| geneid | 65983 |
|---|---|
| ensemblid | ENSG00000155324.10 |
| hgncid | 24911 |
| symbol | GRAMD2B |
| name | GRAM domain containing 2B |
| refseq_nuc | NM_023927.4 |
| refseq_prot | NP_076416.2 |
| ensembl_nuc | ENST00000285689.8 |
| ensembl_prot | ENSP00000285689.3 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 126423409 |
| end | 126494364 |
| strand | + |
| ver | v1.2 |
| region | chr5:126423409-126494364 |
| region5000 | chr5:126418409-126499364 |
| regionname0 | GRAMD2B_chr5_126423409_126494364 |
| regionname5000 | GRAMD2B_chr5_126418409_126499364 |
| 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 | 432 | 331 | 90 | 71 | 116 | 18 | 34 | 76 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| a0002 | 0/0 | 432 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| a0003 | 0/0 | 432 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1299 | 326 | 86 | 71 | 115 | 18 | 34 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| c0002 | 0/0 | 1299 | 3 | 3 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| c0003 | 0/0 | 1299 | 2 | 2 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| c0004 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| c0005 | 0/0 | 1299 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| c0006 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| 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 | 0/1 | 1607 | 187 | 38 | 23 | 94 | 9 | 22 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| t0002 | 1/0 | 1607 | 56 | 12 | 23 | 9 | 5 | 6 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| t0003 | 0/0 | 1608 | 51 | 16 | 17 | 10 | 4 | 4 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| t0004 | 0/0 | 1607 | 11 | 10 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| t0005 | 0/0 | 1607 | 8 | 4 | 3 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| t0006 | 0/0 | 1607 | 4 | 4 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| t0007 | 0/0 | 1608 | 3 | 3 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| t0008 | 0/0 | 1607 | 2 | 2 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| t0009 | 0/0 | 1608 | 2 | 0 | 2 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| t0010 | 0/0 | 1607 | 2 | 0 | 0 | 2 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| t0011 | 0/0 | 1607 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| t0012 | 0/0 | 1607 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| t0013 | 0/0 | 1607 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| t0014 | 0/0 | 1607 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| t0015 | 0/0 | 1607 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| t0016 | 0/0 | 1607 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| t0017 | 0/0 | 1607 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| t0018 | 0/0 | 1575 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0013 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0173 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1299 | 326 | 86 | 71 | 115 | 18 | 34 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| a0001c0002 | 0/0 | 1299 | 3 | 3 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| a0001c0004 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| a0001c0006 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| a0002c0003 | 0/0 | 1299 | 2 | 2 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| a0003c0005 | 0/0 | 1299 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2905 | 181 | 33 | 23 | 93 | 9 | 22 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| a0001c0001t0002 | 1/0 | 2905 | 55 | 12 | 22 | 9 | 5 | 6 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| a0001c0001t0003 | 0/0 | 2906 | 50 | 15 | 17 | 10 | 4 | 4 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| a0001c0001t0004 | 0/0 | 2905 | 11 | 10 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| a0001c0001t0005 | 0/0 | 2905 | 8 | 4 | 3 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| a0001c0001t0006 | 0/0 | 2905 | 4 | 4 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| a0001c0001t0007 | 0/0 | 2906 | 3 | 3 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| a0001c0001t0008 | 0/0 | 2905 | 2 | 2 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| a0001c0001t0009 | 0/0 | 2906 | 2 | 0 | 2 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| a0001c0001t0010 | 0/0 | 2905 | 2 | 0 | 0 | 2 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| a0001c0001t0011 | 0/0 | 2905 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| a0001c0001t0012 | 0/0 | 2905 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| a0001c0001t0013 | 0/0 | 2905 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| a0001c0001t0014 | 0/0 | 2905 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| a0001c0001t0015 | 0/0 | 2905 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| a0001c0001t0016 | 0/0 | 2905 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| a0001c0001t0017 | 0/0 | 2905 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| a0001c0001t0018 | 0/0 | 2873 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| a0001c0002t0001 | 0/0 | 2905 | 3 | 3 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| a0001c0004t0001 | 0/0 | 2905 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| a0001c0006t0001 | 0/0 | 2905 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| a0002c0003t0001 | 0/0 | 2905 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| a0002c0003t0003 | 0/0 | 2906 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| a0003c0005t0002 | 0/0 | 2905 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | copy fasta | chr5 | 126418409 | 126499364 |
| 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 | 2 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0013 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0173 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0005g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0005g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0005g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0005g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0005g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0006g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0006g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0006g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0007g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0007g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0007g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0008g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0008g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0009g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0010g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0010g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0011g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0012g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0013g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0014g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0015g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0016g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0017g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0001t0018g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0002t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0004t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0001c0006t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0002c0003t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0002c0003t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| a0003c0005t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0307 | EUR | GBR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0240 | EUR | GBR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0107 | EUR | GBR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0263 | EUR | GBR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0193 | EUR | FIN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | FIN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0077 | EUR | FIN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0097 | EUR | FIN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0226 | EAS | CHS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | CHS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | CHS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0086 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0267 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0270 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0315 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0108 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00738 | hp1 | a0001 | c0001 | t0009 | g0007 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00738 | hp2 | a0001 | c0001 | t0016 | g0026 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0192 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0085 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0238 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0237 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0306 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0073 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0189 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0159 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0310 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0095 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0190 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0312 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01192 | hp1 | a0001 | c0001 | t0009 | g0007 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01243 | hp2 | a0001 | c0001 | t0012 | g0024 | AMR | PUR | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0314 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0232 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0269 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0261 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0088 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0305 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | IBS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0313 | EUR | IBS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0015 | EUR | IBS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0079 | EUR | IBS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0014 | EUR | IBS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | IBS | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0252 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0316 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | PEL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0094 | AMR | PEL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PEL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PEL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PEL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0101 | AMR | PEL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01981 | hp2 | a0001 | c0001 | t0013 | g0053 | AMR | PEL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0255 | AMR | PEL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0142 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0320 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02074 | hp1 | a0001 | c0001 | t0010 | g0169 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02135 | hp1 | a0001 | c0006 | t0001 | g0059 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0113 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | CDX | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CDX | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CDX | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CDX | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02257 | hp2 | a0002 | c0003 | t0003 | g0284 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0168 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0259 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02273 | hp1 | a0003 | c0005 | t0002 | g0217 | AMR | PEL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PEL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | PEL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02451 | hp2 | a0001 | c0001 | t0017 | g0295 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0171 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0294 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0265 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0136 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0256 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0235 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0103 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0172 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0143 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0139 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0129 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02886 | hp2 | a0001 | c0004 | t0001 | g0293 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0140 | AFR | ESN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0304 | AFR | ESN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0163 | AFR | ESN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | ESN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ESN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | ESN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0115 | AFR | ESN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03041 | hp1 | a0001 | c0001 | t0015 | g0288 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0321 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | MSL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0141 | AFR | MSL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0102 | AFR | ESN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03139 | hp1 | a0001 | c0001 | t0011 | g0180 | AFR | ESN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | ESN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0322 | AFR | ESN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | ESN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | MSL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0178 | AFR | MSL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0268 | AFR | MSL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0299 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0279 | AFR | MSL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0162 | AFR | MSL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | MSL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | MSL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0233 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0023 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0181 | AFR | MSL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03654 | hp2 | a0001 | c0001 | t0005 | g0214 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | STU | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0042 | SAS | STU | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0229 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0118 | SAS | PJL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0111 | SAS | BEB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0224 | SAS | BEB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03942 | hp2 | a0001 | c0001 | t0014 | g0033 | SAS | BEB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | STU | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0318 | SAS | STU | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | STU | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | STU | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | STU | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0206 | SAS | STU | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0297 | AFR | YRI | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0022 | AFR | YRI | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | CHB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | YRI | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18906 | hp2 | a0002 | c0003 | t0001 | g0183 | AFR | YRI | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0302 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0326 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | LWK | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | LWK | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0234 | AFR | LWK | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0292 | AFR | LWK | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19066 | hp2 | a0001 | c0001 | t0010 | g0125 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19084 | hp2 | a0001 | c0001 | t0018 | g0199 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0254 | AFR | YRI | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0005 | AFR | YRI | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0130 | AFR | ASW | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ASW | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0081 | EUR | TSI | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0272 | EUR | TSI | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0308 | EUR | TSI | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0239 | EUR | TSI | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | GIH | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0324 | SAS | GIH | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0311 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | CLM | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0282 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0309 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0179 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | ACB | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0275 | AFR | MSL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0112 | AFR | USA | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | USA | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | USA | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | USA | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | LWK | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | LWK | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0013 | REF | REF | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0173 | REF | REF | GRAMD2B_chr5_126418409_126499364 | GRAMD2B | chr5 | 126418409 | 126499364 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:126485737
|
C | T | 1 | a0003 | 1 | HG02273.hp1 | missense_variant | MODERATE | c.1022C>T | p.Pro341Leu | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 11/14 | 1220/2905 | 1022/1299 | 341/432 | chr5 | 126485737 | ||
| chr5:126488806
|
G | A | 1 | a0002 | 2 | HG02257.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.1171G>A | p.Ala391Thr | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/14 | 1369/2905 | 1171/1299 | 391/432 | chr5 | 126488806 | ||
| chr5:126494364
|
A | G | 1 | a0001 | 11 | HG00642.hp1 HG02622.hp2 HG02809.hp2 others(8): Show |
splice_region_variant | LOW | c.*1408A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 14/14 | chr5 | 126494364 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:126477712
|
G | A | 1 | a0001c0004 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.507G>A | p.Ser169Ser | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/14 | 705/2905 | 507/1299 | 169/432 | chr5 | 126477712 | ||
| chr5:126477730
|
A | G | 1 | a0001c0002 | 3 | HG02055.hp1 HG02976.hp1 HG03041.hp2 |
synonymous_variant | LOW | c.525A>G | p.Lys175Lys | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/14 | 723/2905 | 525/1299 | 175/432 | chr5 | 126477730 | ||
| chr5:126484424
|
A | G | 1 | a0001c0006 | 1 | HG02135.hp1 | synonymous_variant | LOW | c.870A>G | p.Gln290Gln | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/14 | 1068/2905 | 870/1299 | 290/432 | chr5 | 126484424 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:126423439
|
G | C | 1 | a0001c0001t0011 | 1 | HG03139.hp1 | 5_prime_UTR_variant | MODIFIER | c.-168G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/14 | 168 | chr5 | 126423439 | |||||
| chr5:126423478
|
TGGGCGGA others(26): Show |
T | 1 | a0001c0001t0018 | 1 | NA19084.hp2 | 5_prime_UTR_variant | MODIFIER | c.-128_-96delGGGCGGA others(26): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/14 | 96 | chr5 | 126423478 | |||||
| chr5:126423533
|
A | C | 1 | a0001c0001t0017 | 1 | HG02451.hp2 | 5_prime_UTR_variant | MODIFIER | c.-74A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/14 | 74 | chr5 | 126423533 | |||||
| chr5:126423537
|
A | G | 1 | a0001c0001t0016 | 1 | HG00738.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-70A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/14 | chr5 | 126423537 | ||||||
| chr5:126423553
|
C | A | 2 | a0001c0001t0008a0001c0001t0012 | 3 | HG01243.hp2 HG03540.hp1 NA18522.hp2 |
5_prime_UTR_variant | MODIFIER | c.-54C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/14 | 54 | chr5 | 126423553 | |||||
| chr5:126493111
|
A | G | 20 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(17): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(273): Show |
3_prime_UTR_variant | MODIFIER | c.*155A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 14/14 | 155 | chr5 | 126493111 | |||||
| chr5:126493231
|
C | T | 1 | a0001c0001t0010 | 2 | HG02074.hp1 NA19066.hp2 |
3_prime_UTR_variant | MODIFIER | c.*275C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 14/14 | 275 | chr5 | 126493231 | |||||
| chr5:126493337
|
C | T | 1 | a0001c0001t0013 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*381C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 14/14 | 381 | chr5 | 126493337 | |||||
| chr5:126493392
|
A | G | 1 | a0001c0001t0015 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*436A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 14/14 | 436 | chr5 | 126493392 | |||||
| chr5:126493429
|
C | T | 1 | a0001c0001t0005 | 8 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*473C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 14/14 | 473 | chr5 | 126493429 | |||||
| chr5:126493487
|
C | T | 2 | a0001c0001t0006a0001c0001t0012 | 5 | HG01243.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*531C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 14/14 | 531 | chr5 | 126493487 | |||||
| chr5:126493535
|
C | A | 1 | a0001c0001t0009 | 2 | HG00738.hp1 HG01192.hp1 |
3_prime_UTR_variant | MODIFIER | c.*579C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 14/14 | 579 | chr5 | 126493535 | |||||
| chr5:126493600
|
G | A | 1 | a0001c0001t0007 | 3 | HG02615.hp2 HG03225.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*644G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 14/14 | 644 | chr5 | 126493600 | |||||
| chr5:126493720
|
A | C | 1 | a0001c0001t0014 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*764A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 14/14 | 764 | chr5 | 126493720 | |||||
| chr5:126493738
|
T | G | 1 | a0001c0001t0014 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*782T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 14/14 | 782 | chr5 | 126493738 | |||||
| chr5:126493812
|
T | G | 2 | a0001c0001t0006a0001c0001t0012 | 5 | HG01243.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*856T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 14/14 | 856 | chr5 | 126493812 | |||||
| chr5:126494320
|
A | C | 1 | a0001c0001t0004 | 11 | HG00642.hp1 HG02622.hp2 HG02809.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1364A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 14/14 | 1364 | chr5 | 126494320 | |||||
| chr5:126494322
|
C | T | 1 | a0001c0001t0004 | 11 | HG00642.hp1 HG02622.hp2 HG02809.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1366C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 14/14 | 1366 | chr5 | 126494322 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:126423832
|
A | ACT | 111 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(108): Show | 115 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.83+154_83+155dupCT | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126423832 | |||||
| chr5:126424245
|
T | C | 48 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(45): Show | 48 | HG00280.hp2 HG00621.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.83+556T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126424245 | ||||||
| chr5:126424278
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.83+589T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126424278 | ||||||
| chr5:126424330
|
C | T | 35 | a0001c0001t0001g0114a0001c0001t0001g0296a0001c0001t0001g0298others(32): Show | 37 | HG00099.hp1 HG00733.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.83+641C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126424330 | ||||||
| chr5:126424350
|
CT | C | 10 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(7): Show | 11 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.83+662delT | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126424350 | ||||||
| chr5:126424472
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.83+783G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126424472 | ||||||
| chr5:126424474
|
T | C | 2 | a0001c0001t0001g0161a0001c0001t0004g0162 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.83+785T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126424474 | ||||||
| chr5:126424557
|
G | A | 3 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0012g0024 | 3 | HG01243.hp2 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.83+868G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126424557 | ||||||
| chr5:126424626
|
A | G | 3 | a0001c0001t0007g0294a0001c0001t0017g0295a0001c0004t0001g0293 | 3 | HG02451.hp2 HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.83+937A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126424626 | ||||||
| chr5:126424696
|
A | G | 277 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(274): Show | 282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.83+1007A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126424696 | ||||||
| chr5:126425030
|
T | A | 75 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0025others(72): Show | 76 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.83+1341T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126425030 | ||||||
| chr5:126425038
|
G | T | 9 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287others(6): Show | 9 | HG02257.hp2 HG02280.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.83+1349G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126425038 | ||||||
| chr5:126425087
|
A | C | 17 | a0001c0001t0001g0160a0001c0001t0001g0280a0001c0001t0001g0281others(14): Show | 17 | HG02109.hp1 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.83+1398A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126425087 | ||||||
| chr5:126425117
|
T | C | 1 | a0001c0001t0007g0112 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.83+1428T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126425117 | ||||||
| chr5:126425131
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.83+1442A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126425131 | ||||||
| chr5:126425348
|
C | T | 18 | a0001c0001t0001g0160a0001c0001t0001g0280a0001c0001t0001g0281others(15): Show | 18 | HG02109.hp1 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.83+1659C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126425348 | ||||||
| chr5:126425533
|
G | A | 74 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0025others(71): Show | 75 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.83+1844G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126425533 | ||||||
| chr5:126425543
|
G | A | 18 | a0001c0001t0001g0120a0001c0001t0001g0160a0001c0001t0001g0280others(15): Show | 18 | HG00621.hp1 HG02109.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.83+1854G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126425543 | ||||||
| chr5:126425875
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.83+2186G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126425875 | ||||||
| chr5:126425898
|
G | A | 1 | a0001c0001t0006g0235 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.83+2209G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126425898 | ||||||
| chr5:126425985
|
T | A | 271 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(268): Show | 277 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.83+2296T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126425985 | ||||||
| chr5:126426332
|
A | G | 13 | a0001c0001t0001g0120a0001c0001t0001g0160a0001c0001t0001g0273others(10): Show | 14 | HG00621.hp1 HG02109.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.83+2643A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126426332 | ||||||
| chr5:126426455
|
C | T | 4 | a0001c0001t0001g0283a0001c0001t0002g0282a0001c0001t0002g0292others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+2766C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126426455 | ||||||
| chr5:126426608
|
A | C | 14 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(11): Show | 15 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.83+2919A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126426608 | ||||||
| chr5:126426757
|
T | C | 158 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(155): Show | 162 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.83+3068T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126426757 | ||||||
| chr5:126426795
|
C | T | 11 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(8): Show | 12 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.83+3106C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126426795 | ||||||
| chr5:126426826
|
C | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.83+3137C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126426826 | ||||||
| chr5:126426880
|
C | T | 5 | a0001c0001t0003g0141a0001c0001t0003g0143a0001c0001t0008g0023others(2): Show | 5 | HG01243.hp2 HG02055.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.83+3191C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126426880 | ||||||
| chr5:126426933
|
A | T | 10 | a0001c0001t0001g0231a0001c0001t0001g0264a0001c0001t0001g0285others(7): Show | 10 | HG01255.hp2 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.83+3244A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126426933 | ||||||
| chr5:126426937
|
A | C | 1 | a0001c0001t0001g0228 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.83+3248A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126426937 | ||||||
| chr5:126426944
|
G | A | 1 | a0001c0001t0006g0235 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.83+3255G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126426944 | ||||||
| chr5:126427039
|
C | T | 1 | a0001c0001t0003g0227 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.83+3350C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126427039 | ||||||
| chr5:126427045
|
G | A | 112 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(109): Show | 114 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.83+3356G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126427045 | ||||||
| chr5:126427159
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0004g0162 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.83+3470C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126427159 | ||||||
| chr5:126427231
|
A | G | 80 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0031others(77): Show | 81 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.83+3542A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126427231 | ||||||
| chr5:126427387
|
G | GA | 177 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(174): Show | 182 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.83+3699dupA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126427387 | |||||
| chr5:126427437
|
C | T | 14 | a0001c0001t0001g0231a0001c0001t0001g0236a0001c0001t0001g0264others(11): Show | 14 | HG01069.hp1 HG01071.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.83+3748C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126427437 | ||||||
| chr5:126427498
|
A | G | 2 | a0001c0001t0007g0294a0001c0004t0001g0293 | 2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.83+3809A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126427498 | ||||||
| chr5:126427859
|
T | G | 2 | a0001c0001t0001g0032a0001c0001t0014g0033 | 2 | HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.83+4170T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126427859 | ||||||
| chr5:126428094
|
G | C | 2 | a0001c0001t0003g0144a0001c0001t0003g0145 | 2 | NA18940.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.83+4405G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126428094 | ||||||
| chr5:126428220
|
A | G | 3 | a0001c0001t0001g0323a0001c0001t0003g0159a0001c0001t0003g0233 | 3 | HG01106.hp2 HG02257.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.83+4531A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126428220 | ||||||
| chr5:126428447
|
G | T | 74 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0031others(71): Show | 75 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.83+4758G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126428447 | ||||||
| chr5:126428471
|
A | G | 79 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0031others(76): Show | 80 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.83+4782A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126428471 | ||||||
| chr5:126428482
|
T | G | 6 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0283others(3): Show | 6 | HG02109.hp1 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.83+4793T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126428482 | ||||||
| chr5:126428729
|
G | T | 47 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(44): Show | 49 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.83+5040G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126428729 | ||||||
| chr5:126428810
|
G | A | 148 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(145): Show | 151 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.83+5121G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126428810 | ||||||
| chr5:126428815
|
G | A | 56 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(53): Show | 58 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.83+5126G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126428815 | ||||||
| chr5:126428911
|
A | G | 3 | a0001c0001t0001g0236a0001c0001t0003g0237a0001c0001t0003g0238 | 3 | HG01069.hp1 HG01071.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.83+5222A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126428911 | ||||||
| chr5:126428934
|
T | C | 1 | a0001c0001t0001g0273 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.83+5245T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126428934 | ||||||
| chr5:126428936
|
C | G | 135 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(132): Show | 138 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.83+5247C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126428936 | ||||||
| chr5:126428959
|
C | T | 1 | a0001c0001t0003g0097 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.83+5270C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126428959 | ||||||
| chr5:126429078
|
A | T | 3 | a0001c0001t0001g0105a0001c0001t0001g0271a0001c0001t0003g0326 | 3 | HG02155.hp1 NA18973.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.83+5389A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126429078 | ||||||
| chr5:126429119
|
A | G | 1 | a0001c0001t0008g0022 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.83+5430A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126429119 | ||||||
| chr5:126429286
|
A | C | 15 | a0001c0001t0001g0119a0001c0001t0001g0277a0001c0001t0001g0289others(12): Show | 16 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.83+5597A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126429286 | ||||||
| chr5:126429333
|
T | G | 3 | a0001c0001t0001g0236a0001c0001t0003g0237a0001c0001t0003g0238 | 3 | HG01069.hp1 HG01071.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.83+5644T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126429333 | ||||||
| chr5:126429506
|
A | G | 22 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0016others(19): Show | 23 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.83+5817A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126429506 | ||||||
| chr5:126429647
|
T | C | 3 | a0001c0001t0001g0236a0001c0001t0003g0237a0001c0001t0003g0238 | 3 | HG01069.hp1 HG01071.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.83+5958T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126429647 | ||||||
| chr5:126429726
|
C | T | 7 | a0001c0001t0001g0160a0001c0001t0001g0280a0001c0001t0001g0281others(4): Show | 7 | HG02280.hp2 HG02970.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.83+6037C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126429726 | ||||||
| chr5:126429906
|
A | C | 2 | a0001c0001t0003g0163a0001c0001t0006g0005 | 3 | HG02896.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.83+6217A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126429906 | ||||||
| chr5:126430031
|
C | G | 1 | a0001c0001t0002g0004 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.83+6342C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126430031 | ||||||
| chr5:126430203
|
G | A | 65 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0032others(62): Show | 66 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.83+6514G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126430203 | ||||||
| chr5:126430342
|
G | A | 1 | a0001c0001t0001g0239 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.83+6653G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126430342 | ||||||
| chr5:126430487
|
T | G | 199 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(196): Show | 205 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.83+6798T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126430487 | ||||||
| chr5:126430656
|
C | T | 158 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(155): Show | 163 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.83+6967C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126430656 | ||||||
| chr5:126430665
|
C | A | 47 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(44): Show | 48 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.83+6976C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126430665 | ||||||
| chr5:126430671
|
A | G | 1 | a0001c0001t0003g0322 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.83+6982A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126430671 | ||||||
| chr5:126430722
|
G | A | 5 | a0001c0001t0001g0116a0001c0001t0001g0124a0001c0001t0001g0126others(2): Show | 5 | HG00621.hp2 HG02056.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.83+7033G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126430722 | ||||||
| chr5:126430729
|
A | C | 1 | a0001c0001t0001g0029 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.83+7040A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126430729 | ||||||
| chr5:126430738
|
G | A | 10 | a0001c0001t0001g0117a0001c0001t0001g0182a0001c0001t0001g0283others(7): Show | 10 | HG02109.hp1 HG02486.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.83+7049G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126430738 | ||||||
| chr5:126430741
|
T | A | 10 | a0001c0001t0001g0117a0001c0001t0001g0182a0001c0001t0001g0283others(7): Show | 10 | HG02109.hp1 HG02486.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.83+7052T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126430741 | ||||||
| chr5:126430803
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.83+7114T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126430803 | ||||||
| chr5:126430925
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.83+7236T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126430925 | ||||||
| chr5:126431051
|
C | T | 10 | a0001c0001t0001g0117a0001c0001t0001g0182a0001c0001t0001g0283others(7): Show | 10 | HG02109.hp1 HG02486.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.83+7362C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126431051 | ||||||
| chr5:126431108
|
C | G | 10 | a0001c0001t0001g0117a0001c0001t0001g0182a0001c0001t0001g0283others(7): Show | 10 | HG02109.hp1 HG02486.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.83+7419C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126431108 | ||||||
| chr5:126431133
|
C | A | 1 | a0001c0001t0007g0294 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.83+7444C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126431133 | ||||||
| chr5:126431134
|
G | T | 1 | a0001c0001t0001g0319 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.83+7445G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126431134 | ||||||
| chr5:126431424
|
T | C | 82 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0016others(79): Show | 86 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.83+7735T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126431424 | ||||||
| chr5:126431432
|
T | C | 2 | a0001c0001t0003g0163a0001c0001t0006g0005 | 3 | HG02896.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.83+7743T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126431432 | ||||||
| chr5:126431494
|
C | T | 17 | a0001c0001t0001g0231a0001c0001t0001g0264a0001c0001t0001g0266others(14): Show | 17 | HG00639.hp2 HG00642.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.83+7805C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126431494 | ||||||
| chr5:126431553
|
C | G | 10 | a0001c0001t0001g0117a0001c0001t0001g0182a0001c0001t0001g0283others(7): Show | 10 | HG02109.hp1 HG02486.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.83+7864C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126431553 | ||||||
| chr5:126431603
|
A | G | 1 | a0001c0001t0007g0294 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.83+7914A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126431603 | ||||||
| chr5:126431623
|
G | A | 2 | a0001c0001t0001g0283a0001c0001t0002g0282 | 2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.83+7934G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126431623 | ||||||
| chr5:126431773
|
G | GA | 50 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(47): Show | 52 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.83+8092dupA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126431773 | |||||
| chr5:126431913
|
C | T | 1 | a0001c0001t0003g0297 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.83+8224C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126431913 | ||||||
| chr5:126432089
|
T | C | 4 | a0001c0001t0001g0128a0001c0001t0002g0131a0001c0001t0004g0129others(1): Show | 4 | HG02886.hp1 HG02976.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.83+8400T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126432089 | ||||||
| chr5:126432129
|
A | G | 2 | a0001c0001t0001g0176a0001c0001t0005g0140 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.83+8440A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126432129 | ||||||
| chr5:126432156
|
T | G | 98 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0031others(95): Show | 102 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.83+8467T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126432156 | ||||||
| chr5:126432221
|
A | G | 201 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(198): Show | 208 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.83+8532A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126432221 | ||||||
| chr5:126432328
|
C | T | 95 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0031others(92): Show | 97 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.83+8639C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126432328 | ||||||
| chr5:126432559
|
C | T | 48 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(45): Show | 50 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.83+8870C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126432559 | ||||||
| chr5:126432608
|
T | G | 1 | a0001c0001t0003g0185 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.83+8919T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126432608 | ||||||
| chr5:126432715
|
C | T | 2 | a0001c0001t0001g0176a0001c0001t0005g0140 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.83+9026C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126432715 | ||||||
| chr5:126432775
|
G | T | 2 | a0001c0001t0001g0176a0001c0001t0005g0140 | 2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.83+9086G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126432775 | ||||||
| chr5:126432790
|
A | G | 1 | a0001c0001t0003g0103 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.83+9101A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126432790 | ||||||
| chr5:126432808
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.83+9119G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126432808 | ||||||
| chr5:126432838
|
A | G | 49 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(46): Show | 51 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.83+9149A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126432838 | ||||||
| chr5:126433084
|
G | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG00280.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.83+9395G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126433084 | ||||||
| chr5:126433104
|
T | C | 3 | a0001c0001t0001g0013a0001c0001t0003g0014a0001c0001t0003g0015 | 3 | HG01516.hp1 HG01517.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.83+9415T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126433104 | ||||||
| chr5:126433207
|
G | A | 49 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(46): Show | 51 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.83+9518G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126433207 | ||||||
| chr5:126433358
|
A | G | 11 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(8): Show | 12 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.83+9669A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126433358 | ||||||
| chr5:126433423
|
C | T | 1 | a0001c0001t0001g0325 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.83+9734C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126433423 | ||||||
| chr5:126433468
|
G | A | 185 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(182): Show | 190 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.83+9779G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126433468 | ||||||
| chr5:126433685
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.83+9996C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126433685 | ||||||
| chr5:126433987
|
C | T | 193 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(190): Show | 199 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.83+10298C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126433987 | ||||||
| chr5:126434066
|
A | G | 1 | a0001c0001t0002g0123 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.83+10377A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126434066 | ||||||
| chr5:126434284
|
T | A | 188 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(185): Show | 193 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.83+10595T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126434284 | ||||||
| chr5:126434287
|
A | G | 4 | a0001c0001t0003g0101a0001c0001t0004g0270a0001c0001t0005g0269others(1): Show | 4 | HG00642.hp1 HG01257.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.83+10598A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126434287 | ||||||
| chr5:126434377
|
A | G | 7 | a0001c0001t0001g0274a0001c0001t0002g0292a0001c0001t0003g0101others(4): Show | 7 | HG00642.hp1 HG01257.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.83+10688A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126434377 | ||||||
| chr5:126434386
|
T | C | 1 | a0001c0001t0001g0298 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.83+10697T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126434386 | ||||||
| chr5:126434387
|
A | G | 3 | a0001c0001t0001g0301a0001c0001t0002g0164a0001c0001t0002g0165 | 3 | HG00642.hp2 HG01070.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.83+10698A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126434387 | ||||||
| chr5:126434424
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.83+10735A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126434424 | ||||||
| chr5:126434492
|
C | T | 47 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(44): Show | 49 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.83+10803C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126434492 | ||||||
| chr5:126434508
|
T | TTTTTTA | 20 | a0001c0001t0001g0117a0001c0001t0001g0231a0001c0001t0001g0264others(17): Show | 20 | HG01255.hp2 HG02109.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.83+10837_83+10842d others(8): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126434508 | |||||
| chr5:126434531
|
T | G | 2 | a0001c0001t0001g0135a0001c0001t0005g0136 | 2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.83+10842T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126434531 | ||||||
| chr5:126434626
|
A | T | 7 | a0001c0001t0001g0266a0001c0001t0002g0267a0001c0001t0002g0268others(4): Show | 7 | HG00639.hp2 HG00642.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.83+10937A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126434626 | ||||||
| chr5:126434731
|
A | G | 14 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(11): Show | 15 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.83+11042A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126434731 | ||||||
| chr5:126434807
|
G | A | 33 | a0001c0001t0001g0010a0001c0001t0001g0128a0001c0001t0001g0135others(30): Show | 33 | HG00639.hp2 HG00642.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.83+11118G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126434807 | ||||||
| chr5:126435141
|
G | T | 54 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(51): Show | 57 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.83+11452G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126435141 | ||||||
| chr5:126435260
|
T | G | 1 | a0001c0001t0004g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.83+11571T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126435260 | ||||||
| chr5:126435506
|
C | T | 5 | a0001c0001t0001g0116a0001c0001t0001g0126a0001c0001t0001g0127others(2): Show | 5 | HG00621.hp2 NA18965.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.83+11817C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126435506 | ||||||
| chr5:126435547
|
C | G | 54 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(51): Show | 57 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.83+11858C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126435547 | ||||||
| chr5:126435623
|
T | C | 1 | a0001c0001t0007g0294 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.83+11934T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126435623 | ||||||
| chr5:126435811
|
C | G | 25 | a0001c0001t0001g0010a0001c0001t0001g0128a0001c0001t0001g0135others(22): Show | 25 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.83+12122C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126435811 | ||||||
| chr5:126435813
|
T | C | 22 | a0001c0001t0001g0119a0001c0001t0001g0277a0001c0001t0001g0285others(19): Show | 24 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.83+12124T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126435813 | ||||||
| chr5:126435922
|
G | C | 43 | a0001c0001t0001g0117a0001c0001t0001g0119a0001c0001t0001g0231others(40): Show | 45 | HG01243.hp2 HG01255.hp2 HG02055.hp1 others(42): Show |
intron_variant | MODIFIER | c.83+12233G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126435922 | ||||||
| chr5:126435947
|
C | A | 1 | a0001c0001t0003g0279 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.83+12258C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126435947 | ||||||
| chr5:126435989
|
T | C | 14 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(11): Show | 15 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.83+12300T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126435989 | ||||||
| chr5:126436070
|
A | G | 1 | a0001c0001t0001g0251 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.83+12381A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126436070 | ||||||
| chr5:126436153
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.83+12464A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126436153 | ||||||
| chr5:126436190
|
A | G | 9 | a0001c0001t0001g0266a0001c0001t0002g0267a0001c0001t0002g0268others(6): Show | 9 | HG00639.hp2 HG00642.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.83+12501A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126436190 | ||||||
| chr5:126436358
|
A | T | 1 | a0001c0001t0001g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.83+12669A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126436358 | ||||||
| chr5:126436459
|
G | A | 2 | a0001c0001t0002g0075a0001c0001t0002g0076 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.83+12770G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126436459 | ||||||
| chr5:126436601
|
C | G | 5 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.83+12912C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126436601 | ||||||
| chr5:126437015
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.83+13326G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126437015 | ||||||
| chr5:126437016
|
C | G | 1 | a0001c0001t0001g0186 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.83+13327C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126437016 | ||||||
| chr5:126437146
|
G | A | 11 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0191others(8): Show | 11 | HG00280.hp1 HG00558.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.83+13457G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126437146 | ||||||
| chr5:126437309
|
G | A | 8 | a0001c0001t0001g0266a0001c0001t0002g0267a0001c0001t0002g0268others(5): Show | 8 | HG00639.hp2 HG00642.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.83+13620G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126437309 | ||||||
| chr5:126437313
|
T | C | 1 | a0001c0001t0003g0326 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.83+13624T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126437313 | ||||||
| chr5:126437317
|
T | C | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | HG01256.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.83+13628T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126437317 | ||||||
| chr5:126437325
|
G | A | 1 | a0001c0001t0003g0252 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.83+13636G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126437325 | ||||||
| chr5:126437472
|
A | T | 48 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(45): Show | 50 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.83+13783A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126437472 | ||||||
| chr5:126437639
|
A | C | 211 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0012others(208): Show | 217 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.83+13950A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126437639 | ||||||
| chr5:126437641
|
C | T | 8 | a0001c0001t0001g0266a0001c0001t0002g0267a0001c0001t0002g0268others(5): Show | 8 | HG00639.hp2 HG00642.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.83+13952C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126437641 | ||||||
| chr5:126437696
|
A | T | 9 | a0001c0001t0001g0266a0001c0001t0002g0267a0001c0001t0002g0268others(6): Show | 9 | HG00639.hp2 HG00642.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.83+14007A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126437696 | ||||||
| chr5:126437763
|
G | C | 3 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0325 | 3 | NA18965.hp1 NA18995.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.83+14074G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126437763 | ||||||
| chr5:126437817
|
C | G | 29 | a0001c0001t0001g0010a0001c0001t0001g0128a0001c0001t0001g0135others(26): Show | 30 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.83+14128C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126437817 | ||||||
| chr5:126437878
|
G | A | 51 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(48): Show | 53 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.83+14189G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126437878 | ||||||
| chr5:126438463
|
G | A | 64 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0032others(61): Show | 65 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.83+14774G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126438463 | ||||||
| chr5:126438780
|
T | C | 1 | a0001c0001t0001g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.83+15091T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126438780 | ||||||
| chr5:126438783
|
T | C | 13 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(10): Show | 14 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.83+15094T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126438783 | ||||||
| chr5:126438830
|
A | G | 89 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0016others(86): Show | 92 | HG00639.hp2 HG00642.hp1 HG01069.hp1 others(89): Show |
intron_variant | MODIFIER | c.83+15141A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126438830 | ||||||
| chr5:126439009
|
G | A | 13 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(10): Show | 14 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.83+15320G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126439009 | ||||||
| chr5:126439078
|
A | T | 2 | a0001c0001t0001g0278a0001c0001t0001g0281 | 2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.83+15389A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126439078 | ||||||
| chr5:126439328
|
C | CT | 15 | a0001c0001t0001g0011a0001c0001t0001g0070a0001c0001t0001g0264others(12): Show | 15 | HG00735.hp2 HG01109.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.83+15656dupT | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126439328 | |||||
| chr5:126439328
|
C | CTTTTT | 26 | a0001c0001t0001g0266a0001c0001t0001g0277a0001c0001t0001g0285others(23): Show | 27 | HG00639.hp2 HG00642.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.83+15652_83+15656d others(7): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126439328 | |||||
| chr5:126439328
|
C | CTTTTTT | 24 | a0001c0001t0001g0119a0001c0001t0001g0128a0001c0001t0001g0137others(21): Show | 24 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.83+15651_83+15656d others(8): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126439328 | |||||
| chr5:126439372
|
G | A | 4 | a0001c0001t0003g0101a0001c0001t0004g0270a0001c0001t0005g0269others(1): Show | 4 | HG00642.hp1 HG01257.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.83+15683G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126439372 | ||||||
| chr5:126439374
|
T | G | 1 | a0001c0001t0003g0073 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.83+15685T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126439374 | ||||||
| chr5:126439378
|
G | A | 2 | a0001c0001t0003g0163a0001c0001t0006g0005 | 3 | HG02896.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.83+15689G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126439378 | ||||||
| chr5:126439540
|
G | T | 1 | a0001c0001t0001g0149 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.83+15851G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126439540 | ||||||
| chr5:126439559
|
C | A | 1 | a0001c0001t0002g0195 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.83+15870C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126439559 | ||||||
| chr5:126439748
|
T | C | 89 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0016others(86): Show | 92 | HG00639.hp2 HG00642.hp1 HG01069.hp1 others(89): Show |
intron_variant | MODIFIER | c.83+16059T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126439748 | ||||||
| chr5:126439785
|
C | T | 20 | a0001c0001t0001g0119a0001c0001t0001g0277a0001c0001t0001g0285others(17): Show | 21 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.83+16096C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126439785 | ||||||
| chr5:126440058
|
T | C | 9 | a0001c0001t0001g0266a0001c0001t0002g0267a0001c0001t0002g0268others(6): Show | 9 | HG00639.hp2 HG00642.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.83+16369T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126440058 | ||||||
| chr5:126440244
|
G | A | 46 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(43): Show | 48 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.83+16555G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126440244 | ||||||
| chr5:126440270
|
T | C | 1 | a0001c0001t0002g0195 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.83+16581T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126440270 | ||||||
| chr5:126440376
|
T | C | 9 | a0001c0001t0001g0266a0001c0001t0002g0267a0001c0001t0002g0268others(6): Show | 9 | HG00639.hp2 HG00642.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.83+16687T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126440376 | ||||||
| chr5:126440483
|
T | C | 31 | a0001c0001t0001g0119a0001c0001t0001g0266a0001c0001t0001g0277others(28): Show | 33 | HG00639.hp2 HG00642.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.83+16794T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126440483 | ||||||
| chr5:126440494
|
A | AT | 2 | a0001c0001t0003g0163a0001c0001t0006g0005 | 3 | HG02896.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.83+16809dupT | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126440494 | |||||
| chr5:126440574
|
G | A | 2 | a0001c0001t0001g0278a0001c0001t0001g0281 | 2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.83+16885G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126440574 | ||||||
| chr5:126440596
|
CA | C | 8 | a0001c0001t0001g0231a0001c0001t0001g0264a0001c0001t0001g0274others(5): Show | 8 | HG01255.hp2 HG02451.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.83+16909delA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126440596 | |||||
| chr5:126440658
|
A | G | 4 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287others(1): Show | 4 | HG02257.hp2 HG02280.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+16969A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126440658 | ||||||
| chr5:126440660
|
T | C | 1 | a0002c0003t0003g0284 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.83+16971T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126440660 | ||||||
| chr5:126440733
|
A | C | 13 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(10): Show | 14 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.83+17044A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126440733 | ||||||
| chr5:126440735
|
T | C | 31 | a0001c0001t0001g0119a0001c0001t0001g0266a0001c0001t0001g0277others(28): Show | 33 | HG00639.hp2 HG00642.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.83+17046T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126440735 | ||||||
| chr5:126440766
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.83+17077A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126440766 | ||||||
| chr5:126440794
|
G | A | 46 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(43): Show | 48 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.83+17105G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126440794 | ||||||
| chr5:126440871
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0003g0014a0001c0001t0003g0015 | 3 | HG01516.hp1 HG01517.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.83+17182C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126440871 | ||||||
| chr5:126440930
|
A | G | 31 | a0001c0001t0001g0119a0001c0001t0001g0266a0001c0001t0001g0277others(28): Show | 33 | HG00639.hp2 HG00642.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.83+17241A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126440930 | ||||||
| chr5:126441115
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.83+17426G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126441115 | ||||||
| chr5:126441119
|
G | A | 5 | a0001c0001t0001g0231a0001c0001t0001g0264a0001c0001t0001g0296others(2): Show | 5 | HG01255.hp2 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.83+17430G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126441119 | ||||||
| chr5:126441670
|
A | G | 2 | a0001c0001t0001g0318a0001c0001t0003g0108 | 2 | HG00735.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.83+17981A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126441670 | ||||||
| chr5:126441795
|
C | T | 5 | a0001c0001t0001g0231a0001c0001t0001g0264a0001c0001t0001g0296others(2): Show | 5 | HG01255.hp2 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.83+18106C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126441795 | ||||||
| chr5:126441834
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.83+18145T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126441834 | ||||||
| chr5:126441884
|
T | C | 2 | a0001c0001t0002g0292a0001c0001t0017g0295 | 2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.83+18195T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126441884 | ||||||
| chr5:126441991
|
G | A | 1 | a0001c0001t0005g0269 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.83+18302G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126441991 | ||||||
| chr5:126442293
|
CT | C | 62 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(59): Show | 64 | HG00639.hp2 HG00642.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.83+18617delT | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126442293 | |||||
| chr5:126442321
|
C | A | 1 | a0001c0001t0006g0235 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.83+18632C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126442321 | ||||||
| chr5:126442400
|
C | T | 1 | a0002c0003t0001g0183 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.83+18711C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126442400 | ||||||
| chr5:126442437
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.83+18748G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126442437 | ||||||
| chr5:126442454
|
G | C | 1 | a0001c0001t0001g0128 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.83+18765G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126442454 | ||||||
| chr5:126442506
|
A | G | 2 | a0001c0001t0003g0163a0001c0001t0006g0005 | 3 | HG02896.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.83+18817A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126442506 | ||||||
| chr5:126442572
|
G | A | 1 | a0001c0001t0006g0256 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.83+18883G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126442572 | ||||||
| chr5:126442719
|
G | A | 4 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0200others(1): Show | 4 | NA18981.hp1 NA19072.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+19030G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126442719 | ||||||
| chr5:126442857
|
A | T | 9 | a0001c0001t0001g0266a0001c0001t0002g0267a0001c0001t0002g0268others(6): Show | 9 | HG00639.hp2 HG00642.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.83+19168A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126442857 | ||||||
| chr5:126442859
|
A | C | 1 | a0001c0001t0002g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.83+19170A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126442859 | ||||||
| chr5:126443002
|
C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0253a0001c0001t0003g0252others(1): Show | 4 | HG01884.hp1 HG02809.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+19313C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126443002 | ||||||
| chr5:126443096
|
G | A | 2 | a0001c0001t0001g0278a0001c0001t0001g0281 | 2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.83+19407G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126443096 | ||||||
| chr5:126443243
|
T | C | 64 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(61): Show | 67 | HG00639.hp2 HG00642.hp1 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.83+19554T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126443243 | ||||||
| chr5:126443263
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.83+19574G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126443263 | ||||||
| chr5:126443339
|
A | G | 15 | a0001c0001t0001g0119a0001c0001t0001g0277a0001c0001t0001g0289others(12): Show | 16 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.83+19650A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126443339 | ||||||
| chr5:126443417
|
T | G | 2 | a0001c0001t0001g0278a0001c0001t0001g0281 | 2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.83+19728T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126443417 | ||||||
| chr5:126443488
|
A | C | 48 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(45): Show | 50 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.83+19799A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126443488 | ||||||
| chr5:126443659
|
A | T | 2 | a0001c0001t0001g0278a0001c0001t0001g0281 | 2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.83+19970A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126443659 | ||||||
| chr5:126443663
|
C | T | 2 | a0001c0001t0001g0278a0001c0001t0001g0281 | 2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.83+19974C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126443663 | ||||||
| chr5:126443795
|
A | T | 48 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(45): Show | 51 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.83+20106A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126443795 | ||||||
| chr5:126443847
|
C | T | 2 | a0001c0001t0001g0278a0001c0001t0001g0281 | 2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.83+20158C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126443847 | ||||||
| chr5:126443953
|
G | A | 10 | a0001c0001t0001g0117a0001c0001t0001g0273a0001c0001t0001g0283others(7): Show | 10 | HG02109.hp1 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.83+20264G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126443953 | ||||||
| chr5:126443962
|
G | A | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.83+20273G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126443962 | ||||||
| chr5:126444072
|
G | T | 1 | a0001c0001t0003g0227 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.83+20383G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126444072 | ||||||
| chr5:126444173
|
T | C | 25 | a0001c0001t0001g0010a0001c0001t0001g0128a0001c0001t0001g0135others(22): Show | 25 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.83+20484T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126444173 | ||||||
| chr5:126444268
|
C | T | 1 | a0001c0001t0002g0232 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.83+20579C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126444268 | ||||||
| chr5:126444400
|
G | A | 11 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0001g0137others(8): Show | 11 | HG01884.hp2 HG02258.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.83+20711G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126444400 | ||||||
| chr5:126444422
|
T | C | 89 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0016others(86): Show | 92 | HG00639.hp2 HG00642.hp1 HG01069.hp1 others(89): Show |
intron_variant | MODIFIER | c.83+20733T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126444422 | ||||||
| chr5:126444440
|
T | G | 48 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(45): Show | 51 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.83+20751T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126444440 | ||||||
| chr5:126444493
|
T | C | 50 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(47): Show | 53 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.83+20804T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126444493 | ||||||
| chr5:126444758
|
G | A | 33 | a0001c0001t0001g0117a0001c0001t0001g0119a0001c0001t0001g0231others(30): Show | 34 | HG01243.hp2 HG01255.hp2 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.84-20668G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126444758 | ||||||
| chr5:126444760
|
C | T | 15 | a0001c0001t0001g0119a0001c0001t0001g0277a0001c0001t0001g0289others(12): Show | 16 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.84-20666C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126444760 | ||||||
| chr5:126444782
|
C | A | 33 | a0001c0001t0001g0117a0001c0001t0001g0119a0001c0001t0001g0231others(30): Show | 34 | HG01243.hp2 HG01255.hp2 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.84-20644C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126444782 | ||||||
| chr5:126444943
|
C | A | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | NA18954.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.84-20483C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126444943 | ||||||
| chr5:126444943
|
C | T | 1 | a0001c0001t0001g0317 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.84-20483C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126444943 | ||||||
| chr5:126444944
|
G | T | 1 | a0001c0001t0001g0096 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.84-20482G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126444944 | ||||||
| chr5:126444974
|
G | A | 2 | a0001c0001t0003g0163a0001c0001t0006g0005 | 3 | HG02896.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.84-20452G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126444974 | ||||||
| chr5:126444985
|
A | G | 8 | a0001c0001t0001g0231a0001c0001t0001g0264a0001c0001t0001g0274others(5): Show | 8 | HG01255.hp2 HG02451.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.84-20441A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126444985 | ||||||
| chr5:126445046
|
C | T | 1 | a0001c0001t0003g0143 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.84-20380C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126445046 | ||||||
| chr5:126445101
|
T | C | 48 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(45): Show | 51 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.84-20325T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126445101 | ||||||
| chr5:126445120
|
C | T | 1 | a0001c0001t0002g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.84-20306C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126445120 | ||||||
| chr5:126445227
|
T | A | 1 | a0001c0001t0007g0294 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.84-20199T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126445227 | ||||||
| chr5:126445268
|
G | T | 10 | a0001c0001t0001g0117a0001c0001t0001g0273a0001c0001t0001g0283others(7): Show | 10 | HG02109.hp1 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.84-20158G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126445268 | ||||||
| chr5:126445519
|
C | A | 1 | a0001c0001t0001g0105 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.84-19907C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126445519 | ||||||
| chr5:126445522
|
A | C | 54 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(51): Show | 57 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.84-19904A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126445522 | ||||||
| chr5:126445995
|
C | G | 109 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0031others(106): Show | 110 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.84-19431C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126445995 | ||||||
| chr5:126446062
|
C | T | 1 | a0001c0001t0007g0294 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.84-19364C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126446062 | ||||||
| chr5:126446136
|
T | A | 116 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0031others(113): Show | 117 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.84-19290T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126446136 | ||||||
| chr5:126446137
|
A | T | 15 | a0001c0001t0001g0119a0001c0001t0001g0277a0001c0001t0001g0289others(12): Show | 16 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.84-19289A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126446137 | ||||||
| chr5:126446195
|
C | T | 9 | a0001c0001t0001g0117a0001c0001t0001g0273a0001c0001t0001g0283others(6): Show | 9 | HG02109.hp1 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.84-19231C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126446195 | ||||||
| chr5:126446230
|
A | G | 13 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(10): Show | 14 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.84-19196A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126446230 | ||||||
| chr5:126446346
|
A | G | 48 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(45): Show | 51 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(48): Show |
intron_variant | MODIFIER | c.84-19080A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126446346 | ||||||
| chr5:126446433
|
C | A | 10 | a0001c0001t0001g0231a0001c0001t0001g0264a0001c0001t0001g0274others(7): Show | 11 | HG01255.hp2 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.84-18993C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126446433 | ||||||
| chr5:126446532
|
T | G | 2 | a0001c0001t0002g0074a0001c0001t0003g0073 | 2 | HG01074.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.84-18894T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126446532 | ||||||
| chr5:126446594
|
T | C | 317 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(314): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.84-18832T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126446594 | ||||||
| chr5:126446620
|
T | TA | 10 | a0001c0001t0001g0011a0001c0001t0001g0161a0001c0001t0001g0203others(7): Show | 10 | HG00438.hp1 HG01255.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.84-18786dupA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126446620 | |||||
| chr5:126446620
|
TA | T | 102 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0031others(99): Show | 103 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.84-18786delA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126446620 | |||||
| chr5:126446620
|
TAA | T | 46 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(43): Show | 48 | HG00639.hp2 HG00642.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.84-18787_84-18786d others(4): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126446620 | |||||
| chr5:126446620
|
TAAA | T | 44 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(41): Show | 46 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.84-18788_84-18786d others(5): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126446620 | |||||
| chr5:126446634
|
A | C | 2 | a0001c0001t0001g0117a0001c0001t0008g0022 | 2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.84-18792A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126446634 | ||||||
| chr5:126446724
|
G | A | 2 | a0001c0001t0001g0281a0001c0004t0001g0293 | 2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.84-18702G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126446724 | ||||||
| chr5:126446976
|
C | T | 1 | a0001c0001t0001g0182 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.84-18450C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126446976 | ||||||
| chr5:126447104
|
C | A | 24 | a0001c0001t0001g0119a0001c0001t0001g0231a0001c0001t0001g0264others(21): Show | 25 | HG01243.hp2 HG01255.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.84-18322C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447104 | ||||||
| chr5:126447166
|
G | A | 45 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(42): Show | 47 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.84-18260G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447166 | ||||||
| chr5:126447189
|
C | T | 9 | a0001c0001t0001g0117a0001c0001t0001g0273a0001c0001t0001g0283others(6): Show | 9 | HG02109.hp1 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.84-18237C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447189 | ||||||
| chr5:126447385
|
G | A | 47 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(44): Show | 49 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.84-18041G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447385 | ||||||
| chr5:126447453
|
A | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.84-17973A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447453 | ||||||
| chr5:126447458
|
T | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.84-17968T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447458 | ||||||
| chr5:126447478
|
C | T | 1 | a0001c0001t0002g0156 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.84-17948C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447478 | ||||||
| chr5:126447525
|
G | A | 125 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0031others(122): Show | 126 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.84-17901G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447525 | ||||||
| chr5:126447551
|
C | A | 59 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0016others(56): Show | 62 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.84-17875C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447551 | ||||||
| chr5:126447557
|
A | G | 1 | a0001c0001t0002g0107 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.84-17869A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447557 | ||||||
| chr5:126447613
|
G | A | 122 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0031others(119): Show | 123 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.84-17813G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447613 | ||||||
| chr5:126447630
|
C | G | 2 | a0001c0001t0002g0292a0001c0001t0017g0295 | 2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.84-17796C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447630 | ||||||
| chr5:126447642
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.84-17784C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447642 | ||||||
| chr5:126447650
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.84-17776C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447650 | ||||||
| chr5:126447651
|
A | G | 1 | a0001c0001t0002g0224 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.84-17775A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447651 | ||||||
| chr5:126447658
|
C | T | 44 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(41): Show | 46 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.84-17768C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447658 | ||||||
| chr5:126447671
|
G | A | 1 | a0001c0001t0002g0038 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.84-17755G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447671 | ||||||
| chr5:126447671
|
G | GA | 122 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0031others(119): Show | 123 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.84-17740dupA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126447671 | |||||
| chr5:126447671
|
G | GAAA | 36 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(33): Show | 39 | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.84-17742_84-17740d others(5): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126447671 | |||||
| chr5:126447687
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.84-17739G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447687 | ||||||
| chr5:126447698
|
G | C | 2 | a0001c0001t0001g0281a0001c0004t0001g0293 | 2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.84-17728G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447698 | ||||||
| chr5:126447703
|
C | T | 5 | a0001c0001t0001g0263a0001c0001t0002g0309a0001c0001t0002g0311others(2): Show | 5 | HG00140.hp2 HG01109.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.84-17723C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447703 | ||||||
| chr5:126447754
|
T | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0021others(1): Show | 5 | HG01069.hp2 HG01106.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.84-17672T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447754 | ||||||
| chr5:126447761
|
T | C | 86 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0016others(83): Show | 91 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.84-17665T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447761 | ||||||
| chr5:126447873
|
TTTAA | T | 14 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(11): Show | 15 | HG00558.hp1 HG01069.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.84-17552_84-17549d others(6): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447873 | ||||||
| chr5:126447874
|
TTAA | T | 24 | a0001c0001t0001g0119a0001c0001t0001g0231a0001c0001t0001g0264others(21): Show | 25 | HG01243.hp2 HG01255.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.84-17551_84-17549d others(5): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447874 | ||||||
| chr5:126447875
|
TA | T | 5 | a0001c0001t0001g0066a0001c0001t0001g0071a0001c0001t0002g0039others(2): Show | 6 | HG02735.hp1 HG02896.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.84-17545delA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126447875 | |||||
| chr5:126447875
|
TAA | T | 46 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(43): Show | 48 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.84-17546_84-17545d others(4): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126447875 | |||||
| chr5:126447876
|
A | T | 113 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0031others(110): Show | 114 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.84-17550A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447876 | ||||||
| chr5:126447877
|
A | T | 3 | a0001c0001t0002g0069a0001c0001t0003g0163a0001c0001t0006g0005 | 4 | HG02300.hp1 HG02896.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.84-17549A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447877 | ||||||
| chr5:126447882
|
T | G | 86 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0016others(83): Show | 91 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.84-17544T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447882 | ||||||
| chr5:126447920
|
C | T | 86 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0016others(83): Show | 91 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.84-17506C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447920 | ||||||
| chr5:126447927
|
T | A | 86 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0016others(83): Show | 91 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.84-17499T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447927 | ||||||
| chr5:126447948
|
C | T | 44 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(41): Show | 46 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.84-17478C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126447948 | ||||||
| chr5:126448000
|
C | G | 86 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0016others(83): Show | 91 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.84-17426C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448000 | ||||||
| chr5:126448006
|
T | C | 2 | a0001c0001t0001g0109a0001c0001t0001g0303 | 2 | HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.84-17420T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448006 | ||||||
| chr5:126448034
|
AT | A | 86 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0016others(83): Show | 91 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.84-17386delT | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126448034 | |||||
| chr5:126448063
|
G | C | 86 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0016others(83): Show | 91 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.84-17363G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448063 | ||||||
| chr5:126448133
|
A | G | 86 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0016others(83): Show | 91 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.84-17293A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448133 | ||||||
| chr5:126448185
|
C | T | 86 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0016others(83): Show | 91 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.84-17241C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448185 | ||||||
| chr5:126448278
|
A | G | 85 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0016others(82): Show | 90 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.84-17148A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448278 | ||||||
| chr5:126448357
|
G | A | 2 | a0001c0001t0002g0306a0001c0001t0003g0305 | 2 | HG01074.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.84-17069G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448357 | ||||||
| chr5:126448509
|
G | A | 2 | a0001c0001t0001g0207a0001c0001t0002g0206 | 2 | HG02602.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.84-16917G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448509 | ||||||
| chr5:126448539
|
T | C | 4 | a0001c0001t0003g0141a0001c0001t0003g0143a0001c0001t0003g0320others(1): Show | 4 | HG01243.hp2 HG02055.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.84-16887T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448539 | ||||||
| chr5:126448590
|
G | A | 11 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(8): Show | 12 | HG00558.hp1 HG01069.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.84-16836G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448590 | ||||||
| chr5:126448596
|
A | G | 87 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0016others(84): Show | 92 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.84-16830A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448596 | ||||||
| chr5:126448667
|
C | G | 1 | a0001c0001t0003g0073 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.84-16759C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448667 | ||||||
| chr5:126448766
|
G | A | 1 | a0001c0001t0007g0294 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.84-16660G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448766 | ||||||
| chr5:126448800
|
T | C | 85 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0016others(82): Show | 90 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.84-16626T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448800 | ||||||
| chr5:126448839
|
T | C | 1 | a0001c0001t0003g0077 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.84-16587T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448839 | ||||||
| chr5:126448840
|
G | T | 49 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0079others(46): Show | 51 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.84-16586G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448840 | ||||||
| chr5:126448844
|
C | T | 85 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0016others(82): Show | 90 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.84-16582C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126448844 | ||||||
| chr5:126449071
|
G | A | 39 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(36): Show | 41 | HG00323.hp1 HG00408.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.84-16355G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126449071 | ||||||
| chr5:126449073
|
T | A | 2 | a0001c0001t0003g0163a0001c0001t0006g0005 | 3 | HG02896.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.84-16353T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126449073 | ||||||
| chr5:126449075
|
C | T | 92 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0031others(89): Show | 93 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.84-16351C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126449075 | ||||||
| chr5:126449090
|
T | G | 37 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(34): Show | 39 | HG00558.hp1 HG01069.hp2 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.84-16336T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126449090 | ||||||
| chr5:126449424
|
C | G | 2 | a0001c0001t0003g0014a0001c0001t0003g0015 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.84-16002C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126449424 | ||||||
| chr5:126449522
|
AT | A | 130 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0031others(127): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.84-15899delT | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126449522 | |||||
| chr5:126449546
|
G | A | 153 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0031others(150): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.84-15880G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126449546 | ||||||
| chr5:126449568
|
C | A | 1 | a0001c0001t0001g0230 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.84-15858C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126449568 | ||||||
| chr5:126449720
|
G | T | 23 | a0001c0001t0001g0117a0001c0001t0001g0176a0001c0001t0001g0236others(20): Show | 23 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.84-15706G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126449720 | ||||||
| chr5:126449743
|
A | G | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | NA18965.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.84-15683A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126449743 | ||||||
| chr5:126449748
|
G | C | 1 | a0001c0001t0001g0013 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.84-15678G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126449748 | ||||||
| chr5:126449760
|
G | T | 4 | a0001c0001t0001g0031a0001c0001t0002g0063a0001c0001t0002g0064others(1): Show | 4 | HG00735.hp1 HG01934.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.84-15666G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126449760 | ||||||
| chr5:126449889
|
A | C | 1 | a0001c0001t0001g0222 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.84-15537A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126449889 | ||||||
| chr5:126449921
|
G | A | 6 | a0001c0001t0002g0234a0001c0001t0003g0141a0001c0001t0003g0143others(3): Show | 6 | HG02055.hp1 HG02055.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.84-15505G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126449921 | ||||||
| chr5:126449957
|
C | G | 26 | a0001c0001t0001g0031a0001c0001t0001g0058a0001c0001t0001g0060others(23): Show | 26 | HG00438.hp2 HG00642.hp2 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.84-15469C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126449957 | ||||||
| chr5:126450068
|
T | C | 3 | a0001c0001t0001g0109a0001c0001t0001g0303a0001c0001t0002g0299 | 3 | HG03239.hp1 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.84-15358T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450068 | ||||||
| chr5:126450191
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.84-15235A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450191 | ||||||
| chr5:126450221
|
G | C | 1 | a0001c0001t0001g0296 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.84-15205G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450221 | ||||||
| chr5:126450325
|
C | G | 1 | a0001c0001t0001g0062 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.84-15101C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450325 | ||||||
| chr5:126450340
|
A | G | 1 | a0001c0001t0001g0222 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.84-15086A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450340 | ||||||
| chr5:126450420
|
C | T | 1 | a0001c0004t0001g0293 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.84-15006C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450420 | ||||||
| chr5:126450588
|
T | C | 319 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(316): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.84-14838T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450588 | ||||||
| chr5:126450613
|
T | G | 199 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(196): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.84-14813T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450613 | ||||||
| chr5:126450652
|
T | TA | 119 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(116): Show | 123 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.84-14748dupA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126450652 | |||||
| chr5:126450652
|
T | TAA | 19 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0049others(16): Show | 19 | HG00639.hp1 HG00642.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.84-14749_84-14748d others(4): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126450652 | |||||
| chr5:126450652
|
TA | T | 12 | a0001c0001t0001g0016a0001c0001t0001g0079a0001c0001t0001g0093others(9): Show | 12 | HG00140.hp2 HG01258.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.84-14748delA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126450652 | |||||
| chr5:126450652
|
TAA | T | 90 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0018others(87): Show | 93 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.84-14749_84-14748d others(4): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126450652 | |||||
| chr5:126450652
|
TAAA | T | 25 | a0001c0001t0001g0009a0001c0001t0001g0044a0001c0001t0001g0045others(22): Show | 25 | HG00280.hp1 HG00323.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.84-14750_84-14748d others(5): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126450652 | |||||
| chr5:126450652
|
TAAAAAAA others(4): Show |
T | 1 | a0001c0001t0001g0148 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.84-14758_84-14748d others(13): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126450652 | |||||
| chr5:126450652
|
TAAAAAAA others(5): Show |
T | 4 | a0001c0001t0001g0160a0001c0001t0002g0131a0001c0001t0007g0294others(1): Show | 4 | HG02615.hp2 HG02886.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.84-14759_84-14748d others(14): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126450652 | |||||
| chr5:126450689
|
T | C | 3 | a0001c0001t0001g0013a0001c0001t0002g0074a0001c0001t0003g0261 | 3 | HG01261.hp2 HG06807.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.84-14737T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450689 | ||||||
| chr5:126450695
|
C | T | 1 | a0001c0004t0001g0293 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.84-14731C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450695 | ||||||
| chr5:126450707
|
G | A | 1 | a0001c0001t0001g0318 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.84-14719G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450707 | ||||||
| chr5:126450899
|
C | G | 1 | a0001c0001t0001g0174 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.84-14527C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450899 | ||||||
| chr5:126450905
|
G | A | 1 | a0001c0001t0002g0267 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.84-14521G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450905 | ||||||
| chr5:126450907
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.84-14519G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450907 | ||||||
| chr5:126450908
|
C | T | 122 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(119): Show | 126 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.84-14518C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450908 | ||||||
| chr5:126450912
|
G | A | 8 | a0001c0001t0001g0041a0001c0001t0001g0067a0001c0001t0001g0193others(5): Show | 8 | HG00280.hp1 HG01074.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.84-14514G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450912 | ||||||
| chr5:126450969
|
C | T | 4 | a0001c0001t0002g0313a0001c0001t0003g0085a0001c0001t0003g0101others(1): Show | 4 | HG00741.hp2 HG01255.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.84-14457C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450969 | ||||||
| chr5:126450987
|
C | G | 1 | a0001c0004t0001g0293 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.84-14439C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126450987 | ||||||
| chr5:126451119
|
C | T | 8 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0003g0094others(5): Show | 8 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.84-14307C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451119 | ||||||
| chr5:126451161
|
C | T | 144 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(141): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.84-14265C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451161 | ||||||
| chr5:126451162
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0253a0001c0001t0004g0254 | 3 | HG02809.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.84-14264G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451162 | ||||||
| chr5:126451171
|
G | C | 109 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(106): Show | 113 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.84-14255G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451171 | ||||||
| chr5:126451178
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.84-14248A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451178 | ||||||
| chr5:126451244
|
A | C | 7 | a0001c0001t0001g0160a0001c0001t0001g0277a0001c0001t0001g0278others(4): Show | 7 | HG02055.hp1 HG02451.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.84-14182A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451244 | ||||||
| chr5:126451249
|
C | T | 5 | a0001c0001t0001g0277a0001c0001t0001g0281a0001c0002t0001g0115others(2): Show | 5 | HG02055.hp1 HG02451.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.84-14177C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451249 | ||||||
| chr5:126451369
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.84-14057G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451369 | ||||||
| chr5:126451442
|
G | A | 2 | a0001c0001t0001g0273a0001c0001t0005g0140 | 2 | HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.84-13984G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451442 | ||||||
| chr5:126451590
|
C | T | 300 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(297): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.84-13836C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451590 | ||||||
| chr5:126451681
|
G | A | 3 | a0001c0001t0001g0027a0001c0001t0001g0035a0001c0004t0001g0293 | 3 | HG00673.hp2 HG02886.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.84-13745G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451681 | ||||||
| chr5:126451693
|
G | T | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | HG02280.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.84-13733G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451693 | ||||||
| chr5:126451699
|
G | A | 8 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0003g0094others(5): Show | 8 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.84-13727G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451699 | ||||||
| chr5:126451749
|
G | T | 1 | a0001c0001t0003g0159 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.84-13677G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451749 | ||||||
| chr5:126451798
|
G | A | 155 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.84-13628G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451798 | ||||||
| chr5:126451890
|
G | T | 140 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(137): Show | 142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.84-13536G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451890 | ||||||
| chr5:126451927
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.84-13499C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126451927 | ||||||
| chr5:126452021
|
A | C | 7 | a0001c0001t0001g0137a0001c0001t0001g0160a0001c0001t0001g0176others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.84-13405A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126452021 | ||||||
| chr5:126452156
|
G | A | 7 | a0001c0001t0001g0134a0001c0001t0001g0161a0001c0001t0001g0274others(4): Show | 7 | HG02145.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.84-13270G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126452156 | ||||||
| chr5:126452161
|
T | G | 1 | a0001c0001t0002g0315 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.84-13265T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126452161 | ||||||
| chr5:126452271
|
G | T | 17 | a0001c0001t0001g0072a0001c0001t0001g0091a0001c0001t0001g0092others(14): Show | 17 | HG00408.hp1 HG00423.hp2 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.84-13155G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126452271 | ||||||
| chr5:126452320
|
C | T | 5 | a0001c0001t0001g0277a0001c0001t0001g0281a0001c0002t0001g0115others(2): Show | 5 | HG02055.hp1 HG02451.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.84-13106C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126452320 | ||||||
| chr5:126452333
|
A | G | 1 | a0001c0001t0004g0254 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.84-13093A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126452333 | ||||||
| chr5:126452369
|
C | T | 20 | a0001c0001t0001g0135a0001c0001t0001g0231a0001c0001t0001g0239others(17): Show | 21 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.84-13057C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126452369 | ||||||
| chr5:126452446
|
A | G | 5 | a0001c0001t0001g0277a0001c0001t0001g0281a0001c0002t0001g0115others(2): Show | 5 | HG02055.hp1 HG02451.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.84-12980A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126452446 | ||||||
| chr5:126452501
|
T | C | 130 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(127): Show | 134 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.84-12925T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126452501 | ||||||
| chr5:126452580
|
G | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0096a0001c0001t0001g0117others(4): Show | 7 | HG00642.hp1 HG01891.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.84-12846G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126452580 | ||||||
| chr5:126452679
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0253a0001c0001t0004g0254 | 3 | HG02809.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.84-12747G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126452679 | ||||||
| chr5:126452833
|
A | C | 121 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(118): Show | 125 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.84-12593A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126452833 | ||||||
| chr5:126453174
|
A | G | 1 | a0001c0001t0004g0304 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.84-12252A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126453174 | ||||||
| chr5:126453348
|
G | GA | 7 | a0001c0001t0001g0277a0001c0001t0001g0281a0001c0001t0003g0163others(4): Show | 8 | HG02055.hp1 HG02451.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.84-12059dupA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126453348 | |||||
| chr5:126453348
|
GA | G | 164 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(161): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.84-12059delA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126453348 | |||||
| chr5:126453348
|
GAAAA | G | 124 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(121): Show | 128 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.84-12062_84-12059d others(6): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126453348 | |||||
| chr5:126453516
|
A | G | 126 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(123): Show | 130 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.84-11910A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126453516 | ||||||
| chr5:126453812
|
C | G | 4 | a0001c0001t0001g0096a0001c0001t0001g0117a0001c0001t0004g0270others(1): Show | 4 | HG00642.hp1 HG01891.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.84-11614C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126453812 | ||||||
| chr5:126453974
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.84-11452T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126453974 | ||||||
| chr5:126454029
|
A | G | 126 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(123): Show | 130 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.84-11397A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126454029 | ||||||
| chr5:126454133
|
C | T | 1 | a0001c0001t0002g0004 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.84-11293C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126454133 | ||||||
| chr5:126454160
|
C | A | 1 | a0001c0001t0003g0163 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.84-11266C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126454160 | ||||||
| chr5:126454172
|
A | C | 126 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(123): Show | 130 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.84-11254A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126454172 | ||||||
| chr5:126454291
|
C | T | 6 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0003g0094others(3): Show | 6 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.84-11135C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126454291 | ||||||
| chr5:126454311
|
T | C | 3 | a0001c0001t0001g0236a0001c0001t0003g0237a0001c0001t0003g0238 | 3 | HG01069.hp1 HG01071.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.84-11115T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126454311 | ||||||
| chr5:126454476
|
G | A | 126 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(123): Show | 130 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.84-10950G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126454476 | ||||||
| chr5:126454809
|
G | A | 121 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(118): Show | 125 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.84-10617G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126454809 | ||||||
| chr5:126454868
|
T | C | 34 | a0001c0001t0001g0096a0001c0001t0001g0117a0001c0001t0001g0135others(31): Show | 35 | HG00099.hp2 HG00642.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.84-10558T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126454868 | ||||||
| chr5:126454895
|
T | G | 1 | a0001c0001t0001g0079 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.84-10531T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126454895 | ||||||
| chr5:126455029
|
C | G | 126 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(123): Show | 130 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.84-10397C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455029 | ||||||
| chr5:126455076
|
G | A | 122 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(119): Show | 126 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.84-10350G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455076 | ||||||
| chr5:126455118
|
T | A | 1 | a0001c0001t0003g0279 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.84-10308T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455118 | ||||||
| chr5:126455178
|
C | T | 126 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(123): Show | 130 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.84-10248C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455178 | ||||||
| chr5:126455180
|
T | C | 126 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(123): Show | 130 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.84-10246T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455180 | ||||||
| chr5:126455327
|
T | C | 126 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(123): Show | 130 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.84-10099T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455327 | ||||||
| chr5:126455403
|
T | G | 124 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(121): Show | 128 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.84-10023T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455403 | ||||||
| chr5:126455448
|
A | G | 126 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(123): Show | 130 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.84-9978A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455448 | ||||||
| chr5:126455591
|
A | C | 2 | a0001c0001t0003g0163a0001c0001t0006g0005 | 3 | HG02896.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.84-9835A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455591 | ||||||
| chr5:126455598
|
T | C | 126 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(123): Show | 130 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.84-9828T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455598 | ||||||
| chr5:126455599
|
G | A | 122 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(119): Show | 126 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.84-9827G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455599 | ||||||
| chr5:126455625
|
A | G | 132 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(129): Show | 136 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.84-9801A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455625 | ||||||
| chr5:126455782
|
G | A | 2 | a0001c0001t0003g0163a0001c0001t0006g0005 | 3 | HG02896.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.84-9644G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455782 | ||||||
| chr5:126455784
|
A | T | 1 | a0001c0001t0001g0154 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.84-9642A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455784 | ||||||
| chr5:126455919
|
T | C | 128 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(125): Show | 133 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.84-9507T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455919 | ||||||
| chr5:126455947
|
T | C | 128 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(125): Show | 133 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.84-9479T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455947 | ||||||
| chr5:126455981
|
G | C | 24 | a0001c0001t0001g0096a0001c0001t0001g0117a0001c0001t0001g0135others(21): Show | 25 | HG00099.hp2 HG00642.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.84-9445G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126455981 | ||||||
| chr5:126456138
|
A | G | 1 | a0001c0001t0002g0131 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.84-9288A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456138 | ||||||
| chr5:126456200
|
C | G | 1 | a0001c0001t0003g0118 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.84-9226C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456200 | ||||||
| chr5:126456267
|
G | A | 124 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(121): Show | 128 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.84-9159G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456267 | ||||||
| chr5:126456279
|
C | T | 178 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(175): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.84-9147C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456279 | ||||||
| chr5:126456280
|
G | A | 128 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(125): Show | 133 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.84-9146G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456280 | ||||||
| chr5:126456355
|
T | C | 133 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(130): Show | 138 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.84-9071T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456355 | ||||||
| chr5:126456385
|
GT | G | 135 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(132): Show | 140 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.84-9032delT | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126456385 | |||||
| chr5:126456386
|
T | G | 21 | a0001c0001t0001g0096a0001c0001t0001g0117a0001c0001t0001g0135others(18): Show | 22 | HG00642.hp1 HG01243.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.84-9040T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456386 | ||||||
| chr5:126456445
|
C | T | 1 | a0001c0001t0001g0239 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.84-8981C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456445 | ||||||
| chr5:126456452
|
T | C | 1 | a0001c0001t0001g0296 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.84-8974T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456452 | ||||||
| chr5:126456502
|
T | C | 160 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(157): Show | 167 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.84-8924T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456502 | ||||||
| chr5:126456625
|
T | C | 1 | a0001c0004t0001g0293 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.84-8801T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456625 | ||||||
| chr5:126456808
|
A | G | 1 | a0001c0001t0003g0179 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.84-8618A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456808 | ||||||
| chr5:126456812
|
G | T | 8 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0003g0094others(5): Show | 8 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.84-8614G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456812 | ||||||
| chr5:126456813
|
C | T | 8 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0003g0094others(5): Show | 8 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.84-8613C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456813 | ||||||
| chr5:126456856
|
G | T | 299 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(296): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.84-8570G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456856 | ||||||
| chr5:126456914
|
C | T | 7 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0003g0094others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.84-8512C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456914 | ||||||
| chr5:126456917
|
A | G | 287 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(284): Show | 294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.84-8509A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456917 | ||||||
| chr5:126456956
|
G | T | 265 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(262): Show | 271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.84-8470G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456956 | ||||||
| chr5:126456959
|
A | G | 307 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(304): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.84-8467A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456959 | ||||||
| chr5:126456989
|
A | G | 287 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(284): Show | 294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.84-8437A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126456989 | ||||||
| chr5:126457008
|
C | T | 287 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(284): Show | 294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.84-8418C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457008 | ||||||
| chr5:126457065
|
G | A | 8 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0003g0094others(5): Show | 8 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.84-8361G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457065 | ||||||
| chr5:126457097
|
C | T | 287 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(284): Show | 294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.84-8329C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457097 | ||||||
| chr5:126457114
|
T | C | 287 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(284): Show | 294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.84-8312T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457114 | ||||||
| chr5:126457115
|
G | C | 287 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(284): Show | 294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.84-8311G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457115 | ||||||
| chr5:126457146
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.84-8280C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457146 | ||||||
| chr5:126457147
|
G | A | 7 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0003g0094others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.84-8279G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457147 | ||||||
| chr5:126457162
|
A | G | 287 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(284): Show | 294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.84-8264A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457162 | ||||||
| chr5:126457173
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.84-8253C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457173 | ||||||
| chr5:126457187
|
G | A | 2 | a0001c0001t0003g0163a0001c0001t0006g0005 | 3 | HG02896.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.84-8239G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457187 | ||||||
| chr5:126457191
|
C | CA | 6 | a0001c0001t0001g0119a0001c0001t0001g0161a0001c0001t0001g0182others(3): Show | 6 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.84-8205dupA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126457191 | |||||
| chr5:126457191
|
CAAAAAA | C | 31 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0096others(28): Show | 33 | HG00621.hp1 HG00639.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.84-8210_84-8205del others(6): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126457191 | |||||
| chr5:126457191
|
CAAAAAAA | C | 246 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(243): Show | 251 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.84-8211_84-8205del others(7): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126457191 | |||||
| chr5:126457191
|
CAAAAAAA others(1): Show |
C | 9 | a0001c0001t0001g0010a0001c0001t0001g0037a0001c0001t0001g0186others(6): Show | 9 | HG01074.hp1 HG01257.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.84-8212_84-8205del others(8): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126457191 | |||||
| chr5:126457191
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0004t0001g0293 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.84-8215_84-8205del others(11): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126457191 | |||||
| chr5:126457191
|
CAAAAAAA others(6): Show |
C | 6 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0003g0094others(3): Show | 6 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.84-8217_84-8205del others(13): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126457191 | |||||
| chr5:126457191
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0005g0190 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.84-8218_84-8205del others(14): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126457191 | |||||
| chr5:126457219
|
A | G | 17 | a0001c0001t0001g0096a0001c0001t0001g0117a0001c0001t0001g0135others(14): Show | 18 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.84-8207A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457219 | ||||||
| chr5:126457222
|
G | A | 1 | a0001c0001t0004g0304 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.84-8204G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457222 | ||||||
| chr5:126457248
|
T | C | 287 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(284): Show | 294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.84-8178T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457248 | ||||||
| chr5:126457298
|
A | G | 125 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(122): Show | 129 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.84-8128A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457298 | ||||||
| chr5:126457432
|
A | G | 270 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(267): Show | 276 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.84-7994A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457432 | ||||||
| chr5:126457563
|
G | A | 1 | a0001c0001t0001g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.84-7863G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457563 | ||||||
| chr5:126457586
|
G | T | 7 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0003g0094others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.84-7840G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457586 | ||||||
| chr5:126457631
|
G | A | 3 | a0001c0001t0001g0128a0001c0001t0001g0273a0001c0001t0002g0234 | 3 | HG02622.hp1 HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.84-7795G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457631 | ||||||
| chr5:126457642
|
A | C | 282 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(279): Show | 289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.84-7784A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457642 | ||||||
| chr5:126457729
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.84-7697G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457729 | ||||||
| chr5:126457761
|
TG | T | 265 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(262): Show | 271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.84-7660delG | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126457761 | |||||
| chr5:126457812
|
C | T | 17 | a0001c0001t0001g0096a0001c0001t0001g0117a0001c0001t0001g0135others(14): Show | 18 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.84-7614C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457812 | ||||||
| chr5:126457836
|
T | C | 1 | a0001c0001t0004g0304 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.84-7590T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457836 | ||||||
| chr5:126457895
|
G | A | 7 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0003g0094others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.84-7531G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126457895 | ||||||
| chr5:126458156
|
C | T | 262 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(259): Show | 268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.84-7270C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126458156 | ||||||
| chr5:126458157
|
A | G | 286 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(283): Show | 293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.84-7269A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126458157 | ||||||
| chr5:126458263
|
T | G | 3 | a0001c0001t0001g0128a0001c0001t0001g0273a0001c0001t0002g0234 | 3 | HG02622.hp1 HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.84-7163T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126458263 | ||||||
| chr5:126458264
|
G | A | 1 | a0001c0001t0001g0281 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.84-7162G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126458264 | ||||||
| chr5:126458378
|
C | T | 301 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(298): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.84-7048C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126458378 | ||||||
| chr5:126458427
|
A | G | 305 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(302): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.84-6999A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126458427 | ||||||
| chr5:126458444
|
CA | C | 6 | a0001c0001t0001g0043a0001c0001t0001g0116a0001c0001t0001g0250others(3): Show | 6 | HG00544.hp2 HG00621.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.84-6969delA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126458444 | |||||
| chr5:126458448
|
A | AC | 13 | a0001c0001t0001g0137a0001c0001t0001g0176a0001c0001t0001g0239others(10): Show | 13 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.84-6978_84-6977ins others(1): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126458448 | ||||||
| chr5:126458448
|
A | C | 3 | a0001c0001t0002g0313a0001c0001t0002g0315a0001c0001t0003g0314 | 3 | HG00733.hp1 HG01255.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.84-6978A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126458448 | ||||||
| chr5:126458449
|
A | C | 2 | a0001c0001t0001g0124a0001c0001t0003g0202 | 2 | HG00438.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.84-6977A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126458449 | ||||||
| chr5:126458616
|
G | A | 283 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(280): Show | 290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.84-6810G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126458616 | ||||||
| chr5:126458674
|
G | A | 2 | a0001c0001t0003g0163a0001c0001t0006g0005 | 3 | HG02896.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.84-6752G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126458674 | ||||||
| chr5:126458746
|
C | G | 16 | a0001c0001t0001g0096a0001c0001t0001g0117a0001c0001t0001g0135others(13): Show | 17 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.84-6680C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126458746 | ||||||
| chr5:126458751
|
C | A | 300 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(297): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.84-6675C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126458751 | ||||||
| chr5:126458812
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.84-6614C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126458812 | ||||||
| chr5:126458965
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.84-6461C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126458965 | ||||||
| chr5:126458966
|
G | A | 1 | a0001c0001t0003g0261 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.84-6460G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126458966 | ||||||
| chr5:126459033
|
C | T | 1 | a0001c0001t0007g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.84-6393C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126459033 | ||||||
| chr5:126459075
|
T | C | 12 | a0001c0001t0001g0135a0001c0001t0001g0231a0001c0001t0001g0264others(9): Show | 13 | HG01255.hp2 HG02055.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.84-6351T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126459075 | ||||||
| chr5:126459119
|
C | A | 1 | a0001c0001t0001g0110 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.84-6307C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126459119 | ||||||
| chr5:126459130
|
G | A | 2 | a0001c0001t0003g0163a0001c0001t0006g0005 | 3 | HG02896.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.84-6296G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126459130 | ||||||
| chr5:126459230
|
A | G | 2 | a0001c0001t0003g0163a0001c0001t0006g0005 | 3 | HG02896.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.84-6196A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126459230 | ||||||
| chr5:126459318
|
A | C | 7 | a0001c0001t0001g0050a0001c0001t0001g0056a0001c0001t0001g0121others(4): Show | 7 | NA18960.hp2 NA18964.hp1 NA18984.hp2 others(4): Show |
intron_variant | MODIFIER | c.84-6108A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126459318 | ||||||
| chr5:126459346
|
C | G | 284 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(281): Show | 291 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.84-6080C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126459346 | ||||||
| chr5:126459484
|
A | T | 299 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(296): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.84-5942A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126459484 | ||||||
| chr5:126459533
|
A | G | 269 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(266): Show | 275 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.84-5893A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126459533 | ||||||
| chr5:126459613
|
A | G | 315 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(312): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.84-5813A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126459613 | ||||||
| chr5:126459719
|
C | T | 20 | a0001c0001t0001g0096a0001c0001t0001g0117a0001c0001t0001g0128others(17): Show | 21 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.84-5707C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126459719 | ||||||
| chr5:126459823
|
A | G | 279 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(276): Show | 285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.84-5603A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126459823 | ||||||
| chr5:126459849
|
C | T | 12 | a0001c0001t0001g0137a0001c0001t0001g0176a0001c0001t0001g0239others(9): Show | 12 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.84-5577C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126459849 | ||||||
| chr5:126459871
|
T | G | 62 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0029others(59): Show | 64 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.84-5555T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126459871 | ||||||
| chr5:126459888
|
A | AT | 5 | a0001c0001t0001g0137a0001c0001t0001g0176a0001c0001t0001g0283others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.84-5532dupT | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126459888 | |||||
| chr5:126459890
|
T | C | 285 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(282): Show | 292 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.84-5536T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126459890 | ||||||
| chr5:126459913
|
C | T | 283 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(280): Show | 290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.84-5513C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126459913 | ||||||
| chr5:126460059
|
G | A | 297 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(294): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.84-5367G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126460059 | ||||||
| chr5:126460071
|
T | C | 2 | a0001c0001t0001g0296a0001c0001t0004g0304 | 2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.84-5355T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126460071 | ||||||
| chr5:126460105
|
G | T | 1 | a0001c0001t0001g0273 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.84-5321G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126460105 | ||||||
| chr5:126460127
|
A | C | 284 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(281): Show | 291 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.84-5299A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126460127 | ||||||
| chr5:126460153
|
C | T | 302 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(299): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.84-5273C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126460153 | ||||||
| chr5:126460206
|
C | T | 284 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(281): Show | 291 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.84-5220C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126460206 | ||||||
| chr5:126460216
|
C | T | 4 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0071others(1): Show | 4 | HG01256.hp2 HG01496.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.84-5210C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126460216 | ||||||
| chr5:126460285
|
A | C | 5 | a0001c0001t0001g0137a0001c0001t0001g0176a0001c0001t0001g0283others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.84-5141A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126460285 | ||||||
| chr5:126460476
|
G | T | 1 | a0001c0001t0007g0294 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.84-4950G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126460476 | ||||||
| chr5:126460725
|
G | A | 3 | a0001c0001t0001g0135a0001c0001t0003g0163a0001c0001t0006g0005 | 4 | HG02896.hp1 HG02965.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.84-4701G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126460725 | ||||||
| chr5:126460766
|
T | C | 16 | a0001c0001t0001g0096a0001c0001t0001g0117a0001c0001t0001g0135others(13): Show | 17 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.84-4660T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126460766 | ||||||
| chr5:126460973
|
T | C | 1 | a0001c0001t0005g0171 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.84-4453T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126460973 | ||||||
| chr5:126461158
|
T | C | 293 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(290): Show | 300 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.84-4268T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126461158 | ||||||
| chr5:126461175
|
C | T | 301 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(298): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.84-4251C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126461175 | ||||||
| chr5:126461211
|
TC | T | 2 | a0001c0001t0003g0163a0001c0001t0006g0005 | 3 | HG02896.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.84-4212delC | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126461211 | |||||
| chr5:126461284
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.84-4142G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126461284 | ||||||
| chr5:126461379
|
T | G | 302 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(299): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.84-4047T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126461379 | ||||||
| chr5:126461411
|
T | C | 1 | a0001c0001t0007g0294 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.84-4015T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126461411 | ||||||
| chr5:126461419
|
G | T | 1 | a0001c0001t0003g0179 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.84-4007G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126461419 | ||||||
| chr5:126461422
|
C | G | 2 | a0001c0001t0003g0163a0001c0001t0006g0005 | 3 | HG02896.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.84-4004C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126461422 | ||||||
| chr5:126461500
|
T | A | 3 | a0001c0001t0001g0160a0001c0001t0001g0296a0001c0001t0004g0304 | 3 | HG02922.hp2 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.84-3926T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126461500 | ||||||
| chr5:126461629
|
G | A | 125 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(122): Show | 129 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.84-3797G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126461629 | ||||||
| chr5:126461692
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0160 | 2 | NA19091.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.84-3734C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126461692 | ||||||
| chr5:126461757
|
G | A | 3 | a0001c0001t0001g0128a0001c0001t0001g0296a0001c0001t0004g0304 | 3 | HG02922.hp2 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.84-3669G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126461757 | ||||||
| chr5:126461823
|
A | G | 6 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0003g0094others(3): Show | 6 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.84-3603A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126461823 | ||||||
| chr5:126461854
|
G | A | 1 | a0001c0001t0010g0169 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.84-3572G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126461854 | ||||||
| chr5:126461921
|
A | G | 2 | a0001c0001t0003g0008a0001c0001t0004g0265 | 3 | HG02622.hp2 HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.84-3505A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126461921 | ||||||
| chr5:126461939
|
A | G | 1 | a0001c0001t0002g0306 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.84-3487A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126461939 | ||||||
| chr5:126462259
|
G | A | 261 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(258): Show | 267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.84-3167G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126462259 | ||||||
| chr5:126462407
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.84-3019A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126462407 | ||||||
| chr5:126462581
|
A | G | 17 | a0001c0001t0001g0096a0001c0001t0001g0117a0001c0001t0001g0135others(14): Show | 18 | HG00642.hp1 HG01255.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.84-2845A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126462581 | ||||||
| chr5:126462717
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.84-2709C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126462717 | ||||||
| chr5:126462774
|
A | G | 5 | a0001c0001t0001g0277a0001c0001t0005g0140a0001c0002t0001g0115others(2): Show | 5 | HG02055.hp1 HG02451.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.84-2652A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126462774 | ||||||
| chr5:126462879
|
G | A | 6 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0003g0094others(3): Show | 6 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.84-2547G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126462879 | ||||||
| chr5:126462922
|
T | C | 1 | a0001c0001t0001g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.84-2504T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126462922 | ||||||
| chr5:126462945
|
A | G | 5 | a0001c0001t0001g0137a0001c0001t0001g0176a0001c0001t0001g0283others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.84-2481A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126462945 | ||||||
| chr5:126463196
|
C | G | 2 | a0001c0001t0004g0181a0001c0001t0008g0023 | 2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.84-2230C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126463196 | ||||||
| chr5:126463337
|
G | A | 6 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0003g0094others(3): Show | 6 | HG00099.hp2 HG00741.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.84-2089G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126463337 | ||||||
| chr5:126463450
|
A | G | 2 | a0001c0001t0002g0164a0001c0001t0002g0165 | 2 | HG00642.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.84-1976A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126463450 | ||||||
| chr5:126463509
|
T | C | 22 | a0001c0001t0001g0096a0001c0001t0001g0117a0001c0001t0001g0135others(19): Show | 23 | HG00642.hp1 HG01243.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.84-1917T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126463509 | ||||||
| chr5:126463525
|
G | C | 3 | a0001c0001t0001g0128a0001c0001t0001g0273a0001c0001t0002g0234 | 3 | HG02622.hp1 HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.84-1901G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126463525 | ||||||
| chr5:126463620
|
C | A | 1 | a0001c0001t0001g0035 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.84-1806C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126463620 | ||||||
| chr5:126463681
|
T | C | 138 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(135): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.84-1745T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126463681 | ||||||
| chr5:126463756
|
C | A | 1 | a0001c0001t0001g0035 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.84-1670C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126463756 | ||||||
| chr5:126463854
|
A | T | 1 | a0001c0001t0001g0133 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.84-1572A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126463854 | ||||||
| chr5:126463983
|
G | A | 4 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0069others(1): Show | 4 | HG01928.hp2 HG01943.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.84-1443G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126463983 | ||||||
| chr5:126463985
|
G | A | 123 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(120): Show | 127 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.84-1441G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126463985 | ||||||
| chr5:126464024
|
A | G | 1 | a0001c0001t0001g0244 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.84-1402A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126464024 | ||||||
| chr5:126464028
|
C | CA | 7 | a0001c0001t0001g0152a0001c0001t0001g0177a0001c0001t0003g0179others(4): Show | 7 | HG02486.hp2 HG02615.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.84-1384dupA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr5 | 126464028 | |||||
| chr5:126464141
|
A | G | 138 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(135): Show | 143 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.84-1285A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126464141 | ||||||
| chr5:126464165
|
T | G | 3 | a0001c0001t0001g0128a0001c0001t0001g0273a0001c0001t0002g0234 | 3 | HG02622.hp1 HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.84-1261T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126464165 | ||||||
| chr5:126464278
|
C | G | 3 | a0001c0001t0003g0141a0001c0001t0003g0143a0001c0001t0003g0320 | 3 | HG02055.hp2 HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.84-1148C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126464278 | ||||||
| chr5:126464331
|
T | G | 22 | a0001c0001t0001g0096a0001c0001t0001g0117a0001c0001t0001g0135others(19): Show | 23 | HG00642.hp1 HG01243.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.84-1095T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126464331 | ||||||
| chr5:126464473
|
C | G | 3 | a0001c0001t0003g0141a0001c0001t0003g0143a0001c0001t0003g0320 | 3 | HG02055.hp2 HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.84-953C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126464473 | ||||||
| chr5:126464493
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0253a0001c0001t0004g0254 | 3 | HG02809.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.84-933G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126464493 | ||||||
| chr5:126464658
|
A | G | 14 | a0001c0001t0001g0119a0001c0001t0001g0161a0001c0001t0001g0236others(11): Show | 14 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.84-768A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126464658 | ||||||
| chr5:126464709
|
T | C | 10 | a0001c0001t0001g0096a0001c0001t0001g0117a0001c0001t0001g0134others(7): Show | 10 | HG00642.hp1 HG01891.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.84-717T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126464709 | ||||||
| chr5:126464874
|
C | A | 1 | a0001c0001t0001g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.84-552C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126464874 | ||||||
| chr5:126464954
|
T | C | 134 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0017others(131): Show | 138 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.84-472T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126464954 | ||||||
| chr5:126464992
|
A | G | 1 | a0001c0001t0005g0214 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.84-434A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126464992 | ||||||
| chr5:126465105
|
C | T | 5 | a0001c0001t0001g0161a0001c0001t0001g0274a0001c0001t0004g0102others(2): Show | 5 | HG02922.hp2 HG03130.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.84-321C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126465105 | ||||||
| chr5:126465144
|
C | T | 108 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0017others(105): Show | 112 | HG00323.hp2 HG00544.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.84-282C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126465144 | ||||||
| chr5:126465155
|
A | C | 1 | a0001c0001t0001g0055 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.84-271A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126465155 | ||||||
| chr5:126465233
|
G | T | 1 | a0001c0001t0004g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.84-193G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126465233 | ||||||
| chr5:126465237
|
C | A | 1 | a0001c0001t0001g0210 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.84-189C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126465237 | ||||||
| chr5:126465242
|
G | T | 1 | a0001c0001t0002g0267 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.84-184G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126465242 | ||||||
| chr5:126465363
|
C | T | 1 | a0001c0001t0002g0065 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.84-63C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 1/13 | chr5 | 126465363 | ||||||
| chr5:126465631
|
T | C | 1 | a0001c0001t0011g0180 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.203+86T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126465631 | ||||||
| chr5:126465702
|
T | C | 226 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(223): Show | 234 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.203+157T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126465702 | ||||||
| chr5:126465722
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.203+177T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126465722 | ||||||
| chr5:126465724
|
C | T | 107 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0016others(104): Show | 111 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.203+179C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126465724 | ||||||
| chr5:126465898
|
G | A | 1 | a0001c0001t0007g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.203+353G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126465898 | ||||||
| chr5:126465960
|
T | G | 1 | a0001c0001t0006g0256 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.203+415T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126465960 | ||||||
| chr5:126466123
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.203+578C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126466123 | ||||||
| chr5:126466184
|
T | C | 3 | a0001c0001t0001g0046a0001c0001t0001g0052a0001c0001t0005g0140 | 3 | HG02922.hp1 NA18973.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.203+639T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126466184 | ||||||
| chr5:126466335
|
G | A | 68 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0061others(65): Show | 69 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.203+790G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126466335 | ||||||
| chr5:126466355
|
C | T | 2 | a0001c0001t0001g0098a0001c0001t0001g0106 | 2 | HG03492.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.203+810C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126466355 | ||||||
| chr5:126466430
|
CT | C | 23 | a0001c0001t0001g0010a0001c0001t0001g0135a0001c0001t0001g0137others(20): Show | 24 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.203+897delT | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 126466430 | |||||
| chr5:126466443
|
C | T | 25 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(22): Show | 26 | HG00558.hp1 HG00609.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.203+898C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126466443 | ||||||
| chr5:126466460
|
C | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0253a0001c0001t0007g0178 | 3 | HG02809.hp1 HG03225.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.203+915C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126466460 | ||||||
| chr5:126466559
|
G | A | 5 | a0001c0001t0001g0137a0001c0001t0001g0176a0001c0001t0001g0283others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.203+1014G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126466559 | ||||||
| chr5:126466667
|
C | T | 1 | a0001c0001t0014g0033 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.203+1122C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126466667 | ||||||
| chr5:126466712
|
T | C | 10 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0176others(7): Show | 11 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.203+1167T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126466712 | ||||||
| chr5:126466729
|
G | T | 1 | a0001c0001t0002g0107 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.203+1184G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126466729 | ||||||
| chr5:126466776
|
G | A | 6 | a0001c0001t0001g0135a0001c0001t0001g0231a0001c0001t0001g0264others(3): Show | 7 | HG02055.hp2 HG02615.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.203+1231G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126466776 | ||||||
| chr5:126466809
|
G | A | 5 | a0001c0001t0001g0135a0001c0001t0001g0231a0001c0001t0001g0264others(2): Show | 6 | HG02055.hp2 HG02615.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.203+1264G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126466809 | ||||||
| chr5:126466914
|
T | C | 5 | a0001c0001t0004g0129a0001c0001t0004g0130a0001c0001t0004g0254others(2): Show | 5 | HG02886.hp1 HG03471.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.203+1369T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126466914 | ||||||
| chr5:126466986
|
C | G | 7 | a0001c0001t0001g0096a0001c0001t0001g0280a0001c0001t0003g0168others(4): Show | 7 | HG00642.hp1 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.203+1441C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126466986 | ||||||
| chr5:126466993
|
A | C | 21 | a0001c0001t0001g0010a0001c0001t0001g0062a0001c0001t0001g0117others(18): Show | 21 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(18): Show |
intron_variant | MODIFIER | c.203+1448A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126466993 | ||||||
| chr5:126467012
|
A | G | 287 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(284): Show | 295 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.203+1467A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126467012 | ||||||
| chr5:126467110
|
T | C | 48 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0061others(45): Show | 49 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.203+1565T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126467110 | ||||||
| chr5:126467224
|
G | A | 29 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0012others(26): Show | 30 | HG00558.hp1 HG02040.hp2 HG02074.hp2 others(27): Show |
intron_variant | MODIFIER | c.203+1679G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126467224 | ||||||
| chr5:126467427
|
G | A | 97 | a0001c0001t0001g0010a0001c0001t0001g0041a0001c0001t0001g0043others(94): Show | 100 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.203+1882G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126467427 | ||||||
| chr5:126467503
|
A | G | 4 | a0001c0001t0001g0277a0001c0002t0001g0115a0001c0002t0001g0142others(1): Show | 4 | HG02055.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.203+1958A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126467503 | ||||||
| chr5:126467526
|
C | G | 1 | a0001c0004t0001g0293 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.203+1981C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126467526 | ||||||
| chr5:126467614
|
G | C | 1 | a0001c0001t0014g0033 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.204-2063G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126467614 | ||||||
| chr5:126467628
|
A | G | 2 | a0001c0001t0001g0068a0001c0001t0001g0184 | 2 | HG02015.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.204-2049A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126467628 | ||||||
| chr5:126467648
|
T | C | 2 | a0001c0001t0003g0113a0001c0001t0003g0143 | 2 | HG02145.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.204-2029T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126467648 | ||||||
| chr5:126467890
|
T | C | 2 | a0001c0001t0003g0008a0001c0001t0003g0320 | 3 | HG02055.hp2 HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.204-1787T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126467890 | ||||||
| chr5:126467966
|
C | G | 3 | a0001c0001t0004g0129a0001c0001t0004g0130a0001c0001t0004g0275 | 3 | HG02886.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.204-1711C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126467966 | ||||||
| chr5:126468073
|
G | A | 317 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(314): Show | 325 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.204-1604G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126468073 | ||||||
| chr5:126468079
|
C | T | 5 | a0001c0001t0001g0170a0001c0001t0002g0234a0001c0001t0002g0292others(2): Show | 5 | HG02622.hp2 HG03041.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.204-1598C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126468079 | ||||||
| chr5:126468187
|
C | G | 2 | a0001c0001t0001g0035a0001c0001t0014g0033 | 2 | HG00673.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.204-1490C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126468187 | ||||||
| chr5:126468469
|
T | G | 1 | a0001c0004t0001g0293 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.204-1208T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126468469 | ||||||
| chr5:126468677
|
G | A | 2 | a0001c0001t0001g0278a0001c0001t0001g0281 | 2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.204-1000G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126468677 | ||||||
| chr5:126468730
|
C | T | 22 | a0001c0001t0001g0062a0001c0001t0001g0135a0001c0001t0001g0146others(19): Show | 23 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(20): Show |
intron_variant | MODIFIER | c.204-947C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126468730 | ||||||
| chr5:126468935
|
A | G | 1 | a0001c0001t0002g0315 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.204-742A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126468935 | ||||||
| chr5:126469053
|
T | C | 24 | a0001c0001t0001g0010a0001c0001t0001g0160a0001c0001t0001g0253others(21): Show | 25 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.204-624T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126469053 | ||||||
| chr5:126469119
|
A | C | 52 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0061others(49): Show | 53 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.204-558A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126469119 | ||||||
| chr5:126469267
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.204-410A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126469267 | ||||||
| chr5:126469277
|
G | GA | 5 | a0001c0001t0001g0170a0001c0001t0002g0234a0001c0001t0002g0292others(2): Show | 5 | HG02622.hp2 HG03041.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.204-395dupA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 126469277 | |||||
| chr5:126469365
|
G | A | 5 | a0001c0001t0001g0041a0001c0001t0001g0067a0001c0001t0001g0272others(2): Show | 5 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.204-312G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126469365 | ||||||
| chr5:126469546
|
G | A | 1 | a0001c0001t0008g0022 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.204-131G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126469546 | ||||||
| chr5:126469583
|
C | T | 3 | a0001c0002t0001g0115a0001c0002t0001g0142a0001c0002t0001g0321 | 3 | HG02055.hp1 HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.204-94C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126469583 | ||||||
| chr5:126469620
|
G | T | 1 | a0001c0001t0010g0125 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.204-57G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | chr5 | 126469620 | ||||||
| chr5:126469641
|
ATTATC | A | 10 | a0001c0001t0003g0113a0001c0001t0003g0143a0001c0001t0003g0237others(7): Show | 10 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.204-31_204-27delCT others(3): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr5 | 126469641 | |||||
| chr5:126469886
|
A | G | 24 | a0001c0001t0001g0010a0001c0001t0001g0160a0001c0001t0001g0253others(21): Show | 25 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.315+98A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126469886 | ||||||
| chr5:126469917
|
T | G | 2 | a0001c0001t0003g0168a0001c0001t0003g0322 | 2 | HG02258.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.315+129T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126469917 | ||||||
| chr5:126469929
|
C | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0253a0001c0001t0001g0266 | 3 | HG02809.hp1 HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.315+141C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126469929 | ||||||
| chr5:126470060
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.315+272C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126470060 | ||||||
| chr5:126470062
|
C | A | 1 | a0001c0001t0002g0078 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.315+274C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126470062 | ||||||
| chr5:126470237
|
T | C | 24 | a0001c0001t0001g0010a0001c0001t0001g0160a0001c0001t0001g0253others(21): Show | 25 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.315+449T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126470237 | ||||||
| chr5:126470385
|
C | A | 1 | a0001c0001t0001g0298 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.315+597C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126470385 | ||||||
| chr5:126470556
|
A | G | 19 | a0001c0001t0001g0117a0001c0001t0001g0161a0001c0001t0001g0166others(16): Show | 19 | HG00639.hp2 HG02280.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.315+768A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126470556 | ||||||
| chr5:126470709
|
C | T | 22 | a0001c0001t0001g0062a0001c0001t0001g0135a0001c0001t0001g0146others(19): Show | 23 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(20): Show |
intron_variant | MODIFIER | c.315+921C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126470709 | ||||||
| chr5:126470786
|
T | G | 2 | a0001c0001t0002g0164a0001c0001t0002g0165 | 2 | HG00642.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.315+998T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126470786 | ||||||
| chr5:126470842
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.315+1054G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126470842 | ||||||
| chr5:126470931
|
C | T | 1 | a0001c0001t0004g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.315+1143C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126470931 | ||||||
| chr5:126471170
|
A | G | 12 | a0001c0001t0001g0161a0001c0001t0001g0166a0001c0001t0001g0274others(9): Show | 12 | HG00639.hp2 HG02280.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.316-1068A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126471170 | ||||||
| chr5:126471192
|
T | A | 1 | a0001c0001t0014g0033 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.316-1046T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126471192 | ||||||
| chr5:126471334
|
C | T | 141 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0016others(138): Show | 145 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.316-904C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126471334 | ||||||
| chr5:126471555
|
T | A | 2 | a0001c0001t0001g0080a0001c0001t0001g0083 | 2 | HG00609.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.316-683T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126471555 | ||||||
| chr5:126471665
|
A | G | 1 | a0001c0001t0001g0274 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.316-573A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126471665 | ||||||
| chr5:126471946
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.316-292C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126471946 | ||||||
| chr5:126472145
|
A | G | 21 | a0001c0001t0001g0010a0001c0001t0001g0117a0001c0001t0001g0161others(18): Show | 21 | HG00639.hp2 HG02280.hp1 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.316-93A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126472145 | ||||||
| chr5:126472219
|
T | C | 22 | a0001c0001t0001g0062a0001c0001t0001g0135a0001c0001t0001g0146others(19): Show | 23 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(20): Show |
intron_variant | MODIFIER | c.316-19T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126472219 | ||||||
| chr5:126472228
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.316-10C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 3/13 | chr5 | 126472228 | ||||||
| chr5:126472577
|
C | T | 10 | a0001c0001t0003g0113a0001c0001t0003g0143a0001c0001t0003g0237others(7): Show | 10 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.382+273C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 4/13 | chr5 | 126472577 | ||||||
| chr5:126472662
|
CCTT | C | 43 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0061others(40): Show | 44 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.382+359_382+361del others(3): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 4/13 | chr5 | 126472662 | ||||||
| chr5:126472750
|
C | A | 2 | a0001c0001t0002g0259a0001c0001t0008g0023 | 2 | HG02258.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.382+446C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 4/13 | chr5 | 126472750 | ||||||
| chr5:126473060
|
T | A | 2 | a0001c0001t0001g0035a0001c0001t0014g0033 | 2 | HG00673.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.383-205T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 4/13 | chr5 | 126473060 | ||||||
| chr5:126473253
|
A | G | 2 | a0001c0001t0001g0035a0001c0001t0014g0033 | 2 | HG00673.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.383-12A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 4/13 | chr5 | 126473253 | ||||||
| chr5:126473453
|
G | A | 97 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0043others(94): Show | 100 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.486+85G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126473453 | ||||||
| chr5:126473457
|
A | G | 1 | a0001c0001t0001g0240 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.486+89A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126473457 | ||||||
| chr5:126473689
|
T | C | 2 | a0001c0001t0001g0092a0001c0001t0001g0122 | 2 | HG02040.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.486+321T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126473689 | ||||||
| chr5:126473791
|
G | A | 54 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0061others(51): Show | 55 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.486+423G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126473791 | ||||||
| chr5:126473868
|
G | A | 96 | a0001c0001t0001g0010a0001c0001t0001g0041a0001c0001t0001g0043others(93): Show | 99 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.486+500G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126473868 | ||||||
| chr5:126474004
|
G | A | 2 | a0001c0001t0001g0266a0001c0001t0014g0033 | 2 | HG03516.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.486+636G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126474004 | ||||||
| chr5:126474046
|
C | T | 3 | a0001c0001t0001g0160a0001c0001t0014g0033a0002c0003t0003g0284 | 3 | HG02257.hp2 HG03942.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.486+678C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126474046 | ||||||
| chr5:126474066
|
A | G | 1 | a0001c0001t0003g0073 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.486+698A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126474066 | ||||||
| chr5:126474480
|
T | A | 1 | a0001c0001t0001g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.486+1112T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126474480 | ||||||
| chr5:126474606
|
T | A | 1 | a0001c0001t0017g0295 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.486+1238T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126474606 | ||||||
| chr5:126474616
|
A | T | 8 | a0001c0001t0001g0096a0001c0001t0001g0161a0001c0001t0001g0166others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.486+1248A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126474616 | ||||||
| chr5:126474903
|
A | G | 4 | a0001c0001t0003g0113a0001c0001t0003g0143a0001c0001t0004g0162others(1): Show | 4 | HG02145.hp2 HG02723.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.486+1535A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126474903 | ||||||
| chr5:126474996
|
A | G | 54 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0035others(51): Show | 54 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.486+1628A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126474996 | ||||||
| chr5:126475081
|
C | T | 4 | a0001c0001t0001g0161a0001c0001t0001g0166a0001c0001t0001g0274others(1): Show | 4 | HG02486.hp1 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.486+1713C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126475081 | ||||||
| chr5:126475085
|
T | C | 74 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(71): Show | 78 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.486+1717T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126475085 | ||||||
| chr5:126475165
|
T | A | 6 | a0001c0001t0001g0117a0001c0001t0001g0277a0001c0001t0014g0033others(3): Show | 6 | HG02055.hp1 HG02451.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.486+1797T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126475165 | ||||||
| chr5:126475173
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.486+1805C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126475173 | ||||||
| chr5:126475444
|
G | A | 2 | a0002c0003t0001g0183a0002c0003t0003g0284 | 2 | HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.486+2076G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126475444 | ||||||
| chr5:126475498
|
G | A | 52 | a0001c0001t0001g0020a0001c0001t0001g0036a0001c0001t0001g0037others(49): Show | 53 | HG00140.hp1 HG00642.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.486+2130G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126475498 | ||||||
| chr5:126475673
|
G | A | 1 | a0001c0001t0001g0281 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.487-2019G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126475673 | ||||||
| chr5:126475735
|
C | T | 1 | a0001c0001t0001g0222 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.487-1957C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126475735 | ||||||
| chr5:126475754
|
C | T | 9 | a0001c0001t0001g0319a0001c0001t0002g0259a0001c0001t0003g0014others(6): Show | 9 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.487-1938C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126475754 | ||||||
| chr5:126475758
|
C | A | 153 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(150): Show | 157 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.487-1934C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126475758 | ||||||
| chr5:126475834
|
C | T | 9 | a0001c0001t0001g0117a0001c0001t0004g0102a0001c0001t0004g0129others(6): Show | 9 | HG02257.hp2 HG02886.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.487-1858C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126475834 | ||||||
| chr5:126475835
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0253 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.487-1857G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126475835 | ||||||
| chr5:126475846
|
C | T | 2 | a0001c0001t0001g0278a0001c0001t0001g0281 | 2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.487-1846C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126475846 | ||||||
| chr5:126475971
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.487-1721G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126475971 | ||||||
| chr5:126476095
|
C | T | 99 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0056others(96): Show | 102 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.487-1597C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126476095 | ||||||
| chr5:126476199
|
G | T | 1 | a0001c0001t0001g0277 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.487-1493G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126476199 | ||||||
| chr5:126476203
|
A | T | 1 | a0001c0001t0001g0277 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.487-1489A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126476203 | ||||||
| chr5:126476758
|
T | A | 1 | a0001c0001t0003g0305 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.487-934T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126476758 | ||||||
| chr5:126476852
|
A | T | 322 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(319): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.487-840A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126476852 | ||||||
| chr5:126476970
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.487-722G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126476970 | ||||||
| chr5:126477067
|
C | T | 10 | a0001c0001t0003g0113a0001c0001t0004g0162a0001c0001t0004g0181others(7): Show | 11 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.487-625C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126477067 | ||||||
| chr5:126477109
|
T | C | 1 | a0001c0001t0003g0297 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.487-583T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126477109 | ||||||
| chr5:126477423
|
T | A | 1 | a0001c0001t0001g0277 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.487-269T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126477423 | ||||||
| chr5:126477673
|
C | T | 4 | a0001c0001t0001g0018a0001c0001t0001g0091a0001c0001t0001g0133others(1): Show | 4 | HG00408.hp1 NA18949.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.487-19C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 5/13 | chr5 | 126477673 | ||||||
| chr5:126477823
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.582+36G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126477823 | ||||||
| chr5:126477912
|
G | T | 2 | a0001c0001t0001g0035a0001c0001t0014g0033 | 2 | HG00673.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.582+125G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126477912 | ||||||
| chr5:126477982
|
A | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0117a0001c0001t0001g0253 | 3 | HG02809.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.582+195A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126477982 | ||||||
| chr5:126477984
|
A | G | 306 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(303): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.582+197A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126477984 | ||||||
| chr5:126478140
|
G | GA | 161 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(158): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.582+372dupA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr5 | 126478140 | |||||
| chr5:126478140
|
G | GAA | 76 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0050others(73): Show | 78 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.582+371_582+372dup others(2): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr5 | 126478140 | |||||
| chr5:126478314
|
T | A | 1 | a0001c0001t0001g0175 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.582+527T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126478314 | ||||||
| chr5:126478363
|
A | G | 11 | a0001c0001t0001g0193a0001c0001t0001g0307a0001c0001t0001g0319others(8): Show | 11 | HG00099.hp1 HG00280.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.582+576A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126478363 | ||||||
| chr5:126478424
|
A | C | 306 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(303): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.582+637A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126478424 | ||||||
| chr5:126478430
|
C | A | 1 | a0001c0001t0001g0277 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.582+643C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126478430 | ||||||
| chr5:126478561
|
T | C | 156 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(153): Show | 160 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.582+774T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126478561 | ||||||
| chr5:126478583
|
A | C | 1 | a0001c0001t0001g0241 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.582+796A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126478583 | ||||||
| chr5:126478679
|
T | C | 2 | a0001c0001t0001g0174a0001c0001t0001g0263 | 2 | HG00140.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.582+892T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126478679 | ||||||
| chr5:126478692
|
G | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | HG01256.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.582+905G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126478692 | ||||||
| chr5:126478729
|
C | T | 34 | a0001c0001t0001g0061a0001c0001t0001g0158a0001c0001t0001g0200others(31): Show | 35 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.582+942C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126478729 | ||||||
| chr5:126478978
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.582+1191A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126478978 | ||||||
| chr5:126479444
|
T | C | 2 | a0002c0003t0001g0183a0002c0003t0003g0284 | 2 | HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.583-1012T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126479444 | ||||||
| chr5:126479616
|
TAGTA | T | 5 | a0001c0001t0001g0117a0001c0001t0004g0102a0001c0001t0004g0129others(2): Show | 5 | HG02886.hp1 HG03130.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.583-836_583-833del others(4): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr5 | 126479616 | |||||
| chr5:126479780
|
C | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0090 | 2 | NA18999.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.583-676C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126479780 | ||||||
| chr5:126479791
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.583-665A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126479791 | ||||||
| chr5:126479903
|
C | T | 1 | a0001c0001t0002g0292 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.583-553C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126479903 | ||||||
| chr5:126479910
|
A | G | 152 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(149): Show | 156 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.583-546A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126479910 | ||||||
| chr5:126480047
|
G | A | 85 | a0001c0001t0001g0006a0001c0001t0001g0056a0001c0001t0001g0060others(82): Show | 88 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.583-409G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126480047 | ||||||
| chr5:126480054
|
C | T | 3 | a0001c0001t0006g0005a0001c0001t0006g0235a0001c0001t0012g0024 | 4 | HG01243.hp2 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.583-402C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126480054 | ||||||
| chr5:126480072
|
C | G | 1 | a0001c0001t0001g0025 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.583-384C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126480072 | ||||||
| chr5:126480238
|
G | A | 4 | a0001c0001t0001g0175a0001c0001t0001g0271a0001c0001t0001g0290others(1): Show | 4 | HG02080.hp1 HG02155.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.583-218G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | chr5 | 126480238 | ||||||
| chr5:126480257
|
TTTTATGG others(12): Show |
T | 1 | a0001c0001t0001g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.583-193_583-175del others(19): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr5 | 126480257 | |||||
| chr5:126480545
|
G | A | 3 | a0001c0001t0006g0005a0001c0001t0006g0235a0001c0001t0012g0024 | 4 | HG01243.hp2 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.654+18G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 7/13 | chr5 | 126480545 | ||||||
| chr5:126480549
|
C | T | 3 | a0001c0001t0006g0005a0001c0001t0006g0235a0001c0001t0012g0024 | 4 | HG01243.hp2 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.654+22C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 7/13 | chr5 | 126480549 | ||||||
| chr5:126480765
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.735+58C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126480765 | ||||||
| chr5:126480807
|
G | A | 10 | a0001c0001t0003g0008a0001c0001t0003g0143a0001c0001t0003g0163others(7): Show | 11 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.735+100G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126480807 | ||||||
| chr5:126481031
|
T | C | 1 | a0001c0001t0001g0251 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.735+324T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481031 | ||||||
| chr5:126481148
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.735+441C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481148 | ||||||
| chr5:126481170
|
G | C | 1 | a0001c0001t0003g0185 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.735+463G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481170 | ||||||
| chr5:126481202
|
AAAAAGAA others(14): Show |
A | 4 | a0001c0001t0001g0012a0001c0001t0001g0285a0001c0001t0001g0287others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+499_735+519del others(21): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126481202 | |||||
| chr5:126481203
|
A | AAAAGAAA others(5): Show |
2 | a0001c0001t0004g0265a0001c0001t0006g0256 | 2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.735+532_735+543dup others(12): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126481203 | |||||
| chr5:126481203
|
A | AAAAGAAA others(9): Show |
1 | a0001c0001t0008g0023 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.735+528_735+543dup others(16): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126481203 | |||||
| chr5:126481203
|
AAAAG | A | 7 | a0001c0001t0001g0286a0001c0001t0002g0131a0001c0001t0002g0138others(4): Show | 7 | HG00639.hp2 HG02280.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.735+540_735+543del others(4): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126481203 | |||||
| chr5:126481203
|
AAAAGAAA others(1): Show |
A | 11 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0067others(8): Show | 11 | HG00280.hp1 HG01167.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.735+536_735+543del others(8): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126481203 | |||||
| chr5:126481203
|
AAAAGAAA others(5): Show |
A | 136 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(133): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.735+532_735+543del others(12): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126481203 | |||||
| chr5:126481203
|
AAAAGAAA others(9): Show |
A | 50 | a0001c0001t0001g0020a0001c0001t0001g0036a0001c0001t0001g0037others(47): Show | 51 | HG00140.hp1 HG00642.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.735+528_735+543del others(16): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126481203 | |||||
| chr5:126481203
|
AAAAGAAA others(13): Show |
A | 1 | a0001c0001t0001g0221 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.735+524_735+543del others(20): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126481203 | |||||
| chr5:126481203
|
AAAAGAAA others(17): Show |
A | 3 | a0001c0001t0001g0160a0001c0001t0001g0278a0001c0001t0003g0077 | 3 | HG00323.hp1 HG03098.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.735+520_735+543del others(24): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126481203 | |||||
| chr5:126481203
|
AAAAGAAA others(21): Show |
A | 4 | a0001c0001t0001g0161a0001c0001t0001g0166a0001c0001t0001g0274others(1): Show | 4 | HG02486.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+516_735+543del others(28): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126481203 | |||||
| chr5:126481204
|
AAAGAAAG others(4): Show |
A | 2 | a0001c0001t0001g0114a0001c0001t0002g0065 | 2 | HG01934.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.735+500_735+510del others(11): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126481204 | |||||
| chr5:126481204
|
AAAGAAAG others(8): Show |
A | 1 | a0001c0001t0001g0182 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.735+500_735+514del others(15): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126481204 | |||||
| chr5:126481204
|
AAAGAAAG others(16): Show |
A | 81 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0056others(78): Show | 84 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.735+500_735+522del others(23): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126481204 | |||||
| chr5:126481205
|
AAGAAAGA others(7): Show |
A | 9 | a0001c0001t0001g0319a0001c0001t0002g0259a0001c0001t0003g0014others(6): Show | 9 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.735+500_735+513del others(14): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126481205 | |||||
| chr5:126481205
|
AAGAAAGA others(15): Show |
A | 1 | a0001c0001t0003g0051 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.735+500_735+521del others(22): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126481205 | |||||
| chr5:126481223
|
G | A | 9 | a0001c0001t0001g0319a0001c0001t0002g0259a0001c0001t0003g0014others(6): Show | 9 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.735+516G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481223 | ||||||
| chr5:126481231
|
G | A | 83 | a0001c0001t0001g0006a0001c0001t0001g0056a0001c0001t0001g0060others(80): Show | 86 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.735+524G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481231 | ||||||
| chr5:126481237
|
A | G | 51 | a0001c0001t0001g0020a0001c0001t0001g0036a0001c0001t0001g0037others(48): Show | 52 | HG00140.hp1 HG00642.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.735+530A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481237 | ||||||
| chr5:126481529
|
G | A | 3 | a0001c0002t0001g0115a0001c0002t0001g0142a0001c0002t0001g0321 | 3 | HG02055.hp1 HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.735+822G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481529 | ||||||
| chr5:126481531
|
T | G | 9 | a0001c0001t0001g0319a0001c0001t0002g0259a0001c0001t0003g0014others(6): Show | 9 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.735+824T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481531 | ||||||
| chr5:126481622
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.735+915G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481622 | ||||||
| chr5:126481776
|
G | T | 10 | a0001c0001t0003g0008a0001c0001t0003g0143a0001c0001t0003g0163others(7): Show | 11 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.735+1069G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481776 | ||||||
| chr5:126481782
|
A | G | 9 | a0001c0001t0001g0319a0001c0001t0002g0259a0001c0001t0003g0014others(6): Show | 9 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.735+1075A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481782 | ||||||
| chr5:126481836
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0280 | 2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.735+1129C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481836 | ||||||
| chr5:126481868
|
C | T | 3 | a0001c0001t0001g0211a0001c0001t0001g0296a0001c0001t0001g0298 | 3 | HG02280.hp2 NA18949.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.735+1161C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481868 | ||||||
| chr5:126481869
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.735+1162G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481869 | ||||||
| chr5:126481927
|
C | T | 53 | a0001c0001t0001g0010a0001c0001t0001g0020a0001c0001t0001g0036others(50): Show | 54 | HG00140.hp1 HG00642.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.735+1220C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481927 | ||||||
| chr5:126481970
|
CA | C | 52 | a0001c0001t0001g0020a0001c0001t0001g0036a0001c0001t0001g0037others(49): Show | 53 | HG00140.hp1 HG00642.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.735+1279delA | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126481970 | |||||
| chr5:126481985
|
AAG | A | 93 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0056others(90): Show | 96 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.735+1279_735+1280d others(4): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481985 | ||||||
| chr5:126481986
|
A | G | 17 | a0001c0001t0001g0260a0001c0001t0001g0325a0001c0001t0003g0113others(14): Show | 18 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.735+1279A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126481986 | ||||||
| chr5:126482373
|
G | A | 94 | a0001c0001t0001g0006a0001c0001t0001g0035a0001c0001t0001g0056others(91): Show | 97 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.736-1090G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126482373 | ||||||
| chr5:126482604
|
G | C | 4 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0313others(1): Show | 4 | HG00733.hp1 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.736-859G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126482604 | ||||||
| chr5:126482620
|
A | G | 1 | a0001c0001t0001g0289 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.736-843A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126482620 | ||||||
| chr5:126482761
|
T | G | 1 | a0001c0001t0003g0302 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.736-702T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126482761 | ||||||
| chr5:126482853
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.736-610A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126482853 | ||||||
| chr5:126482926
|
A | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0280 | 2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.736-537A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126482926 | ||||||
| chr5:126483006
|
C | T | 149 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(146): Show | 153 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.736-457C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126483006 | ||||||
| chr5:126483035
|
T | A | 1 | a0001c0001t0001g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.736-428T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126483035 | ||||||
| chr5:126483062
|
TTC | T | 53 | a0001c0001t0001g0020a0001c0001t0001g0036a0001c0001t0001g0037others(50): Show | 54 | HG00140.hp1 HG00642.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.736-395_736-394del others(2): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126483062 | |||||
| chr5:126483062
|
TTCTC | T | 10 | a0001c0001t0003g0008a0001c0001t0003g0143a0001c0001t0003g0163others(7): Show | 11 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.736-397_736-394del others(4): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr5 | 126483062 | |||||
| chr5:126483139
|
T | G | 1 | a0001c0001t0001g0029 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.736-324T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126483139 | ||||||
| chr5:126483159
|
A | G | 3 | a0001c0001t0006g0005a0001c0001t0006g0235a0001c0001t0012g0024 | 4 | HG01243.hp2 HG02647.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.736-304A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126483159 | ||||||
| chr5:126483180
|
C | T | 2 | a0001c0001t0001g0119a0001c0001t0001g0236 | 2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.736-283C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126483180 | ||||||
| chr5:126483217
|
C | T | 153 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(150): Show | 157 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.736-246C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126483217 | ||||||
| chr5:126483292
|
A | C | 10 | a0001c0001t0003g0113a0001c0001t0004g0162a0001c0001t0004g0181others(7): Show | 11 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.736-171A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 8/13 | chr5 | 126483292 | ||||||
| chr5:126483731
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0253 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.847+157G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 9/13 | chr5 | 126483731 | ||||||
| chr5:126483914
|
C | T | 10 | a0001c0001t0003g0008a0001c0001t0003g0143a0001c0001t0003g0163others(7): Show | 11 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.847+340C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 9/13 | chr5 | 126483914 | ||||||
| chr5:126483919
|
C | A | 1 | a0001c0001t0002g0259 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.847+345C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 9/13 | chr5 | 126483919 | ||||||
| chr5:126484018
|
C | T | 1 | a0001c0001t0001g0046 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.848-384C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 9/13 | chr5 | 126484018 | ||||||
| chr5:126484584
|
CT | C | 11 | a0001c0001t0001g0060a0001c0001t0003g0113a0001c0001t0004g0162others(8): Show | 12 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.970+75delT | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr5 | 126484584 | |||||
| chr5:126484651
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0253 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.970+127T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126484651 | ||||||
| chr5:126484762
|
T | C | 1 | a0001c0001t0002g0195 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.970+238T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126484762 | ||||||
| chr5:126484804
|
G | A | 4 | a0001c0001t0003g0008a0001c0001t0003g0143a0001c0001t0003g0163others(1): Show | 5 | HG02055.hp2 HG02723.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.970+280G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126484804 | ||||||
| chr5:126484975
|
T | A | 11 | a0001c0001t0001g0296a0001c0001t0001g0298a0001c0001t0001g0319others(8): Show | 11 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.970+451T>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126484975 | ||||||
| chr5:126485031
|
C | T | 7 | a0001c0001t0004g0102a0001c0001t0004g0129a0001c0001t0004g0130others(4): Show | 7 | HG02257.hp2 HG02886.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.970+507C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126485031 | ||||||
| chr5:126485120
|
C | A | 151 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0020others(148): Show | 155 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.971-566C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126485120 | ||||||
| chr5:126485131
|
T | C | 1 | a0001c0001t0001g0025 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.971-555T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126485131 | ||||||
| chr5:126485205
|
T | C | 2 | a0001c0001t0001g0154a0001c0001t0001g0198 | 2 | NA19005.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.971-481T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126485205 | ||||||
| chr5:126485300
|
G | A | 9 | a0001c0001t0004g0162a0001c0001t0004g0181a0001c0001t0005g0140others(6): Show | 10 | HG01243.hp2 HG02055.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.971-386G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126485300 | ||||||
| chr5:126485308
|
G | A | 11 | a0001c0001t0003g0008a0001c0001t0003g0113a0001c0001t0003g0143others(8): Show | 12 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.971-378G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126485308 | ||||||
| chr5:126485404
|
C | G | 7 | a0001c0001t0004g0102a0001c0001t0004g0129a0001c0001t0004g0130others(4): Show | 7 | HG02257.hp2 HG02886.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.971-282C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126485404 | ||||||
| chr5:126485413
|
C | T | 9 | a0001c0001t0001g0319a0001c0001t0002g0259a0001c0001t0003g0014others(6): Show | 9 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.971-273C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126485413 | ||||||
| chr5:126485451
|
T | C | 2 | a0001c0001t0001g0152a0001c0001t0001g0177 | 2 | NA18964.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.971-235T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126485451 | ||||||
| chr5:126485520
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0253 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.971-166A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126485520 | ||||||
| chr5:126485595
|
T | C | 5 | a0001c0001t0003g0077a0001c0001t0003g0094a0001c0001t0003g0192others(2): Show | 5 | HG00323.hp1 HG00741.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.971-91T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126485595 | ||||||
| chr5:126485602
|
T | G | 8 | a0001c0001t0003g0008a0001c0001t0003g0113a0001c0001t0003g0143others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.971-84T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126485602 | ||||||
| chr5:126485663
|
G | A | 1 | a0001c0001t0001g0323 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.971-23G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 10/13 | chr5 | 126485663 | ||||||
| chr5:126485849
|
A | G | 4 | a0001c0001t0001g0161a0001c0001t0001g0166a0001c0001t0001g0274others(1): Show | 4 | HG02486.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1058+76A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 11/13 | chr5 | 126485849 | ||||||
| chr5:126485916
|
C | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0280 | 2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1058+143C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 11/13 | chr5 | 126485916 | ||||||
| chr5:126486057
|
T | C | 4 | a0001c0001t0001g0161a0001c0001t0001g0166a0001c0001t0001g0274others(1): Show | 4 | HG02486.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1058+284T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 11/13 | chr5 | 126486057 | ||||||
| chr5:126486151
|
C | T | 1 | a0001c0001t0002g0259 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1058+378C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 11/13 | chr5 | 126486151 | ||||||
| chr5:126486169
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1058+396A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 11/13 | chr5 | 126486169 | ||||||
| chr5:126486264
|
A | G | 54 | a0001c0001t0001g0020a0001c0001t0001g0036a0001c0001t0001g0037others(51): Show | 54 | HG00140.hp1 HG00642.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1058+491A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 11/13 | chr5 | 126486264 | ||||||
| chr5:126486313
|
G | T | 65 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0056others(62): Show | 67 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.1058+540G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 11/13 | chr5 | 126486313 | ||||||
| chr5:126486651
|
T | C | 1 | a0001c0001t0003g0051 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1059-222T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 11/13 | chr5 | 126486651 | ||||||
| chr5:126486654
|
C | T | 1 | a0001c0001t0005g0269 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1059-219C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 11/13 | chr5 | 126486654 | ||||||
| chr5:126486749
|
C | A | 1 | a0001c0001t0001g0019 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1059-124C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 11/13 | chr5 | 126486749 | ||||||
| chr5:126486835
|
G | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0285a0001c0001t0001g0287others(1): Show | 4 | HG02896.hp2 HG02965.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059-38G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 11/13 | chr5 | 126486835 | ||||||
| chr5:126487066
|
T | C | 2 | a0001c0001t0001g0035a0001c0001t0014g0033 | 2 | HG00673.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1163+89T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 12/13 | chr5 | 126487066 | ||||||
| chr5:126487382
|
T | G | 2 | a0001c0001t0001g0035a0001c0001t0014g0033 | 2 | HG00673.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1163+405T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 12/13 | chr5 | 126487382 | ||||||
| chr5:126487634
|
G | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0280 | 2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1163+657G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 12/13 | chr5 | 126487634 | ||||||
| chr5:126487665
|
A | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0280 | 2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1163+688A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 12/13 | chr5 | 126487665 | ||||||
| chr5:126487699
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1163+722G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 12/13 | chr5 | 126487699 | ||||||
| chr5:126487743
|
G | A | 1 | a0001c0001t0003g0227 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1163+766G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 12/13 | chr5 | 126487743 | ||||||
| chr5:126487787
|
T | C | 4 | a0001c0001t0001g0161a0001c0001t0001g0166a0001c0001t0001g0274others(1): Show | 4 | HG02486.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1163+810T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 12/13 | chr5 | 126487787 | ||||||
| chr5:126487825
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1163+848T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 12/13 | chr5 | 126487825 | ||||||
| chr5:126487892
|
G | A | 256 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(253): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.1164-907G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 12/13 | chr5 | 126487892 | ||||||
| chr5:126487902
|
G | T | 12 | a0001c0001t0001g0278a0001c0001t0003g0008a0001c0001t0003g0113others(9): Show | 13 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1164-897G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 12/13 | chr5 | 126487902 | ||||||
| chr5:126488122
|
G | A | 2 | a0001c0001t0001g0296a0001c0001t0001g0298 | 2 | HG02280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1164-677G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 12/13 | chr5 | 126488122 | ||||||
| chr5:126488163
|
A | G | 1 | a0001c0001t0003g0185 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1164-636A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 12/13 | chr5 | 126488163 | ||||||
| chr5:126488260
|
G | T | 3 | a0001c0001t0004g0162a0001c0001t0004g0181a0001c0001t0005g0140 | 3 | HG02922.hp1 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1164-539G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 12/13 | chr5 | 126488260 | ||||||
| chr5:126488357
|
G | A | 256 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(253): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.1164-442G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 12/13 | chr5 | 126488357 | ||||||
| chr5:126488597
|
G | A | 1 | a0001c0001t0001g0231 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1164-202G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 12/13 | chr5 | 126488597 | ||||||
| chr5:126488994
|
G | A | 3 | a0001c0001t0004g0162a0001c0001t0004g0181a0001c0001t0005g0140 | 3 | HG02922.hp1 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1257+102G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126488994 | ||||||
| chr5:126489018
|
T | C | 1 | a0001c0001t0001g0239 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1257+126T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126489018 | ||||||
| chr5:126489117
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1257+225G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126489117 | ||||||
| chr5:126489127
|
C | T | 256 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(253): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.1257+235C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126489127 | ||||||
| chr5:126489182
|
T | C | 256 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(253): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.1257+290T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126489182 | ||||||
| chr5:126489186
|
G | A | 9 | a0001c0001t0001g0319a0001c0001t0002g0259a0001c0001t0003g0014others(6): Show | 9 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1257+294G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126489186 | ||||||
| chr5:126489208
|
A | G | 1 | a0001c0001t0001g0296 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1257+316A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126489208 | ||||||
| chr5:126489324
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1257+432C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126489324 | ||||||
| chr5:126489387
|
C | G | 263 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(260): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1257+495C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126489387 | ||||||
| chr5:126489403
|
C | T | 1 | a0002c0003t0001g0183 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1257+511C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126489403 | ||||||
| chr5:126489422
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1257+530C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126489422 | ||||||
| chr5:126489427
|
G | A | 9 | a0001c0001t0001g0319a0001c0001t0002g0259a0001c0001t0003g0014others(6): Show | 9 | HG01099.hp2 HG01106.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1257+535G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126489427 | ||||||
| chr5:126489615
|
C | T | 3 | a0001c0001t0004g0102a0001c0001t0004g0130a0001c0001t0004g0275 | 3 | HG03130.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1257+723C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126489615 | ||||||
| chr5:126489630
|
A | T | 256 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(253): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.1257+738A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126489630 | ||||||
| chr5:126489800
|
G | GAGA | 256 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(253): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.1257+910_1257+912d others(5): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr5 | 126489800 | |||||
| chr5:126489997
|
A | G | 4 | a0001c0001t0001g0161a0001c0001t0001g0166a0001c0001t0001g0274others(1): Show | 4 | HG02486.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1257+1105A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126489997 | ||||||
| chr5:126490030
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1257+1138T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490030 | ||||||
| chr5:126490132
|
A | G | 258 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(255): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.1257+1240A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490132 | ||||||
| chr5:126490184
|
G | A | 1 | a0001c0001t0002g0267 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1257+1292G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490184 | ||||||
| chr5:126490240
|
A | G | 258 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(255): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.1257+1348A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490240 | ||||||
| chr5:126490258
|
A | G | 1 | a0001c0001t0004g0130 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1257+1366A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490258 | ||||||
| chr5:126490349
|
G | A | 1 | a0001c0001t0015g0288 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1257+1457G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490349 | ||||||
| chr5:126490351
|
TG | T | 253 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(250): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.1257+1462delG | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr5 | 126490351 | |||||
| chr5:126490362
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1257+1470G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490362 | ||||||
| chr5:126490397
|
A | G | 1 | a0001c0001t0001g0251 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1257+1505A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490397 | ||||||
| chr5:126490469
|
G | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0296 | 2 | HG03209.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1257+1577G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490469 | ||||||
| chr5:126490499
|
T | C | 274 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(271): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.1257+1607T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490499 | ||||||
| chr5:126490532
|
A | G | 1 | a0002c0003t0003g0284 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1257+1640A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490532 | ||||||
| chr5:126490544
|
G | A | 1 | a0001c0001t0003g0246 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1257+1652G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490544 | ||||||
| chr5:126490556
|
C | T | 15 | a0001c0001t0001g0010a0001c0001t0001g0253a0001c0001t0001g0278others(12): Show | 16 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1257+1664C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490556 | ||||||
| chr5:126490557
|
G | A | 1 | a0001c0001t0006g0256 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1257+1665G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490557 | ||||||
| chr5:126490593
|
A | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0280 | 2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1257+1701A>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490593 | ||||||
| chr5:126490634
|
C | A | 5 | a0001c0001t0001g0319a0001c0001t0002g0259a0001c0001t0005g0189others(2): Show | 5 | HG01099.hp2 HG01168.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1257+1742C>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490634 | ||||||
| chr5:126490637
|
C | T | 5 | a0001c0001t0001g0286a0001c0001t0002g0138a0001c0001t0002g0167others(2): Show | 5 | HG00639.hp2 HG02280.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1257+1745C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490637 | ||||||
| chr5:126490642
|
G | A | 18 | a0001c0001t0001g0010a0001c0001t0001g0096a0001c0001t0001g0160others(15): Show | 19 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1257+1750G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490642 | ||||||
| chr5:126490708
|
C | T | 1 | a0001c0001t0003g0233 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1257+1816C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490708 | ||||||
| chr5:126490732
|
T | C | 153 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0016others(150): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.1257+1840T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490732 | ||||||
| chr5:126490839
|
C | T | 1 | a0001c0001t0005g0140 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1257+1947C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490839 | ||||||
| chr5:126490953
|
C | T | 1 | a0001c0001t0004g0254 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1258-1962C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126490953 | ||||||
| chr5:126491080
|
A | C | 1 | a0001c0001t0001g0289 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1258-1835A>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126491080 | ||||||
| chr5:126491097
|
T | C | 271 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(268): Show | 277 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1258-1818T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126491097 | ||||||
| chr5:126491148
|
T | C | 1 | a0001c0001t0014g0033 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1258-1767T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126491148 | ||||||
| chr5:126491332
|
G | A | 128 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(125): Show | 129 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1258-1583G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126491332 | ||||||
| chr5:126491427
|
T | C | 6 | a0001c0001t0001g0117a0001c0001t0001g0319a0001c0001t0006g0005others(3): Show | 7 | HG01243.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1258-1488T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126491427 | ||||||
| chr5:126491538
|
C | T | 83 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0035others(80): Show | 85 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.1258-1377C>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126491538 | ||||||
| chr5:126491542
|
G | A | 1 | a0001c0001t0002g0107 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1258-1373G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126491542 | ||||||
| chr5:126491591
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1258-1324T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126491591 | ||||||
| chr5:126491606
|
C | G | 1 | a0001c0001t0001g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1258-1309C>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126491606 | ||||||
| chr5:126491645
|
T | G | 2 | a0001c0001t0001g0117a0001c0001t0001g0319 | 2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1258-1270T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126491645 | ||||||
| chr5:126491647
|
T | G | 2 | a0001c0001t0001g0117a0001c0001t0001g0319 | 2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1258-1268T>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126491647 | ||||||
| chr5:126491689
|
G | T | 4 | a0001c0001t0006g0005a0001c0001t0006g0235a0001c0001t0006g0256others(1): Show | 5 | HG01243.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1258-1226G>T | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126491689 | ||||||
| chr5:126491827
|
A | G | 4 | a0001c0001t0006g0005a0001c0001t0006g0235a0001c0001t0006g0256others(1): Show | 5 | HG01243.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1258-1088A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126491827 | ||||||
| chr5:126492130
|
G | A | 4 | a0001c0001t0001g0034a0001c0001t0001g0223a0001c0001t0001g0244others(1): Show | 4 | HG02165.hp1 NA18984.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.1258-785G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126492130 | ||||||
| chr5:126492210
|
GTTAAACA others(13): Show |
G | 4 | a0001c0001t0006g0005a0001c0001t0006g0235a0001c0001t0006g0256others(1): Show | 5 | HG01243.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1258-702_1258-683d others(22): Show |
GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr5 | 126492210 | |||||
| chr5:126492224
|
T | C | 266 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.1258-691T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126492224 | ||||||
| chr5:126492229
|
G | C | 266 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.1258-686G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126492229 | ||||||
| chr5:126492392
|
T | C | 1 | a0002c0003t0003g0284 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1258-523T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126492392 | ||||||
| chr5:126492411
|
G | A | 4 | a0001c0001t0006g0005a0001c0001t0006g0235a0001c0001t0006g0256others(1): Show | 5 | HG01243.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1258-504G>A | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126492411 | ||||||
| chr5:126492477
|
T | C | 2 | a0001c0001t0001g0281a0001c0004t0001g0293 | 2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1258-438T>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126492477 | ||||||
| chr5:126492484
|
G | C | 2 | a0001c0001t0002g0081a0001c0001t0002g0316 | 2 | HG01891.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1258-431G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126492484 | ||||||
| chr5:126492512
|
G | C | 6 | a0001c0001t0003g0077a0001c0001t0003g0094a0001c0001t0003g0159others(3): Show | 6 | HG00323.hp1 HG00741.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.1258-403G>C | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126492512 | ||||||
| chr5:126492556
|
A | G | 135 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(132): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.1258-359A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126492556 | ||||||
| chr5:126492769
|
A | G | 4 | a0001c0001t0001g0096a0001c0001t0001g0280a0001c0002t0001g0115others(1): Show | 4 | HG01891.hp1 HG02055.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1258-146A>G | GRAMD2B | ENSG00000155324.10 | transcript | ENST00000285689.8 | protein_coding | 13/13 | chr5 | 126492769 |