| geneid | 54762 |
|---|---|
| ensemblid | ENSG00000178075.20 |
| hgncid | 25252 |
| symbol | GRAMD1C |
| name | GRAM domain containing 1C |
| refseq_nuc | NM_017577.5 |
| refseq_prot | NP_060047.3 |
| ensembl_nuc | ENST00000358160.9 |
| ensembl_prot | ENSP00000350881.4 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 113838788 |
| end | 113947174 |
| strand | + |
| ver | v1.2 |
| region | chr3:113838788-113947174 |
| region5000 | chr3:113833788-113952174 |
| regionname0 | GRAMD1C_chr3_113838788_113947174 |
| regionname5000 | GRAMD1C_chr3_113833788_113952174 |
| 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 | 662 | 310 | 81 | 56 | 125 | 14 | 32 | 87 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0002 | 0/0 | 662 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0003 | 0/0 | 662 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0004 | 0/0 | 662 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0005 | 0/0 | 662 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0006 | 0/0 | 662 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0007 | 0/0 | 662 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0008 | 0/0 | 662 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0009 | 0/0 | 662 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0010 | 0/0 | 662 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0011 | 0/0 | 662 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0012 | 0/0 | 662 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0013 | 0/0 | 662 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| 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 | 1989 | 176 | 66 | 26 | 61 | 8 | 13 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| c0002 | 0/0 | 1989 | 55 | 3 | 16 | 26 | 2 | 8 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| c0003 | 0/0 | 1989 | 41 | 3 | 7 | 21 | 3 | 7 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| c0004 | 0/0 | 1989 | 28 | 0 | 6 | 17 | 1 | 4 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| c0005 | 0/0 | 1989 | 9 | 8 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| c0006 | 0/0 | 1989 | 3 | 3 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| c0007 | 0/0 | 1989 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| c0008 | 0/0 | 1989 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| c0009 | 0/0 | 1989 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| c0010 | 0/0 | 1989 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| c0011 | 0/0 | 1989 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| c0012 | 0/0 | 1989 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| c0013 | 0/0 | 1989 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| c0014 | 0/0 | 1989 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| c0015 | 0/0 | 1989 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| c0016 | 0/0 | 1989 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| c0017 | 0/0 | 1989 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| c0018 | 0/0 | 1989 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1819 | 122 | 25 | 27 | 52 | 6 | 10 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| t0002 | 0/0 | 1819 | 61 | 15 | 10 | 20 | 6 | 10 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| t0003 | 0/0 | 1819 | 46 | 6 | 9 | 24 | 1 | 6 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| t0004 | 0/0 | 1819 | 23 | 1 | 4 | 13 | 1 | 4 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| t0005 | 0/0 | 1819 | 11 | 0 | 2 | 8 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| t0006 | 0/0 | 1819 | 8 | 8 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| t0007 | 0/0 | 1819 | 6 | 0 | 0 | 6 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| t0008 | 0/0 | 1819 | 5 | 5 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| t0009 | 0/0 | 1817 | 5 | 5 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| t0010 | 0/0 | 1814 | 5 | 4 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| t0011 | 0/0 | 1819 | 4 | 0 | 4 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| t0012 | 0/0 | 1822 | 4 | 4 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| t0013 | 0/0 | 1815 | 3 | 0 | 0 | 3 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| t0014 | 0/0 | 1819 | 3 | 3 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| t0015 | 0/0 | 1814 | 2 | 2 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| t0016 | 0/0 | 1814 | 2 | 2 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| t0017 | 0/0 | 1819 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| t0018 | 0/0 | 1819 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| t0019 | 0/0 | 1819 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| t0020 | 0/0 | 1833 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| t0021 | 0/0 | 1819 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| t0022 | 0/0 | 1819 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| t0023 | 0/0 | 1819 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| t0024 | 0/0 | 1817 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| t0025 | 0/0 | 1817 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| t0026 | 0/0 | 1819 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| t0027 | 0/0 | 1819 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| t0028 | 0/0 | 1819 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| t0029 | 0/0 | 1819 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| t0030 | 0/0 | 1814 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| 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 | 1 | 0 | 1 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0012 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0164 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| 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 | 1989 | 176 | 66 | 26 | 61 | 8 | 13 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0002 | 0/0 | 1989 | 55 | 3 | 16 | 26 | 2 | 8 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0003 | 0/0 | 1989 | 41 | 3 | 7 | 21 | 3 | 7 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0004 | 0/0 | 1989 | 28 | 0 | 6 | 17 | 1 | 4 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0005 | 0/0 | 1989 | 9 | 8 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0012 | 0/0 | 1989 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0002c0006 | 0/0 | 1989 | 3 | 3 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0003c0018 | 0/0 | 1989 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0004c0017 | 0/0 | 1989 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0005c0008 | 0/0 | 1989 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0006c0014 | 0/0 | 1989 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0007c0013 | 0/0 | 1989 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0008c0009 | 0/0 | 1989 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0009c0010 | 0/0 | 1989 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0010c0011 | 0/0 | 1989 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0011c0015 | 0/0 | 1989 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0012c0016 | 0/0 | 1989 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0013c0007 | 0/0 | 1989 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3807 | 110 | 22 | 23 | 50 | 5 | 8 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0001t0002 | 0/0 | 3807 | 19 | 9 | 0 | 4 | 3 | 3 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0001t0003 | 0/0 | 3807 | 9 | 4 | 0 | 4 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0001t0006 | 0/0 | 3807 | 8 | 8 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0001t0008 | 0/0 | 3807 | 5 | 5 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0001t0009 | 0/0 | 3805 | 2 | 2 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0001t0010 | 0/0 | 3802 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0001t0011 | 0/0 | 3807 | 2 | 0 | 2 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0001t0012 | 0/0 | 3810 | 4 | 4 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0001t0013 | 0/0 | 3803 | 3 | 0 | 0 | 3 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0001t0014 | 0/0 | 3807 | 3 | 3 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0001t0015 | 0/0 | 3802 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0001t0016 | 0/0 | 3802 | 2 | 2 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0001t0017 | 0/0 | 3807 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0001t0018 | 0/0 | 3807 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0001t0021 | 0/0 | 3807 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0001t0022 | 0/0 | 3807 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0001t0026 | 0/0 | 3807 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0001t0028 | 0/0 | 3807 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0001t0030 | 0/0 | 3802 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0002t0001 | 0/0 | 3807 | 6 | 0 | 3 | 0 | 1 | 2 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0002t0003 | 0/0 | 3807 | 36 | 1 | 9 | 20 | 1 | 5 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0002t0004 | 0/0 | 3807 | 9 | 1 | 2 | 5 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0002t0011 | 0/0 | 3807 | 2 | 0 | 2 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0002t0020 | 0/0 | 3821 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0002t0027 | 0/0 | 3807 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0003t0002 | 0/0 | 3807 | 35 | 3 | 7 | 15 | 3 | 7 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0003t0007 | 0/0 | 3807 | 6 | 0 | 0 | 6 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0004t0002 | 0/0 | 3807 | 2 | 0 | 2 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0004t0004 | 0/0 | 3807 | 14 | 0 | 2 | 8 | 1 | 3 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0004t0005 | 0/0 | 3807 | 11 | 0 | 2 | 8 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0004t0019 | 0/0 | 3807 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0005t0001 | 0/0 | 3807 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0005t0002 | 0/0 | 3807 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0005t0009 | 0/0 | 3805 | 2 | 2 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0005t0010 | 0/0 | 3802 | 4 | 4 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0005t0015 | 0/0 | 3802 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0001c0012t0002 | 0/0 | 3807 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0002c0006t0009 | 0/0 | 3805 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0002c0006t0024 | 0/0 | 3805 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0002c0006t0025 | 0/0 | 3805 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0003c0018t0001 | 0/0 | 3807 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0004c0017t0029 | 0/0 | 3807 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0005c0008t0023 | 0/0 | 3807 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0006c0014t0002 | 0/0 | 3807 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0007c0013t0003 | 0/0 | 3807 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0008c0009t0001 | 0/0 | 3807 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0009c0010t0002 | 0/0 | 3807 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0010c0011t0001 | 0/0 | 3807 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0011c0015t0001 | 0/0 | 3807 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0012c0016t0001 | 0/0 | 3807 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| a0013c0007t0002 | 0/0 | 3807 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | copy fasta | chr3 | 113833788 | 113952174 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0012 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0164 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0006g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0006g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0006g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0006g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0008g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0008g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0008g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0008g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0008g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0009g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0009g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0010g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0011g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0011g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0012g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0012g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0012g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0012g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0013g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0013g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0013g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0014g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0014g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0014g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0015g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0016g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0016g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0017g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0018g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0021g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0022g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0026g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0028g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0001t0030g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0004g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0011g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0011g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0020g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0002t0027g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0007g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0007g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0007g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0007g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0007g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0003t0007g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0004t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0004t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0004t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0004t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0004t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0004t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0004t0004g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0004t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0004t0004g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0004t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0004t0004g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0004t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0004t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0004t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0004t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0004t0004g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0004t0005g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0004t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0004t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0004t0005g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0004t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0004t0005g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0004t0005g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0004t0005g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0004t0005g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0004t0005g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0004t0005g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0004t0019g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0005t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0005t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0005t0009g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0005t0009g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0005t0010g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0005t0010g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0005t0010g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0005t0010g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0005t0015g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0001c0012t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0002c0006t0009g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0002c0006t0024g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0002c0006t0025g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0003c0018t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0004c0017t0029g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0005c0008t0023g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0006c0014t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0007c0013t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0008c0009t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0009c0010t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0010c0011t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0011c0015t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0012c0016t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| a0013c0007t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0303 | EUR | GBR | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | GBR | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0286 | EUR | GBR | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG00280 | hp1 | a0001 | c0003 | t0002 | g0289 | EUR | FIN | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0220 | EUR | FIN | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG00323 | hp2 | a0001 | c0002 | t0003 | g0026 | EUR | FIN | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG00408 | hp2 | a0001 | c0003 | t0002 | g0147 | EAS | CHS | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG00438 | hp1 | a0001 | c0002 | t0004 | g0069 | EAS | CHS | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG00597 | hp1 | a0001 | c0003 | t0002 | g0260 | EAS | CHS | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG00597 | hp2 | a0001 | c0002 | t0003 | g0084 | EAS | CHS | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG00609 | hp1 | a0001 | c0002 | t0020 | g0316 | EAS | CHS | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG00609 | hp2 | a0001 | c0003 | t0002 | g0149 | EAS | CHS | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG00639 | hp2 | a0001 | c0002 | t0003 | g0053 | AMR | PUR | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG00642 | hp1 | a0001 | c0002 | t0003 | g0070 | AMR | PUR | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG00673 | hp1 | a0001 | c0004 | t0004 | g0034 | EAS | CHS | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG00735 | hp1 | a0001 | c0002 | t0004 | g0072 | AMR | PUR | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG00735 | hp2 | a0001 | c0001 | t0010 | g0008 | AMR | PUR | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG00741 | hp1 | a0001 | c0002 | t0003 | g0055 | AMR | PUR | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG00741 | hp2 | a0001 | c0003 | t0002 | g0271 | AMR | PUR | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01071 | hp1 | a0001 | c0002 | t0003 | g0037 | AMR | PUR | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01106 | hp1 | a0001 | c0001 | t0011 | g0240 | AMR | PUR | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01109 | hp2 | a0001 | c0005 | t0002 | g0295 | AMR | PUR | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0052 | AMR | PUR | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01169 | hp1 | a0001 | c0002 | t0003 | g0049 | AMR | PUR | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01192 | hp1 | a0004 | c0017 | t0029 | g0282 | AMR | PUR | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01243 | hp1 | a0001 | c0002 | t0011 | g0138 | AMR | PUR | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01256 | hp1 | a0001 | c0004 | t0002 | g0139 | AMR | CLM | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | CLM | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01258 | hp1 | a0001 | c0003 | t0002 | g0188 | AMR | CLM | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01258 | hp2 | a0001 | c0004 | t0002 | g0137 | AMR | CLM | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01261 | hp1 | a0001 | c0003 | t0002 | g0092 | AMR | CLM | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01346 | hp1 | a0001 | c0001 | t0011 | g0261 | AMR | CLM | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | CLM | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01361 | hp1 | a0001 | c0003 | t0002 | g0217 | AMR | CLM | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01361 | hp2 | a0001 | c0004 | t0004 | g0066 | AMR | CLM | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01433 | hp1 | a0001 | c0004 | t0005 | g0081 | AMR | CLM | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01433 | hp2 | a0001 | c0002 | t0003 | g0080 | AMR | CLM | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01496 | hp1 | a0001 | c0002 | t0003 | g0048 | AMR | CLM | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0257 | EUR | IBS | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | IBS | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01516 | hp1 | a0001 | c0003 | t0002 | g0215 | EUR | IBS | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0263 | EUR | IBS | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01884 | hp1 | a0003 | c0018 | t0001 | g0248 | AFR | ACB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01884 | hp2 | a0002 | c0006 | t0024 | g0133 | AFR | ACB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01891 | hp1 | a0007 | c0013 | t0003 | g0122 | AFR | ACB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0151 | AFR | ACB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01934 | hp2 | a0001 | c0004 | t0004 | g0099 | AMR | PEL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01943 | hp1 | a0001 | c0002 | t0004 | g0059 | AMR | PEL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01943 | hp2 | a0001 | c0003 | t0002 | g0221 | AMR | PEL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01952 | hp2 | a0001 | c0004 | t0005 | g0079 | AMR | PEL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01993 | hp1 | a0001 | c0002 | t0003 | g0043 | AMR | PEL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG01993 | hp2 | a0001 | c0003 | t0002 | g0166 | AMR | PEL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02015 | hp2 | a0001 | c0004 | t0005 | g0064 | EAS | KHV | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02055 | hp1 | a0001 | c0002 | t0004 | g0098 | AFR | ACB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0315 | AFR | ACB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02056 | hp1 | a0001 | c0003 | t0002 | g0239 | EAS | KHV | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02056 | hp2 | a0001 | c0003 | t0002 | g0252 | EAS | KHV | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02080 | hp1 | a0001 | c0002 | t0003 | g0321 | EAS | KHV | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02132 | hp1 | a0001 | c0002 | t0003 | g0057 | EAS | KHV | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02135 | hp1 | a0001 | c0002 | t0003 | g0087 | EAS | KHV | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02145 | hp1 | a0001 | c0001 | t0014 | g0102 | AFR | ACB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CDX | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CDX | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02165 | hp1 | a0001 | c0004 | t0005 | g0035 | EAS | CDX | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02165 | hp2 | a0001 | c0002 | t0003 | g0060 | EAS | CDX | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02257 | hp1 | a0001 | c0005 | t0009 | g0276 | AFR | ACB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0100 | AFR | ACB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02258 | hp1 | a0005 | c0008 | t0023 | g0131 | AFR | ACB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02258 | hp2 | a0001 | c0001 | t0030 | g0155 | AFR | ACB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02273 | hp2 | a0011 | c0015 | t0001 | g0224 | AMR | PEL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02280 | hp1 | a0001 | c0001 | t0016 | g0003 | AFR | ACB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02280 | hp2 | a0001 | c0005 | t0010 | g0007 | AFR | ACB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02293 | hp1 | a0001 | c0003 | t0002 | g0222 | AMR | PEL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02293 | hp2 | a0001 | c0002 | t0003 | g0082 | AMR | PEL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02300 | hp1 | a0001 | c0002 | t0011 | g0141 | AMR | PEL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02451 | hp2 | a0001 | c0001 | t0008 | g0167 | AFR | ACB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02523 | hp1 | a0001 | c0002 | t0003 | g0051 | EAS | KHV | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02615 | hp2 | a0001 | c0001 | t0012 | g0104 | AFR | GWD | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02630 | hp1 | a0001 | c0005 | t0009 | g0294 | AFR | GWD | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0192 | AFR | GWD | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02647 | hp2 | a0001 | c0005 | t0010 | g0010 | AFR | GWD | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02683 | hp1 | a0001 | c0003 | t0002 | g0187 | SAS | PJL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0213 | SAS | PJL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0123 | AFR | GWD | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02723 | hp2 | a0001 | c0002 | t0027 | g0062 | AFR | GWD | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02735 | hp1 | a0001 | c0004 | t0005 | g0036 | SAS | PJL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02738 | hp1 | a0001 | c0002 | t0003 | g0129 | SAS | PJL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02738 | hp2 | a0001 | c0002 | t0003 | g0078 | SAS | PJL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02886 | hp1 | a0001 | c0005 | t0001 | g0292 | AFR | GWD | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0172 | AFR | GWD | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0298 | AFR | GWD | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02895 | hp2 | a0001 | c0003 | t0002 | g0279 | AFR | GWD | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0301 | AFR | GWD | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02896 | hp2 | a0001 | c0001 | t0012 | g0103 | AFR | GWD | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02897 | hp1 | a0001 | c0001 | t0012 | g0116 | AFR | GWD | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0296 | AFR | GWD | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02922 | hp1 | a0001 | c0001 | t0014 | g0143 | AFR | ESN | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | ESN | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0145 | AFR | ESN | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0309 | AFR | ESN | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0005 | AFR | ESN | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0126 | AFR | ESN | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0056 | SAS | PJL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03017 | hp2 | a0001 | c0001 | t0017 | g0259 | SAS | PJL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0089 | AFR | MSL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0124 | AFR | MSL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0106 | AFR | ESN | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03130 | hp2 | a0001 | c0001 | t0018 | g0127 | AFR | ESN | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03139 | hp1 | a0002 | c0006 | t0009 | g0311 | AFR | ESN | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03139 | hp2 | a0001 | c0001 | t0009 | g0267 | AFR | ESN | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0254 | AFR | MSL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03209 | hp2 | a0009 | c0010 | t0002 | g0134 | AFR | MSL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | MSL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0146 | AFR | MSL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0091 | SAS | PJL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0140 | SAS | PJL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0310 | AFR | MSL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03491 | hp1 | a0001 | c0003 | t0002 | g0183 | SAS | PJL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03491 | hp2 | a0001 | c0003 | t0002 | g0119 | SAS | PJL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03540 | hp2 | a0001 | c0003 | t0002 | g0293 | AFR | GWD | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0281 | AFR | MSL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03579 | hp2 | a0001 | c0005 | t0015 | g0128 | AFR | MSL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03669 | hp2 | a0001 | c0002 | t0003 | g0075 | SAS | PJL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03688 | hp1 | a0001 | c0004 | t0004 | g0042 | SAS | STU | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | STU | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0165 | SAS | PJL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03704 | hp2 | a0001 | c0002 | t0003 | g0071 | SAS | PJL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03710 | hp1 | a0001 | c0003 | t0002 | g0204 | SAS | PJL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03710 | hp2 | a0001 | c0003 | t0002 | g0284 | SAS | PJL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03831 | hp2 | a0001 | c0003 | t0002 | g0207 | SAS | BEB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03834 | hp1 | a0001 | c0002 | t0004 | g0038 | SAS | BEB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0117 | SAS | BEB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | BEB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03942 | hp2 | a0001 | c0004 | t0004 | g0076 | SAS | BEB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | STU | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG04228 | hp2 | a0001 | c0004 | t0004 | g0058 | SAS | STU | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18522 | hp1 | a0001 | c0001 | t0015 | g0101 | AFR | YRI | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18522 | hp2 | a0001 | c0001 | t0014 | g0088 | AFR | YRI | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CHB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | CHB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18906 | hp1 | a0001 | c0001 | t0022 | g0132 | AFR | YRI | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18906 | hp2 | a0002 | c0006 | t0025 | g0130 | AFR | YRI | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18939 | hp2 | a0001 | c0004 | t0004 | g0050 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18940 | hp1 | a0001 | c0003 | t0002 | g0142 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18941 | hp1 | a0001 | c0002 | t0003 | g0030 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18946 | hp1 | a0001 | c0003 | t0002 | g0212 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18946 | hp2 | a0001 | c0002 | t0003 | g0045 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18948 | hp1 | a0001 | c0003 | t0002 | g0114 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18948 | hp2 | a0001 | c0002 | t0003 | g0041 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18949 | hp2 | a0001 | c0004 | t0005 | g0068 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18950 | hp1 | a0001 | c0002 | t0003 | g0095 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18950 | hp2 | a0001 | c0003 | t0002 | g0250 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18952 | hp1 | a0001 | c0003 | t0002 | g0201 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18952 | hp2 | a0001 | c0003 | t0002 | g0189 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18959 | hp2 | a0001 | c0003 | t0002 | g0236 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18960 | hp1 | a0001 | c0003 | t0007 | g0242 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18961 | hp1 | a0001 | c0003 | t0007 | g0110 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18961 | hp2 | a0001 | c0002 | t0003 | g0319 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18962 | hp1 | a0001 | c0002 | t0004 | g0047 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18964 | hp1 | a0001 | c0002 | t0003 | g0024 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18964 | hp2 | a0001 | c0001 | t0013 | g0205 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18965 | hp2 | a0001 | c0002 | t0004 | g0073 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18968 | hp2 | a0001 | c0004 | t0005 | g0044 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18969 | hp1 | a0001 | c0003 | t0007 | g0199 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18969 | hp2 | a0001 | c0004 | t0004 | g0029 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18972 | hp1 | a0001 | c0004 | t0005 | g0033 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18978 | hp1 | a0001 | c0002 | t0004 | g0097 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18980 | hp1 | a0001 | c0002 | t0003 | g0318 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18980 | hp2 | a0001 | c0003 | t0002 | g0230 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18982 | hp1 | a0001 | c0004 | t0005 | g0027 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18985 | hp1 | a0001 | c0003 | t0007 | g0159 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18985 | hp2 | a0001 | c0004 | t0004 | g0040 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18986 | hp2 | a0001 | c0002 | t0003 | g0317 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18988 | hp1 | a0001 | c0002 | t0003 | g0065 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19002 | hp1 | a0001 | c0004 | t0004 | g0096 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19002 | hp2 | a0012 | c0016 | t0001 | g0229 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19004 | hp1 | a0001 | c0003 | t0007 | g0154 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19004 | hp2 | a0001 | c0004 | t0004 | g0039 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19007 | hp1 | a0001 | c0003 | t0002 | g0195 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19010 | hp2 | a0001 | c0002 | t0003 | g0083 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19012 | hp1 | a0001 | c0003 | t0002 | g0288 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19030 | hp1 | a0001 | c0001 | t0008 | g0223 | AFR | LWK | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19030 | hp2 | a0013 | c0007 | t0002 | g0255 | AFR | LWK | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | LWK | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19043 | hp2 | a0001 | c0001 | t0026 | g0297 | AFR | LWK | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19056 | hp1 | a0001 | c0002 | t0004 | g0031 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19057 | hp1 | a0001 | c0004 | t0005 | g0028 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19060 | hp1 | a0008 | c0009 | t0001 | g0176 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19065 | hp2 | a0006 | c0014 | t0002 | g0118 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19075 | hp1 | a0001 | c0002 | t0003 | g0320 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19075 | hp2 | a0001 | c0004 | t0004 | g0085 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19079 | hp1 | a0001 | c0003 | t0007 | g0237 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19079 | hp2 | a0001 | c0002 | t0003 | g0322 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19081 | hp1 | a0001 | c0004 | t0005 | g0032 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19084 | hp2 | a0001 | c0002 | t0003 | g0046 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19085 | hp2 | a0001 | c0004 | t0019 | g0054 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19088 | hp2 | a0001 | c0002 | t0003 | g0025 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19090 | hp1 | a0001 | c0004 | t0004 | g0077 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19091 | hp1 | a0001 | c0001 | t0013 | g0245 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19091 | hp2 | a0001 | c0001 | t0013 | g0185 | EAS | JPT | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | YRI | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA19240 | hp2 | a0001 | c0005 | t0010 | g0004 | AFR | YRI | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA20129 | hp1 | a0001 | c0001 | t0028 | g0179 | AFR | ASW | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA20129 | hp2 | a0010 | c0011 | t0001 | g0011 | AFR | ASW | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA20752 | hp1 | a0001 | c0003 | t0002 | g0157 | EUR | TSI | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA20752 | hp2 | a0001 | c0004 | t0004 | g0067 | EUR | TSI | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA20905 | hp1 | a0001 | c0003 | t0002 | g0235 | SAS | GIH | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA20905 | hp2 | a0001 | c0002 | t0003 | g0074 | SAS | GIH | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02109 | hp1 | a0001 | c0001 | t0009 | g0262 | AFR | ACB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02109 | hp2 | a0001 | c0005 | t0010 | g0302 | AFR | ACB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02486 | hp1 | a0001 | c0001 | t0012 | g0300 | AFR | ACB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | ACB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | ACB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG02559 | hp2 | a0001 | c0001 | t0016 | g0009 | AFR | ACB | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | MSL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | MSL | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG06807 | hp1 | a0001 | c0012 | t0002 | g0216 | AFR | USA | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| HG06807 | hp2 | a0001 | c0001 | t0021 | g0287 | AFR | USA | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0125 | AFR | USA | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0280 | AFR | USA | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA21309 | hp1 | a0001 | c0003 | t0002 | g0105 | AFR | LWK | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| NA21309 | hp2 | a0001 | c0002 | t0003 | g0061 | AFR | LWK | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0164 | REF | REF | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0012 | REF | REF | GRAMD1C_chr3_113833788_113952174 | GRAMD1C | chr3 | 113833788 | 113952174 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:113844534
|
C | T | 1 | a0003 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.59C>T | p.Thr20Ile | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/18 | 181/3807 | 59/1989 | 20/662 | chr3 | 113844534 | ||
| chr3:113844550
|
T | G | 1 | a0013 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.75T>G | p.Asp25Glu | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/18 | 197/3807 | 75/1989 | 25/662 | chr3 | 113844550 | ||
| chr3:113876219
|
C | T | 1 | a0004 | 1 | HG01192.hp1 | missense_variant | MODERATE | c.418C>T | p.Leu140Phe | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/18 | 540/3807 | 418/1989 | 140/662 | chr3 | 113876219 | ||
| chr3:113904154
|
G | A | 1 | a0005 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.671G>A | p.Ser224Asn | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/18 | 793/3807 | 671/1989 | 224/662 | chr3 | 113904154 | ||
| chr3:113915721
|
C | G | 1 | a0012 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.973C>G | p.Leu325Val | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/18 | 1095/3807 | 973/1989 | 325/662 | chr3 | 113915721 | ||
| chr3:113915743
|
A | G | 1 | a0011 | 1 | HG02273.hp2 | missense_variant | MODERATE | c.995A>G | p.Asn332Ser | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/18 | 1117/3807 | 995/1989 | 332/662 | chr3 | 113915743 | ||
| chr3:113930733
|
G | T | 1 | a0006 | 1 | NA19065.hp2 | missense_variant | MODERATE | c.1110G>T | p.Trp370Cys | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 11/18 | 1232/3807 | 1110/1989 | 370/662 | chr3 | 113930733 | ||
| chr3:113933520
|
A | G | 2 | a0003a0007 | 2 | HG01884.hp1 HG01891.hp1 |
missense_variant | MODERATE | c.1219A>G | p.Lys407Glu | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 12/18 | 1341/3807 | 1219/1989 | 407/662 | chr3 | 113933520 | ||
| chr3:113933604
|
G | A | 1 | a0008 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.1303G>A | p.Val435Met | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 12/18 | 1425/3807 | 1303/1989 | 435/662 | chr3 | 113933604 | ||
| chr3:113936367
|
G | A | 1 | a0007 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.1558G>A | p.Ala520Thr | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 14/18 | 1680/3807 | 1558/1989 | 520/662 | chr3 | 113936367 | ||
| chr3:113938098
|
A | C | 1 | a0002 | 3 | HG01884.hp2 HG03139.hp1 NA18906.hp2 |
missense_variant | MODERATE | c.1646A>C | p.Glu549Ala | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 15/18 | 1768/3807 | 1646/1989 | 549/662 | chr3 | 113938098 | ||
| chr3:113938115
|
G | A | 1 | a0009 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1663G>A | p.Val555Ile | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 15/18 | 1785/3807 | 1663/1989 | 555/662 | chr3 | 113938115 | ||
| chr3:113940243
|
A | T | 1 | a0010 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.1806A>T | p.Leu602Phe | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/18 | 1928/3807 | 1806/1989 | 602/662 | chr3 | 113940243 | ||
| chr3:113947173
|
G | C | 6 | a0001a0004a0005others(3): Show | 115 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(112): Show |
splice_region_variant | LOW | c.*1695G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 18/18 | chr3 | 113947173 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:113875530
|
A | G | 2 | a0001c0002a0001c0004 | 83 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(80): Show |
synonymous_variant | LOW | c.306A>G | p.Leu102Leu | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 4/18 | 428/3807 | 306/1989 | 102/662 | chr3 | 113875530 | ||
| chr3:113904173
|
G | A | 1 | a0001c0005 | 9 | HG01109.hp2 HG02109.hp2 HG02257.hp1 others(6): Show |
synonymous_variant | LOW | c.690G>A | p.Gly230Gly | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/18 | 812/3807 | 690/1989 | 230/662 | chr3 | 113904173 | ||
| chr3:113933579
|
C | T | 1 | a0001c0012 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.1278C>T | p.Val426Val | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 12/18 | 1400/3807 | 1278/1989 | 426/662 | chr3 | 113933579 | ||
| chr3:113936360
|
C | T | 4 | a0001c0003a0001c0004a0001c0012others(1): Show | 71 | HG00280.hp1 HG00408.hp2 HG00597.hp1 others(68): Show |
synonymous_variant | LOW | c.1551C>T | p.Asn517Asn | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 14/18 | 1673/3807 | 1551/1989 | 517/662 | chr3 | 113936360 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:113838816
|
G | C | 1 | a0001c0001t0017 | 1 | HG03017.hp2 | 5_prime_UTR_variant | MODIFIER | c.-94G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/18 | 94 | chr3 | 113838816 | |||||
| chr3:113838843
|
G | A | 11 | a0001c0001t0003a0001c0001t0015a0001c0001t0018others(8): Show | 85 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(82): Show |
5_prime_UTR_variant | MODIFIER | c.-67G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/18 | 67 | chr3 | 113838843 | |||||
| chr3:113838859
|
G | C | 1 | a0001c0001t0021 | 1 | HG06807.hp2 | 5_prime_UTR_variant | MODIFIER | c.-51G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/18 | 51 | chr3 | 113838859 | |||||
| chr3:113838879
|
G | GGGCGGTG others(7): Show |
1 | a0001c0002t0020 | 1 | HG00609.hp1 | 5_prime_UTR_variant | MODIFIER | c.-25_-12dupTGCCGCGG others(6): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/18 | 11 | INFO_REALIGN_3_PRIME | chr3 | 113838879 | ||||
| chr3:113838892
|
G | A | 4 | a0001c0001t0022a0002c0006t0024a0002c0006t0025others(1): Show | 4 | HG01884.hp2 HG02258.hp1 NA18906.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-18G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/18 | 18 | chr3 | 113838892 | |||||
| chr3:113945499
|
G | A | 1 | a0001c0001t0016 | 2 | HG02280.hp1 HG02559.hp2 |
3_prime_UTR_variant | MODIFIER | c.*21G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 18/18 | 21 | chr3 | 113945499 | |||||
| chr3:113945517
|
TAAAGA | T | 6 | a0001c0001t0010a0001c0001t0015a0001c0001t0016others(3): Show | 10 | HG00735.hp2 HG02109.hp2 HG02258.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*43_*47delGAAAA | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 18/18 | 43 | INFO_REALIGN_3_PRIME | chr3 | 113945517 | ||||
| chr3:113945574
|
CTA | C | 5 | a0001c0001t0009a0001c0005t0009a0002c0006t0009others(2): Show | 7 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*98_*99delAT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 18/18 | 98 | INFO_REALIGN_3_PRIME | chr3 | 113945574 | ||||
| chr3:113945715
|
C | T | 1 | a0004c0017t0029 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*237C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 18/18 | 237 | chr3 | 113945715 | |||||
| chr3:113945838
|
T | A | 1 | a0001c0001t0026 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*360T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 18/18 | 360 | chr3 | 113945838 | |||||
| chr3:113945978
|
A | C | 1 | a0001c0001t0006 | 8 | HG01891.hp2 HG02965.hp1 HG03098.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*500A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 18/18 | 500 | chr3 | 113945978 | |||||
| chr3:113946184
|
C | G | 6 | a0001c0001t0010a0001c0001t0015a0001c0001t0016others(3): Show | 10 | HG00735.hp2 HG02109.hp2 HG02258.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*706C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 18/18 | 706 | chr3 | 113946184 | |||||
| chr3:113946367
|
G | T | 3 | a0001c0003t0007a0001c0004t0005a0001c0004t0019 | 18 | HG01433.hp1 HG01952.hp2 HG02015.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*889G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 18/18 | 889 | chr3 | 113946367 | |||||
| chr3:113946377
|
G | A | 2 | a0001c0001t0011a0001c0002t0011 | 4 | HG01106.hp1 HG01243.hp1 HG01346.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*899G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 18/18 | 899 | chr3 | 113946377 | |||||
| chr3:113946495
|
T | G | 6 | a0001c0001t0010a0001c0001t0015a0001c0001t0016others(3): Show | 10 | HG00735.hp2 HG02109.hp2 HG02258.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1017T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 18/18 | 1017 | chr3 | 113946495 | |||||
| chr3:113946556
|
C | T | 1 | a0001c0001t0028 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1078C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 18/18 | 1078 | chr3 | 113946556 | |||||
| chr3:113946722
|
T | TTTA | 1 | a0001c0001t0012 | 4 | HG02486.hp1 HG02615.hp2 HG02896.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1245_*1247dupTTA | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 18/18 | 1248 | INFO_REALIGN_3_PRIME | chr3 | 113946722 | ||||
| chr3:113946746
|
C | T | 1 | a0001c0004t0019 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1268C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 18/18 | 1268 | chr3 | 113946746 | |||||
| chr3:113946786
|
T | A | 1 | a0002c0006t0024 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1308T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 18/18 | 1308 | chr3 | 113946786 | |||||
| chr3:113946801
|
A | G | 2 | a0001c0001t0014a0001c0001t0018 | 4 | HG02145.hp1 HG02922.hp1 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1323A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 18/18 | 1323 | chr3 | 113946801 | |||||
| chr3:113946844
|
T | C | 1 | a0001c0001t0030 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1366T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 18/18 | 1366 | chr3 | 113946844 | |||||
| chr3:113947017
|
GTTTA | G | 1 | a0001c0001t0013 | 3 | NA18964.hp2 NA19091.hp1 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1544_*1547delTTTA | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 18/18 | 1544 | INFO_REALIGN_3_PRIME | chr3 | 113947017 | ||||
| chr3:113947023
|
T | G | 3 | a0001c0001t0008a0001c0001t0021a0001c0001t0022 | 7 | HG02055.hp2 HG02451.hp2 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1545T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 18/18 | 1545 | chr3 | 113947023 | |||||
| chr3:113947056
|
A | G | 1 | a0001c0002t0027 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1578A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 18/18 | 1578 | chr3 | 113947056 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:113838940
|
AGCC | A | 311 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(308): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
splice_region_variant&intron_variant | LOW | c.27+7_27+9delCGC | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr3 | 113838940 | |||||
| chr3:113838973
|
G | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG03669.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.27+37G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113838973 | ||||||
| chr3:113839053
|
G | C | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(3): Show | 6 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.27+117G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113839053 | ||||||
| chr3:113839075
|
A | G | 7 | a0001c0002t0003g0317a0001c0002t0003g0318a0001c0002t0003g0319others(4): Show | 7 | HG00609.hp1 HG02080.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.27+139A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113839075 | ||||||
| chr3:113839090
|
A | G | 16 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0306others(13): Show | 16 | HG00099.hp1 HG00642.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.27+154A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113839090 | ||||||
| chr3:113839211
|
C | T | 14 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(11): Show | 14 | HG01106.hp2 HG01109.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.27+275C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113839211 | ||||||
| chr3:113839256
|
C | A | 1 | a0001c0001t0001g0022 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.27+320C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113839256 | ||||||
| chr3:113839538
|
A | G | 1 | a0001c0001t0001g0291 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.27+602A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113839538 | ||||||
| chr3:113839745
|
A | G | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(3): Show | 6 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.27+809A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113839745 | ||||||
| chr3:113839875
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.27+939A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113839875 | ||||||
| chr3:113840027
|
C | T | 1 | a0001c0001t0001g0291 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.27+1091C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113840027 | ||||||
| chr3:113840227
|
A | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG03669.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.27+1291A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113840227 | ||||||
| chr3:113840264
|
C | T | 162 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(159): Show | 164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.27+1328C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113840264 | ||||||
| chr3:113840390
|
C | T | 1 | a0001c0003t0002g0289 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.27+1454C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113840390 | ||||||
| chr3:113840711
|
G | T | 1 | a0001c0003t0002g0288 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.27+1775G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113840711 | ||||||
| chr3:113840792
|
G | T | 4 | a0001c0001t0022g0132a0002c0006t0024g0133a0002c0006t0025g0130others(1): Show | 4 | HG01884.hp2 HG02258.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+1856G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113840792 | ||||||
| chr3:113841082
|
A | G | 1 | a0001c0002t0003g0129 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.27+2146A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113841082 | ||||||
| chr3:113841173
|
A | C | 58 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(55): Show | 58 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.27+2237A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113841173 | ||||||
| chr3:113841217
|
C | G | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(3): Show | 6 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.27+2281C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113841217 | ||||||
| chr3:113841285
|
C | CTTTTT | 42 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(39): Show | 42 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.27+2361_27+2365dup others(5): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr3 | 113841285 | |||||
| chr3:113841285
|
C | CTTTTTT | 90 | a0001c0001t0001g0021a0001c0001t0001g0135a0001c0001t0001g0136others(87): Show | 91 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.27+2360_27+2365dup others(6): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr3 | 113841285 | |||||
| chr3:113841285
|
C | CTTTTTTT | 134 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(131): Show | 135 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.27+2359_27+2365dup others(7): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr3 | 113841285 | |||||
| chr3:113841285
|
C | CTTTTTTT others(1): Show |
27 | a0001c0001t0001g0256a0001c0001t0001g0258a0001c0001t0001g0264others(24): Show | 27 | HG00408.hp1 HG00597.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.27+2358_27+2365dup others(8): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr3 | 113841285 | |||||
| chr3:113841285
|
C | CTTTTTTT others(2): Show |
8 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0283others(5): Show | 8 | HG00438.hp2 HG01192.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.27+2357_27+2365dup others(9): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr3 | 113841285 | |||||
| chr3:113841285
|
C | T | 1 | a0001c0005t0015g0128 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.27+2349C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113841285 | ||||||
| chr3:113841285
|
CTT | C | 8 | a0001c0001t0001g0299a0001c0001t0002g0296a0001c0001t0002g0298others(5): Show | 8 | HG01106.hp2 HG01109.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.27+2364_27+2365del others(2): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr3 | 113841285 | |||||
| chr3:113841363
|
G | A | 2 | a0001c0001t0003g0123a0007c0013t0003g0122 | 2 | HG01891.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.27+2427G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113841363 | ||||||
| chr3:113841392
|
T | C | 20 | a0001c0001t0001g0144a0001c0001t0001g0148a0001c0001t0001g0150others(17): Show | 20 | HG00408.hp2 HG00609.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.27+2456T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113841392 | ||||||
| chr3:113841442
|
C | T | 7 | a0001c0001t0001g0253a0001c0001t0001g0275a0001c0001t0022g0132others(4): Show | 7 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.27+2506C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113841442 | ||||||
| chr3:113841547
|
C | T | 2 | a0001c0001t0001g0251a0001c0003t0002g0252 | 2 | HG02056.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.27+2611C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113841547 | ||||||
| chr3:113841632
|
C | T | 1 | a0001c0003t0002g0250 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.27+2696C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113841632 | ||||||
| chr3:113841635
|
T | C | 12 | a0001c0001t0001g0006a0001c0001t0006g0124a0001c0001t0006g0125others(9): Show | 12 | HG00735.hp2 HG02280.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.27+2699T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113841635 | ||||||
| chr3:113841883
|
GA | G | 5 | a0001c0001t0001g0013a0001c0001t0001g0299a0001c0001t0002g0296others(2): Show | 5 | HG01106.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-2619delA | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113841883 | ||||||
| chr3:113841897
|
G | A | 321 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(318): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.28-2606G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113841897 | ||||||
| chr3:113842039
|
G | A | 7 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(4): Show | 7 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.28-2464G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113842039 | ||||||
| chr3:113842485
|
C | T | 4 | a0001c0003t0002g0293a0001c0005t0001g0292a0001c0005t0002g0295others(1): Show | 4 | HG01109.hp2 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-2018C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113842485 | ||||||
| chr3:113842551
|
T | TG | 42 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(39): Show | 42 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.28-1950dupG | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr3 | 113842551 | |||||
| chr3:113842657
|
A | G | 158 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(155): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.28-1846A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113842657 | ||||||
| chr3:113842700
|
C | T | 321 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(318): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.28-1803C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113842700 | ||||||
| chr3:113842754
|
G | A | 1 | a0001c0005t0010g0302 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.28-1749G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113842754 | ||||||
| chr3:113842792
|
A | G | 1 | a0001c0004t0004g0099 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.28-1711A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113842792 | ||||||
| chr3:113842836
|
G | A | 1 | a0001c0001t0021g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.28-1667G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113842836 | ||||||
| chr3:113842911
|
C | T | 157 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(154): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.28-1592C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113842911 | ||||||
| chr3:113842938
|
A | G | 157 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(154): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.28-1565A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113842938 | ||||||
| chr3:113842980
|
A | G | 53 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(50): Show | 53 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.28-1523A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113842980 | ||||||
| chr3:113843049
|
G | GT | 146 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0018others(143): Show | 148 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.28-1428dupT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr3 | 113843049 | |||||
| chr3:113843049
|
G | GTT | 68 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0020others(65): Show | 68 | HG00438.hp1 HG00597.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.28-1429_28-1428dup others(2): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr3 | 113843049 | |||||
| chr3:113843049
|
G | GTTT | 10 | a0001c0001t0001g0274a0001c0001t0006g0125a0001c0001t0010g0008others(7): Show | 10 | HG00735.hp2 HG01934.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.28-1430_28-1428dup others(3): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr3 | 113843049 | |||||
| chr3:113843121
|
C | T | 7 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(4): Show | 7 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.28-1382C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113843121 | ||||||
| chr3:113843148
|
T | C | 4 | a0001c0001t0001g0135a0001c0001t0001g0156a0001c0001t0001g0186others(1): Show | 4 | HG01346.hp2 HG01515.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-1355T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113843148 | ||||||
| chr3:113843345
|
G | T | 42 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(39): Show | 42 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.28-1158G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113843345 | ||||||
| chr3:113843408
|
C | A | 95 | a0001c0001t0001g0253a0001c0001t0001g0275a0001c0001t0003g0063others(92): Show | 96 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.28-1095C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113843408 | ||||||
| chr3:113843446
|
GC | G | 152 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(149): Show | 153 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.28-1055delC | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr3 | 113843446 | |||||
| chr3:113843514
|
C | T | 1 | a0001c0001t0015g0101 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.28-989C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113843514 | ||||||
| chr3:113843575
|
G | A | 1 | a0001c0002t0001g0023 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.28-928G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113843575 | ||||||
| chr3:113843818
|
A | T | 2 | a0001c0001t0003g0063a0001c0001t0003g0086 | 2 | NA18982.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.28-685A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113843818 | ||||||
| chr3:113843905
|
A | T | 5 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0246others(2): Show | 5 | HG02074.hp2 NA18990.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-598A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113843905 | ||||||
| chr3:113844367
|
G | A | 7 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(4): Show | 7 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.28-136G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 1/17 | chr3 | 113844367 | ||||||
| chr3:113844701
|
A | G | 2 | a0001c0001t0011g0261a0001c0003t0002g0271 | 2 | HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.174+52A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113844701 | ||||||
| chr3:113844898
|
G | A | 1 | a0001c0001t0012g0300 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.174+249G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113844898 | ||||||
| chr3:113845009
|
A | T | 1 | a0001c0001t0001g0270 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.174+360A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113845009 | ||||||
| chr3:113845028
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.174+379G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113845028 | ||||||
| chr3:113845034
|
G | A | 115 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(112): Show | 116 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.174+385G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113845034 | ||||||
| chr3:113845072
|
A | G | 1 | a0001c0001t0012g0300 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.174+423A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113845072 | ||||||
| chr3:113845164
|
G | T | 115 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(112): Show | 116 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.174+515G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113845164 | ||||||
| chr3:113845189
|
T | A | 7 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(4): Show | 7 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+540T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113845189 | ||||||
| chr3:113845257
|
T | A | 11 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(8): Show | 11 | HG01109.hp2 HG01934.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.174+608T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113845257 | ||||||
| chr3:113845357
|
A | G | 7 | a0001c0001t0001g0253a0001c0001t0001g0275a0001c0001t0022g0132others(4): Show | 7 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+708A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113845357 | ||||||
| chr3:113845419
|
C | T | 4 | a0001c0001t0022g0132a0002c0006t0024g0133a0002c0006t0025g0130others(1): Show | 4 | HG01884.hp2 HG02258.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+770C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113845419 | ||||||
| chr3:113845429
|
C | T | 115 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(112): Show | 116 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.174+780C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113845429 | ||||||
| chr3:113845594
|
A | G | 3 | a0001c0002t0003g0061a0001c0002t0004g0098a0001c0002t0027g0062 | 3 | HG02055.hp1 HG02723.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.174+945A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113845594 | ||||||
| chr3:113845758
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.174+1109C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113845758 | ||||||
| chr3:113845913
|
G | GT | 157 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(154): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.174+1267dupT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113845913 | |||||
| chr3:113846071
|
T | A | 157 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(154): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.174+1422T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113846071 | ||||||
| chr3:113846110
|
AT | A | 305 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(302): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.174+1474delT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113846110 | |||||
| chr3:113846120
|
T | G | 1 | a0001c0004t0005g0064 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.174+1471T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113846120 | ||||||
| chr3:113846140
|
CTT | C | 12 | a0001c0001t0001g0006a0001c0001t0006g0124a0001c0001t0006g0125others(9): Show | 12 | HG00735.hp2 HG02280.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.174+1492_174+1493d others(4): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113846140 | ||||||
| chr3:113846182
|
T | C | 51 | a0001c0001t0001g0013a0001c0001t0001g0107a0001c0001t0001g0108others(48): Show | 51 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.174+1533T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113846182 | ||||||
| chr3:113846202
|
G | A | 7 | a0001c0001t0001g0253a0001c0001t0001g0275a0001c0001t0022g0132others(4): Show | 7 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+1553G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113846202 | ||||||
| chr3:113846352
|
C | T | 3 | a0001c0001t0001g0225a0001c0001t0013g0185a0001c0004t0004g0085 | 3 | NA18998.hp1 NA19075.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.174+1703C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113846352 | ||||||
| chr3:113846440
|
G | C | 1 | a0001c0001t0001g0158 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.174+1791G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113846440 | ||||||
| chr3:113846539
|
A | G | 12 | a0001c0001t0001g0006a0001c0001t0006g0124a0001c0001t0006g0125others(9): Show | 12 | HG00735.hp2 HG02280.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.174+1890A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113846539 | ||||||
| chr3:113846823
|
A | G | 4 | a0001c0001t0001g0274a0001c0001t0003g0123a0001c0001t0021g0287others(1): Show | 4 | HG01891.hp1 HG02717.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.174+2174A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113846823 | ||||||
| chr3:113847131
|
A | G | 4 | a0001c0003t0002g0293a0001c0005t0001g0292a0001c0005t0002g0295others(1): Show | 4 | HG01109.hp2 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+2482A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113847131 | ||||||
| chr3:113847241
|
T | G | 12 | a0001c0001t0001g0006a0001c0001t0006g0124a0001c0001t0006g0125others(9): Show | 12 | HG00735.hp2 HG02280.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.174+2592T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113847241 | ||||||
| chr3:113847408
|
A | G | 4 | a0001c0003t0002g0293a0001c0005t0001g0292a0001c0005t0002g0295others(1): Show | 4 | HG01109.hp2 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+2759A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113847408 | ||||||
| chr3:113847444
|
C | A | 1 | a0005c0008t0023g0131 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.174+2795C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113847444 | ||||||
| chr3:113847485
|
T | C | 7 | a0001c0001t0001g0253a0001c0001t0001g0275a0001c0001t0022g0132others(4): Show | 7 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+2836T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113847485 | ||||||
| chr3:113847848
|
CA | C | 35 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(32): Show | 35 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.174+3201delA | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113847848 | |||||
| chr3:113847876
|
G | A | 1 | a0001c0004t0004g0085 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.174+3227G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113847876 | ||||||
| chr3:113848126
|
G | A | 1 | a0001c0003t0002g0187 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.174+3477G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113848126 | ||||||
| chr3:113848287
|
C | T | 3 | a0001c0002t0003g0060a0001c0002t0003g0083a0001c0002t0003g0084 | 3 | HG00597.hp2 HG02165.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.174+3638C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113848287 | ||||||
| chr3:113848449
|
T | C | 321 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(318): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.174+3800T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113848449 | ||||||
| chr3:113848484
|
A | C | 1 | a0001c0001t0001g0150 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.174+3835A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113848484 | ||||||
| chr3:113848497
|
G | GT | 303 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0016others(300): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.174+3859dupT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113848497 | |||||
| chr3:113848497
|
G | T | 1 | a0011c0015t0001g0224 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.174+3848G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113848497 | ||||||
| chr3:113848607
|
C | A | 8 | a0001c0001t0008g0005a0001c0001t0010g0008a0001c0001t0016g0003others(5): Show | 8 | HG00735.hp2 HG02280.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.174+3958C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113848607 | ||||||
| chr3:113848752
|
G | A | 9 | a0001c0001t0001g0013a0001c0001t0001g0290a0001c0001t0001g0299others(6): Show | 9 | HG01106.hp2 HG01358.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.174+4103G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113848752 | ||||||
| chr3:113848830
|
T | C | 4 | a0001c0003t0002g0293a0001c0005t0001g0292a0001c0005t0002g0295others(1): Show | 4 | HG01109.hp2 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+4181T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113848830 | ||||||
| chr3:113848897
|
T | C | 1 | a0001c0001t0003g0126 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.174+4248T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113848897 | ||||||
| chr3:113848984
|
A | AAAAC | 321 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(318): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.174+4346_174+4349d others(6): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113848984 | |||||
| chr3:113849025
|
T | TA | 5 | a0001c0001t0001g0013a0001c0001t0001g0299a0001c0001t0002g0296others(2): Show | 5 | HG01106.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.174+4377dupA | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113849025 | |||||
| chr3:113849223
|
A | G | 21 | a0001c0001t0001g0144a0001c0001t0001g0148a0001c0001t0001g0150others(18): Show | 21 | HG00408.hp2 HG00609.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.174+4574A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849223 | ||||||
| chr3:113849261
|
T | C | 1 | a0001c0001t0013g0185 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.174+4612T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849261 | ||||||
| chr3:113849267
|
T | TTTTA | 103 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(100): Show | 104 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.174+4658_174+4661d others(6): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113849267 | |||||
| chr3:113849267
|
T | TTTTATTT others(1): Show |
7 | a0001c0001t0001g0022a0001c0001t0001g0226a0001c0001t0001g0227others(4): Show | 7 | HG00673.hp2 HG02615.hp1 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+4654_174+4661d others(10): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113849267 | |||||
| chr3:113849267
|
TTTTA | T | 26 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(23): Show | 26 | HG00140.hp2 HG00438.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.174+4658_174+4661d others(6): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113849267 | |||||
| chr3:113849267
|
TTTTATTT others(1): Show |
T | 8 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(5): Show | 8 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.174+4654_174+4661d others(10): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113849267 | |||||
| chr3:113849267
|
TTTTATTT others(5): Show |
T | 2 | a0001c0001t0001g0290a0001c0005t0002g0295 | 2 | HG01109.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.174+4650_174+4661d others(14): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113849267 | |||||
| chr3:113849270
|
T | A | 11 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0065others(8): Show | 11 | HG00609.hp1 HG02080.hp1 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.174+4621T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849270 | ||||||
| chr3:113849271
|
A | T | 11 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0065others(8): Show | 11 | HG00609.hp1 HG02080.hp1 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.174+4622A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849271 | ||||||
| chr3:113849299
|
A | T | 11 | a0001c0002t0003g0024a0001c0002t0003g0025a0001c0002t0003g0065others(8): Show | 11 | HG01433.hp1 HG01943.hp1 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.174+4650A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849299 | ||||||
| chr3:113849300
|
T | A | 1 | a0001c0004t0005g0064 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.174+4651T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849300 | ||||||
| chr3:113849301
|
T | A | 2 | a0001c0002t0003g0129a0001c0004t0005g0081 | 2 | HG01433.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.174+4652T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849301 | ||||||
| chr3:113849303
|
A | T | 62 | a0001c0002t0001g0001a0001c0002t0001g0023a0001c0002t0001g0052others(59): Show | 63 | HG00099.hp2 HG00597.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.174+4654A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849303 | ||||||
| chr3:113849307
|
A | T | 82 | a0001c0002t0001g0001a0001c0002t0001g0023a0001c0002t0001g0052others(79): Show | 83 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.174+4658A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849307 | ||||||
| chr3:113849347
|
G | A | 9 | a0001c0001t0001g0013a0001c0001t0001g0290a0001c0001t0001g0299others(6): Show | 9 | HG01106.hp2 HG01358.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.174+4698G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849347 | ||||||
| chr3:113849433
|
A | G | 2 | a0001c0001t0001g0290a0001c0001t0002g0301 | 2 | HG01358.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.174+4784A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849433 | ||||||
| chr3:113849463
|
C | T | 1 | a0001c0001t0003g0126 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.174+4814C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849463 | ||||||
| chr3:113849528
|
T | C | 1 | a0005c0008t0023g0131 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.174+4879T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849528 | ||||||
| chr3:113849552
|
C | G | 1 | a0001c0002t0003g0057 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.174+4903C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849552 | ||||||
| chr3:113849603
|
G | A | 1 | a0001c0001t0002g0280 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.174+4954G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849603 | ||||||
| chr3:113849633
|
T | A | 5 | a0001c0003t0002g0293a0001c0005t0001g0292a0001c0005t0002g0295others(2): Show | 5 | HG01109.hp2 HG01884.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.174+4984T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849633 | ||||||
| chr3:113849640
|
G | T | 12 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(9): Show | 12 | HG01109.hp2 HG01884.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.174+4991G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849640 | ||||||
| chr3:113849686
|
A | C | 4 | a0001c0001t0008g0005a0001c0005t0010g0004a0001c0005t0010g0007others(1): Show | 4 | HG02280.hp2 HG02647.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+5037A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849686 | ||||||
| chr3:113849707
|
G | T | 1 | a0001c0002t0003g0321 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.174+5058G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849707 | ||||||
| chr3:113849749
|
C | G | 1 | a0001c0001t0017g0259 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.174+5100C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849749 | ||||||
| chr3:113849780
|
G | C | 1 | a0001c0001t0001g0150 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.174+5131G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849780 | ||||||
| chr3:113849803
|
T | C | 3 | a0001c0001t0001g0249a0001c0001t0003g0126a0001c0005t0015g0128 | 3 | HG02976.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.174+5154T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849803 | ||||||
| chr3:113849848
|
C | T | 3 | a0001c0001t0006g0310a0001c0001t0008g0315a0002c0006t0009g0311 | 3 | HG02055.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.174+5199C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849848 | ||||||
| chr3:113849862
|
G | T | 1 | a0001c0001t0001g0270 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.174+5213G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849862 | ||||||
| chr3:113849866
|
C | T | 113 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(110): Show | 114 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.174+5217C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849866 | ||||||
| chr3:113849867
|
G | A | 1 | a0001c0003t0002g0188 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.174+5218G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849867 | ||||||
| chr3:113849916
|
G | GGGGGGGC others(239): Show |
1 | a0001c0001t0002g0209 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.174+5344_174+5345i others(248): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113849916 | |||||
| chr3:113849916
|
G | GGGGGGGC others(140): Show |
1 | a0001c0005t0002g0295 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.174+5352_174+5353i others(149): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113849916 | |||||
| chr3:113849916
|
GGGGGGGC others(42): Show |
G | 1 | a0003c0018t0001g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.174+5304_174+5352d others(51): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113849916 | |||||
| chr3:113849926
|
A | AC | 87 | a0001c0001t0001g0253a0001c0001t0001g0275a0001c0001t0022g0132others(84): Show | 88 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.174+5284dupC | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113849926 | |||||
| chr3:113849926
|
A | ACCCCCCC others(76): Show |
1 | a0001c0002t0003g0026 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.174+5284_174+5285i others(85): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113849926 | |||||
| chr3:113849929
|
C | CA | 4 | a0001c0001t0003g0100a0001c0001t0014g0102a0001c0001t0015g0101others(1): Show | 4 | HG02145.hp1 HG02257.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.174+5280_174+5281i others(3): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849929 | ||||||
| chr3:113849948
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.174+5299C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849948 | ||||||
| chr3:113849953
|
C | T | 3 | a0001c0002t0001g0056a0001c0002t0003g0055a0001c0002t0003g0080 | 3 | HG00741.hp1 HG01433.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.174+5304C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849953 | ||||||
| chr3:113849959
|
A | G | 3 | a0001c0002t0001g0056a0001c0002t0003g0055a0001c0002t0003g0080 | 3 | HG00741.hp1 HG01433.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.174+5310A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849959 | ||||||
| chr3:113849964
|
G | GCGGGGGG others(25): Show |
42 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(39): Show | 42 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.174+5321_174+5352d others(34): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113849964 | |||||
| chr3:113849964
|
GCGGGGGG others(90): Show |
G | 1 | a0001c0001t0001g0019 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.174+5327_174+5423d others(99): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113849964 | |||||
| chr3:113849969
|
G | A | 1 | a0001c0002t0003g0037 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.174+5320G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849969 | ||||||
| chr3:113849984
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.174+5335C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849984 | ||||||
| chr3:113849994
|
G | A | 151 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(148): Show | 152 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.174+5345G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113849994 | ||||||
| chr3:113850002
|
T | C | 4 | a0001c0001t0002g0301a0001c0002t0001g0056a0001c0002t0003g0055others(1): Show | 4 | HG00741.hp1 HG01433.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+5353T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113850002 | ||||||
| chr3:113850008
|
G | A | 1 | a0001c0001t0002g0301 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.174+5359G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113850008 | ||||||
| chr3:113850013
|
G | A | 45 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(42): Show | 45 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.174+5364G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113850013 | ||||||
| chr3:113850025
|
C | A | 3 | a0001c0002t0001g0056a0001c0002t0003g0055a0001c0002t0003g0080 | 3 | HG00741.hp1 HG01433.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.174+5376C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113850025 | ||||||
| chr3:113850032
|
C | A | 3 | a0001c0002t0001g0056a0001c0002t0003g0055a0001c0002t0003g0080 | 3 | HG00741.hp1 HG01433.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.174+5383C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113850032 | ||||||
| chr3:113850039
|
C | T | 1 | a0001c0001t0001g0270 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.174+5390C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113850039 | ||||||
| chr3:113850183
|
C | CT | 7 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(4): Show | 7 | HG02135.hp2 HG02293.hp1 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+5545dupT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113850183 | |||||
| chr3:113850268
|
A | G | 4 | a0001c0001t0003g0100a0001c0001t0014g0102a0001c0001t0015g0101others(1): Show | 4 | HG02145.hp1 HG02257.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.174+5619A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113850268 | ||||||
| chr3:113850318
|
T | G | 1 | a0001c0003t0002g0189 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.174+5669T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113850318 | ||||||
| chr3:113850425
|
GC | G | 4 | a0001c0001t0003g0100a0001c0001t0014g0102a0001c0001t0015g0101others(1): Show | 4 | HG02145.hp1 HG02257.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.174+5778delC | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113850425 | |||||
| chr3:113850710
|
G | A | 154 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(151): Show | 155 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.174+6061G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113850710 | ||||||
| chr3:113850750
|
C | T | 1 | a0003c0018t0001g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.174+6101C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113850750 | ||||||
| chr3:113850823
|
A | T | 1 | a0001c0004t0019g0054 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.174+6174A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113850823 | ||||||
| chr3:113850891
|
TC | T | 321 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(318): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.174+6246delC | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113850891 | |||||
| chr3:113850950
|
G | C | 82 | a0001c0002t0001g0001a0001c0002t0001g0023a0001c0002t0001g0052others(79): Show | 83 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.174+6301G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113850950 | ||||||
| chr3:113850964
|
G | A | 7 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(4): Show | 7 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+6315G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113850964 | ||||||
| chr3:113851004
|
A | G | 148 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(145): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.174+6355A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113851004 | ||||||
| chr3:113851148
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.174+6499T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113851148 | ||||||
| chr3:113851522
|
C | CT | 21 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(18): Show | 21 | HG00735.hp2 HG01934.hp1 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.174+6889dupT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113851522 | |||||
| chr3:113851522
|
CT | C | 89 | a0001c0001t0001g0190a0001c0001t0002g0257a0001c0001t0003g0100others(86): Show | 90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.174+6889delT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113851522 | |||||
| chr3:113851756
|
G | A | 7 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(4): Show | 7 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+7107G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113851756 | ||||||
| chr3:113851891
|
T | C | 321 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(318): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.174+7242T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113851891 | ||||||
| chr3:113851993
|
C | T | 4 | a0001c0001t0001g0290a0001c0001t0002g0301a0001c0001t0012g0300others(1): Show | 4 | HG01358.hp2 HG02486.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+7344C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113851993 | ||||||
| chr3:113852116
|
A | AT | 7 | a0001c0002t0003g0053a0001c0002t0003g0082a0001c0002t0004g0059others(4): Show | 7 | HG00639.hp2 HG01433.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+7476dupT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113852116 | |||||
| chr3:113852211
|
T | G | 148 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(145): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.174+7562T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113852211 | ||||||
| chr3:113852397
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.174+7748A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113852397 | ||||||
| chr3:113852496
|
C | T | 6 | a0001c0001t0003g0100a0001c0001t0015g0101a0001c0001t0018g0127others(3): Show | 6 | HG02165.hp1 HG02257.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.174+7847C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113852496 | ||||||
| chr3:113852521
|
G | T | 1 | a0001c0001t0002g0117 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.174+7872G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113852521 | ||||||
| chr3:113852562
|
A | C | 1 | a0001c0001t0001g0022 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.174+7913A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113852562 | ||||||
| chr3:113852673
|
C | T | 1 | a0003c0018t0001g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.174+8024C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113852673 | ||||||
| chr3:113852682
|
C | T | 11 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(8): Show | 11 | HG01109.hp2 HG01934.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.174+8033C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113852682 | ||||||
| chr3:113852887
|
G | T | 1 | a0001c0002t0001g0052 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.174+8238G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113852887 | ||||||
| chr3:113852985
|
G | A | 12 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0002g0257others(9): Show | 12 | HG00741.hp2 HG01192.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.174+8336G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113852985 | ||||||
| chr3:113853106
|
A | C | 5 | a0001c0001t0006g0106a0001c0001t0012g0103a0001c0001t0012g0104others(2): Show | 5 | HG02615.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.174+8457A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113853106 | ||||||
| chr3:113853209
|
C | T | 4 | a0001c0001t0003g0100a0001c0001t0014g0102a0001c0001t0015g0101others(1): Show | 4 | HG02145.hp1 HG02257.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.174+8560C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113853209 | ||||||
| chr3:113853274
|
A | G | 9 | a0001c0001t0001g0013a0001c0001t0001g0290a0001c0001t0001g0299others(6): Show | 9 | HG01106.hp2 HG01358.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.174+8625A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113853274 | ||||||
| chr3:113853318
|
AAG | A | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0003t0007g0159 | 3 | HG00558.hp1 HG00558.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.174+8675_174+8676d others(4): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113853318 | |||||
| chr3:113853346
|
T | G | 1 | a0001c0001t0001g0150 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.174+8697T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113853346 | ||||||
| chr3:113853925
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.174+9276G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113853925 | ||||||
| chr3:113854102
|
C | A | 42 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(39): Show | 42 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.174+9453C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113854102 | ||||||
| chr3:113854130
|
G | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.174+9481G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113854130 | ||||||
| chr3:113854230
|
C | T | 4 | a0001c0001t0001g0182a0001c0001t0001g0227a0001c0001t0002g0175others(1): Show | 4 | HG00673.hp2 NA18612.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+9581C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113854230 | ||||||
| chr3:113854286
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.174+9637A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113854286 | ||||||
| chr3:113854330
|
AT | A | 3 | a0001c0001t0001g0290a0001c0001t0002g0301a0001c0001t0012g0300 | 3 | HG01358.hp2 HG02486.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.174+9682delT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113854330 | ||||||
| chr3:113854358
|
C | A | 1 | a0001c0001t0001g0177 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.174+9709C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113854358 | ||||||
| chr3:113854426
|
G | A | 86 | a0001c0001t0003g0100a0001c0001t0014g0102a0001c0001t0015g0101others(83): Show | 87 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.174+9777G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113854426 | ||||||
| chr3:113854509
|
G | C | 2 | a0001c0001t0001g0019a0001c0001t0001g0020 | 2 | NA18972.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.174+9860G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113854509 | ||||||
| chr3:113854590
|
A | G | 12 | a0001c0001t0001g0006a0001c0001t0006g0124a0001c0001t0006g0125others(9): Show | 12 | HG00735.hp2 HG02280.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.174+9941A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113854590 | ||||||
| chr3:113854709
|
A | G | 1 | a0001c0001t0003g0126 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.174+10060A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113854709 | ||||||
| chr3:113854884
|
G | A | 4 | a0001c0003t0002g0293a0001c0005t0001g0292a0001c0005t0002g0295others(1): Show | 4 | HG01109.hp2 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+10235G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113854884 | ||||||
| chr3:113855045
|
C | G | 4 | a0001c0003t0002g0293a0001c0005t0001g0292a0001c0005t0002g0295others(1): Show | 4 | HG01109.hp2 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+10396C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113855045 | ||||||
| chr3:113855050
|
G | A | 1 | a0001c0005t0015g0128 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.174+10401G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113855050 | ||||||
| chr3:113855170
|
G | C | 1 | a0001c0001t0002g0175 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.174+10521G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113855170 | ||||||
| chr3:113855234
|
C | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(151): Show | 155 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.174+10585C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113855234 | ||||||
| chr3:113855586
|
T | C | 9 | a0001c0001t0001g0013a0001c0001t0001g0290a0001c0001t0001g0299others(6): Show | 9 | HG01106.hp2 HG01358.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.174+10937T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113855586 | ||||||
| chr3:113855705
|
G | GAAA | 7 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(4): Show | 7 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+11066_174+1106 others(7): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113855705 | |||||
| chr3:113855869
|
C | T | 2 | a0002c0006t0024g0133a0002c0006t0025g0130 | 2 | HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.174+11220C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113855869 | ||||||
| chr3:113855896
|
A | T | 2 | a0001c0003t0002g0188a0001c0003t0002g0289 | 2 | HG00280.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.174+11247A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113855896 | ||||||
| chr3:113856041
|
A | G | 7 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(4): Show | 7 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+11392A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113856041 | ||||||
| chr3:113856140
|
G | A | 7 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(4): Show | 7 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+11491G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113856140 | ||||||
| chr3:113856226
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.174+11577C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113856226 | ||||||
| chr3:113856276
|
G | C | 7 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(4): Show | 7 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+11627G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113856276 | ||||||
| chr3:113856383
|
T | C | 1 | a0001c0001t0003g0094 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.174+11734T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113856383 | ||||||
| chr3:113856523
|
T | TTATG | 155 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(152): Show | 156 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.174+11894_174+1189 others(8): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113856523 | |||||
| chr3:113856523
|
T | TTATGTAT others(5): Show |
1 | a0012c0016t0001g0229 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.174+11886_174+1189 others(16): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113856523 | |||||
| chr3:113856543
|
G | T | 5 | a0001c0001t0001g0013a0001c0001t0001g0299a0001c0001t0002g0296others(2): Show | 5 | HG01106.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.174+11894G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113856543 | ||||||
| chr3:113856547
|
T | G | 13 | a0001c0001t0001g0006a0001c0001t0006g0124a0001c0001t0006g0125others(10): Show | 13 | HG00735.hp2 HG01884.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.174+11898T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113856547 | ||||||
| chr3:113856570
|
T | C | 148 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(145): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.174+11921T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113856570 | ||||||
| chr3:113856586
|
C | T | 12 | a0001c0001t0001g0006a0001c0001t0006g0124a0001c0001t0006g0125others(9): Show | 12 | HG00735.hp2 HG02280.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.174+11937C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113856586 | ||||||
| chr3:113856599
|
G | C | 1 | a0001c0002t0001g0001 | 2 | HG00099.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.174+11950G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113856599 | ||||||
| chr3:113856623
|
T | G | 1 | a0001c0004t0004g0066 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.174+11974T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113856623 | ||||||
| chr3:113856843
|
AT | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0135others(17): Show | 20 | HG00735.hp2 HG01074.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.174+12211delT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113856843 | |||||
| chr3:113856843
|
ATT | A | 86 | a0001c0001t0003g0100a0001c0001t0014g0102a0001c0001t0015g0101others(83): Show | 87 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.174+12210_174+1221 others(6): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113856843 | |||||
| chr3:113856860
|
T | A | 1 | a0001c0003t0002g0230 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.174+12211T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113856860 | ||||||
| chr3:113856860
|
TA | T | 13 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(10): Show | 13 | HG01109.hp2 HG01934.hp1 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.174+12215delA | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113856860 | |||||
| chr3:113856861
|
A | T | 40 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(37): Show | 40 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.174+12212A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113856861 | ||||||
| chr3:113856864
|
A | G | 85 | a0001c0001t0003g0100a0001c0001t0014g0102a0001c0001t0015g0101others(82): Show | 86 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.174+12215A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113856864 | ||||||
| chr3:113856920
|
A | G | 2 | a0001c0001t0001g0181a0001c0001t0017g0259 | 2 | HG03017.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.174+12271A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113856920 | ||||||
| chr3:113857118
|
C | T | 4 | a0001c0001t0001g0274a0001c0001t0003g0123a0001c0001t0021g0287others(1): Show | 4 | HG01891.hp1 HG02717.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.175-12389C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113857118 | ||||||
| chr3:113857119
|
G | A | 38 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(35): Show | 38 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.175-12388G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113857119 | ||||||
| chr3:113857172
|
C | CA | 10 | a0001c0001t0001g0286a0001c0001t0001g0304a0001c0001t0001g0305others(7): Show | 10 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(7): Show |
intron_variant | MODIFIER | c.175-12332dupA | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113857172 | |||||
| chr3:113857176
|
C | A | 10 | a0001c0001t0001g0286a0001c0001t0001g0304a0001c0001t0001g0305others(7): Show | 10 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(7): Show |
intron_variant | MODIFIER | c.175-12331C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113857176 | ||||||
| chr3:113857176
|
C | CA | 137 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(134): Show | 138 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.175-12324dupA | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113857176 | |||||
| chr3:113857202
|
G | A | 147 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(144): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.175-12305G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113857202 | ||||||
| chr3:113857244
|
G | A | 7 | a0001c0001t0001g0253a0001c0001t0001g0275a0001c0001t0022g0132others(4): Show | 7 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.175-12263G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113857244 | ||||||
| chr3:113857265
|
C | G | 4 | a0001c0002t0003g0051a0001c0004t0004g0034a0001c0004t0005g0035others(1): Show | 4 | HG00673.hp1 HG02165.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-12242C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113857265 | ||||||
| chr3:113857355
|
A | G | 12 | a0001c0001t0001g0006a0001c0001t0006g0124a0001c0001t0006g0125others(9): Show | 12 | HG00735.hp2 HG02280.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-12152A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113857355 | ||||||
| chr3:113857361
|
G | A | 7 | a0001c0001t0001g0253a0001c0001t0001g0275a0001c0001t0022g0132others(4): Show | 7 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.175-12146G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113857361 | ||||||
| chr3:113857378
|
CT | C | 271 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(268): Show | 273 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.175-12114delT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113857378 | |||||
| chr3:113857398
|
C | T | 12 | a0001c0001t0001g0006a0001c0001t0006g0124a0001c0001t0006g0125others(9): Show | 12 | HG00735.hp2 HG02280.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-12109C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113857398 | ||||||
| chr3:113857409
|
T | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(151): Show | 155 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.175-12098T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113857409 | ||||||
| chr3:113857444
|
T | C | 314 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.175-12063T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113857444 | ||||||
| chr3:113857517
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.175-11990G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113857517 | ||||||
| chr3:113857520
|
C | T | 1 | a0001c0001t0006g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.175-11987C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113857520 | ||||||
| chr3:113857566
|
C | T | 1 | a0001c0003t0002g0149 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.175-11941C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113857566 | ||||||
| chr3:113857597
|
C | T | 2 | a0001c0001t0003g0123a0007c0013t0003g0122 | 2 | HG01891.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.175-11910C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113857597 | ||||||
| chr3:113857728
|
C | A | 4 | a0001c0001t0003g0100a0001c0001t0014g0102a0001c0001t0015g0101others(1): Show | 4 | HG02145.hp1 HG02257.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.175-11779C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113857728 | ||||||
| chr3:113857875
|
T | G | 2 | a0001c0004t0005g0027a0001c0004t0005g0028 | 2 | NA18982.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.175-11632T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113857875 | ||||||
| chr3:113858060
|
A | G | 7 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(4): Show | 7 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.175-11447A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113858060 | ||||||
| chr3:113858106
|
A | C | 3 | a0001c0002t0003g0061a0001c0002t0004g0098a0001c0002t0027g0062 | 3 | HG02055.hp1 HG02723.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.175-11401A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113858106 | ||||||
| chr3:113858255
|
CAG | C | 3 | a0001c0002t0003g0053a0001c0002t0003g0082a0001c0002t0004g0059 | 3 | HG00639.hp2 HG01943.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.175-11249_175-1124 others(6): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113858255 | |||||
| chr3:113858267
|
C | T | 1 | a0001c0001t0001g0314 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.175-11240C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113858267 | ||||||
| chr3:113858393
|
C | CGT | 69 | a0001c0002t0001g0001a0001c0002t0001g0023a0001c0002t0001g0052others(66): Show | 70 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.175-11114_175-1111 others(6): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113858393 | ||||||
| chr3:113858393
|
C | CGTT | 13 | a0001c0002t0003g0025a0001c0002t0003g0026a0001c0002t0003g0078others(10): Show | 13 | HG00323.hp2 HG00597.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.175-11114_175-1111 others(7): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113858393 | ||||||
| chr3:113858394
|
A | AT | 139 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(136): Show | 140 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.175-11094dupT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113858394 | |||||
| chr3:113858394
|
A | ATT | 48 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(45): Show | 48 | HG00140.hp2 HG00597.hp1 HG01243.hp2 others(45): Show |
intron_variant | MODIFIER | c.175-11095_175-1109 others(6): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113858394 | |||||
| chr3:113858394
|
A | ATTT | 28 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0121others(25): Show | 28 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.175-11096_175-1109 others(7): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113858394 | |||||
| chr3:113858394
|
A | ATTTT | 6 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(3): Show | 6 | HG01934.hp1 HG02273.hp1 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.175-11097_175-1109 others(8): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113858394 | |||||
| chr3:113858394
|
A | T | 82 | a0001c0002t0001g0001a0001c0002t0001g0023a0001c0002t0001g0052others(79): Show | 83 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.175-11113A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113858394 | ||||||
| chr3:113858551
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.175-10956C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113858551 | ||||||
| chr3:113858811
|
G | A | 2 | a0001c0001t0001g0006a0010c0011t0001g0011 | 2 | HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.175-10696G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113858811 | ||||||
| chr3:113858835
|
A | AG | 4 | a0001c0001t0001g0277a0001c0001t0002g0281a0001c0003t0002g0279others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-10670dupG | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113858835 | |||||
| chr3:113859047
|
T | A | 53 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(50): Show | 53 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.175-10460T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113859047 | ||||||
| chr3:113859408
|
G | T | 106 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(103): Show | 107 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.175-10099G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113859408 | ||||||
| chr3:113859687
|
G | T | 1 | a0001c0001t0017g0259 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.175-9820G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113859687 | ||||||
| chr3:113859821
|
G | A | 8 | a0001c0001t0008g0005a0001c0001t0010g0008a0001c0001t0016g0003others(5): Show | 8 | HG00735.hp2 HG02280.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.175-9686G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113859821 | ||||||
| chr3:113859884
|
C | T | 1 | a0001c0002t0027g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.175-9623C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113859884 | ||||||
| chr3:113859987
|
A | G | 4 | a0001c0001t0008g0005a0001c0005t0010g0004a0001c0005t0010g0007others(1): Show | 4 | HG02280.hp2 HG02647.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-9520A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113859987 | ||||||
| chr3:113860230
|
C | T | 5 | a0001c0001t0001g0013a0001c0001t0001g0299a0001c0001t0002g0296others(2): Show | 5 | HG01106.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.175-9277C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113860230 | ||||||
| chr3:113860366
|
T | A | 42 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(39): Show | 42 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.175-9141T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113860366 | ||||||
| chr3:113860483
|
A | G | 1 | a0003c0018t0001g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.175-9024A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113860483 | ||||||
| chr3:113860549
|
A | G | 2 | a0001c0002t0001g0023a0001c0002t0001g0052 | 2 | HG00639.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.175-8958A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113860549 | ||||||
| chr3:113860706
|
C | T | 86 | a0001c0001t0003g0100a0001c0001t0014g0102a0001c0001t0015g0101others(83): Show | 87 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.175-8801C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113860706 | ||||||
| chr3:113860747
|
C | T | 1 | a0001c0001t0001g0249 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.175-8760C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113860747 | ||||||
| chr3:113860862
|
A | T | 1 | a0001c0001t0002g0301 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.175-8645A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113860862 | ||||||
| chr3:113860874
|
G | A | 9 | a0001c0001t0001g0013a0001c0001t0001g0290a0001c0001t0001g0299others(6): Show | 9 | HG01106.hp2 HG01358.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.175-8633G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113860874 | ||||||
| chr3:113860943
|
G | T | 1 | a0001c0004t0005g0033 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.175-8564G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113860943 | ||||||
| chr3:113860967
|
TA | T | 160 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(157): Show | 161 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.175-8525delA | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113860967 | |||||
| chr3:113861035
|
G | T | 3 | a0001c0001t0001g0290a0001c0001t0002g0301a0001c0001t0012g0300 | 3 | HG01358.hp2 HG02486.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.175-8472G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113861035 | ||||||
| chr3:113861062
|
T | C | 5 | a0001c0001t0001g0013a0001c0001t0001g0299a0001c0001t0002g0296others(2): Show | 5 | HG01106.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.175-8445T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113861062 | ||||||
| chr3:113861301
|
C | T | 10 | a0001c0002t0001g0140a0001c0002t0003g0026a0001c0002t0003g0048others(7): Show | 10 | HG00323.hp2 HG01169.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.175-8206C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113861301 | ||||||
| chr3:113861324
|
G | T | 1 | a0001c0002t0001g0056 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.175-8183G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113861324 | ||||||
| chr3:113861349
|
T | C | 1 | a0001c0004t0004g0058 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.175-8158T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113861349 | ||||||
| chr3:113861557
|
A | T | 86 | a0001c0001t0003g0100a0001c0001t0014g0102a0001c0001t0015g0101others(83): Show | 87 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.175-7950A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113861557 | ||||||
| chr3:113861910
|
G | A | 86 | a0001c0001t0003g0100a0001c0001t0014g0102a0001c0001t0015g0101others(83): Show | 87 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.175-7597G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113861910 | ||||||
| chr3:113861935
|
A | T | 3 | a0001c0001t0001g0290a0001c0001t0002g0301a0001c0001t0012g0300 | 3 | HG01358.hp2 HG02486.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.175-7572A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113861935 | ||||||
| chr3:113861938
|
A | G | 50 | a0001c0001t0001g0022a0001c0001t0001g0136a0001c0001t0001g0161others(47): Show | 50 | HG00280.hp2 HG00558.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.175-7569A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113861938 | ||||||
| chr3:113861956
|
G | A | 7 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(4): Show | 7 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.175-7551G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113861956 | ||||||
| chr3:113861961
|
G | A | 7 | a0001c0001t0001g0253a0001c0001t0001g0275a0001c0001t0022g0132others(4): Show | 7 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.175-7546G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113861961 | ||||||
| chr3:113862012
|
A | G | 3 | a0001c0001t0001g0290a0001c0001t0002g0301a0001c0001t0012g0300 | 3 | HG01358.hp2 HG02486.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.175-7495A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113862012 | ||||||
| chr3:113862193
|
C | G | 69 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(66): Show | 70 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.175-7314C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113862193 | ||||||
| chr3:113862352
|
T | G | 1 | a0001c0002t0003g0083 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.175-7155T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113862352 | ||||||
| chr3:113862557
|
G | A | 1 | a0013c0007t0002g0255 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.175-6950G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113862557 | ||||||
| chr3:113862571
|
T | C | 1 | a0003c0018t0001g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.175-6936T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113862571 | ||||||
| chr3:113862600
|
C | T | 2 | a0001c0001t0001g0160a0001c0003t0007g0159 | 2 | HG00558.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.175-6907C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113862600 | ||||||
| chr3:113862605
|
G | A | 9 | a0001c0001t0001g0013a0001c0001t0001g0290a0001c0001t0001g0299others(6): Show | 9 | HG01106.hp2 HG01358.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.175-6902G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113862605 | ||||||
| chr3:113862692
|
C | A | 7 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(4): Show | 7 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.175-6815C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113862692 | ||||||
| chr3:113862718
|
A | G | 1 | a0001c0001t0002g0301 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.175-6789A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113862718 | ||||||
| chr3:113862742
|
T | G | 9 | a0001c0001t0001g0013a0001c0001t0001g0290a0001c0001t0001g0299others(6): Show | 9 | HG01106.hp2 HG01358.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.175-6765T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113862742 | ||||||
| chr3:113862759
|
G | T | 1 | a0001c0001t0001g0253 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.175-6748G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113862759 | ||||||
| chr3:113862859
|
C | T | 2 | a0001c0001t0001g0290a0001c0001t0002g0301 | 2 | HG01358.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.175-6648C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113862859 | ||||||
| chr3:113863051
|
A | G | 86 | a0001c0001t0003g0100a0001c0001t0014g0102a0001c0001t0015g0101others(83): Show | 87 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.175-6456A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113863051 | ||||||
| chr3:113863114
|
G | A | 82 | a0001c0002t0001g0001a0001c0002t0001g0023a0001c0002t0001g0052others(79): Show | 83 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.175-6393G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113863114 | ||||||
| chr3:113863314
|
G | A | 3 | a0001c0001t0006g0310a0001c0001t0008g0315a0002c0006t0009g0311 | 3 | HG02055.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.175-6193G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113863314 | ||||||
| chr3:113863652
|
A | AGT | 82 | a0001c0002t0001g0001a0001c0002t0001g0023a0001c0002t0001g0052others(79): Show | 83 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.175-5853_175-5852d others(4): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113863652 | |||||
| chr3:113863674
|
C | T | 4 | a0001c0001t0002g0257a0001c0001t0002g0263a0001c0001t0011g0261others(1): Show | 4 | HG00741.hp2 HG01346.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-5833C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113863674 | ||||||
| chr3:113863696
|
C | T | 5 | a0001c0001t0001g0274a0001c0001t0003g0123a0001c0001t0021g0287others(2): Show | 5 | HG01891.hp1 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.175-5811C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113863696 | ||||||
| chr3:113863697
|
C | T | 86 | a0001c0001t0003g0100a0001c0001t0014g0102a0001c0001t0015g0101others(83): Show | 87 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.175-5810C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113863697 | ||||||
| chr3:113863920
|
A | G | 68 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(65): Show | 69 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.175-5587A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113863920 | ||||||
| chr3:113863960
|
T | C | 9 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0243others(6): Show | 9 | HG02074.hp2 NA18941.hp2 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.175-5547T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113863960 | ||||||
| chr3:113864170
|
T | G | 2 | a0001c0001t0012g0103a0001c0001t0012g0116 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.175-5337T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113864170 | ||||||
| chr3:113864330
|
T | G | 7 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(4): Show | 7 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.175-5177T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113864330 | ||||||
| chr3:113864457
|
C | T | 1 | a0001c0005t0010g0302 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.175-5050C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113864457 | ||||||
| chr3:113864458
|
A | G | 1 | a0001c0002t0001g0023 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.175-5049A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113864458 | ||||||
| chr3:113864799
|
T | C | 12 | a0001c0001t0001g0006a0001c0001t0006g0124a0001c0001t0006g0125others(9): Show | 12 | HG00735.hp2 HG02280.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-4708T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113864799 | ||||||
| chr3:113864825
|
C | T | 2 | a0001c0001t0006g0145a0001c0001t0006g0151 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.175-4682C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113864825 | ||||||
| chr3:113864902
|
G | A | 154 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(151): Show | 155 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.175-4605G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113864902 | ||||||
| chr3:113864948
|
T | A | 13 | a0001c0001t0001g0161a0001c0001t0001g0200a0001c0001t0001g0210others(10): Show | 13 | HG00558.hp2 HG02074.hp2 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.175-4559T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113864948 | ||||||
| chr3:113865012
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.175-4495T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113865012 | ||||||
| chr3:113865022
|
A | T | 2 | a0001c0003t0002g0142a0001c0003t0007g0237 | 2 | NA18940.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.175-4485A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113865022 | ||||||
| chr3:113865123
|
G | A | 8 | a0001c0001t0001g0022a0001c0001t0001g0202a0001c0001t0001g0203others(5): Show | 8 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.175-4384G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113865123 | ||||||
| chr3:113865326
|
G | A | 1 | a0003c0018t0001g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.175-4181G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113865326 | ||||||
| chr3:113865425
|
C | T | 1 | a0003c0018t0001g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.175-4082C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113865425 | ||||||
| chr3:113865640
|
T | A | 160 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(157): Show | 161 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.175-3867T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113865640 | ||||||
| chr3:113865923
|
T | C | 1 | a0001c0003t0002g0212 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.175-3584T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113865923 | ||||||
| chr3:113866022
|
G | C | 1 | a0001c0001t0001g0274 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.175-3485G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113866022 | ||||||
| chr3:113866201
|
A | G | 321 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(318): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.175-3306A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113866201 | ||||||
| chr3:113866288
|
G | T | 1 | a0001c0003t0002g0183 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.175-3219G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113866288 | ||||||
| chr3:113866307
|
A | C | 196 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(193): Show | 197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.175-3200A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113866307 | ||||||
| chr3:113866389
|
A | G | 42 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(39): Show | 42 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.175-3118A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113866389 | ||||||
| chr3:113866786
|
T | C | 98 | a0001c0001t0001g0006a0001c0001t0003g0100a0001c0001t0006g0124others(95): Show | 99 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.175-2721T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113866786 | ||||||
| chr3:113866827
|
C | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(151): Show | 155 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.175-2680C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113866827 | ||||||
| chr3:113866835
|
C | CT | 151 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0017others(148): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.175-2661dupT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113866835 | |||||
| chr3:113866921
|
C | T | 3 | a0001c0001t0001g0144a0001c0001t0001g0153a0001c0001t0014g0088 | 3 | HG02717.hp1 HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.175-2586C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113866921 | ||||||
| chr3:113866931
|
G | C | 314 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.175-2576G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113866931 | ||||||
| chr3:113866959
|
G | T | 4 | a0001c0003t0002g0293a0001c0005t0001g0292a0001c0005t0002g0295others(1): Show | 4 | HG01109.hp2 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-2548G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113866959 | ||||||
| chr3:113867115
|
C | T | 1 | a0003c0018t0001g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.175-2392C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113867115 | ||||||
| chr3:113867167
|
G | A | 1 | a0005c0008t0023g0131 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.175-2340G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113867167 | ||||||
| chr3:113867180
|
T | C | 154 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(151): Show | 155 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.175-2327T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113867180 | ||||||
| chr3:113867219
|
C | T | 4 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(1): Show | 4 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-2288C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113867219 | ||||||
| chr3:113867596
|
C | T | 82 | a0001c0002t0001g0001a0001c0002t0001g0023a0001c0002t0001g0052others(79): Show | 83 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.175-1911C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113867596 | ||||||
| chr3:113867631
|
G | C | 2 | a0001c0001t0011g0261a0001c0003t0002g0271 | 2 | HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.175-1876G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113867631 | ||||||
| chr3:113867640
|
A | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(151): Show | 155 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.175-1867A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113867640 | ||||||
| chr3:113867654
|
A | G | 314 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.175-1853A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113867654 | ||||||
| chr3:113867660
|
AC | A | 12 | a0001c0001t0001g0006a0001c0001t0006g0124a0001c0001t0006g0125others(9): Show | 12 | HG00735.hp2 HG02280.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.175-1844delC | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113867660 | |||||
| chr3:113867756
|
A | T | 1 | a0001c0002t0004g0047 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.175-1751A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113867756 | ||||||
| chr3:113867764
|
G | A | 1 | a0001c0002t0001g0001 | 2 | HG00099.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.175-1743G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113867764 | ||||||
| chr3:113867929
|
C | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(151): Show | 155 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.175-1578C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113867929 | ||||||
| chr3:113868171
|
T | G | 4 | a0001c0003t0002g0293a0001c0005t0001g0292a0001c0005t0002g0295others(1): Show | 4 | HG01109.hp2 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-1336T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113868171 | ||||||
| chr3:113868369
|
A | T | 1 | a0001c0001t0002g0280 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.175-1138A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113868369 | ||||||
| chr3:113868508
|
A | C | 2 | a0001c0001t0001g0198a0001c0003t0002g0189 | 2 | NA18952.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.175-999A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113868508 | ||||||
| chr3:113868560
|
T | A | 82 | a0001c0002t0001g0001a0001c0002t0001g0023a0001c0002t0001g0052others(79): Show | 83 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.175-947T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113868560 | ||||||
| chr3:113868679
|
T | C | 7 | a0001c0001t0001g0253a0001c0001t0001g0275a0001c0001t0022g0132others(4): Show | 7 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.175-828T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | chr3 | 113868679 | ||||||
| chr3:113868979
|
CAG | C | 9 | a0001c0001t0001g0013a0001c0001t0001g0290a0001c0001t0001g0299others(6): Show | 9 | HG01106.hp2 HG01358.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.175-525_175-524del others(2): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 113868979 | |||||
| chr3:113869598
|
T | C | 42 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(39): Show | 42 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(39): Show |
splice_region_variant&intron_variant | LOW | c.259+7T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113869598 | ||||||
| chr3:113869840
|
G | C | 1 | a0001c0001t0001g0247 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.259+249G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113869840 | ||||||
| chr3:113870032
|
C | A | 196 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(193): Show | 197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.259+441C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113870032 | ||||||
| chr3:113870227
|
G | A | 3 | a0001c0004t0005g0064a0001c0004t0005g0079a0001c0004t0005g0081 | 3 | HG01433.hp1 HG01952.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.259+636G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113870227 | ||||||
| chr3:113870353
|
C | A | 1 | a0001c0004t0004g0050 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.259+762C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113870353 | ||||||
| chr3:113870426
|
A | G | 321 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(318): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.259+835A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113870426 | ||||||
| chr3:113870508
|
G | T | 1 | a0001c0001t0001g0153 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.259+917G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113870508 | ||||||
| chr3:113870604
|
G | A | 5 | a0001c0001t0001g0013a0001c0001t0001g0299a0001c0001t0002g0296others(2): Show | 5 | HG01106.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+1013G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113870604 | ||||||
| chr3:113870819
|
A | AT | 21 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(18): Show | 21 | HG00558.hp1 HG01106.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.259+1243dupT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 113870819 | |||||
| chr3:113870859
|
G | T | 1 | a0001c0001t0001g0022 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.259+1268G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113870859 | ||||||
| chr3:113870953
|
CAAAT | C | 20 | a0001c0001t0001g0006a0001c0001t0001g0253a0001c0001t0001g0275others(17): Show | 20 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.259+1378_259+1381d others(6): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 113870953 | |||||
| chr3:113870969
|
T | A | 1 | a0001c0001t0010g0008 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.259+1378T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113870969 | ||||||
| chr3:113870970
|
A | C | 1 | a0001c0001t0010g0008 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.259+1379A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113870970 | ||||||
| chr3:113870972
|
A | C | 1 | a0001c0001t0010g0008 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.259+1381A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113870972 | ||||||
| chr3:113870974
|
G | C | 1 | a0001c0001t0010g0008 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.259+1383G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113870974 | ||||||
| chr3:113870974
|
G | GAC | 4 | a0001c0001t0001g0274a0001c0001t0001g0285a0001c0001t0001g0286others(1): Show | 4 | HG00140.hp2 HG01256.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.259+1431_259+1432d others(4): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 113870974 | |||||
| chr3:113871004
|
CACACACA others(13): Show |
C | 2 | a0001c0001t0003g0100a0001c0001t0014g0102 | 2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.259+1415_259+1434d others(22): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 113871004 | |||||
| chr3:113871006
|
CACACACA others(11): Show |
C | 4 | a0001c0001t0001g0006a0001c0001t0012g0300a0001c0001t0018g0127others(1): Show | 4 | HG02486.hp1 HG02630.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.259+1417_259+1434d others(20): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 113871006 | |||||
| chr3:113871007
|
A | G | 2 | a0001c0001t0002g0209a0001c0003t0002g0204 | 2 | HG03710.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.259+1416A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113871007 | ||||||
| chr3:113871008
|
CACACACA others(9): Show |
C | 1 | a0001c0001t0015g0101 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.259+1419_259+1434d others(18): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 113871008 | |||||
| chr3:113871009
|
A | G | 3 | a0001c0001t0001g0203a0001c0001t0001g0251a0001c0003t0002g0252 | 3 | HG02056.hp2 HG02523.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.259+1418A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113871009 | ||||||
| chr3:113871010
|
CACACACA others(7): Show |
C | 2 | a0001c0002t0001g0140a0001c0004t0004g0076 | 2 | HG03239.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.259+1421_259+1434d others(16): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 113871010 | |||||
| chr3:113871011
|
A | G | 95 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(92): Show | 96 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.259+1420A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113871011 | ||||||
| chr3:113871013
|
A | G | 32 | a0001c0001t0001g0148a0001c0001t0001g0164a0001c0001t0001g0178others(29): Show | 32 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.259+1422A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113871013 | ||||||
| chr3:113871014
|
CACACACA others(3): Show |
C | 73 | a0001c0001t0003g0123a0001c0002t0001g0001a0001c0002t0001g0023others(70): Show | 74 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.259+1425_259+1434d others(12): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 113871014 | |||||
| chr3:113871015
|
A | G | 20 | a0001c0001t0001g0144a0001c0001t0001g0152a0001c0001t0001g0153others(17): Show | 20 | HG00408.hp2 HG01261.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.259+1424A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113871015 | ||||||
| chr3:113871016
|
CACACACA others(1): Show |
C | 17 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0107others(14): Show | 17 | HG00735.hp1 HG01358.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.259+1427_259+1434d others(10): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 113871016 | |||||
| chr3:113871018
|
CACACAG | C | 14 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(11): Show | 14 | HG00642.hp1 HG01496.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.259+1429_259+1434d others(8): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 113871018 | |||||
| chr3:113871020
|
CACAG | C | 119 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(116): Show | 120 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.259+1431_259+1434d others(6): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 113871020 | |||||
| chr3:113871022
|
CAG | C | 46 | a0001c0001t0001g0148a0001c0001t0001g0164a0001c0001t0001g0178others(43): Show | 46 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.259+1434_259+1435d others(4): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 113871022 | |||||
| chr3:113871024
|
G | C | 43 | a0001c0001t0001g0144a0001c0001t0001g0152a0001c0001t0001g0153others(40): Show | 43 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(40): Show |
intron_variant | MODIFIER | c.259+1433G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113871024 | ||||||
| chr3:113871026
|
G | C | 1 | a0001c0001t0021g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.259+1435G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113871026 | ||||||
| chr3:113871261
|
A | C | 4 | a0001c0003t0002g0293a0001c0005t0001g0292a0001c0005t0002g0295others(1): Show | 4 | HG01109.hp2 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+1670A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113871261 | ||||||
| chr3:113871353
|
T | A | 7 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(4): Show | 7 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.259+1762T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113871353 | ||||||
| chr3:113871465
|
C | T | 4 | a0001c0003t0002g0293a0001c0005t0001g0292a0001c0005t0002g0295others(1): Show | 4 | HG01109.hp2 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+1874C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113871465 | ||||||
| chr3:113871478
|
G | C | 1 | a0001c0004t0005g0027 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.259+1887G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113871478 | ||||||
| chr3:113871530
|
G | A | 1 | a0001c0001t0012g0300 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.259+1939G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113871530 | ||||||
| chr3:113871596
|
T | G | 2 | a0001c0004t0004g0039a0001c0004t0004g0040 | 2 | NA18985.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.259+2005T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113871596 | ||||||
| chr3:113871667
|
C | A | 86 | a0001c0001t0003g0100a0001c0001t0014g0102a0001c0001t0015g0101others(83): Show | 87 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.259+2076C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113871667 | ||||||
| chr3:113871724
|
A | G | 1 | a0001c0003t0002g0230 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.259+2133A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113871724 | ||||||
| chr3:113871744
|
C | CAA | 139 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(136): Show | 140 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.259+2174_259+2175d others(4): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 113871744 | |||||
| chr3:113871744
|
C | CAAA | 12 | a0001c0001t0001g0163a0001c0001t0001g0193a0001c0001t0001g0226others(9): Show | 12 | HG00673.hp2 HG00741.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.259+2173_259+2175d others(5): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 113871744 | |||||
| chr3:113871744
|
CA | C | 16 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0019others(13): Show | 16 | HG01358.hp2 HG01934.hp1 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.259+2175delA | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 113871744 | |||||
| chr3:113871744
|
CAA | C | 6 | a0001c0001t0001g0013a0001c0001t0001g0113a0001c0001t0001g0120others(3): Show | 6 | HG01106.hp2 HG02897.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.259+2174_259+2175d others(4): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 113871744 | |||||
| chr3:113871757
|
A | C | 85 | a0001c0001t0003g0100a0001c0001t0014g0102a0001c0001t0015g0101others(82): Show | 86 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.259+2166A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113871757 | ||||||
| chr3:113871811
|
T | C | 196 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(193): Show | 197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.259+2220T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113871811 | ||||||
| chr3:113871860
|
G | A | 154 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(151): Show | 155 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.259+2269G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113871860 | ||||||
| chr3:113872312
|
A | G | 8 | a0001c0001t0003g0100a0001c0001t0014g0102a0001c0001t0015g0101others(5): Show | 8 | HG01109.hp2 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.259+2721A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113872312 | ||||||
| chr3:113872370
|
A | G | 94 | a0001c0001t0001g0006a0001c0001t0006g0124a0001c0001t0006g0125others(91): Show | 95 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.259+2779A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113872370 | ||||||
| chr3:113872391
|
C | CT | 60 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0021others(57): Show | 60 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.259+2821dupT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 113872391 | |||||
| chr3:113872391
|
CT | C | 92 | a0001c0001t0001g0006a0001c0001t0006g0124a0001c0001t0006g0125others(89): Show | 93 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.259+2821delT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 113872391 | |||||
| chr3:113872391
|
CTTTTTTT others(5): Show |
C | 9 | a0001c0001t0001g0013a0001c0001t0001g0290a0001c0001t0001g0299others(6): Show | 9 | HG01106.hp2 HG01358.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.259+2810_259+2821d others(14): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 113872391 | |||||
| chr3:113872401
|
T | C | 82 | a0001c0002t0001g0001a0001c0002t0001g0023a0001c0002t0001g0052others(79): Show | 83 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.259+2810T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113872401 | ||||||
| chr3:113872440
|
A | G | 305 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(302): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.259+2849A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113872440 | ||||||
| chr3:113872463
|
C | T | 2 | a0001c0001t0003g0123a0007c0013t0003g0122 | 2 | HG01891.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.259+2872C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113872463 | ||||||
| chr3:113872786
|
C | G | 42 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(39): Show | 42 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.260-2698C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113872786 | ||||||
| chr3:113872791
|
G | A | 3 | a0001c0002t0003g0060a0001c0002t0003g0083a0001c0002t0003g0084 | 3 | HG00597.hp2 HG02165.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.260-2693G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113872791 | ||||||
| chr3:113872843
|
G | A | 154 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(151): Show | 155 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.260-2641G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113872843 | ||||||
| chr3:113872849
|
A | G | 1 | a0001c0003t0002g0250 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.260-2635A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113872849 | ||||||
| chr3:113872917
|
C | CA | 21 | a0001c0001t0001g0022a0001c0001t0001g0107a0001c0001t0001g0109others(18): Show | 21 | HG00741.hp2 HG01952.hp2 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.260-2549dupA | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 113872917 | |||||
| chr3:113872917
|
CA | C | 24 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(21): Show | 24 | HG01106.hp2 HG01256.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.260-2549delA | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 113872917 | |||||
| chr3:113872957
|
C | T | 5 | a0001c0001t0006g0106a0001c0001t0012g0103a0001c0001t0012g0104others(2): Show | 5 | HG02615.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.260-2527C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113872957 | ||||||
| chr3:113873050
|
G | A | 1 | a0001c0002t0003g0129 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.260-2434G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113873050 | ||||||
| chr3:113873071
|
C | T | 3 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0002g0273 | 3 | NA18941.hp2 NA18986.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.260-2413C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113873071 | ||||||
| chr3:113873092
|
C | CAAAAAA | 41 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(38): Show | 41 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.260-2379_260-2374d others(8): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 113873092 | |||||
| chr3:113873092
|
C | CAAAAAAA | 11 | a0001c0001t0001g0113a0001c0001t0001g0290a0001c0001t0001g0299others(8): Show | 11 | HG01106.hp2 HG01109.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.260-2380_260-2374d others(9): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 113873092 | |||||
| chr3:113873092
|
C | CAAAAAAA others(1): Show |
99 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0016others(96): Show | 100 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.260-2381_260-2374d others(10): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 113873092 | |||||
| chr3:113873092
|
C | CAAAAAAA others(2): Show |
134 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0019others(131): Show | 135 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.260-2382_260-2374d others(11): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 113873092 | |||||
| chr3:113873092
|
C | CAAAAAAA others(3): Show |
28 | a0001c0001t0001g0015a0001c0001t0001g0150a0001c0001t0001g0198others(25): Show | 28 | HG00438.hp2 HG00741.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.260-2383_260-2374d others(12): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 113873092 | |||||
| chr3:113873116
|
C | T | 1 | a0001c0003t0002g0236 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.260-2368C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113873116 | ||||||
| chr3:113873144
|
C | T | 69 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(66): Show | 70 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.260-2340C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113873144 | ||||||
| chr3:113873174
|
A | C | 203 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(200): Show | 204 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.260-2310A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113873174 | ||||||
| chr3:113873238
|
C | T | 82 | a0001c0002t0001g0001a0001c0002t0001g0023a0001c0002t0001g0052others(79): Show | 83 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.260-2246C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113873238 | ||||||
| chr3:113873278
|
G | GCAA | 4 | a0001c0003t0002g0293a0001c0005t0001g0292a0001c0005t0002g0295others(1): Show | 4 | HG01109.hp2 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-2199_260-2197d others(5): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 113873278 | |||||
| chr3:113873603
|
T | C | 314 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.260-1881T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113873603 | ||||||
| chr3:113873635
|
C | T | 1 | a0001c0001t0021g0287 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.260-1849C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113873635 | ||||||
| chr3:113873808
|
C | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(151): Show | 155 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.260-1676C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113873808 | ||||||
| chr3:113874029
|
A | G | 1 | a0003c0018t0001g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.260-1455A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113874029 | ||||||
| chr3:113874226
|
T | G | 86 | a0001c0001t0003g0100a0001c0001t0014g0102a0001c0001t0015g0101others(83): Show | 87 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.260-1258T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113874226 | ||||||
| chr3:113874400
|
G | C | 3 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0002g0303 | 3 | HG00099.hp1 HG00642.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.260-1084G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113874400 | ||||||
| chr3:113874461
|
A | G | 314 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.260-1023A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113874461 | ||||||
| chr3:113874564
|
T | C | 305 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(302): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.260-920T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113874564 | ||||||
| chr3:113874799
|
T | G | 1 | a0001c0001t0001g0268 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.260-685T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113874799 | ||||||
| chr3:113874943
|
G | A | 1 | a0001c0003t0002g0279 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.260-541G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113874943 | ||||||
| chr3:113875137
|
G | GTT | 154 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(151): Show | 155 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.260-340_260-339dup others(2): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 113875137 | |||||
| chr3:113875349
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.260-135C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113875349 | ||||||
| chr3:113875444
|
A | T | 1 | a0001c0001t0001g0274 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.260-40A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113875444 | ||||||
| chr3:113875450
|
G | A | 14 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(11): Show | 14 | HG02004.hp1 HG02040.hp2 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.260-34G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 3/17 | chr3 | 113875450 | ||||||
| chr3:113875730
|
C | CAT | 320 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(317): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.363+143_363+144ins others(2): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 4/17 | chr3 | 113875730 | ||||||
| chr3:113875730
|
C | T | 1 | a0001c0004t0004g0058 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.363+143C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 4/17 | chr3 | 113875730 | ||||||
| chr3:113875859
|
T | C | 1 | a0001c0003t0002g0293 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.363+272T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 4/17 | chr3 | 113875859 | ||||||
| chr3:113875970
|
T | C | 4 | a0001c0003t0002g0293a0001c0005t0001g0292a0001c0005t0002g0295others(1): Show | 4 | HG01109.hp2 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-195T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 4/17 | chr3 | 113875970 | ||||||
| chr3:113876059
|
T | C | 1 | a0001c0001t0006g0124 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.364-106T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 4/17 | chr3 | 113876059 | ||||||
| chr3:113876296
|
G | A | 4 | a0001c0001t0003g0100a0001c0001t0014g0102a0001c0001t0015g0101others(1): Show | 4 | HG02145.hp1 HG02257.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.459+36G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113876296 | ||||||
| chr3:113876309
|
C | G | 314 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.459+49C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113876309 | ||||||
| chr3:113876422
|
A | G | 82 | a0001c0002t0001g0001a0001c0002t0001g0023a0001c0002t0001g0052others(79): Show | 83 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.459+162A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113876422 | ||||||
| chr3:113876533
|
C | T | 5 | a0001c0001t0001g0161a0001c0001t0001g0200a0001c0001t0001g0228others(2): Show | 5 | HG00558.hp2 HG02155.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.459+273C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113876533 | ||||||
| chr3:113876537
|
A | G | 36 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(33): Show | 36 | HG00140.hp2 HG01243.hp2 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.459+277A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113876537 | ||||||
| chr3:113876542
|
T | A | 2 | a0001c0002t0003g0048a0001c0002t0003g0078 | 2 | HG01496.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.459+282T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113876542 | ||||||
| chr3:113876621
|
CA | C | 34 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(31): Show | 34 | HG00140.hp2 HG01169.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.459+362delA | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113876621 | ||||||
| chr3:113876758
|
C | T | 4 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0021others(1): Show | 4 | HG01934.hp1 HG01952.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.459+498C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113876758 | ||||||
| chr3:113876849
|
G | GA | 63 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0144others(60): Show | 63 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.459+599dupA | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr3 | 113876849 | |||||
| chr3:113876882
|
G | A | 1 | a0001c0003t0007g0237 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.459+622G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113876882 | ||||||
| chr3:113877054
|
C | T | 1 | a0001c0001t0002g0172 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.459+794C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113877054 | ||||||
| chr3:113877062
|
A | G | 143 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(140): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.459+802A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113877062 | ||||||
| chr3:113877085
|
G | A | 3 | a0001c0001t0003g0100a0001c0001t0014g0102a0001c0001t0015g0101 | 3 | HG02145.hp1 HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.459+825G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113877085 | ||||||
| chr3:113877299
|
A | G | 1 | a0001c0003t0007g0154 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.459+1039A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113877299 | ||||||
| chr3:113877370
|
C | T | 1 | a0001c0002t0003g0082 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.459+1110C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113877370 | ||||||
| chr3:113877479
|
T | C | 117 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(114): Show | 119 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.459+1219T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113877479 | ||||||
| chr3:113877483
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.459+1223G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113877483 | ||||||
| chr3:113877511
|
A | G | 4 | a0001c0001t0002g0301a0001c0003t0002g0293a0001c0005t0001g0292others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+1251A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113877511 | ||||||
| chr3:113877627
|
A | G | 1 | a0001c0003t0002g0142 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.459+1367A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113877627 | ||||||
| chr3:113877707
|
C | T | 1 | a0001c0002t0003g0080 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.459+1447C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113877707 | ||||||
| chr3:113877712
|
G | A | 1 | a0004c0017t0029g0282 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.459+1452G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113877712 | ||||||
| chr3:113877782
|
GT | G | 8 | a0001c0001t0001g0168a0001c0001t0001g0173a0001c0001t0001g0180others(5): Show | 8 | HG02004.hp2 HG02132.hp2 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.459+1534delT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr3 | 113877782 | |||||
| chr3:113877848
|
G | A | 1 | a0009c0010t0002g0134 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.459+1588G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113877848 | ||||||
| chr3:113877858
|
A | G | 2 | a0001c0001t0003g0089a0001c0001t0030g0155 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.459+1598A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113877858 | ||||||
| chr3:113877863
|
C | T | 5 | a0001c0001t0008g0005a0001c0005t0010g0004a0001c0005t0010g0007others(2): Show | 5 | HG02109.hp2 HG02280.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+1603C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113877863 | ||||||
| chr3:113877881
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.459+1621G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113877881 | ||||||
| chr3:113877938
|
C | A | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.459+1678C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113877938 | ||||||
| chr3:113878079
|
C | T | 2 | a0001c0001t0001g0277a0001c0001t0002g0281 | 2 | HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.459+1819C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113878079 | ||||||
| chr3:113878122
|
C | T | 1 | a0001c0002t0003g0051 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.459+1862C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113878122 | ||||||
| chr3:113878145
|
C | A | 269 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(266): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.459+1885C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113878145 | ||||||
| chr3:113878217
|
T | C | 13 | a0001c0001t0001g0136a0001c0001t0001g0152a0001c0001t0001g0206others(10): Show | 13 | HG00408.hp2 HG02027.hp2 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.459+1957T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113878217 | ||||||
| chr3:113878441
|
A | G | 269 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(266): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.459+2181A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113878441 | ||||||
| chr3:113878630
|
C | T | 5 | a0001c0001t0001g0013a0001c0001t0001g0299a0001c0001t0002g0296others(2): Show | 5 | HG01106.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+2370C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113878630 | ||||||
| chr3:113878650
|
C | T | 1 | a0001c0001t0001g0182 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.459+2390C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113878650 | ||||||
| chr3:113878824
|
C | T | 1 | a0008c0009t0001g0176 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.459+2564C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113878824 | ||||||
| chr3:113878859
|
C | A | 2 | a0002c0006t0024g0133a0002c0006t0025g0130 | 2 | HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.459+2599C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113878859 | ||||||
| chr3:113878932
|
C | T | 1 | a0001c0003t0002g0142 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.459+2672C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113878932 | ||||||
| chr3:113878989
|
G | A | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.459+2729G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113878989 | ||||||
| chr3:113878990
|
C | T | 34 | a0001c0001t0001g0196a0001c0001t0001g0219a0001c0001t0001g0225others(31): Show | 34 | HG00323.hp2 HG00438.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.459+2730C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113878990 | ||||||
| chr3:113879020
|
A | C | 1 | a0001c0001t0001g0163 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.459+2760A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113879020 | ||||||
| chr3:113879046
|
A | C | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.459+2786A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113879046 | ||||||
| chr3:113879159
|
C | A | 4 | a0001c0001t0006g0145a0001c0001t0006g0146a0001c0001t0006g0151others(1): Show | 4 | HG01891.hp2 HG02965.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+2899C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113879159 | ||||||
| chr3:113879164
|
C | A | 5 | a0001c0001t0008g0005a0001c0005t0010g0004a0001c0005t0010g0007others(2): Show | 5 | HG02109.hp2 HG02280.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+2904C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113879164 | ||||||
| chr3:113879204
|
CA | C | 257 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(254): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.459+2956delA | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr3 | 113879204 | |||||
| chr3:113879236
|
A | G | 5 | a0001c0001t0001g0013a0001c0001t0001g0299a0001c0001t0002g0296others(2): Show | 5 | HG01106.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+2976A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113879236 | ||||||
| chr3:113879266
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.459+3006C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113879266 | ||||||
| chr3:113879376
|
T | G | 232 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(229): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.459+3116T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113879376 | ||||||
| chr3:113879389
|
A | C | 2 | a0001c0001t0008g0167a0001c0001t0008g0192 | 2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.459+3129A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113879389 | ||||||
| chr3:113879463
|
G | C | 1 | a0001c0001t0003g0123 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.459+3203G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113879463 | ||||||
| chr3:113879689
|
C | CT | 22 | a0001c0001t0001g0020a0001c0001t0001g0202a0001c0001t0001g0218others(19): Show | 22 | HG00597.hp1 HG00597.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.460-3042dupT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr3 | 113879689 | |||||
| chr3:113879989
|
C | T | 2 | a0001c0001t0022g0132a0005c0008t0023g0131 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.460-2763C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113879989 | ||||||
| chr3:113880091
|
C | G | 4 | a0001c0001t0001g0144a0001c0001t0001g0153a0001c0001t0014g0088others(1): Show | 4 | HG01109.hp2 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-2661C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113880091 | ||||||
| chr3:113880102
|
A | G | 1 | a0001c0002t0003g0084 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.460-2650A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113880102 | ||||||
| chr3:113880389
|
C | G | 1 | a0001c0001t0001g0019 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.460-2363C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113880389 | ||||||
| chr3:113880424
|
A | T | 286 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(283): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.460-2328A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113880424 | ||||||
| chr3:113880441
|
T | C | 4 | a0001c0001t0001g0196a0001c0002t0001g0023a0001c0002t0001g0052others(1): Show | 4 | HG00639.hp1 HG00639.hp2 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-2311T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113880441 | ||||||
| chr3:113880740
|
G | A | 158 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0020others(155): Show | 158 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.460-2012G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113880740 | ||||||
| chr3:113880960
|
A | G | 65 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0144others(62): Show | 65 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.460-1792A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113880960 | ||||||
| chr3:113881139
|
T | A | 2 | a0001c0001t0003g0089a0001c0001t0030g0155 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.460-1613T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113881139 | ||||||
| chr3:113881147
|
A | T | 1 | a0001c0001t0001g0249 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.460-1605A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113881147 | ||||||
| chr3:113881171
|
C | G | 2 | a0001c0001t0003g0126a0001c0001t0012g0300 | 2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.460-1581C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113881171 | ||||||
| chr3:113881204
|
G | A | 1 | a0001c0001t0001g0019 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.460-1548G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113881204 | ||||||
| chr3:113881217
|
C | T | 2 | a0001c0001t0008g0005a0001c0005t0010g0010 | 2 | HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.460-1535C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113881217 | ||||||
| chr3:113881240
|
C | T | 2 | a0001c0001t0008g0167a0001c0001t0008g0192 | 2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.460-1512C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113881240 | ||||||
| chr3:113881559
|
G | A | 2 | a0001c0001t0022g0132a0005c0008t0023g0131 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.460-1193G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113881559 | ||||||
| chr3:113881794
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.460-958T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113881794 | ||||||
| chr3:113882024
|
T | A | 1 | a0002c0006t0009g0311 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.460-728T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113882024 | ||||||
| chr3:113882123
|
G | T | 268 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(265): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.460-629G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 5/17 | chr3 | 113882123 | ||||||
| chr3:113882914
|
T | A | 54 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0090others(51): Show | 56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.540+82T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113882914 | ||||||
| chr3:113883039
|
A | G | 1 | a0001c0001t0001g0299 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.540+207A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113883039 | ||||||
| chr3:113883085
|
T | C | 1 | a0001c0002t0003g0030 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.540+253T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113883085 | ||||||
| chr3:113883208
|
G | A | 2 | a0001c0001t0003g0089a0001c0001t0030g0155 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.540+376G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113883208 | ||||||
| chr3:113883215
|
T | C | 2 | a0001c0001t0003g0089a0001c0001t0030g0155 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.540+383T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113883215 | ||||||
| chr3:113883307
|
T | G | 1 | a0001c0001t0012g0300 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.540+475T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113883307 | ||||||
| chr3:113883524
|
C | CA | 7 | a0001c0001t0001g0090a0001c0001t0001g0285a0001c0001t0002g0172others(4): Show | 7 | HG01106.hp1 HG01192.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.540+708dupA | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 113883524 | |||||
| chr3:113883525
|
A | C | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02559.hp1 HG02622.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+693A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113883525 | ||||||
| chr3:113883555
|
C | G | 2 | a0001c0001t0001g0277a0001c0001t0002g0281 | 2 | HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.540+723C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113883555 | ||||||
| chr3:113883729
|
G | A | 5 | a0001c0001t0008g0005a0001c0005t0010g0004a0001c0005t0010g0007others(2): Show | 5 | HG02109.hp2 HG02280.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.540+897G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113883729 | ||||||
| chr3:113883948
|
C | A | 5 | a0001c0001t0008g0005a0001c0005t0010g0004a0001c0005t0010g0007others(2): Show | 5 | HG02109.hp2 HG02280.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.540+1116C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113883948 | ||||||
| chr3:113883956
|
G | T | 5 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0203others(2): Show | 5 | HG01168.hp2 HG01169.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.540+1124G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113883956 | ||||||
| chr3:113884078
|
A | G | 6 | a0001c0001t0002g0301a0001c0001t0003g0089a0001c0001t0030g0155others(3): Show | 6 | HG02258.hp2 HG02630.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.540+1246A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113884078 | ||||||
| chr3:113884080
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.540+1248A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113884080 | ||||||
| chr3:113884087
|
GAA | G | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.540+1256_540+1257d others(4): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113884087 | ||||||
| chr3:113884119
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.540+1287A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113884119 | ||||||
| chr3:113884560
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.540+1728C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113884560 | ||||||
| chr3:113884637
|
C | G | 4 | a0001c0001t0002g0301a0001c0005t0001g0292a0001c0005t0009g0294others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+1805C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113884637 | ||||||
| chr3:113884645
|
A | C | 6 | a0001c0001t0001g0169a0001c0001t0001g0171a0001c0001t0001g0174others(3): Show | 6 | HG02486.hp2 HG02622.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.540+1813A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113884645 | ||||||
| chr3:113884659
|
G | A | 142 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(139): Show | 142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.540+1827G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113884659 | ||||||
| chr3:113884852
|
A | G | 1 | a0002c0006t0009g0311 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.540+2020A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113884852 | ||||||
| chr3:113884970
|
A | G | 1 | a0001c0003t0002g0279 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.540+2138A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113884970 | ||||||
| chr3:113885192
|
C | A | 1 | a0001c0001t0001g0203 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.540+2360C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113885192 | ||||||
| chr3:113885259
|
G | T | 1 | a0001c0003t0002g0284 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.540+2427G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113885259 | ||||||
| chr3:113885279
|
C | T | 1 | a0001c0001t0001g0291 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.540+2447C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113885279 | ||||||
| chr3:113885317
|
T | C | 37 | a0001c0001t0001g0196a0001c0001t0001g0219a0001c0001t0001g0225others(34): Show | 37 | HG00323.hp2 HG00438.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.540+2485T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113885317 | ||||||
| chr3:113885370
|
A | G | 2 | a0001c0005t0001g0292a0001c0005t0009g0294 | 2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.540+2538A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113885370 | ||||||
| chr3:113885515
|
T | C | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0002t0001g0056 | 3 | HG00140.hp2 HG01256.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.540+2683T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113885515 | ||||||
| chr3:113885829
|
A | G | 2 | a0001c0001t0008g0167a0001c0001t0008g0192 | 2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.540+2997A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113885829 | ||||||
| chr3:113886051
|
T | G | 54 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0090others(51): Show | 56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.540+3219T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113886051 | ||||||
| chr3:113886062
|
G | C | 1 | a0001c0001t0002g0175 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.540+3230G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113886062 | ||||||
| chr3:113886409
|
T | A | 139 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(136): Show | 139 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.540+3577T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113886409 | ||||||
| chr3:113886463
|
G | C | 1 | a0001c0001t0001g0268 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.540+3631G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113886463 | ||||||
| chr3:113886516
|
C | T | 2 | a0001c0001t0008g0167a0001c0001t0008g0192 | 2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.540+3684C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113886516 | ||||||
| chr3:113886528
|
T | C | 269 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(266): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.540+3696T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113886528 | ||||||
| chr3:113886594
|
C | T | 5 | a0001c0001t0001g0013a0001c0001t0001g0299a0001c0001t0002g0296others(2): Show | 5 | HG01106.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.540+3762C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113886594 | ||||||
| chr3:113886777
|
G | GT | 13 | a0001c0001t0001g0108a0001c0001t0001g0243a0001c0001t0001g0314others(10): Show | 13 | HG00741.hp1 HG01243.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.540+3968dupT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 113886777 | |||||
| chr3:113886777
|
GT | G | 48 | a0001c0001t0001g0006a0001c0001t0001g0196a0001c0001t0001g0202others(45): Show | 48 | HG00323.hp2 HG00438.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.540+3968delT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 113886777 | |||||
| chr3:113886777
|
GTT | G | 141 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(138): Show | 141 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.540+3967_540+3968d others(4): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 113886777 | |||||
| chr3:113886777
|
GTTT | G | 50 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0090others(47): Show | 52 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.540+3966_540+3968d others(5): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 113886777 | |||||
| chr3:113886782
|
T | G | 1 | a0001c0001t0002g0296 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.540+3950T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113886782 | ||||||
| chr3:113886783
|
T | G | 4 | a0001c0001t0001g0013a0001c0001t0001g0299a0001c0001t0002g0298others(1): Show | 4 | HG01106.hp2 HG02895.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+3951T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113886783 | ||||||
| chr3:113886830
|
A | G | 1 | a0001c0001t0001g0299 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.540+3998A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113886830 | ||||||
| chr3:113886875
|
T | C | 2 | a0001c0001t0003g0126a0001c0001t0012g0300 | 2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.540+4043T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113886875 | ||||||
| chr3:113887022
|
C | T | 1 | a0001c0004t0005g0044 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.540+4190C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113887022 | ||||||
| chr3:113887085
|
G | GT | 15 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(12): Show | 15 | HG01358.hp2 HG01934.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.540+4263dupT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 113887085 | |||||
| chr3:113887085
|
G | GTT | 45 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0090others(42): Show | 47 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.540+4262_540+4263d others(4): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 113887085 | |||||
| chr3:113887085
|
G | GTTT | 15 | a0001c0001t0001g0014a0001c0001t0001g0135a0001c0001t0001g0169others(12): Show | 15 | HG01106.hp2 HG01361.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.540+4261_540+4263d others(5): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 113887085 | |||||
| chr3:113887085
|
GTTTTTTT others(5): Show |
G | 1 | a0001c0001t0001g0268 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.540+4264_540+4275d others(14): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 113887085 | |||||
| chr3:113887086
|
TTTTTTTT others(3): Show |
T | 1 | a0001c0001t0002g0172 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.540+4264_540+4273d others(12): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 113887086 | |||||
| chr3:113887087
|
T | G | 1 | a0001c0003t0002g0187 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.540+4255T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113887087 | ||||||
| chr3:113887092
|
T | G | 33 | a0001c0001t0001g0196a0001c0001t0001g0208a0001c0001t0001g0219others(30): Show | 33 | HG00323.hp2 HG00438.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.540+4260T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113887092 | ||||||
| chr3:113887095
|
T | G | 5 | a0001c0001t0003g0100a0001c0001t0003g0123a0001c0001t0014g0102others(2): Show | 5 | HG02145.hp1 HG02257.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.540+4263T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113887095 | ||||||
| chr3:113887095
|
TG | T | 109 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0109others(106): Show | 109 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.540+4264delG | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113887095 | ||||||
| chr3:113887096
|
G | T | 153 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(150): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.540+4264G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113887096 | ||||||
| chr3:113887097
|
T | G | 1 | a0001c0001t0002g0172 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.540+4265T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113887097 | ||||||
| chr3:113887236
|
G | A | 1 | a0001c0002t0003g0053 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.540+4404G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113887236 | ||||||
| chr3:113887245
|
C | G | 34 | a0001c0001t0001g0196a0001c0001t0001g0208a0001c0001t0001g0219others(31): Show | 34 | HG00323.hp2 HG00438.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.540+4413C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113887245 | ||||||
| chr3:113887382
|
A | G | 269 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(266): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.540+4550A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113887382 | ||||||
| chr3:113887499
|
G | C | 3 | a0001c0001t0001g0109a0001c0003t0002g0114a0006c0014t0002g0118 | 3 | HG02040.hp2 NA18948.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.540+4667G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113887499 | ||||||
| chr3:113887570
|
G | A | 2 | a0001c0001t0003g0089a0001c0001t0030g0155 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.540+4738G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113887570 | ||||||
| chr3:113887609
|
GAGAA | G | 152 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0020others(149): Show | 152 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.540+4780_540+4783d others(6): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 113887609 | |||||
| chr3:113887702
|
C | T | 152 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0020others(149): Show | 152 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.540+4870C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113887702 | ||||||
| chr3:113887708
|
C | CA | 65 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0022others(62): Show | 65 | HG00558.hp2 HG00609.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.540+4896dupA | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 113887708 | |||||
| chr3:113887708
|
CA | C | 12 | a0001c0001t0001g0152a0001c0001t0001g0168a0001c0001t0001g0181others(9): Show | 12 | HG00741.hp2 HG01169.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.540+4896delA | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 113887708 | |||||
| chr3:113887728
|
A | T | 1 | a0001c0001t0001g0163 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.540+4896A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113887728 | ||||||
| chr3:113887981
|
G | C | 12 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(9): Show | 12 | HG01106.hp2 HG01934.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.540+5149G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113887981 | ||||||
| chr3:113888077
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.540+5245A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113888077 | ||||||
| chr3:113888111
|
A | G | 5 | a0001c0001t0001g0013a0001c0001t0001g0299a0001c0001t0002g0296others(2): Show | 5 | HG01106.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.540+5279A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113888111 | ||||||
| chr3:113888123
|
T | G | 265 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(262): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.540+5291T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113888123 | ||||||
| chr3:113888172
|
A | G | 153 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0020others(150): Show | 153 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.540+5340A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113888172 | ||||||
| chr3:113888442
|
C | G | 1 | a0001c0001t0001g0274 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.540+5610C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113888442 | ||||||
| chr3:113888578
|
C | T | 1 | a0001c0002t0003g0321 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.540+5746C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113888578 | ||||||
| chr3:113888754
|
G | A | 1 | a0001c0002t0004g0047 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.540+5922G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113888754 | ||||||
| chr3:113888775
|
G | A | 1 | a0001c0003t0002g0236 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.540+5943G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113888775 | ||||||
| chr3:113888822
|
T | C | 2 | a0001c0001t0003g0089a0001c0001t0030g0155 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.540+5990T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113888822 | ||||||
| chr3:113889057
|
G | A | 2 | a0001c0001t0008g0167a0001c0001t0008g0192 | 2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.540+6225G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113889057 | ||||||
| chr3:113889060
|
C | T | 3 | a0001c0003t0002g0215a0001c0003t0002g0284a0001c0012t0002g0216 | 3 | HG01516.hp1 HG03710.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.540+6228C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113889060 | ||||||
| chr3:113889090
|
C | T | 1 | a0001c0002t0004g0038 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.540+6258C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113889090 | ||||||
| chr3:113889154
|
C | T | 2 | a0001c0001t0003g0126a0001c0001t0012g0300 | 2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.540+6322C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113889154 | ||||||
| chr3:113889199
|
T | TA | 267 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(264): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.540+6376dupA | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 113889199 | |||||
| chr3:113889209
|
C | T | 1 | a0001c0001t0002g0301 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.540+6377C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113889209 | ||||||
| chr3:113889328
|
A | G | 1 | a0001c0003t0002g0195 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.540+6496A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113889328 | ||||||
| chr3:113889701
|
C | T | 2 | a0001c0002t0003g0030a0001c0002t0003g0041 | 2 | NA18941.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.540+6869C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113889701 | ||||||
| chr3:113889748
|
C | T | 15 | a0001c0001t0001g0109a0001c0001t0001g0161a0001c0001t0001g0200others(12): Show | 15 | HG00558.hp2 HG02040.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.540+6916C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113889748 | ||||||
| chr3:113889853
|
G | T | 1 | a0001c0002t0001g0140 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.540+7021G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113889853 | ||||||
| chr3:113889962
|
C | A | 5 | a0001c0001t0001g0013a0001c0001t0001g0299a0001c0001t0002g0296others(2): Show | 5 | HG01106.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.540+7130C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113889962 | ||||||
| chr3:113890033
|
T | C | 2 | a0001c0001t0003g0089a0001c0001t0030g0155 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.540+7201T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113890033 | ||||||
| chr3:113890062
|
GC | G | 3 | a0001c0001t0001g0160a0001c0001t0001g0181a0001c0001t0017g0259 | 3 | HG00558.hp1 HG03017.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.540+7232delC | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 113890062 | |||||
| chr3:113890077
|
C | CA | 229 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(226): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.540+7245_540+7246i others(3): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113890077 | ||||||
| chr3:113890128
|
A | G | 268 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(265): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.540+7296A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113890128 | ||||||
| chr3:113890194
|
G | C | 5 | a0001c0001t0001g0013a0001c0001t0001g0299a0001c0001t0002g0296others(2): Show | 5 | HG01106.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.540+7362G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113890194 | ||||||
| chr3:113890537
|
A | G | 1 | a0001c0001t0003g0093 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.540+7705A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113890537 | ||||||
| chr3:113890556
|
G | A | 53 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0090others(50): Show | 55 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.540+7724G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113890556 | ||||||
| chr3:113890873
|
C | A | 1 | a0001c0005t0015g0128 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.540+8041C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113890873 | ||||||
| chr3:113891049
|
T | C | 1 | a0001c0002t0003g0051 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.540+8217T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113891049 | ||||||
| chr3:113891392
|
G | A | 71 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(68): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.540+8560G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113891392 | ||||||
| chr3:113891496
|
A | G | 1 | a0001c0002t0003g0095 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.540+8664A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113891496 | ||||||
| chr3:113891497
|
T | TA | 5 | a0001c0001t0008g0005a0001c0005t0010g0004a0001c0005t0010g0007others(2): Show | 5 | HG02109.hp2 HG02280.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.540+8671dupA | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 113891497 | |||||
| chr3:113891517
|
T | C | 1 | a0001c0001t0003g0123 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.540+8685T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113891517 | ||||||
| chr3:113891562
|
T | A | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.540+8730T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113891562 | ||||||
| chr3:113891712
|
TA | T | 143 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0109others(140): Show | 143 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.540+8894delA | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 113891712 | |||||
| chr3:113891813
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0181 | 2 | HG00558.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.540+8981G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113891813 | ||||||
| chr3:113891841
|
C | T | 3 | a0001c0001t0001g0170a0001c0001t0001g0234a0001c0003t0002g0207 | 3 | HG02015.hp1 HG03831.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.540+9009C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113891841 | ||||||
| chr3:113891851
|
C | T | 3 | a0001c0001t0001g0290a0001c0003t0002g0221a0001c0003t0002g0222 | 3 | HG01358.hp2 HG01943.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.540+9019C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113891851 | ||||||
| chr3:113891869
|
A | G | 1 | a0001c0001t0001g0274 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.540+9037A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113891869 | ||||||
| chr3:113892026
|
A | G | 153 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0020others(150): Show | 153 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.541-9005A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113892026 | ||||||
| chr3:113892231
|
G | A | 1 | a0001c0002t0001g0056 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.541-8800G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113892231 | ||||||
| chr3:113892316
|
A | G | 2 | a0001c0003t0002g0293a0003c0018t0001g0248 | 2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.541-8715A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113892316 | ||||||
| chr3:113892337
|
T | C | 2 | a0001c0001t0003g0126a0001c0001t0012g0300 | 2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.541-8694T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113892337 | ||||||
| chr3:113892386
|
C | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02559.hp1 HG02622.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.541-8645C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113892386 | ||||||
| chr3:113892391
|
G | A | 1 | a0001c0001t0002g0301 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.541-8640G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113892391 | ||||||
| chr3:113892621
|
C | T | 72 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(69): Show | 74 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.541-8410C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113892621 | ||||||
| chr3:113892666
|
T | A | 11 | a0001c0001t0001g0006a0001c0001t0003g0100a0001c0001t0003g0123others(8): Show | 11 | HG00735.hp2 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.541-8365T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113892666 | ||||||
| chr3:113892732
|
G | A | 5 | a0001c0002t0003g0070a0001c0002t0003g0071a0001c0002t0004g0038others(2): Show | 5 | HG00642.hp1 HG00735.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.541-8299G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113892732 | ||||||
| chr3:113892832
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.541-8199C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113892832 | ||||||
| chr3:113893059
|
G | T | 1 | a0001c0001t0001g0194 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.541-7972G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113893059 | ||||||
| chr3:113893221
|
T | A | 1 | a0001c0001t0006g0254 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.541-7810T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113893221 | ||||||
| chr3:113893222
|
A | T | 4 | a0001c0002t0003g0048a0001c0002t0003g0049a0001c0002t0003g0078others(1): Show | 4 | HG01169.hp1 HG01496.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.541-7809A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113893222 | ||||||
| chr3:113893300
|
G | T | 1 | a0001c0001t0001g0218 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.541-7731G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113893300 | ||||||
| chr3:113893308
|
T | G | 154 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0020others(151): Show | 154 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.541-7723T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113893308 | ||||||
| chr3:113893381
|
C | CT | 58 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0019others(55): Show | 60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.541-7638dupT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 113893381 | |||||
| chr3:113893388
|
T | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(1): Show | 4 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.541-7643T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113893388 | ||||||
| chr3:113893783
|
C | T | 1 | a0001c0001t0002g0172 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.541-7248C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113893783 | ||||||
| chr3:113893907
|
G | T | 2 | a0001c0001t0022g0132a0005c0008t0023g0131 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.541-7124G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113893907 | ||||||
| chr3:113893981
|
T | C | 1 | a0001c0001t0011g0261 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.541-7050T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113893981 | ||||||
| chr3:113894025
|
G | A | 1 | a0001c0003t0002g0204 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.541-7006G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113894025 | ||||||
| chr3:113894077
|
T | C | 2 | a0001c0001t0022g0132a0005c0008t0023g0131 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.541-6954T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113894077 | ||||||
| chr3:113894165
|
T | A | 2 | a0001c0001t0003g0126a0001c0001t0012g0300 | 2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.541-6866T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113894165 | ||||||
| chr3:113894337
|
G | GGCATGAT others(34): Show |
1 | a0001c0001t0001g0019 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.541-6693_541-6653d others(43): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 113894337 | |||||
| chr3:113894365
|
G | A | 2 | a0001c0001t0022g0132a0005c0008t0023g0131 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.541-6666G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113894365 | ||||||
| chr3:113894412
|
G | A | 2 | a0001c0003t0002g0293a0003c0018t0001g0248 | 2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.541-6619G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113894412 | ||||||
| chr3:113894460
|
A | C | 2 | a0001c0001t0008g0167a0001c0001t0008g0192 | 2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.541-6571A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113894460 | ||||||
| chr3:113894499
|
G | A | 1 | a0001c0003t0002g0236 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.541-6532G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113894499 | ||||||
| chr3:113894528
|
C | G | 1 | a0001c0001t0002g0172 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.541-6503C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113894528 | ||||||
| chr3:113894537
|
C | G | 1 | a0001c0004t0004g0039 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.541-6494C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113894537 | ||||||
| chr3:113894575
|
G | A | 2 | a0001c0001t0008g0167a0001c0001t0008g0192 | 2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.541-6456G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113894575 | ||||||
| chr3:113894615
|
C | G | 1 | a0001c0001t0017g0259 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.541-6416C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113894615 | ||||||
| chr3:113894811
|
C | G | 2 | a0001c0001t0001g0278a0001c0001t0002g0280 | 2 | HG02451.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.541-6220C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113894811 | ||||||
| chr3:113894812
|
A | C | 3 | a0001c0001t0006g0310a0001c0001t0008g0315a0001c0001t0021g0287 | 3 | HG02055.hp2 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.541-6219A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113894812 | ||||||
| chr3:113894874
|
T | A | 3 | a0001c0001t0006g0310a0001c0001t0008g0315a0001c0001t0021g0287 | 3 | HG02055.hp2 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.541-6157T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113894874 | ||||||
| chr3:113895014
|
C | T | 2 | a0001c0002t0003g0030a0001c0002t0003g0041 | 2 | NA18941.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.541-6017C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113895014 | ||||||
| chr3:113895110
|
A | G | 2 | a0001c0001t0022g0132a0005c0008t0023g0131 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.541-5921A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113895110 | ||||||
| chr3:113895261
|
G | A | 1 | a0001c0002t0003g0321 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.541-5770G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113895261 | ||||||
| chr3:113895389
|
G | A | 6 | a0001c0001t0001g0108a0001c0002t0001g0140a0001c0002t0011g0138others(3): Show | 6 | HG00741.hp2 HG01243.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.541-5642G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113895389 | ||||||
| chr3:113895493
|
G | A | 51 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0090others(48): Show | 53 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.541-5538G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113895493 | ||||||
| chr3:113895498
|
C | T | 1 | a0001c0002t0001g0023 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.541-5533C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113895498 | ||||||
| chr3:113895642
|
C | T | 11 | a0001c0001t0001g0006a0001c0001t0003g0100a0001c0001t0003g0123others(8): Show | 11 | HG00735.hp2 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.541-5389C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113895642 | ||||||
| chr3:113895668
|
A | G | 53 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0090others(50): Show | 55 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.541-5363A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113895668 | ||||||
| chr3:113895937
|
G | A | 2 | a0001c0001t0008g0167a0001c0001t0008g0192 | 2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.541-5094G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113895937 | ||||||
| chr3:113896164
|
G | T | 3 | a0001c0002t0003g0080a0001c0004t0004g0058a0001c0004t0004g0076 | 3 | HG01433.hp2 HG03942.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.541-4867G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113896164 | ||||||
| chr3:113896258
|
C | G | 2 | a0001c0001t0022g0132a0005c0008t0023g0131 | 2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.541-4773C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113896258 | ||||||
| chr3:113896369
|
C | G | 1 | a0001c0001t0002g0301 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.541-4662C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113896369 | ||||||
| chr3:113896396
|
G | A | 39 | a0001c0001t0001g0196a0001c0001t0001g0208a0001c0001t0001g0219others(36): Show | 39 | HG00323.hp2 HG00438.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.541-4635G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113896396 | ||||||
| chr3:113896524
|
T | G | 2 | a0001c0001t0001g0168a0001c0001t0001g0265 | 2 | NA18965.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.541-4507T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113896524 | ||||||
| chr3:113896530
|
A | G | 1 | a0001c0004t0005g0044 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.541-4501A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113896530 | ||||||
| chr3:113896662
|
T | G | 71 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(68): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.541-4369T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113896662 | ||||||
| chr3:113896890
|
A | G | 1 | a0001c0001t0001g0249 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.541-4141A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113896890 | ||||||
| chr3:113896986
|
C | A | 2 | a0001c0001t0001g0090a0001c0003t0002g0092 | 2 | HG01192.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.541-4045C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113896986 | ||||||
| chr3:113897058
|
T | C | 2 | a0001c0001t0008g0167a0001c0001t0008g0192 | 2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.541-3973T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113897058 | ||||||
| chr3:113897103
|
CTT | C | 3 | a0001c0001t0001g0253a0001c0001t0001g0275a0001c0005t0009g0276 | 3 | HG02257.hp1 HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.541-3927_541-3926d others(4): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113897103 | ||||||
| chr3:113897388
|
C | T | 2 | a0001c0001t0016g0003a0001c0001t0016g0009 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.541-3643C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113897388 | ||||||
| chr3:113897669
|
A | C | 1 | a0001c0001t0001g0107 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.541-3362A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113897669 | ||||||
| chr3:113897737
|
T | C | 1 | a0001c0001t0001g0243 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.541-3294T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113897737 | ||||||
| chr3:113898019
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.541-3012A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113898019 | ||||||
| chr3:113898074
|
A | G | 1 | a0001c0003t0002g0239 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.541-2957A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113898074 | ||||||
| chr3:113898122
|
T | G | 1 | a0001c0001t0001g0290 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.541-2909T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113898122 | ||||||
| chr3:113898227
|
G | A | 66 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(63): Show | 68 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.541-2804G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113898227 | ||||||
| chr3:113898430
|
G | A | 5 | a0001c0001t0002g0172a0001c0001t0002g0301a0001c0005t0001g0292others(2): Show | 5 | HG02630.hp1 HG02886.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.541-2601G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113898430 | ||||||
| chr3:113898748
|
G | A | 4 | a0001c0001t0002g0301a0001c0005t0001g0292a0001c0005t0009g0294others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.541-2283G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113898748 | ||||||
| chr3:113898852
|
C | A | 4 | a0001c0001t0010g0008a0001c0001t0016g0003a0001c0001t0016g0009others(1): Show | 4 | HG00735.hp2 HG02280.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.541-2179C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113898852 | ||||||
| chr3:113899029
|
G | T | 1 | a0001c0001t0001g0265 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.541-2002G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113899029 | ||||||
| chr3:113899030
|
A | T | 1 | a0001c0001t0001g0265 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.541-2001A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113899030 | ||||||
| chr3:113899062
|
A | G | 138 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(135): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.541-1969A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113899062 | ||||||
| chr3:113899139
|
C | T | 1 | a0001c0001t0006g0124 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.541-1892C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113899139 | ||||||
| chr3:113899142
|
A | G | 4 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(1): Show | 4 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.541-1889A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113899142 | ||||||
| chr3:113899196
|
G | C | 86 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0107others(83): Show | 86 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.541-1835G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113899196 | ||||||
| chr3:113899220
|
C | T | 14 | a0001c0001t0001g0115a0001c0001t0001g0136a0001c0001t0001g0152others(11): Show | 14 | HG00408.hp2 HG00609.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.541-1811C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113899220 | ||||||
| chr3:113899241
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.541-1790G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113899241 | ||||||
| chr3:113899409
|
A | C | 7 | a0001c0001t0002g0257a0001c0001t0002g0263a0001c0001t0011g0261others(4): Show | 7 | HG01346.hp1 HG01515.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.541-1622A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113899409 | ||||||
| chr3:113899411
|
A | G | 2 | a0001c0001t0003g0126a0001c0001t0012g0300 | 2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.541-1620A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113899411 | ||||||
| chr3:113899454
|
A | AT | 128 | a0001c0001t0001g0022a0001c0001t0001g0109a0001c0001t0001g0115others(125): Show | 128 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.541-1577_541-1576i others(3): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113899454 | ||||||
| chr3:113899455
|
A | G | 128 | a0001c0001t0001g0022a0001c0001t0001g0109a0001c0001t0001g0115others(125): Show | 128 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.541-1576A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113899455 | ||||||
| chr3:113899456
|
C | G | 128 | a0001c0001t0001g0022a0001c0001t0001g0109a0001c0001t0001g0115others(125): Show | 128 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.541-1575C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113899456 | ||||||
| chr3:113899457
|
T | G | 128 | a0001c0001t0001g0022a0001c0001t0001g0109a0001c0001t0001g0115others(125): Show | 128 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.541-1574T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113899457 | ||||||
| chr3:113899659
|
T | G | 1 | a0001c0001t0002g0301 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.541-1372T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113899659 | ||||||
| chr3:113899733
|
G | A | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.541-1298G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113899733 | ||||||
| chr3:113899760
|
G | C | 88 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(85): Show | 88 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.541-1271G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113899760 | ||||||
| chr3:113899802
|
T | C | 1 | a0001c0001t0002g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.541-1229T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113899802 | ||||||
| chr3:113899868
|
C | T | 2 | a0001c0003t0002g0293a0003c0018t0001g0248 | 2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.541-1163C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113899868 | ||||||
| chr3:113899869
|
A | G | 319 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(316): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.541-1162A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113899869 | ||||||
| chr3:113899918
|
A | C | 88 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(85): Show | 88 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.541-1113A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113899918 | ||||||
| chr3:113900028
|
A | G | 1 | a0001c0003t0002g0293 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.541-1003A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113900028 | ||||||
| chr3:113900036
|
T | C | 2 | a0001c0004t0002g0137a0001c0004t0002g0139 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.541-995T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113900036 | ||||||
| chr3:113900130
|
G | C | 3 | a0001c0001t0022g0132a0001c0001t0028g0179a0005c0008t0023g0131 | 3 | HG02258.hp1 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.541-901G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113900130 | ||||||
| chr3:113900138
|
C | T | 4 | a0001c0001t0001g0196a0001c0001t0001g0285a0001c0001t0001g0286others(1): Show | 4 | HG00140.hp2 HG01256.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.541-893C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113900138 | ||||||
| chr3:113900175
|
A | G | 4 | a0001c0001t0003g0100a0001c0001t0014g0102a0001c0001t0015g0101others(1): Show | 4 | HG02145.hp1 HG02257.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.541-856A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113900175 | ||||||
| chr3:113900252
|
G | A | 13 | a0001c0001t0001g0196a0001c0001t0001g0285a0001c0001t0001g0286others(10): Show | 13 | HG00140.hp2 HG01192.hp1 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.541-779G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113900252 | ||||||
| chr3:113900259
|
T | C | 1 | a0001c0003t0002g0212 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.541-772T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113900259 | ||||||
| chr3:113900409
|
A | AATT | 55 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0090others(52): Show | 57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.541-597_541-595dup others(3): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 113900409 | |||||
| chr3:113900409
|
A | AATTATT | 9 | a0001c0001t0001g0006a0001c0001t0001g0249a0001c0001t0001g0264others(6): Show | 9 | HG00735.hp2 HG01361.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.541-600_541-595dup others(6): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 113900409 | |||||
| chr3:113900409
|
A | AATTATTA others(2): Show |
4 | a0001c0001t0016g0003a0001c0001t0016g0009a0001c0003t0002g0222others(1): Show | 4 | HG02280.hp1 HG02293.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.541-603_541-595dup others(9): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 113900409 | |||||
| chr3:113900409
|
A | AATTATTA others(5): Show |
3 | a0001c0001t0009g0262a0001c0001t0009g0267a0001c0003t0002g0230 | 3 | HG02109.hp1 HG03139.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.541-606_541-595dup others(12): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 113900409 | |||||
| chr3:113900409
|
A | AATTATTA others(8): Show |
20 | a0001c0001t0001g0022a0001c0001t0001g0144a0001c0001t0001g0153others(17): Show | 20 | HG00280.hp2 HG01346.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.541-609_541-595dup others(15): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 113900409 | |||||
| chr3:113900409
|
A | AATTATTA others(11): Show |
13 | a0001c0001t0001g0013a0001c0001t0001g0238a0001c0001t0001g0290others(10): Show | 13 | HG01106.hp1 HG01106.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.541-612_541-595dup others(18): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 113900409 | |||||
| chr3:113900409
|
A | AATTATTA others(14): Show |
50 | a0001c0001t0001g0109a0001c0001t0001g0115a0001c0001t0001g0160others(47): Show | 50 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.541-615_541-595dup others(21): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 113900409 | |||||
| chr3:113900409
|
A | AATTATTA others(17): Show |
7 | a0001c0001t0001g0246a0001c0001t0014g0143a0001c0001t0021g0287others(4): Show | 7 | HG00323.hp2 HG02074.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.541-618_541-595dup others(24): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 113900409 | |||||
| chr3:113900409
|
A | AATTATTA others(20): Show |
1 | a0002c0006t0025g0130 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.541-621_541-595dup others(27): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 113900409 | |||||
| chr3:113900451
|
C | T | 1 | a0001c0001t0001g0270 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.541-580C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113900451 | ||||||
| chr3:113900468
|
T | C | 97 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0109others(94): Show | 97 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.541-563T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113900468 | ||||||
| chr3:113900545
|
T | C | 319 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(316): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.541-486T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113900545 | ||||||
| chr3:113900595
|
A | AT | 41 | a0001c0001t0001g0022a0001c0001t0001g0148a0001c0001t0001g0158others(38): Show | 41 | HG00438.hp2 HG00639.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.541-424dupT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 113900595 | |||||
| chr3:113900873
|
T | C | 1 | a0001c0003t0007g0154 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.541-158T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113900873 | ||||||
| chr3:113900948
|
G | T | 2 | a0001c0001t0003g0089a0001c0001t0030g0155 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.541-83G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113900948 | ||||||
| chr3:113901025
|
C | T | 319 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(316): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
splice_region_variant&intron_variant | LOW | c.541-6C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 6/17 | chr3 | 113901025 | ||||||
| chr3:113901470
|
T | C | 2 | a0001c0001t0008g0167a0001c0001t0008g0192 | 2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.656+324T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 7/17 | chr3 | 113901470 | ||||||
| chr3:113901497
|
C | T | 303 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(300): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.656+351C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 7/17 | chr3 | 113901497 | ||||||
| chr3:113901594
|
C | T | 4 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(1): Show | 4 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.656+448C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 7/17 | chr3 | 113901594 | ||||||
| chr3:113901678
|
A | G | 5 | a0001c0001t0001g0253a0001c0001t0001g0275a0001c0001t0022g0132others(2): Show | 5 | HG02258.hp1 HG02615.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.656+532A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 7/17 | chr3 | 113901678 | ||||||
| chr3:113901888
|
T | C | 1 | a0001c0004t0005g0035 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.656+742T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 7/17 | chr3 | 113901888 | ||||||
| chr3:113901991
|
GAC | G | 303 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(300): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.656+846_656+847del others(2): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 7/17 | chr3 | 113901991 | ||||||
| chr3:113901994
|
T | G | 303 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(300): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.656+848T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 7/17 | chr3 | 113901994 | ||||||
| chr3:113901996
|
C | G | 303 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(300): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.656+850C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 7/17 | chr3 | 113901996 | ||||||
| chr3:113901998
|
A | C | 303 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(300): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.656+852A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 7/17 | chr3 | 113901998 | ||||||
| chr3:113902014
|
G | A | 52 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0150others(49): Show | 52 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.656+868G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 7/17 | chr3 | 113902014 | ||||||
| chr3:113902020
|
T | A | 1 | a0011c0015t0001g0224 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.656+874T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 7/17 | chr3 | 113902020 | ||||||
| chr3:113902149
|
A | G | 3 | a0001c0001t0002g0301a0001c0001t0008g0167a0001c0001t0008g0192 | 3 | HG02451.hp2 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.656+1003A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 7/17 | chr3 | 113902149 | ||||||
| chr3:113902152
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.656+1006G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 7/17 | chr3 | 113902152 | ||||||
| chr3:113902171
|
T | C | 2 | a0001c0001t0006g0124a0001c0001t0006g0125 | 2 | HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.656+1025T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 7/17 | chr3 | 113902171 | ||||||
| chr3:113902214
|
A | G | 5 | a0001c0001t0001g0253a0001c0001t0001g0275a0001c0001t0022g0132others(2): Show | 5 | HG02258.hp1 HG02615.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.656+1068A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 7/17 | chr3 | 113902214 | ||||||
| chr3:113902342
|
T | G | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.656+1196T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 7/17 | chr3 | 113902342 | ||||||
| chr3:113902879
|
G | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0265 | 2 | NA18965.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.657-1261G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 7/17 | chr3 | 113902879 | ||||||
| chr3:113902893
|
C | T | 89 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(86): Show | 89 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.657-1247C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 7/17 | chr3 | 113902893 | ||||||
| chr3:113902990
|
G | C | 214 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(211): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.657-1150G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 7/17 | chr3 | 113902990 | ||||||
| chr3:113903056
|
C | T | 1 | a0001c0001t0001g0020 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.657-1084C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 7/17 | chr3 | 113903056 | ||||||
| chr3:113903057
|
C | T | 82 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0108others(79): Show | 82 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.657-1083C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 7/17 | chr3 | 113903057 | ||||||
| chr3:113903139
|
A | AT | 81 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0108others(78): Show | 81 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.657-986dupT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 113903139 | |||||
| chr3:113903264
|
T | C | 3 | a0001c0001t0022g0132a0001c0001t0028g0179a0005c0008t0023g0131 | 3 | HG02258.hp1 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.657-876T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 7/17 | chr3 | 113903264 | ||||||
| chr3:113903272
|
C | T | 2 | a0001c0001t0001g0277a0001c0001t0002g0281 | 2 | HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.657-868C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 7/17 | chr3 | 113903272 | ||||||
| chr3:113903748
|
G | C | 1 | a0001c0001t0001g0019 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.657-392G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 7/17 | chr3 | 113903748 | ||||||
| chr3:113903938
|
G | GTA | 82 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0108others(79): Show | 82 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.657-200_657-199dup others(2): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 113903938 | |||||
| chr3:113904016
|
T | A | 2 | a0001c0001t0009g0262a0001c0001t0009g0267 | 2 | HG02109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.657-124T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 7/17 | chr3 | 113904016 | ||||||
| chr3:113904437
|
G | A | 1 | a0001c0001t0001g0219 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.789+165G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113904437 | ||||||
| chr3:113904449
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.789+177G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113904449 | ||||||
| chr3:113904484
|
C | T | 5 | a0001c0001t0003g0089a0001c0001t0022g0132a0001c0001t0028g0179others(2): Show | 5 | HG02258.hp1 HG02258.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.789+212C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113904484 | ||||||
| chr3:113904610
|
G | GT | 11 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0268others(8): Show | 11 | HG01106.hp2 HG01358.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+351dupT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 113904610 | |||||
| chr3:113904610
|
GT | G | 6 | a0001c0001t0001g0016a0001c0001t0001g0274a0001c0003t0002g0293others(3): Show | 6 | HG01192.hp1 HG01884.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.789+351delT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 113904610 | |||||
| chr3:113904610
|
GTT | G | 82 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0108others(79): Show | 82 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.789+350_789+351del others(2): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 113904610 | |||||
| chr3:113904620
|
T | C | 6 | a0001c0001t0001g0006a0001c0001t0010g0008a0001c0001t0016g0003others(3): Show | 6 | HG00735.hp2 HG02280.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.789+348T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113904620 | ||||||
| chr3:113904806
|
A | T | 1 | a0001c0001t0001g0169 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.789+534A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113904806 | ||||||
| chr3:113904834
|
T | C | 5 | a0001c0001t0001g0253a0001c0001t0001g0275a0001c0001t0022g0132others(2): Show | 5 | HG02258.hp1 HG02615.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.789+562T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113904834 | ||||||
| chr3:113905226
|
A | G | 6 | a0001c0001t0001g0006a0001c0001t0010g0008a0001c0001t0016g0003others(3): Show | 6 | HG00735.hp2 HG02280.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.789+954A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113905226 | ||||||
| chr3:113905612
|
A | G | 1 | a0001c0001t0002g0172 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.789+1340A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113905612 | ||||||
| chr3:113905781
|
C | T | 1 | a0001c0004t0004g0099 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.789+1509C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113905781 | ||||||
| chr3:113905844
|
C | T | 14 | a0001c0001t0001g0015a0001c0001t0001g0196a0001c0001t0001g0285others(11): Show | 14 | HG00140.hp2 HG01192.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.789+1572C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113905844 | ||||||
| chr3:113905911
|
G | T | 10 | a0001c0001t0001g0013a0001c0001t0001g0249a0001c0001t0001g0274others(7): Show | 10 | HG01106.hp2 HG02818.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.789+1639G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113905911 | ||||||
| chr3:113905916
|
C | G | 2 | a0001c0001t0003g0089a0001c0001t0030g0155 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.789+1644C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113905916 | ||||||
| chr3:113905947
|
T | A | 38 | a0001c0001t0001g0148a0001c0001t0001g0158a0001c0001t0001g0214others(35): Show | 38 | HG00438.hp2 HG00639.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.789+1675T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113905947 | ||||||
| chr3:113905978
|
T | G | 2 | a0002c0006t0024g0133a0002c0006t0025g0130 | 2 | HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.789+1706T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113905978 | ||||||
| chr3:113906084
|
G | A | 53 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0090others(50): Show | 55 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.789+1812G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113906084 | ||||||
| chr3:113906214
|
C | T | 1 | a0001c0001t0013g0185 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.789+1942C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113906214 | ||||||
| chr3:113906232
|
G | A | 1 | a0001c0005t0015g0128 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.789+1960G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113906232 | ||||||
| chr3:113906396
|
G | A | 14 | a0001c0001t0003g0100a0001c0001t0003g0123a0001c0001t0014g0102others(11): Show | 14 | HG01109.hp2 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.789+2124G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113906396 | ||||||
| chr3:113906411
|
C | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.789+2139C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113906411 | ||||||
| chr3:113906504
|
T | C | 4 | a0001c0001t0001g0156a0001c0001t0001g0186a0001c0001t0001g0220others(1): Show | 4 | HG00280.hp2 HG01346.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.789+2232T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113906504 | ||||||
| chr3:113906652
|
A | AT | 54 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0090others(51): Show | 56 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.790-2297dupT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 113906652 | |||||
| chr3:113906676
|
A | G | 5 | a0001c0001t0001g0253a0001c0001t0001g0275a0001c0001t0022g0132others(2): Show | 5 | HG02258.hp1 HG02615.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.790-2282A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113906676 | ||||||
| chr3:113906775
|
A | G | 1 | a0001c0001t0001g0274 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.790-2183A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113906775 | ||||||
| chr3:113906877
|
C | T | 5 | a0001c0001t0001g0253a0001c0001t0001g0275a0001c0001t0022g0132others(2): Show | 5 | HG02258.hp1 HG02615.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.790-2081C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113906877 | ||||||
| chr3:113906878
|
G | A | 3 | a0001c0002t0001g0023a0001c0002t0001g0052a0001c0002t0003g0053 | 3 | HG00639.hp1 HG00639.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.790-2080G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113906878 | ||||||
| chr3:113906899
|
C | T | 2 | a0001c0001t0001g0253a0001c0001t0001g0275 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.790-2059C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113906899 | ||||||
| chr3:113907086
|
C | G | 82 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0108others(79): Show | 82 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.790-1872C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113907086 | ||||||
| chr3:113907112
|
G | A | 82 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0108others(79): Show | 82 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.790-1846G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113907112 | ||||||
| chr3:113907438
|
C | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.790-1520C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113907438 | ||||||
| chr3:113907587
|
T | G | 1 | a0001c0001t0003g0089 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.790-1371T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113907587 | ||||||
| chr3:113907638
|
A | T | 102 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0022others(99): Show | 102 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.790-1320A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113907638 | ||||||
| chr3:113907661
|
T | C | 51 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0090others(48): Show | 53 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.790-1297T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113907661 | ||||||
| chr3:113907798
|
C | G | 89 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(86): Show | 89 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.790-1160C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113907798 | ||||||
| chr3:113907832
|
A | G | 3 | a0001c0001t0011g0240a0001c0003t0002g0221a0001c0003t0002g0222 | 3 | HG01106.hp1 HG01943.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.790-1126A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113907832 | ||||||
| chr3:113907846
|
A | G | 2 | a0001c0001t0001g0090a0001c0003t0002g0092 | 2 | HG01192.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.790-1112A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113907846 | ||||||
| chr3:113907918
|
G | A | 1 | a0001c0001t0001g0164 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.790-1040G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113907918 | ||||||
| chr3:113908140
|
G | A | 12 | a0001c0001t0001g0278a0001c0001t0001g0304a0001c0001t0001g0305others(9): Show | 12 | HG00099.hp1 HG00642.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.790-818G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113908140 | ||||||
| chr3:113908204
|
T | A | 1 | a0001c0001t0003g0123 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.790-754T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113908204 | ||||||
| chr3:113908480
|
G | A | 82 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0108others(79): Show | 82 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.790-478G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113908480 | ||||||
| chr3:113908485
|
C | T | 15 | a0001c0001t0001g0136a0001c0001t0001g0152a0001c0001t0001g0177others(12): Show | 15 | HG00408.hp2 HG00609.hp1 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.790-473C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113908485 | ||||||
| chr3:113908568
|
T | A | 3 | a0001c0001t0002g0301a0001c0001t0008g0167a0001c0001t0008g0192 | 3 | HG02451.hp2 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.790-390T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113908568 | ||||||
| chr3:113908695
|
T | C | 2 | a0001c0001t0009g0262a0001c0001t0009g0267 | 2 | HG02109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.790-263T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113908695 | ||||||
| chr3:113908789
|
C | T | 1 | a0001c0002t0003g0129 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.790-169C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113908789 | ||||||
| chr3:113908810
|
G | T | 32 | a0001c0001t0001g0015a0001c0001t0001g0196a0001c0001t0001g0285others(29): Show | 32 | HG00140.hp2 HG01109.hp2 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.790-148G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 8/17 | chr3 | 113908810 | ||||||
| chr3:113909234
|
A | G | 1 | a0001c0001t0030g0155 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.952+114A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113909234 | ||||||
| chr3:113909371
|
A | G | 4 | a0001c0001t0001g0115a0001c0003t0002g0215a0001c0003t0002g0284others(1): Show | 4 | HG01516.hp1 HG03710.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.952+251A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113909371 | ||||||
| chr3:113909706
|
C | T | 3 | a0001c0004t0004g0077a0001c0004t0004g0096a0001c0005t0010g0302 | 3 | HG02109.hp2 NA19002.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.952+586C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113909706 | ||||||
| chr3:113909909
|
GT | G | 223 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(220): Show | 223 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.952+795delT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113909909 | |||||
| chr3:113910121
|
C | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.952+1001C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113910121 | ||||||
| chr3:113910155
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.952+1035G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113910155 | ||||||
| chr3:113910241
|
G | A | 51 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0090others(48): Show | 53 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.952+1121G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113910241 | ||||||
| chr3:113910248
|
C | T | 1 | a0001c0002t0003g0095 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.952+1128C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113910248 | ||||||
| chr3:113910282
|
C | T | 1 | a0001c0003t0002g0212 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.952+1162C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113910282 | ||||||
| chr3:113910315
|
G | A | 2 | a0001c0001t0009g0262a0001c0001t0009g0267 | 2 | HG02109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.952+1195G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113910315 | ||||||
| chr3:113910339
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.952+1219C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113910339 | ||||||
| chr3:113910404
|
A | G | 1 | a0001c0001t0014g0102 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.952+1284A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113910404 | ||||||
| chr3:113910693
|
A | G | 1 | a0001c0003t0002g0230 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.952+1573A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113910693 | ||||||
| chr3:113910707
|
C | T | 1 | a0001c0004t0005g0033 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.952+1587C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113910707 | ||||||
| chr3:113911121
|
T | A | 217 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0019others(214): Show | 217 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.952+2001T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113911121 | ||||||
| chr3:113911171
|
G | GACACACA others(7): Show |
1 | a0001c0001t0006g0146 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.952+2052_952+2053i others(16): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113911171 | |||||
| chr3:113911171
|
G | GACACACA others(13): Show |
2 | a0001c0001t0003g0089a0001c0001t0030g0155 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.952+2052_952+2053i others(22): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113911171 | |||||
| chr3:113911173
|
G | C | 3 | a0001c0001t0003g0089a0001c0001t0006g0146a0001c0001t0030g0155 | 3 | HG02258.hp2 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.952+2053G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113911173 | ||||||
| chr3:113911173
|
G | GACACACA others(5): Show |
13 | a0001c0001t0001g0290a0001c0001t0001g0306a0001c0001t0001g0307others(10): Show | 13 | HG01192.hp1 HG01358.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.952+2058_952+2069d others(14): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113911173 | |||||
| chr3:113911173
|
G | GACACACA others(7): Show |
176 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(173): Show | 176 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.952+2056_952+2069d others(16): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113911173 | |||||
| chr3:113911173
|
G | GACACACA others(9): Show |
19 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0178others(16): Show | 19 | HG00280.hp1 HG00642.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.952+2054_952+2069d others(18): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113911173 | |||||
| chr3:113911173
|
G | GACACACA others(11): Show |
53 | a0001c0001t0001g0014a0001c0001t0001g0090a0001c0001t0001g0107others(50): Show | 53 | HG01109.hp2 HG01168.hp2 HG01169.hp2 others(50): Show |
intron_variant | MODIFIER | c.952+2069_952+2070i others(20): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113911173 | |||||
| chr3:113911173
|
G | GACACACA others(13): Show |
11 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(8): Show | 13 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(10): Show |
intron_variant | MODIFIER | c.952+2069_952+2070i others(22): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113911173 | |||||
| chr3:113911173
|
G | GACACACA others(15): Show |
35 | a0001c0001t0001g0148a0001c0001t0001g0158a0001c0001t0001g0214others(32): Show | 35 | HG00438.hp2 HG00639.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.952+2069_952+2070i others(24): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113911173 | |||||
| chr3:113911173
|
G | GACACACA others(17): Show |
1 | a0001c0002t0003g0095 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.952+2069_952+2070i others(26): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113911173 | |||||
| chr3:113911173
|
G | GACACACA others(19): Show |
1 | a0001c0001t0001g0243 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.952+2069_952+2070i others(28): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113911173 | |||||
| chr3:113911173
|
G | GAGACACA others(5): Show |
6 | a0001c0001t0001g0196a0001c0001t0001g0285a0001c0001t0001g0286others(3): Show | 6 | HG00140.hp2 HG01256.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.952+2054_952+2055i others(14): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113911173 | |||||
| chr3:113911190
|
G | A | 1 | a0001c0002t0003g0057 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.952+2070G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113911190 | ||||||
| chr3:113911191
|
C | T | 1 | a0001c0002t0004g0098 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.952+2071C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113911191 | ||||||
| chr3:113911221
|
C | T | 3 | a0001c0001t0002g0301a0001c0001t0008g0167a0001c0001t0008g0192 | 3 | HG02451.hp2 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.952+2101C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113911221 | ||||||
| chr3:113911234
|
A | T | 3 | a0001c0001t0001g0219a0001c0001t0001g0225a0001c0002t0003g0024 | 3 | NA18747.hp1 NA18964.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.952+2114A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113911234 | ||||||
| chr3:113911474
|
G | A | 2 | a0001c0001t0001g0253a0001c0001t0001g0275 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.952+2354G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113911474 | ||||||
| chr3:113911475
|
G | C | 1 | a0001c0003t0002g0250 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.952+2355G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113911475 | ||||||
| chr3:113911612
|
TCCTTC | T | 6 | a0001c0001t0001g0006a0001c0001t0010g0008a0001c0001t0016g0003others(3): Show | 6 | HG00735.hp2 HG02280.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.952+2503_952+2507d others(7): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113911612 | |||||
| chr3:113911627
|
C | G | 1 | a0001c0001t0003g0123 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.952+2507C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113911627 | ||||||
| chr3:113911689
|
C | A | 4 | a0001c0001t0001g0247a0001c0001t0001g0283a0001c0002t0003g0095others(1): Show | 4 | HG00438.hp2 HG02080.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.952+2569C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113911689 | ||||||
| chr3:113911696
|
T | TTTCCTTC others(34): Show |
1 | a0005c0008t0023g0131 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.952+2595_952+2596i others(43): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113911696 | |||||
| chr3:113911696
|
T | TTTCCTTC others(38): Show |
2 | a0001c0001t0022g0132a0001c0001t0028g0179 | 2 | NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.952+2595_952+2596i others(47): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113911696 | |||||
| chr3:113911696
|
T | TTTCCTTC others(18): Show |
17 | a0001c0001t0001g0013a0001c0001t0001g0184a0001c0001t0001g0249others(14): Show | 17 | HG01106.hp2 HG02109.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.952+2595_952+2596i others(27): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113911696 | |||||
| chr3:113911696
|
T | TTTCCTTC others(22): Show |
12 | a0001c0001t0001g0006a0001c0001t0001g0304a0001c0001t0001g0305others(9): Show | 12 | HG00642.hp2 HG01074.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.952+2595_952+2596i others(31): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113911696 | |||||
| chr3:113911696
|
T | TTTCCTTC others(34): Show |
1 | a0011c0015t0001g0224 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.952+2595_952+2596i others(43): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113911696 | |||||
| chr3:113911696
|
T | TTTCCTTC others(38): Show |
8 | a0001c0001t0001g0194a0001c0001t0001g0227a0001c0001t0001g0251others(5): Show | 8 | HG00408.hp1 HG00673.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.952+2595_952+2596i others(47): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113911696 | |||||
| chr3:113911696
|
T | TTTCCTTC others(42): Show |
27 | a0001c0001t0001g0108a0001c0001t0001g0136a0001c0001t0001g0150others(24): Show | 27 | HG00408.hp2 HG00438.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.952+2595_952+2596i others(51): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113911696 | |||||
| chr3:113911696
|
T | TTTCCTTC others(46): Show |
19 | a0001c0001t0001g0177a0001c0001t0001g0182a0001c0001t0002g0175others(16): Show | 19 | HG00597.hp2 HG01433.hp1 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.952+2595_952+2596i others(55): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113911696 | |||||
| chr3:113911696
|
T | TTTCCTTC others(50): Show |
7 | a0001c0001t0001g0020a0001c0001t0003g0093a0001c0002t0003g0030others(4): Show | 7 | HG00673.hp1 NA18941.hp1 NA18985.hp2 others(4): Show |
intron_variant | MODIFIER | c.952+2595_952+2596i others(59): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113911696 | |||||
| chr3:113911696
|
T | TTTCCTTC others(26): Show |
36 | a0001c0001t0001g0202a0001c0001t0001g0208a0001c0001t0001g0219others(33): Show | 36 | HG00099.hp1 HG00438.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.952+2595_952+2596i others(35): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113911696 | |||||
| chr3:113911696
|
T | TTTCCTTC others(30): Show |
16 | a0001c0001t0001g0158a0001c0001t0001g0214a0001c0001t0001g0241others(13): Show | 16 | HG00280.hp1 HG01109.hp1 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.952+2595_952+2596i others(39): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113911696 | |||||
| chr3:113911696
|
T | TTTCCTTC others(34): Show |
14 | a0001c0001t0001g0148a0001c0001t0001g0160a0001c0001t0001g0181others(11): Show | 14 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.952+2595_952+2596i others(43): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113911696 | |||||
| chr3:113911696
|
T | TTTCCTTC others(38): Show |
41 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0109others(38): Show | 41 | HG00280.hp2 HG00609.hp2 HG01346.hp2 others(38): Show |
intron_variant | MODIFIER | c.952+2595_952+2596i others(47): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113911696 | |||||
| chr3:113911696
|
T | TTTCCTTC others(42): Show |
22 | a0001c0001t0001g0153a0001c0001t0001g0161a0001c0001t0001g0178others(19): Show | 22 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(19): Show |
intron_variant | MODIFIER | c.952+2595_952+2596i others(51): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113911696 | |||||
| chr3:113911696
|
T | TTTCCTTC others(46): Show |
6 | a0001c0001t0001g0163a0001c0001t0008g0315a0001c0001t0014g0088others(3): Show | 6 | HG01261.hp2 HG02055.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.952+2595_952+2596i others(55): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113911696 | |||||
| chr3:113911696
|
T | TTTCCTTC others(50): Show |
1 | a0001c0003t0002g0188 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.952+2595_952+2596i others(59): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113911696 | |||||
| chr3:113911696
|
T | TTTCTTTC others(38): Show |
2 | a0001c0003t0002g0293a0003c0018t0001g0248 | 2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.952+2579_952+2580i others(47): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113911696 | |||||
| chr3:113911699
|
C | CCTTCCTT others(14): Show |
4 | a0001c0001t0010g0008a0001c0001t0016g0003a0001c0001t0016g0009others(1): Show | 4 | HG00735.hp2 HG02280.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.952+2595_952+2596i others(23): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113911699 | |||||
| chr3:113911703
|
C | CCTTCCTT others(10): Show |
81 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(78): Show | 83 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.952+2595_952+2596i others(19): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113911703 | |||||
| chr3:113911707
|
C | CCTTCCTT others(6): Show |
1 | a0001c0005t0015g0128 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.952+2595_952+2596i others(15): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113911707 | |||||
| chr3:113911727
|
C | T | 227 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(224): Show | 227 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.952+2607C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113911727 | ||||||
| chr3:113911770
|
T | C | 245 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(242): Show | 245 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.952+2650T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113911770 | ||||||
| chr3:113911797
|
G | A | 2 | a0001c0001t0001g0253a0001c0001t0001g0275 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.952+2677G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113911797 | ||||||
| chr3:113911827
|
A | G | 2 | a0001c0001t0001g0006a0010c0011t0001g0011 | 2 | HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.952+2707A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113911827 | ||||||
| chr3:113911889
|
A | G | 2 | a0001c0001t0003g0089a0001c0001t0030g0155 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.952+2769A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113911889 | ||||||
| chr3:113911948
|
T | C | 14 | a0001c0001t0001g0015a0001c0001t0001g0196a0001c0001t0001g0285others(11): Show | 14 | HG00140.hp2 HG01192.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.952+2828T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113911948 | ||||||
| chr3:113911960
|
C | T | 1 | a0001c0001t0002g0281 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.952+2840C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113911960 | ||||||
| chr3:113911963
|
G | A | 51 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0090others(48): Show | 53 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.952+2843G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113911963 | ||||||
| chr3:113911970
|
G | C | 2 | a0001c0001t0003g0089a0001c0001t0030g0155 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.952+2850G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113911970 | ||||||
| chr3:113911973
|
C | T | 53 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0090others(50): Show | 55 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+2853C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113911973 | ||||||
| chr3:113912244
|
T | C | 3 | a0001c0001t0002g0172a0001c0001t0003g0126a0001c0001t0012g0300 | 3 | HG02486.hp1 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.952+3124T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113912244 | ||||||
| chr3:113912335
|
T | G | 6 | a0001c0001t0001g0006a0001c0001t0010g0008a0001c0001t0016g0003others(3): Show | 6 | HG00735.hp2 HG02280.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.952+3215T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113912335 | ||||||
| chr3:113912435
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.953-3266G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113912435 | ||||||
| chr3:113912472
|
G | T | 9 | a0001c0005t0001g0292a0001c0005t0002g0295a0001c0005t0009g0276others(6): Show | 9 | HG01109.hp2 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.953-3229G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113912472 | ||||||
| chr3:113912485
|
C | T | 1 | a0001c0003t0002g0207 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.953-3216C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113912485 | ||||||
| chr3:113912506
|
G | A | 2 | a0001c0001t0001g0251a0001c0003t0002g0252 | 2 | HG02056.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.953-3195G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113912506 | ||||||
| chr3:113912739
|
C | CA | 63 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(60): Show | 65 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.953-2950dupA | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113912739 | |||||
| chr3:113912799
|
A | T | 16 | a0001c0001t0001g0150a0001c0001t0001g0233a0001c0001t0001g0251others(13): Show | 16 | HG01358.hp1 HG01433.hp1 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.953-2902A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113912799 | ||||||
| chr3:113912933
|
A | G | 44 | a0001c0001t0001g0108a0001c0001t0001g0136a0001c0001t0001g0152others(41): Show | 44 | HG00408.hp2 HG00609.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.953-2768A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113912933 | ||||||
| chr3:113912952
|
G | T | 1 | a0001c0001t0001g0307 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.953-2749G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113912952 | ||||||
| chr3:113913018
|
G | A | 52 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0150others(49): Show | 52 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.953-2683G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113913018 | ||||||
| chr3:113913037
|
A | C | 102 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(99): Show | 104 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.953-2664A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113913037 | ||||||
| chr3:113913247
|
G | C | 3 | a0001c0001t0002g0301a0001c0001t0008g0167a0001c0001t0008g0192 | 3 | HG02451.hp2 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.953-2454G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113913247 | ||||||
| chr3:113913261
|
G | A | 58 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(55): Show | 60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.953-2440G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113913261 | ||||||
| chr3:113913296
|
A | G | 1 | a0001c0001t0006g0254 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.953-2405A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113913296 | ||||||
| chr3:113913302
|
G | T | 44 | a0001c0001t0001g0108a0001c0001t0001g0136a0001c0001t0001g0152others(41): Show | 44 | HG00408.hp2 HG00609.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.953-2399G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113913302 | ||||||
| chr3:113913429
|
C | CA | 73 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.953-2250dupA | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113913429 | |||||
| chr3:113913429
|
CA | C | 47 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0090others(44): Show | 49 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.953-2250delA | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113913429 | |||||
| chr3:113913429
|
CAA | C | 10 | a0001c0001t0001g0135a0001c0001t0001g0190a0001c0001t0001g0191others(7): Show | 10 | HG01168.hp2 HG01169.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.953-2251_953-2250d others(4): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113913429 | |||||
| chr3:113913436
|
A | G | 3 | a0001c0001t0022g0132a0001c0001t0028g0179a0005c0008t0023g0131 | 3 | HG02258.hp1 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.953-2265A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113913436 | ||||||
| chr3:113913558
|
G | A | 30 | a0001c0001t0001g0108a0001c0001t0001g0136a0001c0001t0001g0152others(27): Show | 30 | HG00408.hp2 HG00609.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.953-2143G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113913558 | ||||||
| chr3:113913624
|
A | G | 6 | a0001c0001t0002g0172a0001c0001t0002g0301a0001c0001t0003g0126others(3): Show | 6 | HG02451.hp2 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.953-2077A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113913624 | ||||||
| chr3:113913796
|
G | T | 306 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(303): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.953-1905G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113913796 | ||||||
| chr3:113913813
|
G | A | 1 | a0001c0004t0005g0064 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.953-1888G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113913813 | ||||||
| chr3:113913896
|
C | T | 96 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(93): Show | 98 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.953-1805C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113913896 | ||||||
| chr3:113914103
|
T | C | 52 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0090others(49): Show | 54 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.953-1598T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113914103 | ||||||
| chr3:113914293
|
G | A | 58 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(55): Show | 60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.953-1408G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113914293 | ||||||
| chr3:113914388
|
A | G | 1 | a0001c0001t0001g0182 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.953-1313A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113914388 | ||||||
| chr3:113914680
|
G | GT | 7 | a0001c0001t0002g0172a0001c0001t0002g0301a0001c0001t0003g0126others(4): Show | 7 | HG02451.hp2 HG02486.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.953-1009dupT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113914680 | |||||
| chr3:113914680
|
GT | G | 10 | a0001c0001t0001g0013a0001c0001t0001g0249a0001c0001t0001g0274others(7): Show | 10 | HG02818.hp2 HG02895.hp1 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.953-1009delT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 113914680 | |||||
| chr3:113914818
|
G | A | 50 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0090others(47): Show | 52 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.953-883G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113914818 | ||||||
| chr3:113914892
|
G | A | 3 | a0001c0001t0002g0172a0001c0001t0003g0126a0001c0001t0012g0300 | 3 | HG02486.hp1 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.953-809G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113914892 | ||||||
| chr3:113915019
|
T | C | 3 | a0001c0001t0002g0301a0001c0001t0008g0167a0001c0001t0008g0192 | 3 | HG02451.hp2 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.953-682T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113915019 | ||||||
| chr3:113915112
|
T | C | 58 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(55): Show | 60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.953-589T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113915112 | ||||||
| chr3:113915157
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.953-544G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113915157 | ||||||
| chr3:113915185
|
C | T | 58 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(55): Show | 60 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.953-516C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113915185 | ||||||
| chr3:113915235
|
G | C | 2 | a0002c0006t0024g0133a0002c0006t0025g0130 | 2 | HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.953-466G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113915235 | ||||||
| chr3:113915325
|
A | G | 4 | a0001c0001t0010g0008a0001c0001t0016g0003a0001c0001t0016g0009others(1): Show | 4 | HG00735.hp2 HG02280.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.953-376A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113915325 | ||||||
| chr3:113915484
|
A | G | 6 | a0001c0001t0001g0135a0001c0001t0001g0190a0001c0001t0001g0191others(3): Show | 6 | HG01168.hp2 HG01169.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.953-217A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113915484 | ||||||
| chr3:113915513
|
A | G | 15 | a0001c0001t0001g0136a0001c0001t0001g0152a0001c0001t0001g0177others(12): Show | 15 | HG00408.hp2 HG00609.hp1 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.953-188A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 9/17 | chr3 | 113915513 | ||||||
| chr3:113915916
|
G | C | 6 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(3): Show | 6 | HG02135.hp2 NA18945.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.1090+78G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113915916 | ||||||
| chr3:113916105
|
G | A | 319 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(316): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.1090+267G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113916105 | ||||||
| chr3:113916257
|
A | G | 1 | a0001c0001t0002g0301 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1090+419A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113916257 | ||||||
| chr3:113916302
|
G | C | 6 | a0001c0001t0001g0006a0001c0001t0010g0008a0001c0001t0016g0003others(3): Show | 6 | HG00735.hp2 HG02280.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1090+464G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113916302 | ||||||
| chr3:113916412
|
A | G | 1 | a0009c0010t0002g0134 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1090+574A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113916412 | ||||||
| chr3:113916488
|
A | G | 1 | a0001c0001t0008g0315 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1090+650A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113916488 | ||||||
| chr3:113916687
|
C | T | 14 | a0001c0001t0003g0100a0001c0001t0003g0123a0001c0001t0014g0102others(11): Show | 14 | HG01109.hp2 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1090+849C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113916687 | ||||||
| chr3:113916696
|
A | T | 3 | a0001c0002t0004g0059a0001c0003t0002g0221a0001c0003t0002g0222 | 3 | HG01943.hp1 HG01943.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1090+858A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113916696 | ||||||
| chr3:113916823
|
TAAG | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 5 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.1090+991_1090+993d others(5): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr3 | 113916823 | |||||
| chr3:113916864
|
T | G | 3 | a0001c0001t0002g0172a0001c0001t0003g0126a0001c0001t0012g0300 | 3 | HG02486.hp1 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1090+1026T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113916864 | ||||||
| chr3:113916873
|
G | T | 1 | a0001c0004t0004g0066 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1090+1035G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113916873 | ||||||
| chr3:113916990
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1090+1152G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113916990 | ||||||
| chr3:113917209
|
CTT | C | 44 | a0001c0001t0001g0108a0001c0001t0001g0136a0001c0001t0001g0152others(41): Show | 44 | HG00408.hp2 HG00609.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.1090+1373_1090+137 others(6): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr3 | 113917209 | |||||
| chr3:113917472
|
C | T | 2 | a0001c0003t0002g0293a0003c0018t0001g0248 | 2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1090+1634C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113917472 | ||||||
| chr3:113917556
|
A | G | 1 | a0001c0001t0003g0089 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1090+1718A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113917556 | ||||||
| chr3:113917573
|
C | T | 2 | a0001c0001t0001g0253a0001c0001t0001g0275 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1090+1735C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113917573 | ||||||
| chr3:113917671
|
C | T | 3 | a0001c0002t0003g0087a0001c0003t0002g0149a0001c0003t0007g0154 | 3 | HG00609.hp2 HG02135.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1090+1833C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113917671 | ||||||
| chr3:113917795
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1090+1957C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113917795 | ||||||
| chr3:113917856
|
C | CT | 39 | a0001c0001t0001g0014a0001c0001t0001g0090a0001c0001t0001g0107others(36): Show | 40 | HG00099.hp2 HG01070.hp2 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.1090+2043dupT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr3 | 113917856 | |||||
| chr3:113917856
|
C | CTT | 14 | a0001c0001t0001g0002a0001c0001t0001g0121a0001c0001t0001g0171others(11): Show | 15 | HG00140.hp1 HG00323.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.1090+2042_1090+204 others(6): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr3 | 113917856 | |||||
| chr3:113917856
|
CT | C | 35 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0109others(32): Show | 35 | HG00438.hp2 HG00735.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.1090+2043delT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr3 | 113917856 | |||||
| chr3:113917856
|
CTT | C | 176 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(173): Show | 176 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.1090+2042_1090+204 others(6): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr3 | 113917856 | |||||
| chr3:113917856
|
CTTT | C | 38 | a0001c0001t0001g0019a0001c0001t0001g0150a0001c0001t0001g0163others(35): Show | 38 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.1090+2041_1090+204 others(7): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr3 | 113917856 | |||||
| chr3:113917856
|
CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0001g0006a0010c0011t0001g0011 | 2 | HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1090+2030_1090+204 others(18): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr3 | 113917856 | |||||
| chr3:113917890
|
C | G | 3 | a0001c0001t0002g0172a0001c0001t0003g0126a0001c0001t0012g0300 | 3 | HG02486.hp1 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1090+2052C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113917890 | ||||||
| chr3:113918176
|
C | A | 2 | a0001c0001t0003g0089a0001c0001t0030g0155 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1090+2338C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113918176 | ||||||
| chr3:113918327
|
C | G | 1 | a0001c0004t0005g0036 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1090+2489C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113918327 | ||||||
| chr3:113918577
|
G | A | 46 | a0001c0001t0001g0006a0001c0001t0001g0148a0001c0001t0001g0158others(43): Show | 46 | HG00438.hp2 HG00639.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.1090+2739G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113918577 | ||||||
| chr3:113918612
|
A | G | 1 | a0001c0001t0015g0101 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1090+2774A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113918612 | ||||||
| chr3:113918676
|
C | A | 2 | a0001c0001t0003g0089a0001c0001t0030g0155 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1090+2838C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113918676 | ||||||
| chr3:113918747
|
G | A | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(53): Show | 56 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1090+2909G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113918747 | ||||||
| chr3:113918877
|
T | C | 1 | a0001c0002t0003g0026 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1090+3039T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113918877 | ||||||
| chr3:113918954
|
C | T | 38 | a0001c0001t0001g0148a0001c0001t0001g0158a0001c0001t0001g0214others(35): Show | 38 | HG00438.hp2 HG00639.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.1090+3116C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113918954 | ||||||
| chr3:113919029
|
T | A | 2 | a0001c0001t0008g0167a0001c0001t0008g0192 | 2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1090+3191T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113919029 | ||||||
| chr3:113919040
|
A | C | 1 | a0001c0001t0001g0227 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1090+3202A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113919040 | ||||||
| chr3:113919086
|
C | G | 3 | a0001c0001t0001g0308a0001c0001t0001g0312a0001c0001t0001g0313 | 3 | HG02559.hp1 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1090+3248C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113919086 | ||||||
| chr3:113919284
|
G | A | 38 | a0001c0001t0001g0148a0001c0001t0001g0158a0001c0001t0001g0214others(35): Show | 38 | HG00438.hp2 HG00639.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.1090+3446G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113919284 | ||||||
| chr3:113919545
|
T | C | 149 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0022others(146): Show | 149 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.1090+3707T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113919545 | ||||||
| chr3:113919601
|
T | C | 1 | a0001c0001t0001g0243 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1090+3763T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113919601 | ||||||
| chr3:113920183
|
C | G | 161 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(158): Show | 161 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.1090+4345C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113920183 | ||||||
| chr3:113920312
|
A | T | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1090+4474A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113920312 | ||||||
| chr3:113920517
|
T | G | 3 | a0001c0001t0006g0124a0001c0001t0006g0125a0001c0001t0006g0310 | 3 | HG03098.hp2 HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1090+4679T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113920517 | ||||||
| chr3:113920535
|
CTTTATTT | C | 4 | a0001c0001t0001g0258a0001c0001t0001g0269a0001c0002t0004g0031others(1): Show | 4 | HG00408.hp1 HG00438.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.1090+4714_1090+472 others(11): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr3 | 113920535 | |||||
| chr3:113920574
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1090+4736T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113920574 | ||||||
| chr3:113920628
|
G | A | 145 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0022others(142): Show | 145 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.1090+4790G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113920628 | ||||||
| chr3:113920693
|
A | G | 3 | a0001c0001t0001g0156a0001c0001t0001g0186a0001c0003t0002g0157 | 3 | HG01346.hp2 HG01515.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1090+4855A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113920693 | ||||||
| chr3:113920830
|
C | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0181 | 2 | HG00558.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1090+4992C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113920830 | ||||||
| chr3:113921111
|
C | T | 2 | a0001c0001t0009g0262a0001c0001t0009g0267 | 2 | HG02109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1090+5273C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113921111 | ||||||
| chr3:113921189
|
G | T | 50 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0090others(47): Show | 52 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.1090+5351G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113921189 | ||||||
| chr3:113921218
|
A | G | 1 | a0001c0001t0003g0123 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1090+5380A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113921218 | ||||||
| chr3:113921231
|
G | T | 4 | a0001c0001t0003g0100a0001c0001t0014g0102a0001c0001t0015g0101others(1): Show | 4 | HG02145.hp1 HG02257.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1090+5393G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113921231 | ||||||
| chr3:113921451
|
A | G | 3 | a0001c0001t0022g0132a0001c0001t0028g0179a0005c0008t0023g0131 | 3 | HG02258.hp1 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1090+5613A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113921451 | ||||||
| chr3:113921474
|
C | A | 4 | a0001c0005t0001g0292a0001c0005t0002g0295a0001c0005t0009g0276others(1): Show | 4 | HG01109.hp2 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090+5636C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113921474 | ||||||
| chr3:113921810
|
T | C | 1 | a0001c0003t0002g0142 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1090+5972T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113921810 | ||||||
| chr3:113922003
|
G | T | 2 | a0002c0006t0024g0133a0002c0006t0025g0130 | 2 | HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1090+6165G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113922003 | ||||||
| chr3:113922042
|
G | A | 46 | a0001c0001t0001g0006a0001c0001t0001g0148a0001c0001t0001g0158others(43): Show | 46 | HG00438.hp2 HG00639.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.1090+6204G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113922042 | ||||||
| chr3:113922297
|
T | C | 8 | a0001c0005t0001g0292a0001c0005t0002g0295a0001c0005t0009g0276others(5): Show | 8 | HG01109.hp2 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1090+6459T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113922297 | ||||||
| chr3:113922500
|
C | G | 96 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0109others(93): Show | 96 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.1090+6662C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113922500 | ||||||
| chr3:113922527
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1090+6689T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113922527 | ||||||
| chr3:113922587
|
G | C | 1 | a0013c0007t0002g0255 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1090+6749G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113922587 | ||||||
| chr3:113922688
|
A | G | 38 | a0001c0001t0001g0148a0001c0001t0001g0158a0001c0001t0001g0214others(35): Show | 38 | HG00438.hp2 HG00639.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.1090+6850A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113922688 | ||||||
| chr3:113922711
|
A | G | 38 | a0001c0001t0001g0148a0001c0001t0001g0158a0001c0001t0001g0214others(35): Show | 38 | HG00438.hp2 HG00639.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.1090+6873A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113922711 | ||||||
| chr3:113922739
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1090+6901G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113922739 | ||||||
| chr3:113922783
|
T | A | 5 | a0001c0001t0001g0233a0001c0003t0007g0110a0001c0004t0005g0064others(2): Show | 5 | HG01358.hp1 HG01433.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1090+6945T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113922783 | ||||||
| chr3:113923442
|
T | C | 3 | a0001c0001t0002g0172a0001c0001t0003g0126a0001c0001t0012g0300 | 3 | HG02486.hp1 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1091-7272T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113923442 | ||||||
| chr3:113923561
|
G | A | 6 | a0001c0001t0001g0006a0001c0001t0010g0008a0001c0001t0016g0003others(3): Show | 6 | HG00735.hp2 HG02280.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1091-7153G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113923561 | ||||||
| chr3:113923620
|
A | G | 60 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0150others(57): Show | 60 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.1091-7094A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113923620 | ||||||
| chr3:113923622
|
T | C | 1 | a0001c0001t0001g0266 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1091-7092T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113923622 | ||||||
| chr3:113923624
|
T | G | 319 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(316): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.1091-7090T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113923624 | ||||||
| chr3:113923728
|
C | T | 246 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0019others(243): Show | 246 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.1091-6986C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113923728 | ||||||
| chr3:113923901
|
C | T | 142 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0107others(139): Show | 142 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.1091-6813C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113923901 | ||||||
| chr3:113923988
|
C | A | 6 | a0001c0001t0001g0006a0001c0001t0010g0008a0001c0001t0016g0003others(3): Show | 6 | HG00735.hp2 HG02280.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1091-6726C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113923988 | ||||||
| chr3:113924015
|
A | G | 5 | a0001c0001t0002g0301a0001c0001t0003g0089a0001c0001t0008g0167others(2): Show | 5 | HG02258.hp2 HG02451.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1091-6699A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113924015 | ||||||
| chr3:113924029
|
T | G | 1 | a0001c0002t0004g0097 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1091-6685T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113924029 | ||||||
| chr3:113924054
|
G | C | 1 | a0001c0001t0002g0263 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1091-6660G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113924054 | ||||||
| chr3:113924073
|
T | A | 6 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(3): Show | 6 | HG01934.hp1 HG01952.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.1091-6641T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113924073 | ||||||
| chr3:113924091
|
G | GT | 55 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(52): Show | 57 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.1091-6608dupT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr3 | 113924091 | |||||
| chr3:113924091
|
G | GTT | 61 | a0001c0001t0001g0019a0001c0001t0001g0150a0001c0001t0001g0163others(58): Show | 61 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1091-6609_1091-660 others(6): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr3 | 113924091 | |||||
| chr3:113924091
|
G | T | 1 | a0001c0002t0003g0129 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1091-6623G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113924091 | ||||||
| chr3:113924091
|
GT | G | 36 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0136others(33): Show | 36 | HG00408.hp2 HG00609.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.1091-6608delT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr3 | 113924091 | |||||
| chr3:113924116
|
C | T | 47 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0090others(44): Show | 49 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.1091-6598C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113924116 | ||||||
| chr3:113924213
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1091-6501C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113924213 | ||||||
| chr3:113924389
|
A | G | 5 | a0001c0001t0001g0253a0001c0001t0001g0275a0001c0001t0022g0132others(2): Show | 5 | HG02258.hp1 HG02615.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1091-6325A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113924389 | ||||||
| chr3:113924413
|
A | G | 2 | a0001c0003t0002g0284a0001c0012t0002g0216 | 2 | HG03710.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1091-6301A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113924413 | ||||||
| chr3:113924434
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1091-6280T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113924434 | ||||||
| chr3:113924579
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1091-6135T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113924579 | ||||||
| chr3:113924769
|
A | T | 1 | a0001c0001t0003g0126 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1091-5945A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113924769 | ||||||
| chr3:113924796
|
A | G | 3 | a0001c0001t0002g0172a0001c0001t0003g0126a0001c0001t0012g0300 | 3 | HG02486.hp1 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1091-5918A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113924796 | ||||||
| chr3:113925108
|
T | C | 3 | a0001c0001t0002g0172a0001c0001t0003g0126a0001c0001t0012g0300 | 3 | HG02486.hp1 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1091-5606T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113925108 | ||||||
| chr3:113925290
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1091-5424C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113925290 | ||||||
| chr3:113925315
|
G | A | 1 | a0001c0001t0001g0200 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1091-5399G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113925315 | ||||||
| chr3:113925410
|
A | C | 10 | a0001c0001t0003g0123a0001c0005t0001g0292a0001c0005t0002g0295others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1091-5304A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113925410 | ||||||
| chr3:113925433
|
C | T | 3 | a0001c0001t0022g0132a0001c0001t0028g0179a0005c0008t0023g0131 | 3 | HG02258.hp1 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1091-5281C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113925433 | ||||||
| chr3:113925474
|
A | AAAAC | 158 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(155): Show | 160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.1091-5212_1091-520 others(8): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr3 | 113925474 | |||||
| chr3:113925474
|
A | AAAACAAA others(1): Show |
8 | a0001c0001t0002g0272a0001c0005t0001g0292a0001c0005t0009g0276others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1091-5216_1091-520 others(12): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr3 | 113925474 | |||||
| chr3:113925474
|
A | AAAACAAA others(5): Show |
1 | a0001c0001t0003g0123 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1091-5220_1091-520 others(16): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr3 | 113925474 | |||||
| chr3:113925474
|
AAAAC | A | 136 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0109others(133): Show | 136 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.1091-5212_1091-520 others(8): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr3 | 113925474 | |||||
| chr3:113925879
|
T | G | 15 | a0001c0001t0001g0015a0001c0001t0001g0196a0001c0001t0001g0285others(12): Show | 15 | HG00140.hp2 HG01192.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.1091-4835T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113925879 | ||||||
| chr3:113926052
|
A | T | 1 | a0001c0002t0027g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1091-4662A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113926052 | ||||||
| chr3:113926082
|
T | C | 1 | a0010c0011t0001g0011 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1091-4632T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113926082 | ||||||
| chr3:113926237
|
T | C | 7 | a0001c0001t0001g0148a0001c0001t0001g0158a0001c0001t0001g0214others(4): Show | 7 | HG01071.hp1 HG02040.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.1091-4477T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113926237 | ||||||
| chr3:113926355
|
A | G | 38 | a0001c0001t0001g0148a0001c0001t0001g0158a0001c0001t0001g0214others(35): Show | 38 | HG00438.hp2 HG00639.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.1091-4359A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113926355 | ||||||
| chr3:113926661
|
T | C | 3 | a0001c0001t0022g0132a0001c0001t0028g0179a0005c0008t0023g0131 | 3 | HG02258.hp1 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1091-4053T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113926661 | ||||||
| chr3:113926792
|
G | A | 3 | a0001c0002t0003g0071a0001c0002t0004g0038a0001c0002t0004g0072 | 3 | HG00735.hp1 HG03704.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1091-3922G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113926792 | ||||||
| chr3:113927011
|
G | T | 170 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(167): Show | 170 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.1091-3703G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113927011 | ||||||
| chr3:113927081
|
G | A | 1 | a0001c0001t0002g0301 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1091-3633G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113927081 | ||||||
| chr3:113927277
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1091-3437C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113927277 | ||||||
| chr3:113927326
|
C | T | 100 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0109others(97): Show | 100 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.1091-3388C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113927326 | ||||||
| chr3:113927608
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1091-3106C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113927608 | ||||||
| chr3:113927810
|
C | T | 86 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0020others(83): Show | 86 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.1091-2904C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113927810 | ||||||
| chr3:113927868
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1091-2846G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113927868 | ||||||
| chr3:113927877
|
A | G | 2 | a0001c0003t0007g0199a0001c0004t0019g0054 | 2 | NA18969.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1091-2837A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113927877 | ||||||
| chr3:113927878
|
T | C | 10 | a0001c0001t0003g0123a0001c0005t0001g0292a0001c0005t0002g0295others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1091-2836T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113927878 | ||||||
| chr3:113927904
|
C | T | 29 | a0001c0001t0001g0108a0001c0001t0001g0136a0001c0001t0001g0152others(26): Show | 29 | HG00408.hp2 HG00609.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.1091-2810C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113927904 | ||||||
| chr3:113928108
|
A | C | 4 | a0001c0001t0022g0132a0001c0001t0028g0179a0001c0005t0002g0295others(1): Show | 4 | HG01109.hp2 HG02258.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1091-2606A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113928108 | ||||||
| chr3:113928282
|
C | T | 3 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0002g0303 | 3 | HG00099.hp1 HG00642.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.1091-2432C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113928282 | ||||||
| chr3:113928283
|
G | A | 1 | a0001c0003t0002g0204 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1091-2431G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113928283 | ||||||
| chr3:113928286
|
CA | C | 7 | a0001c0001t0001g0013a0001c0001t0001g0274a0001c0001t0006g0124others(4): Show | 7 | HG02486.hp1 HG02818.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1091-2427delA | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113928286 | ||||||
| chr3:113928307
|
G | A | 162 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(159): Show | 162 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.1091-2407G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113928307 | ||||||
| chr3:113928386
|
T | C | 1 | a0001c0001t0001g0244 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1091-2328T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113928386 | ||||||
| chr3:113928515
|
G | A | 7 | a0001c0001t0001g0169a0001c0001t0001g0174a0001c0001t0001g0193others(4): Show | 7 | HG02451.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1091-2199G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113928515 | ||||||
| chr3:113928650
|
T | C | 3 | a0001c0001t0002g0296a0001c0001t0002g0298a0001c0001t0026g0297 | 3 | HG02895.hp1 HG02897.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1091-2064T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113928650 | ||||||
| chr3:113928711
|
G | A | 1 | a0001c0003t0002g0230 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1091-2003G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113928711 | ||||||
| chr3:113928782
|
G | A | 64 | a0001c0001t0001g0019a0001c0001t0001g0113a0001c0001t0001g0120others(61): Show | 64 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.1091-1932G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113928782 | ||||||
| chr3:113928788
|
G | A | 1 | a0001c0002t0004g0031 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1091-1926G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113928788 | ||||||
| chr3:113928863
|
C | T | 6 | a0001c0001t0001g0013a0001c0001t0001g0153a0001c0001t0001g0249others(3): Show | 6 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1091-1851C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113928863 | ||||||
| chr3:113928937
|
A | T | 1 | a0001c0003t0002g0119 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1091-1777A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113928937 | ||||||
| chr3:113928942
|
A | ACTGT | 4 | a0001c0001t0006g0106a0001c0001t0012g0103a0001c0001t0012g0104others(1): Show | 4 | HG02615.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1091-1767_1091-176 others(8): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr3 | 113928942 | |||||
| chr3:113928969
|
TTC | T | 183 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0109others(180): Show | 183 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1091-1743_1091-174 others(6): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr3 | 113928969 | |||||
| chr3:113928972
|
T | C | 183 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0109others(180): Show | 183 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1091-1742T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113928972 | ||||||
| chr3:113929169
|
G | T | 4 | a0001c0005t0010g0004a0001c0005t0010g0007a0001c0005t0010g0010others(1): Show | 4 | HG02109.hp2 HG02280.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1091-1545G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113929169 | ||||||
| chr3:113929263
|
C | A | 14 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(11): Show | 14 | HG00558.hp1 HG01934.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.1091-1451C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113929263 | ||||||
| chr3:113929554
|
C | T | 21 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(18): Show | 21 | HG00558.hp1 HG01106.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1091-1160C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113929554 | ||||||
| chr3:113929647
|
A | G | 1 | a0001c0001t0017g0259 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1091-1067A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113929647 | ||||||
| chr3:113929856
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1091-858A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113929856 | ||||||
| chr3:113930181
|
C | T | 1 | a0001c0001t0018g0127 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1091-533C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113930181 | ||||||
| chr3:113930497
|
T | A | 45 | a0001c0001t0001g0020a0001c0001t0001g0108a0001c0001t0001g0148others(42): Show | 45 | HG00438.hp2 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1091-217T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113930497 | ||||||
| chr3:113930608
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1091-106T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 10/17 | chr3 | 113930608 | ||||||
| chr3:113930869
|
G | GT | 18 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0002g0172others(15): Show | 18 | HG00735.hp2 HG00741.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1209+38dupT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 113930869 | |||||
| chr3:113930995
|
C | T | 30 | a0001c0001t0001g0019a0001c0001t0001g0136a0001c0001t0001g0163others(27): Show | 30 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.1209+163C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 11/17 | chr3 | 113930995 | ||||||
| chr3:113930996
|
G | A | 6 | a0001c0001t0003g0100a0001c0001t0014g0088a0001c0001t0014g0102others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1209+164G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 11/17 | chr3 | 113930996 | ||||||
| chr3:113931081
|
A | G | 1 | a0001c0003t0002g0201 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1209+249A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 11/17 | chr3 | 113931081 | ||||||
| chr3:113931213
|
A | T | 1 | a0001c0001t0002g0172 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1209+381A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 11/17 | chr3 | 113931213 | ||||||
| chr3:113931294
|
G | A | 1 | a0013c0007t0002g0255 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1209+462G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 11/17 | chr3 | 113931294 | ||||||
| chr3:113931362
|
A | AT | 9 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0144others(6): Show | 9 | HG01891.hp2 HG02040.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.1209+546dupT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 113931362 | |||||
| chr3:113931362
|
AT | A | 58 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(55): Show | 58 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.1209+546delT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 113931362 | |||||
| chr3:113931599
|
C | T | 8 | a0001c0001t0001g0312a0001c0001t0006g0106a0001c0001t0012g0103others(5): Show | 8 | HG00741.hp2 HG01934.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1209+767C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 11/17 | chr3 | 113931599 | ||||||
| chr3:113931818
|
C | T | 6 | a0001c0001t0001g0013a0001c0001t0001g0153a0001c0001t0001g0249others(3): Show | 6 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1209+986C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 11/17 | chr3 | 113931818 | ||||||
| chr3:113931870
|
G | A | 1 | a0001c0001t0001g0307 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1209+1038G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 11/17 | chr3 | 113931870 | ||||||
| chr3:113932019
|
T | C | 6 | a0001c0001t0001g0019a0001c0001t0001g0306a0001c0001t0001g0308others(3): Show | 6 | HG02559.hp1 HG02622.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1209+1187T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 11/17 | chr3 | 113932019 | ||||||
| chr3:113932194
|
T | C | 3 | a0001c0001t0002g0172a0001c0001t0008g0315a0001c0001t0021g0287 | 3 | HG02055.hp2 HG02886.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1210-1317T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 11/17 | chr3 | 113932194 | ||||||
| chr3:113932297
|
A | G | 20 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0153others(17): Show | 20 | HG00735.hp2 HG02109.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.1210-1214A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 11/17 | chr3 | 113932297 | ||||||
| chr3:113932401
|
G | C | 26 | a0001c0001t0001g0013a0001c0001t0001g0144a0001c0001t0001g0184others(23): Show | 26 | HG00140.hp2 HG00639.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.1210-1110G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 11/17 | chr3 | 113932401 | ||||||
| chr3:113932508
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1210-1003C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 11/17 | chr3 | 113932508 | ||||||
| chr3:113932614
|
A | T | 1 | a0001c0001t0001g0150 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1210-897A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 11/17 | chr3 | 113932614 | ||||||
| chr3:113932666
|
G | C | 57 | a0001c0001t0001g0019a0001c0001t0001g0113a0001c0001t0001g0120others(54): Show | 57 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.1210-845G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 11/17 | chr3 | 113932666 | ||||||
| chr3:113932683
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1210-828G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 11/17 | chr3 | 113932683 | ||||||
| chr3:113932712
|
C | G | 1 | a0013c0007t0002g0255 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1210-799C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 11/17 | chr3 | 113932712 | ||||||
| chr3:113932770
|
G | A | 215 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(212): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1210-741G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 11/17 | chr3 | 113932770 | ||||||
| chr3:113932886
|
C | CT | 293 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(290): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1210-611dupT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 113932886 | |||||
| chr3:113933037
|
G | A | 6 | a0001c0001t0001g0253a0001c0001t0014g0088a0001c0001t0014g0102others(3): Show | 6 | HG02145.hp1 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1210-474G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 11/17 | chr3 | 113933037 | ||||||
| chr3:113933180
|
T | C | 196 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(193): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.1210-331T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 11/17 | chr3 | 113933180 | ||||||
| chr3:113933202
|
A | G | 1 | a0001c0005t0015g0128 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1210-309A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 11/17 | chr3 | 113933202 | ||||||
| chr3:113933204
|
A | T | 2 | a0001c0001t0001g0244a0001c0003t0002g0119 | 2 | HG03491.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1210-307A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 11/17 | chr3 | 113933204 | ||||||
| chr3:113933214
|
T | C | 27 | a0001c0001t0001g0171a0001c0001t0001g0253a0001c0001t0001g0268others(24): Show | 27 | HG00735.hp2 HG01106.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1210-297T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 11/17 | chr3 | 113933214 | ||||||
| chr3:113933238
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1210-273G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 11/17 | chr3 | 113933238 | ||||||
| chr3:113933270
|
A | G | 311 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(308): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1210-241A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 11/17 | chr3 | 113933270 | ||||||
| chr3:113933367
|
T | C | 28 | a0001c0001t0001g0002a0001c0001t0001g0169a0001c0001t0001g0174others(25): Show | 29 | HG00140.hp1 HG00323.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1210-144T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 11/17 | chr3 | 113933367 | ||||||
| chr3:113933478
|
T | C | 5 | a0001c0005t0001g0292a0001c0005t0009g0276a0001c0005t0009g0294others(2): Show | 5 | HG01891.hp1 HG02257.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1210-33T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 11/17 | chr3 | 113933478 | ||||||
| chr3:113933741
|
C | T | 1 | a0001c0001t0028g0179 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1352+88C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 12/17 | chr3 | 113933741 | ||||||
| chr3:113933927
|
A | G | 127 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0019others(124): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.1352+274A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 12/17 | chr3 | 113933927 | ||||||
| chr3:113934080
|
A | C | 9 | a0001c0001t0006g0106a0001c0001t0006g0124a0001c0001t0006g0125others(6): Show | 9 | HG01891.hp2 HG02965.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.1353-352A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 12/17 | chr3 | 113934080 | ||||||
| chr3:113934167
|
T | C | 3 | a0001c0001t0001g0006a0001c0001t0003g0100a0010c0011t0001g0011 | 3 | HG02257.hp2 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1353-265T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 12/17 | chr3 | 113934167 | ||||||
| chr3:113934374
|
A | G | 8 | a0001c0001t0006g0106a0001c0001t0006g0124a0001c0001t0006g0125others(5): Show | 8 | HG01891.hp2 HG02965.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1353-58A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 12/17 | chr3 | 113934374 | ||||||
| chr3:113934619
|
C | G | 11 | a0001c0001t0010g0008a0001c0001t0015g0101a0001c0001t0016g0003others(8): Show | 11 | HG00735.hp2 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1456+84C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 13/17 | chr3 | 113934619 | ||||||
| chr3:113934671
|
G | C | 1 | a0001c0001t0026g0297 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1456+136G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 13/17 | chr3 | 113934671 | ||||||
| chr3:113934750
|
T | C | 1 | a0001c0001t0002g0172 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1456+215T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 13/17 | chr3 | 113934750 | ||||||
| chr3:113934769
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1456+234A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 13/17 | chr3 | 113934769 | ||||||
| chr3:113934835
|
G | A | 3 | a0001c0001t0006g0124a0001c0001t0006g0125a0001c0001t0006g0310 | 3 | HG03098.hp2 HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1456+300G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 13/17 | chr3 | 113934835 | ||||||
| chr3:113934984
|
C | T | 1 | a0001c0001t0026g0297 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1456+449C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 13/17 | chr3 | 113934984 | ||||||
| chr3:113934985
|
A | G | 130 | a0001c0001t0001g0006a0001c0001t0002g0117a0001c0001t0002g0162others(127): Show | 130 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.1456+450A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 13/17 | chr3 | 113934985 | ||||||
| chr3:113935046
|
A | G | 6 | a0001c0001t0001g0182a0001c0001t0001g0227a0001c0001t0001g0247others(3): Show | 6 | HG00673.hp2 NA18612.hp2 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.1456+511A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 13/17 | chr3 | 113935046 | ||||||
| chr3:113935189
|
G | A | 1 | a0007c0013t0003g0122 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1456+654G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 13/17 | chr3 | 113935189 | ||||||
| chr3:113935310
|
T | G | 9 | a0001c0001t0002g0162a0001c0001t0002g0280a0001c0001t0002g0281others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1456+775T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 13/17 | chr3 | 113935310 | ||||||
| chr3:113935487
|
A | AAT | 23 | a0001c0001t0001g0090a0001c0001t0001g0136a0001c0001t0001g0171others(20): Show | 23 | HG00140.hp2 HG01070.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.1457-765_1457-764d others(4): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 113935487 | |||||
| chr3:113935487
|
AAT | A | 106 | a0001c0001t0001g0006a0001c0001t0002g0117a0001c0001t0002g0165others(103): Show | 106 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1457-765_1457-764d others(4): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 113935487 | |||||
| chr3:113935499
|
T | TACAC | 4 | a0001c0001t0012g0103a0001c0001t0012g0104a0001c0001t0012g0116others(1): Show | 4 | HG02486.hp1 HG02615.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1457-766_1457-765i others(6): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 113935499 | |||||
| chr3:113935501
|
T | C | 16 | a0001c0001t0001g0006a0001c0001t0002g0162a0001c0001t0002g0280others(13): Show | 16 | HG01109.hp2 HG02055.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1457-765T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 13/17 | chr3 | 113935501 | ||||||
| chr3:113935503
|
C | T | 12 | a0001c0001t0001g0169a0001c0001t0001g0174a0001c0001t0001g0193others(9): Show | 12 | HG02055.hp2 HG02451.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1457-763C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 13/17 | chr3 | 113935503 | ||||||
| chr3:113935517
|
CAT | C | 8 | a0001c0001t0006g0106a0001c0001t0006g0124a0001c0001t0006g0125others(5): Show | 8 | HG01891.hp2 HG02965.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1457-744_1457-743d others(4): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 113935517 | |||||
| chr3:113935519
|
T | C | 120 | a0001c0001t0001g0006a0001c0001t0002g0117a0001c0001t0002g0162others(117): Show | 120 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.1457-747T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 13/17 | chr3 | 113935519 | ||||||
| chr3:113935537
|
C | T | 127 | a0001c0001t0001g0006a0001c0001t0002g0117a0001c0001t0002g0162others(124): Show | 127 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.1457-729C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 13/17 | chr3 | 113935537 | ||||||
| chr3:113935555
|
T | C | 1 | a0001c0003t0007g0237 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1457-711T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 13/17 | chr3 | 113935555 | ||||||
| chr3:113935574
|
G | A | 2 | a0001c0002t0003g0045a0001c0002t0003g0046 | 2 | NA18946.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1457-692G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 13/17 | chr3 | 113935574 | ||||||
| chr3:113935611
|
A | C | 3 | a0001c0001t0006g0124a0001c0001t0006g0125a0001c0001t0006g0310 | 3 | HG03098.hp2 HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1457-655A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 13/17 | chr3 | 113935611 | ||||||
| chr3:113935701
|
C | G | 1 | a0001c0001t0001g0161 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1457-565C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 13/17 | chr3 | 113935701 | ||||||
| chr3:113935858
|
T | C | 128 | a0001c0001t0001g0006a0001c0001t0002g0117a0001c0001t0002g0162others(125): Show | 128 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1457-408T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 13/17 | chr3 | 113935858 | ||||||
| chr3:113935954
|
A | G | 8 | a0001c0001t0002g0162a0001c0001t0002g0280a0001c0001t0002g0281others(5): Show | 8 | HG01109.hp2 HG02055.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1457-312A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 13/17 | chr3 | 113935954 | ||||||
| chr3:113935990
|
T | G | 1 | a0001c0001t0026g0297 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1457-276T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 13/17 | chr3 | 113935990 | ||||||
| chr3:113936001
|
A | G | 3 | a0001c0001t0006g0124a0001c0001t0006g0125a0001c0001t0006g0310 | 3 | HG03098.hp2 HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1457-265A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 13/17 | chr3 | 113936001 | ||||||
| chr3:113936096
|
G | T | 3 | a0001c0001t0001g0006a0001c0001t0003g0100a0010c0011t0001g0011 | 3 | HG02257.hp2 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1457-170G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 13/17 | chr3 | 113936096 | ||||||
| chr3:113936185
|
A | C | 2 | a0001c0005t0009g0276a0001c0005t0009g0294 | 2 | HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1457-81A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 13/17 | chr3 | 113936185 | ||||||
| chr3:113936847
|
C | A | 1 | a0001c0001t0001g0274 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1633+405C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 14/17 | chr3 | 113936847 | ||||||
| chr3:113936974
|
C | T | 4 | a0001c0001t0010g0008a0001c0001t0016g0003a0001c0001t0016g0009others(1): Show | 4 | HG00735.hp2 HG02280.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1633+532C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 14/17 | chr3 | 113936974 | ||||||
| chr3:113936995
|
C | A | 1 | a0001c0003t0002g0147 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1633+553C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 14/17 | chr3 | 113936995 | ||||||
| chr3:113937049
|
G | A | 2 | a0001c0001t0001g0006a0010c0011t0001g0011 | 2 | HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1633+607G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 14/17 | chr3 | 113937049 | ||||||
| chr3:113937235
|
G | A | 8 | a0001c0001t0006g0106a0001c0001t0006g0124a0001c0001t0006g0125others(5): Show | 8 | HG01891.hp2 HG02965.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1633+793G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 14/17 | chr3 | 113937235 | ||||||
| chr3:113937435
|
A | C | 111 | a0001c0001t0002g0117a0001c0001t0002g0162a0001c0001t0002g0165others(108): Show | 111 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.1634-651A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 14/17 | chr3 | 113937435 | ||||||
| chr3:113937732
|
C | T | 2 | a0004c0017t0029g0282a0013c0007t0002g0255 | 2 | HG01192.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1634-354C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 14/17 | chr3 | 113937732 | ||||||
| chr3:113937874
|
G | A | 1 | a0001c0003t0002g0201 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1634-212G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 14/17 | chr3 | 113937874 | ||||||
| chr3:113937911
|
A | G | 1 | a0001c0004t0004g0058 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1634-175A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 14/17 | chr3 | 113937911 | ||||||
| chr3:113937922
|
T | C | 1 | a0001c0001t0028g0179 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1634-164T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 14/17 | chr3 | 113937922 | ||||||
| chr3:113937986
|
C | G | 129 | a0001c0001t0001g0006a0001c0001t0002g0117a0001c0001t0002g0162others(126): Show | 129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1634-100C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 14/17 | chr3 | 113937986 | ||||||
| chr3:113938005
|
C | CA | 109 | a0001c0001t0001g0015a0001c0001t0001g0170a0001c0001t0001g0181others(106): Show | 109 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1634-61dupA | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr3 | 113938005 | |||||
| chr3:113938005
|
C | CAA | 6 | a0001c0001t0002g0257a0001c0001t0002g0263a0001c0001t0026g0297others(3): Show | 6 | HG00673.hp1 HG01515.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1634-62_1634-61dup others(2): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr3 | 113938005 | |||||
| chr3:113938005
|
CA | C | 10 | a0001c0001t0001g0158a0001c0001t0001g0173a0001c0001t0001g0202others(7): Show | 10 | HG00140.hp2 HG00408.hp1 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.1634-61delA | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr3 | 113938005 | |||||
| chr3:113938025
|
A | AT | 7 | a0001c0001t0006g0106a0001c0001t0006g0124a0001c0001t0006g0125others(4): Show | 7 | HG01891.hp2 HG03098.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1634-58dupT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr3 | 113938025 | |||||
| chr3:113938025
|
A | T | 1 | a0001c0001t0006g0145 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1634-61A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 14/17 | chr3 | 113938025 | ||||||
| chr3:113938159
|
G | A | 1 | a0001c0001t0010g0008 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1691+16G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 15/17 | chr3 | 113938159 | ||||||
| chr3:113938235
|
G | A | 1 | a0001c0001t0001g0211 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1691+92G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 15/17 | chr3 | 113938235 | ||||||
| chr3:113938612
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1691+469G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 15/17 | chr3 | 113938612 | ||||||
| chr3:113938776
|
G | A | 99 | a0001c0001t0002g0117a0001c0001t0002g0165a0001c0001t0002g0172others(96): Show | 99 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.1691+633G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 15/17 | chr3 | 113938776 | ||||||
| chr3:113938862
|
T | C | 16 | a0001c0001t0002g0117a0001c0001t0002g0172a0001c0001t0002g0175others(13): Show | 16 | HG00438.hp1 HG00609.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.1691+719T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 15/17 | chr3 | 113938862 | ||||||
| chr3:113938873
|
A | G | 129 | a0001c0001t0001g0006a0001c0001t0002g0117a0001c0001t0002g0162others(126): Show | 129 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1691+730A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 15/17 | chr3 | 113938873 | ||||||
| chr3:113938980
|
C | T | 1 | a0001c0003t0002g0250 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1691+837C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 15/17 | chr3 | 113938980 | ||||||
| chr3:113939243
|
G | A | 4 | a0001c0001t0010g0008a0001c0001t0016g0003a0001c0001t0016g0009others(1): Show | 4 | HG00735.hp2 HG02280.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1692-643G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 15/17 | chr3 | 113939243 | ||||||
| chr3:113939267
|
T | C | 2 | a0001c0005t0009g0276a0001c0005t0009g0294 | 2 | HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1692-619T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 15/17 | chr3 | 113939267 | ||||||
| chr3:113939392
|
A | AT | 305 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(302): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.1692-481dupT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr3 | 113939392 | |||||
| chr3:113939439
|
C | T | 1 | a0001c0003t0007g0154 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1692-447C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 15/17 | chr3 | 113939439 | ||||||
| chr3:113939632
|
C | G | 1 | a0001c0001t0001g0211 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1692-254C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 15/17 | chr3 | 113939632 | ||||||
| chr3:113939646
|
C | T | 8 | a0001c0001t0006g0106a0001c0001t0006g0124a0001c0001t0006g0125others(5): Show | 8 | HG01891.hp2 HG02965.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1692-240C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 15/17 | chr3 | 113939646 | ||||||
| chr3:113939649
|
A | C | 3 | a0001c0001t0001g0006a0001c0001t0003g0100a0010c0011t0001g0011 | 3 | HG02257.hp2 HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1692-237A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 15/17 | chr3 | 113939649 | ||||||
| chr3:113939758
|
T | C | 9 | a0001c0001t0002g0162a0001c0001t0002g0280a0001c0001t0002g0281others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1692-128T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 15/17 | chr3 | 113939758 | ||||||
| chr3:113939758
|
T | G | 9 | a0001c0001t0010g0008a0001c0001t0015g0101a0001c0001t0016g0003others(6): Show | 9 | HG00735.hp2 HG02109.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1692-128T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 15/17 | chr3 | 113939758 | ||||||
| chr3:113940002
|
T | C | 1 | a0001c0002t0003g0026 | 1 | HG00323.hp2 | splice_region_variant&intron_variant | LOW | c.1802+6T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 16/17 | chr3 | 113940002 | ||||||
| chr3:113940045
|
T | G | 1 | a0004c0017t0029g0282 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1802+49T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 16/17 | chr3 | 113940045 | ||||||
| chr3:113940356
|
C | T | 22 | a0001c0001t0001g0090a0001c0001t0001g0136a0001c0001t0001g0171others(19): Show | 22 | HG00140.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1908+11C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113940356 | ||||||
| chr3:113940454
|
C | T | 1 | a0001c0003t0002g0235 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1908+109C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113940454 | ||||||
| chr3:113940461
|
G | C | 71 | a0001c0001t0002g0303a0001c0003t0002g0092a0001c0003t0002g0105others(68): Show | 71 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.1908+116G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113940461 | ||||||
| chr3:113940473
|
C | T | 1 | a0001c0002t0001g0052 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1908+128C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113940473 | ||||||
| chr3:113940645
|
A | G | 1 | a0003c0018t0001g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1908+300A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113940645 | ||||||
| chr3:113940649
|
ATCTT | A | 77 | a0001c0001t0002g0165a0001c0001t0002g0197a0001c0001t0002g0257others(74): Show | 77 | HG00280.hp1 HG00408.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.1908+308_1908+311d others(6): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr3 | 113940649 | |||||
| chr3:113940702
|
T | G | 113 | a0001c0001t0001g0006a0001c0001t0002g0117a0001c0001t0002g0162others(110): Show | 113 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.1908+357T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113940702 | ||||||
| chr3:113941067
|
A | G | 1 | a0001c0001t0001g0274 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1908+722A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113941067 | ||||||
| chr3:113941183
|
A | AT | 4 | a0001c0001t0012g0103a0001c0001t0012g0104a0001c0001t0012g0116others(1): Show | 4 | HG02486.hp1 HG02615.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1908+843dupT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr3 | 113941183 | |||||
| chr3:113941337
|
T | C | 1 | a0001c0001t0026g0297 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1908+992T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113941337 | ||||||
| chr3:113941397
|
C | G | 1 | a0001c0001t0001g0180 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1908+1052C>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113941397 | ||||||
| chr3:113941620
|
A | AT | 110 | a0001c0001t0001g0022a0001c0001t0001g0108a0001c0001t0001g0163others(107): Show | 110 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1908+1291dupT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr3 | 113941620 | |||||
| chr3:113941620
|
A | ATT | 24 | a0001c0001t0001g0006a0001c0001t0001g0136a0001c0001t0001g0171others(21): Show | 24 | HG01243.hp2 HG01884.hp2 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.1908+1290_1908+129 others(6): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr3 | 113941620 | |||||
| chr3:113941620
|
A | ATTT | 6 | a0001c0001t0001g0090a0001c0001t0001g0178a0001c0001t0001g0202others(3): Show | 6 | HG00140.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1908+1289_1908+129 others(7): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr3 | 113941620 | |||||
| chr3:113941620
|
AT | A | 6 | a0001c0001t0006g0106a0001c0001t0006g0145a0001c0001t0006g0146others(3): Show | 6 | HG01192.hp1 HG01891.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1908+1291delT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr3 | 113941620 | |||||
| chr3:113941764
|
G | A | 1 | a0001c0001t0002g0213 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1908+1419G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113941764 | ||||||
| chr3:113941870
|
CGGCCTCC others(288): Show |
C | 8 | a0001c0001t0006g0106a0001c0001t0006g0124a0001c0001t0006g0125others(5): Show | 8 | HG01891.hp2 HG02965.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1908+1548_1908+184 others(4): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr3 | 113941870 | |||||
| chr3:113941921
|
C | CT | 12 | a0001c0001t0002g0162a0001c0001t0002g0280a0001c0001t0002g0281others(9): Show | 12 | HG01109.hp2 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1908+1588dupT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr3 | 113941921 | |||||
| chr3:113941926
|
T | A | 4 | a0001c0001t0014g0088a0001c0001t0014g0102a0001c0001t0014g0143others(1): Show | 4 | HG02145.hp1 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1908+1581T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113941926 | ||||||
| chr3:113941969
|
G | T | 4 | a0001c0001t0010g0008a0001c0001t0016g0003a0001c0001t0016g0009others(1): Show | 4 | HG00735.hp2 HG02280.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1908+1624G>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113941969 | ||||||
| chr3:113942150
|
C | A | 1 | a0001c0001t0001g0177 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1908+1805C>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113942150 | ||||||
| chr3:113942217
|
A | AT | 10 | a0001c0001t0001g0214a0001c0001t0002g0162a0001c0001t0002g0280others(7): Show | 10 | HG01109.hp2 HG02055.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1908+1888dupT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr3 | 113942217 | |||||
| chr3:113942217
|
AT | A | 20 | a0001c0001t0001g0210a0001c0001t0001g0241a0001c0001t0001g0290others(17): Show | 20 | HG00735.hp2 HG01109.hp1 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.1908+1888delT | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr3 | 113942217 | |||||
| chr3:113942264
|
A | T | 1 | a0001c0001t0006g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1908+1919A>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113942264 | ||||||
| chr3:113942288
|
T | A | 16 | a0001c0001t0001g0090a0001c0001t0001g0136a0001c0001t0001g0171others(13): Show | 16 | HG00140.hp2 HG01070.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1908+1943T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113942288 | ||||||
| chr3:113942305
|
T | C | 1 | a0001c0003t0002g0235 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1908+1960T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113942305 | ||||||
| chr3:113942588
|
G | A | 2 | a0001c0001t0009g0262a0001c0001t0009g0267 | 2 | HG02109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1908+2243G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113942588 | ||||||
| chr3:113942629
|
A | G | 4 | a0001c0001t0010g0008a0001c0001t0016g0003a0001c0001t0016g0009others(1): Show | 4 | HG00735.hp2 HG02280.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1908+2284A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113942629 | ||||||
| chr3:113942674
|
T | A | 1 | a0001c0001t0001g0290 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1908+2329T>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113942674 | ||||||
| chr3:113942735
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1908+2390T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113942735 | ||||||
| chr3:113942743
|
T | C | 15 | a0001c0001t0002g0117a0001c0001t0002g0175a0001c0001t0002g0209others(12): Show | 15 | HG00438.hp1 HG00609.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.1908+2398T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113942743 | ||||||
| chr3:113942799
|
G | A | 29 | a0001c0001t0001g0006a0001c0001t0001g0090a0001c0001t0001g0136others(26): Show | 29 | HG00140.hp2 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1908+2454G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113942799 | ||||||
| chr3:113942816
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1908+2471C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113942816 | ||||||
| chr3:113942916
|
A | G | 9 | a0001c0001t0002g0162a0001c0001t0002g0280a0001c0001t0002g0281others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1909-2482A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113942916 | ||||||
| chr3:113942967
|
A | G | 1 | a0001c0001t0002g0172 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1909-2431A>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113942967 | ||||||
| chr3:113942976
|
C | T | 4 | a0001c0001t0010g0008a0001c0001t0016g0003a0001c0001t0016g0009others(1): Show | 4 | HG00735.hp2 HG02280.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1909-2422C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113942976 | ||||||
| chr3:113943044
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1909-2354C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113943044 | ||||||
| chr3:113943159
|
C | T | 2 | a0001c0001t0003g0089a0001c0001t0003g0126 | 2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1909-2239C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113943159 | ||||||
| chr3:113943301
|
T | G | 4 | a0001c0001t0010g0008a0001c0001t0016g0003a0001c0001t0016g0009others(1): Show | 4 | HG00735.hp2 HG02280.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1909-2097T>G | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113943301 | ||||||
| chr3:113943415
|
A | C | 1 | a0009c0010t0002g0134 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1909-1983A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113943415 | ||||||
| chr3:113943472
|
C | T | 4 | a0001c0001t0010g0008a0001c0001t0016g0003a0001c0001t0016g0009others(1): Show | 4 | HG00735.hp2 HG02280.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1909-1926C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113943472 | ||||||
| chr3:113943900
|
C | T | 11 | a0001c0001t0010g0008a0001c0001t0012g0103a0001c0001t0012g0104others(8): Show | 11 | HG00735.hp2 HG01192.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1909-1498C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113943900 | ||||||
| chr3:113943969
|
G | C | 1 | a0001c0003t0002g0260 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1909-1429G>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113943969 | ||||||
| chr3:113944086
|
C | T | 7 | a0001c0001t0002g0162a0001c0001t0002g0280a0001c0001t0002g0301others(4): Show | 7 | HG01109.hp2 HG02055.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1909-1312C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113944086 | ||||||
| chr3:113944209
|
T | C | 4 | a0001c0001t0010g0008a0001c0001t0016g0003a0001c0001t0016g0009others(1): Show | 4 | HG00735.hp2 HG02280.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1909-1189T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113944209 | ||||||
| chr3:113944300
|
C | T | 4 | a0001c0001t0014g0088a0001c0001t0014g0102a0001c0001t0014g0143others(1): Show | 4 | HG02145.hp1 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1909-1098C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113944300 | ||||||
| chr3:113944433
|
C | T | 1 | a0001c0003t0002g0204 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1909-965C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113944433 | ||||||
| chr3:113944500
|
T | C | 1 | a0003c0018t0001g0248 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1909-898T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113944500 | ||||||
| chr3:113944798
|
T | C | 2 | a0001c0001t0001g0152a0001c0001t0001g0226 | 2 | NA18940.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.1909-600T>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113944798 | ||||||
| chr3:113944978
|
C | T | 4 | a0001c0001t0012g0103a0001c0001t0012g0104a0001c0001t0012g0116others(1): Show | 4 | HG02486.hp1 HG02615.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1909-420C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113944978 | ||||||
| chr3:113944999
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1909-399G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113944999 | ||||||
| chr3:113945046
|
C | T | 1 | a0001c0001t0017g0259 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1909-352C>T | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113945046 | ||||||
| chr3:113945234
|
A | C | 3 | a0001c0001t0010g0008a0001c0001t0016g0003a0001c0001t0016g0009 | 3 | HG00735.hp2 HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1909-164A>C | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113945234 | ||||||
| chr3:113945324
|
G | A | 2 | a0001c0002t0003g0045a0001c0002t0003g0046 | 2 | NA18946.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1909-74G>A | GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | chr3 | 113945324 | ||||||
| chr3:113945336
|
CAG | C | 97 | a0001c0001t0002g0117a0001c0001t0002g0165a0001c0001t0002g0172others(94): Show | 97 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.1909-60_1909-59del others(2): Show |
GRAMD1C | ENSG00000178075.20 | transcript | ENST00000358160.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr3 | 113945336 |