t0008g0014a0001c0001t0008g0016others(9): Show | 12 | HG01433.hp1 HG01891.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.284-9244G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648943 | ||||||
| chr22:46648943
|
G | GATGGATG others(21): Show |
2 | a0001c0001t0004g0061a0001c0001t0019g0062 | 2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.284-9217_284-9216i others(30): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648943 | |||||
| chr22:46648947
|
G | C | 16 | a0001c0001t0003g0215a0001c0001t0005g0105a0001c0001t0005g0111others(13): Show | 16 | HG00323.hp2 HG01168.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.284-9240G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648947 | ||||||
| chr22:46648947
|
G | GATGGATG others(9): Show |
1 | a0001c0001t0004g0021 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.284-9233_284-9232i others(18): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648947 | |||||
| chr22:46648947
|
G | GATGGATG others(21): Show |
12 | a0001c0001t0005g0063a0001c0001t0007g0022a0001c0001t0007g0023others(9): Show | 12 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.284-9221_284-9220i others(30): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648947 | |||||
| chr22:46648947
|
G | GATGGATG others(17): Show |
7 | a0001c0001t0005g0144a0001c0001t0005g0211a0001c0001t0005g0258others(4): Show | 7 | HG00738.hp2 HG01106.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-9217_284-9216i others(26): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648947 | |||||
| chr22:46648951
|
G | C | 5 | a0001c0001t0002g0281a0001c0001t0002g0290a0001c0001t0006g0199others(2): Show | 5 | HG00639.hp1 HG02145.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-9236G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648951 | ||||||
| chr22:46648951
|
G | GATGGATG others(13): Show |
91 | a0001c0001t0001g0197a0001c0001t0001g0255a0001c0001t0001g0261others(88): Show | 93 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.284-9217_284-9216i others(22): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648951 | |||||
| chr22:46648951
|
G | GATGGATG others(33): Show |
1 | a0001c0001t0002g0312 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.284-9217_284-9216i others(42): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648951 | |||||
| chr22:46648967
|
G | GATGCATG others(17): Show |
4 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0010g0034others(1): Show | 4 | HG02622.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-9217_284-9216i others(26): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46648967 | |||||
| chr22:46648986
|
A | G | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.284-9201A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46648986 | ||||||
| chr22:46649127
|
G | A | 4 | a0001c0001t0003g0229a0001c0001t0003g0245a0001c0001t0014g0052others(1): Show | 4 | HG00733.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-9060G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46649127 | ||||||
| chr22:46649272
|
G | C | 2 | a0001c0001t0002g0171a0001c0001t0002g0257 | 2 | NA18982.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.284-8915G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46649272 | ||||||
| chr22:46649383
|
C | T | 1 | a0001c0001t0014g0058 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.284-8804C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46649383 | ||||||
| chr22:46649384
|
G | A | 1 | a0001c0001t0009g0056 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.284-8803G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46649384 | ||||||
| chr22:46649659
|
T | A | 94 | a0001c0001t0001g0197a0001c0001t0001g0255a0001c0001t0001g0261others(91): Show | 96 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.284-8528T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46649659 | ||||||
| chr22:46649685
|
C | T | 1 | a0001c0001t0003g0212 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.284-8502C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46649685 | ||||||
| chr22:46649858
|
A | T | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.284-8329A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46649858 | ||||||
| chr22:46649896
|
C | T | 1 | a0001c0001t0056g0313 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.284-8291C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46649896 | ||||||
| chr22:46649941
|
G | T | 1 | a0001c0002t0004g0099 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.284-8246G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46649941 | ||||||
| chr22:46650058
|
G | A | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.284-8129G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46650058 | ||||||
| chr22:46650208
|
C | T | 1 | a0001c0001t0003g0245 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.284-7979C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46650208 | ||||||
| chr22:46650308
|
A | AGTGTCGA others(18): Show |
1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.284-7829_284-7805d others(27): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46650308 | |||||
| chr22:46650308
|
AGTGTCGA others(18): Show |
A | 15 | a0001c0001t0001g0273a0001c0001t0004g0021a0001c0001t0005g0063others(12): Show | 15 | HG00642.hp2 HG01070.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.284-7829_284-7805d others(27): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46650308 | |||||
| chr22:46650349
|
G | A | 1 | a0001c0001t0003g0207 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.284-7838G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46650349 | ||||||
| chr22:46650379
|
G | T | 12 | a0001c0001t0005g0063a0001c0001t0007g0022a0001c0001t0007g0023others(9): Show | 12 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.284-7808G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46650379 | ||||||
| chr22:46650430
|
C | G | 1 | a0001c0001t0002g0266 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.284-7757C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46650430 | ||||||
| chr22:46650433
|
AGCATTGA others(6): Show |
A | 13 | a0001c0001t0004g0021a0001c0001t0005g0063a0001c0001t0007g0022others(10): Show | 13 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.284-7752_284-7740d others(15): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46650433 | |||||
| chr22:46650495
|
G | A | 1 | a0001c0001t0064g0306 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.284-7692G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46650495 | ||||||
| chr22:46650497
|
C | G | 2 | a0001c0001t0015g0189a0001c0001t0015g0190 | 2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.284-7690C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46650497 | ||||||
| chr22:46650498
|
G | A | 1 | a0001c0001t0003g0240 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.284-7689G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46650498 | ||||||
| chr22:46650500
|
T | C | 232 | a0001c0001t0001g0098a0001c0001t0001g0197a0001c0001t0001g0220others(229): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.284-7687T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46650500 | ||||||
| chr22:46650529
|
C | G | 22 | a0001c0001t0004g0021a0001c0001t0005g0063a0001c0001t0007g0022others(19): Show | 22 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.284-7658C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46650529 | ||||||
| chr22:46650615
|
T | C | 117 | a0001c0001t0001g0197a0001c0001t0001g0255a0001c0001t0001g0261others(114): Show | 119 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.284-7572T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46650615 | ||||||
| chr22:46650671
|
A | G | 3 | a0001c0001t0003g0234a0001c0003t0003g0235a0001c0003t0003g0236 | 3 | HG02109.hp2 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.284-7516A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46650671 | ||||||
| chr22:46650718
|
C | T | 2 | a0001c0001t0001g0110a0001c0001t0038g0180 | 2 | HG03579.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.284-7469C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46650718 | ||||||
| chr22:46650926
|
G | A | 17 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0083others(14): Show | 17 | HG01243.hp2 HG01496.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.284-7261G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46650926 | ||||||
| chr22:46650931
|
G | A | 2 | a0001c0001t0030g0044a0001c0001t0048g0191 | 2 | HG01433.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.284-7256G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46650931 | ||||||
| chr22:46651039
|
T | G | 1 | a0001c0001t0001g0167 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.284-7148T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46651039 | ||||||
| chr22:46651040
|
G | A | 8 | a0001c0001t0010g0185a0001c0001t0010g0186a0001c0001t0010g0187others(5): Show | 8 | HG01433.hp1 HG01884.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-7147G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46651040 | ||||||
| chr22:46651138
|
AG | A | 21 | a0001c0001t0001g0098a0001c0002t0002g0071a0001c0002t0004g0002others(18): Show | 22 | HG01109.hp1 HG01361.hp2 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.284-7048delG | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46651138 | ||||||
| chr22:46651214
|
T | G | 12 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0010g0034others(9): Show | 12 | HG01433.hp1 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.284-6973T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46651214 | ||||||
| chr22:46651454
|
C | T | 4 | a0001c0001t0010g0185a0001c0001t0010g0186a0001c0001t0010g0187others(1): Show | 4 | HG01884.hp2 HG02572.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-6733C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46651454 | ||||||
| chr22:46651512
|
T | C | 3 | a0001c0001t0011g0183a0001c0001t0011g0184a0001c0001t0028g0060 | 3 | HG02723.hp2 HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.284-6675T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46651512 | ||||||
| chr22:46651527
|
G | T | 1 | a0001c0001t0008g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.284-6660G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46651527 | ||||||
| chr22:46651557
|
C | T | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.284-6630C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46651557 | ||||||
| chr22:46651571
|
G | C | 1 | a0001c0001t0001g0074 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.284-6616G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46651571 | ||||||
| chr22:46651640
|
A | C | 1 | a0001c0001t0058g0277 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.284-6547A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46651640 | ||||||
| chr22:46651650
|
C | G | 2 | a0001c0001t0030g0044a0001c0001t0054g0251 | 2 | HG02647.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.284-6537C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46651650 | ||||||
| chr22:46651737
|
G | T | 3 | a0001c0001t0002g0172a0001c0001t0002g0293a0001c0001t0061g0289 | 3 | HG01943.hp1 HG02148.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.284-6450G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46651737 | ||||||
| chr22:46651850
|
G | C | 1 | a0001c0002t0002g0071 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.284-6337G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46651850 | ||||||
| chr22:46651850
|
G | T | 1 | a0001c0001t0006g0198 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.284-6337G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46651850 | ||||||
| chr22:46651852
|
G | A | 41 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0001g0106others(38): Show | 42 | HG00423.hp1 HG00642.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-6335G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46651852 | ||||||
| chr22:46651977
|
G | C | 10 | a0001c0002t0002g0071a0001c0002t0004g0002a0001c0002t0004g0070others(7): Show | 11 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.284-6210G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46651977 | ||||||
| chr22:46652045
|
G | T | 2 | a0001c0001t0005g0258a0001c0001t0009g0050 | 2 | HG00738.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.284-6142G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652045 | ||||||
| chr22:46652159
|
G | A | 4 | a0001c0001t0005g0111a0001c0001t0005g0142a0001c0001t0005g0143others(1): Show | 4 | HG01168.hp2 HG02735.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-6028G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652159 | ||||||
| chr22:46652227
|
G | A | 13 | a0001c0001t0004g0021a0001c0001t0005g0063a0001c0001t0007g0022others(10): Show | 13 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.284-5960G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652227 | ||||||
| chr22:46652283
|
A | G | 2 | a0001c0001t0027g0038a0002c0011t0053g0019 | 2 | HG02145.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.284-5904A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652283 | ||||||
| chr22:46652305
|
G | A | 10 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0010g0034others(7): Show | 10 | HG01433.hp1 HG01884.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.284-5882G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652305 | ||||||
| chr22:46652368
|
C | T | 6 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0083others(3): Show | 6 | HG01243.hp2 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-5819C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652368 | ||||||
| chr22:46652403
|
T | C | 2 | a0001c0001t0030g0044a0001c0001t0048g0191 | 2 | HG01433.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.284-5784T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652403 | ||||||
| chr22:46652481
|
A | G | 140 | a0001c0001t0001g0197a0001c0001t0001g0308a0001c0001t0002g0007others(137): Show | 142 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.284-5706A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652481 | ||||||
| chr22:46652579
|
G | A | 7 | a0001c0001t0003g0206a0001c0001t0003g0224a0001c0001t0003g0225others(4): Show | 7 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.284-5608G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652579 | ||||||
| chr22:46652632
|
G | A | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.284-5555G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652632 | ||||||
| chr22:46652659
|
G | A | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.284-5528G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652659 | ||||||
| chr22:46652736
|
C | T | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.284-5451C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652736 | ||||||
| chr22:46652737
|
A | G | 322 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(319): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.284-5450A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652737 | ||||||
| chr22:46652768
|
G | A | 1 | a0001c0001t0012g0079 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.284-5419G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652768 | ||||||
| chr22:46652874
|
T | A | 1 | a0001c0001t0010g0034 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.284-5313T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652874 | ||||||
| chr22:46652874
|
T | G | 133 | a0001c0001t0001g0197a0001c0001t0001g0308a0001c0001t0002g0007others(130): Show | 134 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.284-5313T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652874 | ||||||
| chr22:46652895
|
A | G | 84 | a0001c0001t0001g0197a0001c0001t0001g0308a0001c0001t0002g0007others(81): Show | 85 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.284-5292A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46652895 | ||||||
| chr22:46653189
|
C | T | 92 | a0001c0001t0001g0168a0001c0001t0001g0197a0001c0001t0001g0308others(89): Show | 93 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.284-4998C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653189 | ||||||
| chr22:46653207
|
G | C | 1 | a0001c0001t0001g0152 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.284-4980G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653207 | ||||||
| chr22:46653227
|
C | T | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.284-4960C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653227 | ||||||
| chr22:46653241
|
C | A | 107 | a0001c0001t0001g0197a0001c0001t0001g0308a0001c0001t0002g0007others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.284-4946C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653241 | ||||||
| chr22:46653244
|
C | G | 8 | a0001c0001t0001g0074a0001c0001t0001g0112a0001c0001t0001g0125others(5): Show | 8 | HG00438.hp1 HG00639.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-4943C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653244 | ||||||
| chr22:46653254
|
G | C | 2 | a0001c0001t0023g0121a0001c0001t0023g0122 | 2 | HG01952.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.284-4933G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653254 | ||||||
| chr22:46653328
|
T | C | 26 | a0001c0001t0004g0021a0001c0001t0004g0035a0001c0001t0004g0036others(23): Show | 26 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.284-4859T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653328 | ||||||
| chr22:46653366
|
C | T | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.284-4821C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653366 | ||||||
| chr22:46653413
|
G | A | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.284-4774G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653413 | ||||||
| chr22:46653577
|
G | A | 227 | a0001c0001t0001g0197a0001c0001t0001g0220a0001c0001t0001g0308others(224): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.284-4610G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653577 | ||||||
| chr22:46653588
|
C | G | 1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.284-4599C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653588 | ||||||
| chr22:46653607
|
C | T | 2 | a0001c0001t0004g0061a0001c0001t0019g0062 | 2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.284-4580C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653607 | ||||||
| chr22:46653619
|
C | T | 1 | a0001c0001t0002g0276 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.284-4568C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653619 | ||||||
| chr22:46653776
|
G | A | 14 | a0001c0001t0004g0021a0001c0001t0005g0063a0001c0001t0007g0022others(11): Show | 14 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.284-4411G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653776 | ||||||
| chr22:46653859
|
C | T | 1 | a0001c0001t0006g0202 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.284-4328C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653859 | ||||||
| chr22:46653910
|
A | G | 1 | a0001c0002t0004g0091 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.284-4277A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653910 | ||||||
| chr22:46653961
|
G | A | 10 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0010g0034others(7): Show | 10 | HG01433.hp1 HG01884.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.284-4226G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46653961 | ||||||
| chr22:46654044
|
T | G | 1 | a0001c0001t0009g0054 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.284-4143T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46654044 | ||||||
| chr22:46654069
|
C | G | 1 | a0001c0001t0002g0310 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.284-4118C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46654069 | ||||||
| chr22:46654070
|
G | A | 13 | a0001c0001t0004g0021a0001c0001t0005g0063a0001c0001t0007g0022others(10): Show | 13 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.284-4117G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46654070 | ||||||
| chr22:46654179
|
G | A | 2 | a0001c0001t0015g0189a0001c0001t0015g0190 | 2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.284-4008G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46654179 | ||||||
| chr22:46654313
|
G | A | 85 | a0001c0001t0001g0197a0001c0001t0001g0308a0001c0001t0002g0007others(82): Show | 86 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.284-3874G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46654313 | ||||||
| chr22:46654400
|
C | G | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.284-3787C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46654400 | ||||||
| chr22:46654423
|
C | T | 2 | a0001c0001t0002g0171a0001c0001t0002g0257 | 2 | NA18982.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.284-3764C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46654423 | ||||||
| chr22:46654439
|
C | T | 99 | a0001c0001t0001g0197a0001c0001t0001g0308a0001c0001t0002g0007others(96): Show | 100 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.284-3748C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46654439 | ||||||
| chr22:46654490
|
G | A | 84 | a0001c0001t0001g0197a0001c0001t0001g0308a0001c0001t0002g0007others(81): Show | 85 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.284-3697G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46654490 | ||||||
| chr22:46654637
|
C | T | 20 | a0001c0002t0002g0071a0001c0002t0004g0002a0001c0002t0004g0032others(17): Show | 21 | HG01109.hp1 HG01361.hp2 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.284-3550C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46654637 | ||||||
| chr22:46654726
|
C | T | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.284-3461C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46654726 | ||||||
| chr22:46654736
|
C | G | 1 | a0001c0001t0001g0134 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.284-3451C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46654736 | ||||||
| chr22:46654847
|
G | A | 85 | a0001c0001t0001g0197a0001c0001t0001g0308a0001c0001t0002g0007others(82): Show | 86 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.284-3340G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46654847 | ||||||
| chr22:46654956
|
A | G | 2 | a0001c0001t0004g0061a0001c0001t0019g0062 | 2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.284-3231A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46654956 | ||||||
| chr22:46655008
|
C | T | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.284-3179C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655008 | ||||||
| chr22:46655052
|
A | G | 1 | a0001c0002t0004g0099 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.284-3135A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655052 | ||||||
| chr22:46655081
|
G | C | 2 | a0001c0001t0003g0006a0001c0001t0041g0006 | 2 | HG02559.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.284-3106G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655081 | ||||||
| chr22:46655137
|
A | C | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-3050A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655137 | ||||||
| chr22:46655141
|
C | T | 1 | a0001c0001t0029g0053 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.284-3046C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655141 | ||||||
| chr22:46655144
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-3043G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655144 | ||||||
| chr22:46655150
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-3037G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655150 | ||||||
| chr22:46655151
|
G | T | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-3036G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655151 | ||||||
| chr22:46655153
|
C | G | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-3034C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655153 | ||||||
| chr22:46655156
|
A | G | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-3031A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655156 | ||||||
| chr22:46655157
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-3030C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655157 | ||||||
| chr22:46655158
|
C | G | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-3029C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655158 | ||||||
| chr22:46655159
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-3028C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655159 | ||||||
| chr22:46655242
|
G | A | 2 | a0001c0001t0030g0044a0001c0001t0048g0191 | 2 | HG01433.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.284-2945G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655242 | ||||||
| chr22:46655303
|
A | C | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.284-2884A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655303 | ||||||
| chr22:46655342
|
T | C | 7 | a0001c0001t0010g0185a0001c0001t0010g0186a0001c0001t0010g0187others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-2845T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655342 | ||||||
| chr22:46655441
|
G | A | 3 | a0001c0001t0010g0185a0001c0001t0010g0186a0001c0001t0010g0187 | 3 | HG01884.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.284-2746G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655441 | ||||||
| chr22:46655451
|
A | G | 4 | a0001c0001t0003g0208a0001c0001t0003g0214a0001c0001t0003g0215others(1): Show | 4 | HG00099.hp2 HG01081.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-2736A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655451 | ||||||
| chr22:46655600
|
C | T | 98 | a0001c0001t0001g0197a0001c0001t0001g0308a0001c0001t0002g0007others(95): Show | 99 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.284-2587C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655600 | ||||||
| chr22:46655735
|
G | C | 1 | a0001c0001t0003g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.284-2452G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655735 | ||||||
| chr22:46655866
|
G | A | 13 | a0001c0001t0004g0021a0001c0001t0005g0063a0001c0001t0007g0022others(10): Show | 13 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.284-2321G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655866 | ||||||
| chr22:46655890
|
G | GCCAGGTG others(6): Show |
112 | a0001c0001t0001g0197a0001c0001t0001g0308a0001c0001t0002g0007others(109): Show | 114 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.284-2295_284-2294i others(15): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 46655890 | |||||
| chr22:46655927
|
G | A | 4 | a0001c0001t0001g0112a0001c0001t0001g0125a0001c0001t0001g0127others(1): Show | 4 | HG00438.hp1 HG02135.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-2260G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655927 | ||||||
| chr22:46655955
|
C | T | 6 | a0001c0001t0002g0285a0001c0001t0002g0291a0001c0001t0002g0320others(3): Show | 6 | NA18970.hp1 NA18980.hp1 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.284-2232C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655955 | ||||||
| chr22:46655976
|
C | T | 10 | a0001c0001t0007g0022a0001c0001t0007g0023a0001c0001t0007g0024others(7): Show | 10 | HG00642.hp2 HG01243.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.284-2211C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46655976 | ||||||
| chr22:46656010
|
C | A | 1 | a0001c0001t0010g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.284-2177C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46656010 | ||||||
| chr22:46656021
|
T | C | 112 | a0001c0001t0001g0197a0001c0001t0001g0308a0001c0001t0002g0007others(109): Show | 114 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.284-2166T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46656021 | ||||||
| chr22:46656022
|
G | A | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.284-2165G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46656022 | ||||||
| chr22:46656031
|
G | A | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.284-2156G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46656031 | ||||||
| chr22:46656178
|
G | A | 2 | a0001c0001t0002g0305a0001c0001t0057g0304 | 2 | HG01069.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.284-2009G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46656178 | ||||||
| chr22:46656380
|
G | A | 1 | a0001c0001t0022g0138 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.284-1807G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46656380 | ||||||
| chr22:46656796
|
T | G | 107 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0308others(104): Show | 109 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.284-1391T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46656796 | ||||||
| chr22:46656844
|
C | T | 2 | a0001c0001t0003g0218a0001c0001t0003g0242 | 2 | HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.284-1343C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46656844 | ||||||
| chr22:46656949
|
C | T | 1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.284-1238C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46656949 | ||||||
| chr22:46656950
|
C | G | 2 | a0001c0001t0001g0271a0001c0001t0001g0309 | 2 | NA18955.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.284-1237C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46656950 | ||||||
| chr22:46656961
|
T | C | 13 | a0001c0001t0004g0021a0001c0001t0005g0063a0001c0001t0007g0022others(10): Show | 13 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.284-1226T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46656961 | ||||||
| chr22:46657162
|
G | A | 2 | a0001c0001t0015g0189a0001c0001t0015g0190 | 2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.284-1025G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657162 | ||||||
| chr22:46657225
|
A | T | 3 | a0001c0001t0010g0185a0001c0001t0010g0186a0001c0001t0010g0187 | 3 | HG01884.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.284-962A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657225 | ||||||
| chr22:46657231
|
T | C | 2 | a0001c0001t0001g0129a0001c0001t0001g0132 | 2 | HG02148.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.284-956T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657231 | ||||||
| chr22:46657268
|
G | A | 26 | a0001c0001t0001g0220a0001c0001t0003g0006a0001c0001t0003g0104others(23): Show | 26 | HG00140.hp1 HG00741.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.284-919G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657268 | ||||||
| chr22:46657336
|
A | G | 135 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0308others(132): Show | 137 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.284-851A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657336 | ||||||
| chr22:46657368
|
C | T | 1 | a0001c0001t0007g0025 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.284-819C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657368 | ||||||
| chr22:46657406
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-781G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657406 | ||||||
| chr22:46657407
|
A | C | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-780A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657407 | ||||||
| chr22:46657408
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-779G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657408 | ||||||
| chr22:46657409
|
G | C | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-778G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657409 | ||||||
| chr22:46657410
|
A | T | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-777A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657410 | ||||||
| chr22:46657413
|
C | A | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-774C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657413 | ||||||
| chr22:46657414
|
G | T | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-773G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657414 | ||||||
| chr22:46657415
|
G | C | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-772G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657415 | ||||||
| chr22:46657417
|
A | C | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-770A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657417 | ||||||
| chr22:46657419
|
A | T | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-768A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657419 | ||||||
| chr22:46657421
|
A | T | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-766A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657421 | ||||||
| chr22:46657422
|
G | T | 1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-765G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657422 | ||||||
| chr22:46657425
|
C | G | 1 | a0001c0001t0003g0207 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.284-762C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657425 | ||||||
| chr22:46657512
|
T | C | 4 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0010g0034others(1): Show | 4 | HG02622.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-675T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657512 | ||||||
| chr22:46657821
|
T | C | 173 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0308others(170): Show | 176 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.284-366T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657821 | ||||||
| chr22:46657829
|
G | A | 1 | a0001c0001t0004g0035 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.284-358G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657829 | ||||||
| chr22:46657836
|
C | T | 1 | a0001c0001t0029g0053 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.284-351C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657836 | ||||||
| chr22:46657852
|
C | T | 2 | a0001c0001t0003g0210a0001c0001t0003g0239 | 2 | NA18946.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.284-335C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46657852 | ||||||
| chr22:46658019
|
G | A | 3 | a0001c0001t0007g0024a0001c0001t0007g0025a0001c0001t0007g0029 | 3 | HG02451.hp2 HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.284-168G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46658019 | ||||||
| chr22:46658033
|
G | A | 1 | a0002c0010t0047g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.284-154G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46658033 | ||||||
| chr22:46658064
|
A | G | 3 | a0001c0001t0015g0189a0001c0001t0015g0190a0001c0001t0054g0251 | 3 | HG02647.hp2 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.284-123A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46658064 | ||||||
| chr22:46658119
|
C | T | 8 | a0001c0001t0010g0185a0001c0001t0010g0186a0001c0001t0010g0187others(5): Show | 8 | HG01433.hp1 HG01884.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.284-68C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46658119 | ||||||
| chr22:46658161
|
T | C | 10 | a0001c0001t0003g0243a0001c0001t0008g0008a0001c0001t0008g0009others(7): Show | 10 | HG01891.hp1 HG02723.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.284-26T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 3/18 | chr22 | 46658161 | ||||||
| chr22:46658451
|
C | T | 1 | a0001c0001t0001g0255 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.404+144C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46658451 | ||||||
| chr22:46658517
|
A | G | 18 | a0001c0001t0005g0105a0001c0001t0005g0111a0001c0001t0005g0142others(15): Show | 18 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.404+210A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46658517 | ||||||
| chr22:46658535
|
C | T | 1 | a0001c0007t0019g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.404+228C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46658535 | ||||||
| chr22:46658612
|
T | C | 4 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0010g0034others(1): Show | 4 | HG02622.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.404+305T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46658612 | ||||||
| chr22:46658774
|
C | T | 190 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0220others(187): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.404+467C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46658774 | ||||||
| chr22:46658782
|
TGCCCCAG others(16): Show |
T | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.404+481_404+503del others(23): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr22 | 46658782 | |||||
| chr22:46658786
|
C | CCAGCCGC others(19): Show |
1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.404+484_404+485ins others(26): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr22 | 46658786 | |||||
| chr22:46658792
|
A | G | 91 | a0001c0001t0001g0220a0001c0001t0003g0006a0001c0001t0003g0030others(88): Show | 93 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(90): Show |
intron_variant | MODIFIER | c.404+485A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46658792 | ||||||
| chr22:46658798
|
T | C | 32 | a0001c0001t0003g0243a0001c0001t0004g0017a0001c0001t0008g0008others(29): Show | 33 | HG01109.hp1 HG01361.hp2 HG01496.hp2 others(30): Show |
intron_variant | MODIFIER | c.404+491T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46658798 | ||||||
| chr22:46658799
|
G | A | 32 | a0001c0001t0003g0243a0001c0001t0004g0017a0001c0001t0008g0008others(29): Show | 33 | HG01109.hp1 HG01361.hp2 HG01496.hp2 others(30): Show |
intron_variant | MODIFIER | c.404+492G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46658799 | ||||||
| chr22:46658806
|
G | A | 13 | a0001c0001t0004g0021a0001c0001t0005g0063a0001c0001t0007g0022others(10): Show | 13 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.404+499G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46658806 | ||||||
| chr22:46658845
|
G | A | 2 | a0001c0001t0006g0174a0001c0001t0006g0302 | 2 | NA19081.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.404+538G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46658845 | ||||||
| chr22:46658915
|
T | C | 1 | a0001c0001t0004g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.404+608T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46658915 | ||||||
| chr22:46659082
|
G | A | 5 | a0001c0002t0004g0032a0001c0002t0004g0069a0001c0002t0004g0092others(2): Show | 5 | HG01891.hp2 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.404+775G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46659082 | ||||||
| chr22:46659141
|
C | T | 1 | a0001c0007t0019g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.404+834C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46659141 | ||||||
| chr22:46659235
|
TCCCTCAG others(6): Show |
T | 13 | a0001c0001t0004g0021a0001c0001t0005g0063a0001c0001t0007g0022others(10): Show | 13 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.404+936_404+948del others(13): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr22 | 46659235 | |||||
| chr22:46659245
|
T | G | 4 | a0001c0001t0010g0185a0001c0001t0010g0186a0001c0001t0010g0187others(1): Show | 4 | HG01884.hp2 HG03471.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.404+938T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46659245 | ||||||
| chr22:46659254
|
A | G | 1 | a0001c0001t0013g0055 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.404+947A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46659254 | ||||||
| chr22:46659276
|
C | T | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.404+969C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46659276 | ||||||
| chr22:46659308
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0113a0001c0001t0001g0163 | 4 | NA18969.hp1 NA18970.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.404+1001G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46659308 | ||||||
| chr22:46659316
|
A | C | 2 | a0001c0001t0003g0006a0001c0001t0041g0006 | 2 | HG02559.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.404+1009A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46659316 | ||||||
| chr22:46659482
|
C | T | 1 | a0001c0005t0002g0294 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.404+1175C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46659482 | ||||||
| chr22:46659668
|
C | T | 7 | a0001c0001t0003g0243a0001c0001t0008g0008a0001c0001t0008g0009others(4): Show | 7 | HG01891.hp1 HG02723.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.404+1361C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46659668 | ||||||
| chr22:46659707
|
GGGGGGCT others(5): Show |
G | 2 | a0001c0001t0027g0038a0002c0011t0053g0019 | 2 | HG02145.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.404+1419_404+1430d others(14): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr22 | 46659707 | |||||
| chr22:46659739
|
T | C | 15 | a0001c0001t0004g0021a0001c0001t0005g0063a0001c0001t0007g0022others(12): Show | 15 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.404+1432T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46659739 | ||||||
| chr22:46659761
|
G | A | 11 | a0001c0001t0003g0243a0001c0001t0004g0017a0001c0001t0008g0008others(8): Show | 11 | HG01891.hp1 HG02572.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.404+1454G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46659761 | ||||||
| chr22:46659782
|
G | A | 1 | a0001c0001t0002g0300 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.404+1475G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46659782 | ||||||
| chr22:46659978
|
A | G | 5 | a0001c0001t0006g0102a0001c0001t0006g0174a0001c0001t0006g0302others(2): Show | 5 | HG00597.hp1 HG02040.hp2 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.405-1403A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46659978 | ||||||
| chr22:46659990
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.405-1391G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46659990 | ||||||
| chr22:46660000
|
G | T | 1 | a0001c0001t0002g0278 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.405-1381G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46660000 | ||||||
| chr22:46660042
|
C | T | 2 | a0001c0001t0002g0286a0001c0001t0002g0287 | 2 | NA18964.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.405-1339C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46660042 | ||||||
| chr22:46660183
|
C | T | 18 | a0001c0001t0005g0105a0001c0001t0005g0111a0001c0001t0005g0142others(15): Show | 18 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.405-1198C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46660183 | ||||||
| chr22:46660317
|
G | A | 11 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0010g0034others(8): Show | 11 | HG01433.hp1 HG01884.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.405-1064G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46660317 | ||||||
| chr22:46660454
|
A | G | 4 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0010g0034others(1): Show | 4 | HG02622.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.405-927A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46660454 | ||||||
| chr22:46660478
|
A | C | 13 | a0001c0001t0004g0021a0001c0001t0005g0063a0001c0001t0007g0022others(10): Show | 13 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.405-903A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46660478 | ||||||
| chr22:46660493
|
C | T | 5 | a0001c0002t0004g0032a0001c0002t0004g0069a0001c0002t0004g0092others(2): Show | 5 | HG01891.hp2 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.405-888C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46660493 | ||||||
| chr22:46660505
|
A | G | 1 | a0001c0001t0002g0298 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.405-876A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46660505 | ||||||
| chr22:46660632
|
G | A | 10 | a0001c0001t0007g0022a0001c0001t0007g0023a0001c0001t0007g0024others(7): Show | 10 | HG00642.hp2 HG01243.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.405-749G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46660632 | ||||||
| chr22:46660659
|
A | G | 11 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0010g0034others(8): Show | 11 | HG01433.hp1 HG01884.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.405-722A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46660659 | ||||||
| chr22:46660715
|
C | T | 1 | a0001c0007t0019g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.405-666C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46660715 | ||||||
| chr22:46660809
|
A | C | 1 | a0001c0001t0004g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.405-572A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46660809 | ||||||
| chr22:46660904
|
C | T | 1 | a0001c0001t0012g0079 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.405-477C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46660904 | ||||||
| chr22:46660934
|
T | A | 5 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0010g0034others(2): Show | 5 | HG02622.hp2 HG02922.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.405-447T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46660934 | ||||||
| chr22:46660940
|
C | T | 5 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0010g0034others(2): Show | 5 | HG02622.hp2 HG02922.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.405-441C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46660940 | ||||||
| chr22:46660945
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0037g0065 | 2 | NA18948.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.405-436C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46660945 | ||||||
| chr22:46661027
|
AAC | A | 13 | a0001c0001t0004g0021a0001c0001t0005g0063a0001c0001t0007g0022others(10): Show | 13 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.405-350_405-349del others(2): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr22 | 46661027 | |||||
| chr22:46661028
|
A | G | 8 | a0001c0001t0010g0185a0001c0001t0010g0186a0001c0001t0010g0187others(5): Show | 8 | HG01433.hp1 HG01884.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.405-353A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46661028 | ||||||
| chr22:46661050
|
C | A | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.405-331C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46661050 | ||||||
| chr22:46661178
|
C | T | 11 | a0001c0001t0003g0243a0001c0001t0004g0017a0001c0001t0008g0008others(8): Show | 11 | HG01891.hp1 HG02572.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.405-203C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46661178 | ||||||
| chr22:46661179
|
G | A | 31 | a0001c0001t0004g0021a0001c0001t0005g0063a0001c0001t0005g0105others(28): Show | 31 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.405-202G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46661179 | ||||||
| chr22:46661224
|
G | A | 1 | a0001c0001t0063g0227 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.405-157G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46661224 | ||||||
| chr22:46661294
|
C | T | 101 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0308others(98): Show | 103 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.405-87C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46661294 | ||||||
| chr22:46661300
|
C | T | 104 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0308others(101): Show | 106 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.405-81C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46661300 | ||||||
| chr22:46661315
|
G | C | 4 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0010g0034others(1): Show | 4 | HG02622.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.405-66G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46661315 | ||||||
| chr22:46661321
|
G | T | 3 | a0001c0001t0004g0036a0001c0001t0010g0034a0001c0001t0033g0037 | 3 | HG02622.hp2 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.405-60G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 4/18 | chr22 | 46661321 | ||||||
| chr22:46661542
|
C | T | 1 | a0001c0001t0031g0059 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.466+100C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46661542 | ||||||
| chr22:46661546
|
C | A | 1 | a0001c0007t0019g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.466+104C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46661546 | ||||||
| chr22:46661565
|
C | T | 16 | a0001c0001t0004g0061a0001c0001t0010g0185a0001c0001t0010g0186others(13): Show | 16 | HG01433.hp1 HG01884.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.466+123C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46661565 | ||||||
| chr22:46661594
|
C | G | 2 | a0001c0001t0001g0271a0001c0001t0001g0309 | 2 | NA18955.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.466+152C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46661594 | ||||||
| chr22:46661630
|
G | A | 7 | a0001c0001t0001g0115a0001c0001t0001g0139a0001c0001t0001g0255others(4): Show | 7 | HG02027.hp1 NA18612.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.466+188G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46661630 | ||||||
| chr22:46661648
|
G | A | 2 | a0001c0001t0003g0218a0001c0001t0003g0242 | 2 | HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.466+206G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46661648 | ||||||
| chr22:46661676
|
A | G | 164 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0308others(161): Show | 167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.466+234A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46661676 | ||||||
| chr22:46661676
|
A | T | 1 | a0001c0002t0004g0093 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.466+234A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46661676 | ||||||
| chr22:46661748
|
C | A | 1 | a0001c0001t0004g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.466+306C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46661748 | ||||||
| chr22:46661795
|
T | C | 1 | a0001c0007t0019g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.466+353T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46661795 | ||||||
| chr22:46661811
|
C | T | 1 | a0001c0001t0009g0049 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.466+369C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46661811 | ||||||
| chr22:46661849
|
G | C | 4 | a0001c0001t0001g0112a0001c0001t0001g0125a0001c0001t0001g0127others(1): Show | 4 | HG00438.hp1 HG02135.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+407G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46661849 | ||||||
| chr22:46661883
|
A | T | 8 | a0001c0001t0001g0308a0001c0001t0002g0296a0001c0001t0002g0297others(5): Show | 8 | HG00099.hp1 HG00642.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.466+441A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46661883 | ||||||
| chr22:46661959
|
C | T | 1 | a0001c0001t0004g0021 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.466+517C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46661959 | ||||||
| chr22:46661979
|
A | C | 18 | a0001c0001t0005g0105a0001c0001t0005g0111a0001c0001t0005g0142others(15): Show | 18 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.466+537A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46661979 | ||||||
| chr22:46662103
|
C | G | 1 | a0001c0001t0001g0167 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.466+661C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662103 | ||||||
| chr22:46662273
|
G | A | 18 | a0001c0001t0005g0105a0001c0001t0005g0111a0001c0001t0005g0142others(15): Show | 18 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.467-767G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662273 | ||||||
| chr22:46662348
|
G | A | 4 | a0001c0001t0010g0185a0001c0001t0010g0186a0001c0001t0010g0187others(1): Show | 4 | HG01884.hp2 HG03471.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-692G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662348 | ||||||
| chr22:46662360
|
G | A | 1 | a0001c0001t0007g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.467-680G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662360 | ||||||
| chr22:46662368
|
C | T | 6 | a0001c0001t0002g0285a0001c0001t0002g0291a0001c0001t0002g0320others(3): Show | 6 | NA18970.hp1 NA18980.hp1 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.467-672C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662368 | ||||||
| chr22:46662477
|
G | A | 2 | a0001c0001t0004g0061a0001c0001t0019g0062 | 2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.467-563G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662477 | ||||||
| chr22:46662497
|
G | A | 1 | a0001c0001t0005g0188 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.467-543G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662497 | ||||||
| chr22:46662507
|
C | G | 3 | a0001c0001t0003g0210a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | NA18946.hp1 NA18952.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.467-533C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662507 | ||||||
| chr22:46662517
|
G | A | 1 | a0001c0001t0002g0257 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.467-523G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662517 | ||||||
| chr22:46662520
|
C | A | 3 | a0001c0002t0004g0032a0001c0002t0004g0093a0001c0002t0004g0094 | 3 | HG02965.hp1 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.467-520C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662520 | ||||||
| chr22:46662636
|
A | C | 18 | a0001c0001t0005g0105a0001c0001t0005g0111a0001c0001t0005g0142others(15): Show | 18 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.467-404A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662636 | ||||||
| chr22:46662658
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.467-382G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662658 | ||||||
| chr22:46662696
|
C | T | 7 | a0001c0001t0010g0185a0001c0001t0010g0186a0001c0001t0010g0187others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.467-344C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662696 | ||||||
| chr22:46662744
|
G | A | 1 | a0001c0001t0004g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.467-296G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662744 | ||||||
| chr22:46662760
|
A | G | 5 | a0001c0002t0004g0002a0001c0002t0004g0086a0001c0002t0004g0117others(2): Show | 6 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.467-280A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662760 | ||||||
| chr22:46662787
|
C | T | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.467-253C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662787 | ||||||
| chr22:46662974
|
C | T | 2 | a0001c0001t0021g0155a0001c0001t0021g0156 | 2 | HG00673.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.467-66C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662974 | ||||||
| chr22:46662981
|
G | A | 7 | a0001c0001t0003g0243a0001c0001t0008g0008a0001c0001t0008g0009others(4): Show | 7 | HG01891.hp1 HG02723.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.467-59G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46662981 | ||||||
| chr22:46663000
|
C | T | 2 | a0001c0001t0005g0105a0001c0001t0005g0211 | 2 | HG03669.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.467-40C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 5/18 | chr22 | 46663000 | ||||||
| chr22:46663182
|
C | T | 1 | a0001c0001t0002g0262 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.599+10C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 6/18 | chr22 | 46663182 | ||||||
| chr22:46663246
|
G | A | 4 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0010g0034others(1): Show | 4 | HG02622.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.599+74G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 6/18 | chr22 | 46663246 | ||||||
| chr22:46663313
|
T | C | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.599+141T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 6/18 | chr22 | 46663313 | ||||||
| chr22:46663385
|
C | T | 136 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0308others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.599+213C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 6/18 | chr22 | 46663385 | ||||||
| chr22:46663475
|
C | A | 149 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0308others(146): Show | 151 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.599+303C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 6/18 | chr22 | 46663475 | ||||||
| chr22:46663574
|
C | A | 1 | a0001c0001t0043g0311 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.600-264C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 6/18 | chr22 | 46663574 | ||||||
| chr22:46663642
|
G | T | 4 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0010g0034others(1): Show | 4 | HG02622.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.600-196G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 6/18 | chr22 | 46663642 | ||||||
| chr22:46663700
|
A | G | 175 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0308others(172): Show | 178 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.600-138A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 6/18 | chr22 | 46663700 | ||||||
| chr22:46663736
|
G | A | 7 | a0001c0001t0010g0185a0001c0001t0010g0186a0001c0001t0010g0187others(4): Show | 7 | HG01433.hp1 HG01884.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.600-102G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 6/18 | chr22 | 46663736 | ||||||
| chr22:46663769
|
G | A | 1 | a0001c0001t0052g0136 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.600-69G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 6/18 | chr22 | 46663769 | ||||||
| chr22:46664128
|
C | A | 1 | a0001c0001t0001g0134 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.717+11C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46664128 | ||||||
| chr22:46664311
|
G | A | 2 | a0001c0001t0015g0189a0001c0001t0015g0190 | 2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.717+194G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46664311 | ||||||
| chr22:46664380
|
T | C | 166 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0308others(163): Show | 168 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.717+263T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46664380 | ||||||
| chr22:46664449
|
G | A | 3 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254 | 3 | HG01256.hp2 HG01258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.717+332G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46664449 | ||||||
| chr22:46664487
|
C | CA | 230 | a0001c0001t0001g0161a0001c0001t0001g0196a0001c0001t0001g0197others(227): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.717+370_717+371ins others(1): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46664487 | ||||||
| chr22:46664496
|
T | C | 154 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0308others(151): Show | 156 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.717+379T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46664496 | ||||||
| chr22:46664550
|
G | A | 1 | a0001c0002t0002g0071 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.717+433G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46664550 | ||||||
| chr22:46664646
|
G | T | 6 | a0001c0001t0003g0206a0001c0001t0003g0224a0001c0001t0003g0225others(3): Show | 6 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.717+529G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46664646 | ||||||
| chr22:46664650
|
C | T | 2 | a0001c0001t0001g0129a0001c0001t0001g0132 | 2 | HG02148.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.717+533C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46664650 | ||||||
| chr22:46664693
|
C | G | 9 | a0001c0001t0002g0249a0001c0001t0002g0260a0001c0001t0002g0272others(6): Show | 9 | HG02015.hp2 NA18951.hp2 NA18970.hp1 others(6): Show |
intron_variant | MODIFIER | c.717+576C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46664693 | ||||||
| chr22:46664717
|
T | C | 1 | a0001c0001t0054g0251 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.717+600T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46664717 | ||||||
| chr22:46664728
|
G | A | 4 | a0001c0001t0010g0185a0001c0001t0010g0186a0001c0001t0010g0187others(1): Show | 4 | HG01884.hp2 HG03471.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.717+611G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46664728 | ||||||
| chr22:46665019
|
C | T | 38 | a0001c0001t0003g0243a0001c0001t0004g0017a0001c0001t0004g0021others(35): Show | 39 | HG01109.hp1 HG01361.hp2 HG01496.hp2 others(36): Show |
intron_variant | MODIFIER | c.718-596C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46665019 | ||||||
| chr22:46665052
|
G | A | 1 | a0001c0001t0003g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.718-563G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46665052 | ||||||
| chr22:46665056
|
G | A | 1 | a0001c0001t0050g0147 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.718-559G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46665056 | ||||||
| chr22:46665079
|
C | T | 131 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0308others(128): Show | 133 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.718-536C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46665079 | ||||||
| chr22:46665092
|
T | C | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.718-523T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46665092 | ||||||
| chr22:46665246
|
C | G | 1 | a0001c0007t0019g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.718-369C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46665246 | ||||||
| chr22:46665362
|
C | T | 22 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0083others(19): Show | 23 | HG01243.hp2 HG01496.hp1 HG01943.hp2 others(20): Show |
intron_variant | MODIFIER | c.718-253C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46665362 | ||||||
| chr22:46665367
|
G | A | 1 | a0001c0001t0011g0183 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.718-248G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 8/18 | chr22 | 46665367 | ||||||
| chr22:46665744
|
C | T | 20 | a0001c0002t0002g0071a0001c0002t0004g0002a0001c0002t0004g0032others(17): Show | 21 | HG01109.hp1 HG01361.hp2 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.809+38C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46665744 | ||||||
| chr22:46665762
|
G | A | 2 | a0001c0001t0005g0258a0001c0001t0009g0050 | 2 | HG00738.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.809+56G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46665762 | ||||||
| chr22:46665782
|
C | T | 2 | a0001c0001t0030g0044a0001c0001t0048g0191 | 2 | HG01433.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.809+76C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46665782 | ||||||
| chr22:46665797
|
G | A | 4 | a0001c0001t0010g0185a0001c0001t0010g0186a0001c0001t0010g0187others(1): Show | 4 | HG01884.hp2 HG03471.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.809+91G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46665797 | ||||||
| chr22:46665862
|
C | T | 5 | a0001c0001t0004g0061a0001c0001t0011g0183a0001c0001t0011g0184others(2): Show | 5 | HG01884.hp1 HG02723.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.809+156C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46665862 | ||||||
| chr22:46665894
|
C | T | 135 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0308others(132): Show | 137 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.809+188C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46665894 | ||||||
| chr22:46665937
|
G | A | 4 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0010g0034others(1): Show | 4 | HG02622.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.809+231G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46665937 | ||||||
| chr22:46666019
|
A | T | 123 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0308others(120): Show | 125 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.809+313A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46666019 | ||||||
| chr22:46666089
|
G | T | 1 | a0001c0001t0009g0054 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.809+383G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46666089 | ||||||
| chr22:46666179
|
C | T | 5 | a0001c0001t0010g0034a0001c0001t0010g0185a0001c0001t0010g0186others(2): Show | 5 | HG01884.hp2 HG03471.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.809+473C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46666179 | ||||||
| chr22:46666294
|
A | G | 2 | a0001c0001t0003g0006a0001c0001t0041g0006 | 2 | HG02559.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.810-531A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46666294 | ||||||
| chr22:46666389
|
C | G | 2 | a0001c0001t0030g0044a0001c0001t0048g0191 | 2 | HG01433.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.810-436C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46666389 | ||||||
| chr22:46666492
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.810-333C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46666492 | ||||||
| chr22:46666493
|
G | C | 3 | a0001c0002t0004g0091a0001c0002t0004g0095a0001c0002t0004g0096 | 3 | HG01109.hp1 HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.810-332G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46666493 | ||||||
| chr22:46666494
|
TTGGTACC others(33): Show |
T | 1 | a0001c0001t0003g0283 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.810-328_810-289del others(40): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr22 | 46666494 | |||||
| chr22:46666676
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.810-149G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46666676 | ||||||
| chr22:46666683
|
C | A | 1 | a0001c0001t0001g0168 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.810-142C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46666683 | ||||||
| chr22:46666737
|
C | T | 1 | a0001c0001t0001g0219 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.810-88C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46666737 | ||||||
| chr22:46666745
|
C | G | 3 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0033g0037 | 3 | HG02622.hp2 HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.810-80C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46666745 | ||||||
| chr22:46666746
|
G | A | 1 | a0001c0001t0003g0283 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.810-79G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46666746 | ||||||
| chr22:46666805
|
G | A | 1 | a0001c0001t0005g0041 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.810-20G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 9/18 | chr22 | 46666805 | ||||||
| chr22:46666904
|
C | T | 1 | a0001c0001t0012g0079 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.858+31C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 10/18 | chr22 | 46666904 | ||||||
| chr22:46666997
|
G | T | 31 | a0001c0001t0005g0063a0001c0001t0005g0105a0001c0001t0005g0111others(28): Show | 31 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.858+124G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 10/18 | chr22 | 46666997 | ||||||
| chr22:46667241
|
T | G | 1 | a0001c0002t0004g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.858+368T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 10/18 | chr22 | 46667241 | ||||||
| chr22:46667433
|
A | G | 91 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0308others(88): Show | 93 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.858+560A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 10/18 | chr22 | 46667433 | ||||||
| chr22:46667462
|
T | C | 175 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0308others(172): Show | 178 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.858+589T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 10/18 | chr22 | 46667462 | ||||||
| chr22:46667478
|
G | A | 5 | a0001c0002t0004g0002a0001c0002t0004g0086a0001c0002t0004g0117others(2): Show | 6 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.858+605G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 10/18 | chr22 | 46667478 | ||||||
| chr22:46667515
|
T | C | 1 | a0001c0002t0004g0099 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.859-581T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 10/18 | chr22 | 46667515 | ||||||
| chr22:46667595
|
G | A | 11 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0010g0034others(8): Show | 11 | HG01433.hp1 HG01884.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.859-501G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 10/18 | chr22 | 46667595 | ||||||
| chr22:46667600
|
C | T | 1 | a0001c0009t0062g0303 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.859-496C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 10/18 | chr22 | 46667600 | ||||||
| chr22:46667611
|
C | T | 1 | a0001c0001t0002g0269 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.859-485C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 10/18 | chr22 | 46667611 | ||||||
| chr22:46667677
|
G | A | 12 | a0001c0001t0005g0063a0001c0001t0007g0022a0001c0001t0007g0023others(9): Show | 12 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.859-419G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 10/18 | chr22 | 46667677 | ||||||
| chr22:46667712
|
C | T | 1 | a0001c0002t0002g0071 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.859-384C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 10/18 | chr22 | 46667712 | ||||||
| chr22:46667784
|
G | C | 2 | a0001c0001t0002g0305a0001c0001t0057g0304 | 2 | HG01069.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.859-312G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 10/18 | chr22 | 46667784 | ||||||
| chr22:46667985
|
G | A | 1 | a0002c0010t0047g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.859-111G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 10/18 | chr22 | 46667985 | ||||||
| chr22:46668178
|
G | A | 1 | a0001c0001t0003g0212 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.930+11G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 11/18 | chr22 | 46668178 | ||||||
| chr22:46668267
|
C | A | 168 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0308others(165): Show | 170 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.930+100C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 11/18 | chr22 | 46668267 | ||||||
| chr22:46668288
|
G | A | 12 | a0001c0001t0005g0063a0001c0001t0007g0022a0001c0001t0007g0023others(9): Show | 12 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.930+121G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 11/18 | chr22 | 46668288 | ||||||
| chr22:46668417
|
G | A | 5 | a0001c0001t0010g0034a0001c0001t0010g0185a0001c0001t0010g0186others(2): Show | 5 | HG01884.hp2 HG03471.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.930+250G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 11/18 | chr22 | 46668417 | ||||||
| chr22:46668419
|
G | A | 1 | a0001c0001t0028g0060 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.930+252G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 11/18 | chr22 | 46668419 | ||||||
| chr22:46668430
|
T | C | 317 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0066others(314): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.931-259T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 11/18 | chr22 | 46668430 | ||||||
| chr22:46668489
|
C | T | 1 | a0001c0001t0004g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.931-200C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 11/18 | chr22 | 46668489 | ||||||
| chr22:46668768
|
C | T | 99 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0253others(96): Show | 100 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.975-31C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 12/18 | chr22 | 46668768 | ||||||
| chr22:46668937
|
T | G | 1 | a0001c0001t0007g0027 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1084+29T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46668937 | ||||||
| chr22:46668940
|
A | C | 87 | a0001c0001t0001g0163a0001c0001t0001g0196a0001c0001t0001g0197others(84): Show | 88 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.1084+32A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46668940 | ||||||
| chr22:46668953
|
C | T | 6 | a0001c0001t0004g0061a0001c0001t0009g0049a0001c0001t0011g0183others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1084+45C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46668953 | ||||||
| chr22:46669048
|
A | G | 1 | a0001c0007t0019g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1084+140A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669048 | ||||||
| chr22:46669073
|
G | A | 3 | a0001c0001t0003g0083a0001c0001t0003g0084a0001c0001t0003g0085 | 3 | HG01243.hp2 HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1084+165G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669073 | ||||||
| chr22:46669187
|
A | C | 38 | a0001c0001t0003g0243a0001c0001t0004g0035a0001c0001t0004g0036others(35): Show | 38 | HG00738.hp2 HG01106.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.1084+279A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669187 | ||||||
| chr22:46669413
|
G | A | 1 | a0001c0001t0052g0136 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1084+505G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669413 | ||||||
| chr22:46669443
|
GC | G | 24 | a0001c0001t0003g0083a0001c0001t0003g0084a0001c0001t0003g0226others(21): Show | 24 | HG00642.hp2 HG01243.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.1084+542delC | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr22 | 46669443 | |||||
| chr22:46669464
|
C | T | 1 | a0001c0001t0003g0240 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1084+556C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669464 | ||||||
| chr22:46669553
|
T | C | 80 | a0001c0001t0003g0226a0001c0001t0003g0243a0001c0001t0003g0250others(77): Show | 82 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.1084+645T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669553 | ||||||
| chr22:46669577
|
C | G | 86 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0002g0007others(83): Show | 87 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.1084+669C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669577 | ||||||
| chr22:46669579
|
CT | C | 11 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0004g0061others(8): Show | 11 | HG01884.hp1 HG02572.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1084+684delT | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr22 | 46669579 | |||||
| chr22:46669713
|
C | T | 1 | a0001c0001t0007g0029 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1084+805C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669713 | ||||||
| chr22:46669725
|
G | A | 5 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0027g0038others(2): Show | 5 | HG02145.hp1 HG02572.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1084+817G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669725 | ||||||
| chr22:46669733
|
G | A | 1 | a0001c0001t0002g0281 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1084+825G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669733 | ||||||
| chr22:46669767
|
C | T | 157 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0002g0007others(154): Show | 160 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.1084+859C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669767 | ||||||
| chr22:46669787
|
T | C | 179 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0002g0007others(176): Show | 182 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.1084+879T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669787 | ||||||
| chr22:46669816
|
C | T | 12 | a0001c0001t0005g0063a0001c0001t0007g0022a0001c0001t0007g0023others(9): Show | 12 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1084+908C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669816 | ||||||
| chr22:46669851
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1084+943T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669851 | ||||||
| chr22:46669858
|
C | T | 117 | a0001c0001t0002g0007a0001c0001t0002g0081a0001c0001t0002g0100others(114): Show | 119 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.1084+950C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669858 | ||||||
| chr22:46669959
|
T | C | 1 | a0001c0001t0004g0295 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1084+1051T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669959 | ||||||
| chr22:46669990
|
C | T | 2 | a0001c0001t0004g0061a0001c0001t0019g0062 | 2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1084+1082C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669990 | ||||||
| chr22:46669991
|
G | A | 1 | a0001c0001t0002g0257 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1084+1083G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669991 | ||||||
| chr22:46669993
|
C | T | 8 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0011g0183others(5): Show | 8 | HG02572.hp2 HG02622.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1084+1085C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46669993 | ||||||
| chr22:46670050
|
G | A | 2 | a0001c0001t0004g0061a0001c0001t0019g0062 | 2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1084+1142G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46670050 | ||||||
| chr22:46670150
|
C | G | 1 | a0001c0001t0002g0301 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1084+1242C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46670150 | ||||||
| chr22:46670151
|
G | A | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1084+1243G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46670151 | ||||||
| chr22:46670229
|
C | T | 2 | a0001c0001t0002g0305a0001c0001t0057g0304 | 2 | HG01069.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1084+1321C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46670229 | ||||||
| chr22:46670397
|
T | C | 86 | a0001c0001t0002g0007a0001c0001t0002g0081a0001c0001t0002g0100others(83): Show | 87 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.1084+1489T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46670397 | ||||||
| chr22:46670450
|
C | G | 3 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153 | 3 | HG02040.hp1 HG02074.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.1084+1542C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46670450 | ||||||
| chr22:46670460
|
C | T | 1 | a0001c0007t0019g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1084+1552C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46670460 | ||||||
| chr22:46670525
|
C | G | 2 | a0001c0001t0015g0189a0001c0001t0015g0190 | 2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1084+1617C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46670525 | ||||||
| chr22:46670629
|
C | T | 1 | a0001c0001t0001g0220 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1084+1721C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46670629 | ||||||
| chr22:46670729
|
G | A | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1084+1821G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46670729 | ||||||
| chr22:46670733
|
G | A | 4 | a0001c0001t0003g0208a0001c0001t0003g0214a0001c0001t0003g0215others(1): Show | 4 | HG00099.hp2 HG01081.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1084+1825G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46670733 | ||||||
| chr22:46670899
|
G | A | 11 | a0001c0001t0007g0022a0001c0001t0007g0023a0001c0001t0007g0024others(8): Show | 11 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1085-1944G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46670899 | ||||||
| chr22:46670907
|
C | CT | 26 | a0001c0001t0005g0001a0001c0001t0005g0039a0001c0001t0005g0040others(23): Show | 27 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1085-1935dupT | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr22 | 46670907 | |||||
| chr22:46671018
|
T | C | 3 | a0001c0001t0011g0057a0001c0001t0038g0180a0001c0001t0054g0251 | 3 | HG02647.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1085-1825T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671018 | ||||||
| chr22:46671023
|
T | C | 29 | a0001c0001t0004g0061a0001c0001t0005g0001a0001c0001t0005g0039others(26): Show | 30 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1085-1820T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671023 | ||||||
| chr22:46671026
|
C | T | 2 | a0001c0001t0004g0061a0001c0001t0019g0062 | 2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1085-1817C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671026 | ||||||
| chr22:46671264
|
C | T | 11 | a0001c0001t0007g0022a0001c0001t0007g0023a0001c0001t0007g0024others(8): Show | 11 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1085-1579C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671264 | ||||||
| chr22:46671267
|
A | G | 29 | a0001c0001t0004g0061a0001c0001t0005g0001a0001c0001t0005g0039others(26): Show | 30 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1085-1576A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671267 | ||||||
| chr22:46671271
|
G | A | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1085-1572G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671271 | ||||||
| chr22:46671328
|
A | G | 29 | a0001c0001t0004g0061a0001c0001t0005g0001a0001c0001t0005g0039others(26): Show | 30 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1085-1515A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671328 | ||||||
| chr22:46671362
|
G | A | 29 | a0001c0001t0004g0061a0001c0001t0005g0001a0001c0001t0005g0039others(26): Show | 30 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1085-1481G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671362 | ||||||
| chr22:46671371
|
C | T | 8 | a0001c0001t0004g0035a0001c0001t0004g0036a0001c0001t0011g0183others(5): Show | 8 | HG02572.hp2 HG02622.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1085-1472C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671371 | ||||||
| chr22:46671399
|
C | T | 1 | a0001c0001t0048g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1085-1444C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671399 | ||||||
| chr22:46671424
|
A | T | 1 | a0002c0011t0053g0019 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1085-1419A>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671424 | ||||||
| chr22:46671615
|
T | C | 157 | a0001c0001t0002g0007a0001c0001t0002g0081a0001c0001t0002g0100others(154): Show | 160 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.1085-1228T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671615 | ||||||
| chr22:46671634
|
C | T | 1 | a0001c0001t0021g0156 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1085-1209C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671634 | ||||||
| chr22:46671650
|
C | T | 11 | a0001c0001t0007g0022a0001c0001t0007g0023a0001c0001t0007g0024others(8): Show | 11 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1085-1193C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671650 | ||||||
| chr22:46671651
|
G | A | 5 | a0001c0001t0004g0061a0001c0001t0015g0189a0001c0001t0015g0190others(2): Show | 5 | HG01884.hp1 HG02896.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1085-1192G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671651 | ||||||
| chr22:46671656
|
AAAAATAA others(3): Show |
A | 226 | a0001c0001t0002g0007a0001c0001t0002g0081a0001c0001t0002g0100others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1085-1157_1085-114 others(14): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr22 | 46671656 | |||||
| chr22:46671762
|
C | T | 3 | a0001c0001t0011g0057a0001c0001t0038g0180a0001c0001t0054g0251 | 3 | HG02647.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1085-1081C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671762 | ||||||
| chr22:46671861
|
T | C | 1 | a0001c0001t0003g0248 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1085-982T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46671861 | ||||||
| chr22:46672083
|
C | T | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1085-760C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46672083 | ||||||
| chr22:46672084
|
G | A | 9 | a0001c0001t0002g0171a0001c0001t0002g0257a0001c0001t0002g0262others(6): Show | 9 | HG00423.hp2 HG02056.hp2 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.1085-759G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46672084 | ||||||
| chr22:46672111
|
T | C | 29 | a0001c0001t0004g0061a0001c0001t0005g0001a0001c0001t0005g0039others(26): Show | 30 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1085-732T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46672111 | ||||||
| chr22:46672243
|
G | A | 28 | a0001c0001t0004g0061a0001c0001t0005g0001a0001c0001t0005g0039others(25): Show | 29 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1085-600G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46672243 | ||||||
| chr22:46672301
|
T | C | 29 | a0001c0001t0004g0061a0001c0001t0005g0001a0001c0001t0005g0039others(26): Show | 30 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1085-542T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46672301 | ||||||
| chr22:46672340
|
A | G | 12 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0001g0106others(9): Show | 13 | HG00673.hp2 HG02056.hp1 NA18612.hp2 others(10): Show |
intron_variant | MODIFIER | c.1085-503A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46672340 | ||||||
| chr22:46672355
|
G | T | 1 | a0001c0001t0027g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1085-488G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46672355 | ||||||
| chr22:46672359
|
G | T | 21 | a0001c0001t0004g0233a0001c0001t0064g0306a0001c0002t0004g0002others(18): Show | 22 | HG00741.hp2 HG01109.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.1085-484G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46672359 | ||||||
| chr22:46672394
|
A | G | 28 | a0001c0001t0004g0061a0001c0001t0005g0001a0001c0001t0005g0039others(25): Show | 29 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1085-449A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46672394 | ||||||
| chr22:46672468
|
T | C | 25 | a0001c0001t0002g0266a0001c0001t0005g0001a0001c0001t0005g0039others(22): Show | 26 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.1085-375T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 13/18 | chr22 | 46672468 | ||||||
| chr22:46673025
|
G | C | 1 | a0001c0001t0048g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1239+28G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 14/18 | chr22 | 46673025 | ||||||
| chr22:46673032
|
TG | T | 88 | a0001c0001t0001g0005a0001c0001t0001g0080a0001c0001t0001g0098others(85): Show | 89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.1239+41delG | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr22 | 46673032 | |||||
| chr22:46673038
|
G | T | 88 | a0001c0001t0001g0005a0001c0001t0001g0080a0001c0001t0001g0098others(85): Show | 89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.1239+41G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 14/18 | chr22 | 46673038 | ||||||
| chr22:46673129
|
C | A | 20 | a0001c0001t0005g0001a0001c0001t0005g0039a0001c0001t0005g0040others(17): Show | 21 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1239+132C>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 14/18 | chr22 | 46673129 | ||||||
| chr22:46673130
|
T | TA | 20 | a0001c0001t0005g0001a0001c0001t0005g0039a0001c0001t0005g0040others(17): Show | 21 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1239+133_1239+134i others(3): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 14/18 | chr22 | 46673130 | ||||||
| chr22:46673136
|
G | GT | 6 | a0001c0001t0001g0074a0001c0001t0001g0120a0001c0001t0001g0131others(3): Show | 6 | HG01257.hp1 HG01981.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.1239+149dupT | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr22 | 46673136 | |||||
| chr22:46673137
|
T | G | 18 | a0001c0001t0005g0001a0001c0001t0005g0039a0001c0001t0005g0041others(15): Show | 19 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.1239+140T>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 14/18 | chr22 | 46673137 | ||||||
| chr22:46673304
|
G | A | 21 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0083others(18): Show | 21 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1239+307G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 14/18 | chr22 | 46673304 | ||||||
| chr22:46673326
|
A | G | 93 | a0001c0001t0001g0072a0001c0001t0001g0115a0001c0001t0001g0116others(90): Show | 94 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.1239+329A>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 14/18 | chr22 | 46673326 | ||||||
| chr22:46673422
|
G | C | 1 | a0001c0001t0002g0264 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1240-248G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 14/18 | chr22 | 46673422 | ||||||
| chr22:46673439
|
C | G | 6 | a0001c0001t0002g0259a0001c0001t0002g0266a0001c0001t0002g0267others(3): Show | 6 | HG00735.hp1 HG01109.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240-231C>G | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 14/18 | chr22 | 46673439 | ||||||
| chr22:46673451
|
C | T | 3 | a0001c0001t0005g0111a0001c0001t0005g0143a0001c0001t0050g0147 | 3 | HG02735.hp1 HG03688.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1240-219C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 14/18 | chr22 | 46673451 | ||||||
| chr22:46673452
|
G | A | 10 | a0001c0001t0007g0022a0001c0001t0007g0023a0001c0001t0007g0024others(7): Show | 10 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1240-218G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 14/18 | chr22 | 46673452 | ||||||
| chr22:46673874
|
G | A | 3 | a0001c0001t0006g0192a0001c0001t0006g0194a0001c0007t0019g0182 | 3 | HG00438.hp2 HG02015.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1384+60G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46673874 | ||||||
| chr22:46673896
|
C | T | 1 | a0001c0001t0019g0062 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1384+82C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46673896 | ||||||
| chr22:46673943
|
C | T | 1 | a0001c0001t0022g0138 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1384+129C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46673943 | ||||||
| chr22:46673994
|
C | T | 1 | a0001c0001t0005g0213 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1384+180C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46673994 | ||||||
| chr22:46674003
|
G | C | 2 | a0001c0001t0001g0005a0001c0001t0012g0005 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1384+189G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46674003 | ||||||
| chr22:46674015
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1384+201G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46674015 | ||||||
| chr22:46674065
|
G | T | 3 | a0001c0001t0007g0024a0001c0001t0007g0025a0001c0001t0007g0029 | 3 | HG02451.hp2 HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1384+251G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46674065 | ||||||
| chr22:46674093
|
C | T | 5 | a0001c0001t0002g0285a0001c0001t0002g0320a0001c0001t0026g0292others(2): Show | 5 | NA18970.hp1 NA18980.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.1384+279C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46674093 | ||||||
| chr22:46674108
|
G | A | 2 | a0001c0001t0015g0189a0001c0001t0015g0190 | 2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1384+294G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46674108 | ||||||
| chr22:46674121
|
G | A | 23 | a0001c0001t0005g0001a0001c0001t0005g0039a0001c0001t0005g0040others(20): Show | 24 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1384+307G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46674121 | ||||||
| chr22:46674182
|
A | C | 1 | a0001c0001t0005g0142 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1384+368A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46674182 | ||||||
| chr22:46674305
|
C | T | 1 | a0001c0001t0014g0058 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1385-352C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46674305 | ||||||
| chr22:46674327
|
C | T | 2 | a0001c0001t0030g0044a0001c0001t0048g0191 | 2 | HG01433.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1385-330C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46674327 | ||||||
| chr22:46674349
|
C | T | 1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1385-308C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46674349 | ||||||
| chr22:46674511
|
C | T | 1 | a0001c0001t0003g0223 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1385-146C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46674511 | ||||||
| chr22:46674516
|
C | T | 1 | a0001c0001t0008g0009 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1385-141C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46674516 | ||||||
| chr22:46674535
|
G | C | 84 | a0001c0001t0002g0007a0001c0001t0002g0081a0001c0001t0002g0100others(81): Show | 85 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1385-122G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46674535 | ||||||
| chr22:46674551
|
G | A | 1 | a0001c0001t0002g0298 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1385-106G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46674551 | ||||||
| chr22:46674563
|
C | T | 21 | a0001c0001t0004g0061a0001c0001t0004g0295a0001c0002t0004g0002others(18): Show | 22 | HG01109.hp1 HG01361.hp2 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.1385-94C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46674563 | ||||||
| chr22:46674653
|
T | A | 1 | a0001c0001t0011g0057 | 1 | NA19043.hp1 | splice_region_variant&intron_variant | LOW | c.1385-4T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 15/18 | chr22 | 46674653 | ||||||
| chr22:46674850
|
G | T | 52 | a0001c0001t0003g0006a0001c0001t0003g0030a0001c0001t0003g0031others(49): Show | 52 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.1478+100G>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 16/18 | chr22 | 46674850 | ||||||
| chr22:46674856
|
T | A | 1 | a0001c0002t0004g0069 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1478+106T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 16/18 | chr22 | 46674856 | ||||||
| chr22:46675013
|
C | T | 2 | a0001c0001t0019g0062a0001c0007t0019g0182 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1478+263C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 16/18 | chr22 | 46675013 | ||||||
| chr22:46675113
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1479-355G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 16/18 | chr22 | 46675113 | ||||||
| chr22:46675153
|
GCAGAGCA others(20): Show |
G | 1 | a0001c0001t0005g0145 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1479-289_1479-263d others(29): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr22 | 46675153 | |||||
| chr22:46675262
|
TGTGA | T | 33 | a0001c0001t0003g0243a0001c0001t0004g0021a0001c0001t0004g0061others(30): Show | 34 | HG01109.hp1 HG01361.hp2 HG01496.hp2 others(31): Show |
intron_variant | MODIFIER | c.1479-202_1479-199d others(6): Show |
GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr22 | 46675262 | |||||
| chr22:46675343
|
G | C | 5 | a0001c0001t0011g0057a0001c0001t0011g0183a0001c0001t0011g0184others(2): Show | 5 | HG02723.hp2 HG03041.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1479-125G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 16/18 | chr22 | 46675343 | ||||||
| chr22:46675444
|
C | T | 2 | a0001c0001t0003g0218a0001c0001t0003g0242 | 2 | HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1479-24C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 16/18 | chr22 | 46675444 | ||||||
| chr22:46675570
|
C | T | 3 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254 | 3 | HG01256.hp2 HG01258.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1563+18C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 17/18 | chr22 | 46675570 | ||||||
| chr22:46675615
|
C | T | 2 | a0001c0001t0019g0062a0001c0007t0019g0182 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1563+63C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 17/18 | chr22 | 46675615 | ||||||
| chr22:46675634
|
T | C | 106 | a0001c0001t0002g0007a0001c0001t0002g0081a0001c0001t0002g0100others(103): Show | 107 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.1563+82T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 17/18 | chr22 | 46675634 | ||||||
| chr22:46675741
|
G | C | 23 | a0001c0001t0005g0001a0001c0001t0005g0039a0001c0001t0005g0040others(20): Show | 24 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1563+189G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 17/18 | chr22 | 46675741 | ||||||
| chr22:46675839
|
G | A | 1 | a0001c0001t0002g0310 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1563+287G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 17/18 | chr22 | 46675839 | ||||||
| chr22:46675963
|
A | C | 136 | a0001c0001t0002g0007a0001c0001t0002g0081a0001c0001t0002g0100others(133): Show | 138 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.1563+411A>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 17/18 | chr22 | 46675963 | ||||||
| chr22:46676159
|
T | A | 1 | a0001c0001t0019g0062 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1564-441T>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 17/18 | chr22 | 46676159 | ||||||
| chr22:46676173
|
C | T | 89 | a0001c0001t0002g0007a0001c0001t0002g0081a0001c0001t0002g0100others(86): Show | 90 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1564-427C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 17/18 | chr22 | 46676173 | ||||||
| chr22:46676276
|
C | T | 2 | a0001c0003t0003g0235a0001c0003t0003g0236 | 2 | HG02109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1564-324C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 17/18 | chr22 | 46676276 | ||||||
| chr22:46676299
|
C | T | 11 | a0001c0001t0007g0022a0001c0001t0007g0023a0001c0001t0007g0024others(8): Show | 11 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1564-301C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 17/18 | chr22 | 46676299 | ||||||
| chr22:46676423
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1564-177G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 17/18 | chr22 | 46676423 | ||||||
| chr22:46676423
|
G | C | 1 | a0001c0007t0019g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1564-177G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 17/18 | chr22 | 46676423 | ||||||
| chr22:46676580
|
G | A | 122 | a0001c0001t0001g0115a0001c0001t0001g0139a0001c0001t0001g0255others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.1564-20G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 17/18 | chr22 | 46676580 | ||||||
| chr22:46676716
|
G | C | 1 | a0001c0001t0019g0062 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1632+48G>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 18/18 | chr22 | 46676716 | ||||||
| chr22:46676723
|
T | C | 32 | a0001c0001t0004g0021a0001c0001t0004g0061a0001c0001t0004g0233others(29): Show | 33 | HG01109.hp1 HG01361.hp2 HG01496.hp2 others(30): Show |
intron_variant | MODIFIER | c.1632+55T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 18/18 | chr22 | 46676723 | ||||||
| chr22:46676741
|
C | T | 1 | a0001c0001t0005g0143 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1632+73C>T | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 18/18 | chr22 | 46676741 | ||||||
| chr22:46676823
|
G | A | 2 | a0001c0001t0019g0062a0001c0007t0019g0182 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1632+155G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 18/18 | chr22 | 46676823 | ||||||
| chr22:46676830
|
G | A | 11 | a0001c0001t0007g0022a0001c0001t0007g0023a0001c0001t0007g0024others(8): Show | 11 | HG00642.hp2 HG01070.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1632+162G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 18/18 | chr22 | 46676830 | ||||||
| chr22:46676873
|
G | A | 2 | a0001c0001t0001g0129a0001c0001t0001g0132 | 2 | HG02148.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1632+205G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 18/18 | chr22 | 46676873 | ||||||
| chr22:46676889
|
T | C | 9 | a0001c0001t0009g0049a0001c0001t0011g0057a0001c0001t0011g0183others(6): Show | 9 | HG02145.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1632+221T>C | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 18/18 | chr22 | 46676889 | ||||||
| chr22:46676890
|
G | A | 1 | a0001c0001t0038g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1632+222G>A | GRAMD4 | ENSG00000075240.17 | transcript | ENST00000406902.6 | protein_coding | 18/18 | chr22 | 46676890 |