Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g26270 | A01 | 14588883 | G | A | upstream_gene_variant | MODIFIER | c.-4017G>A| |
S195 |
2 | BAA01g26270 | A01 | 14589566 | C | T | upstream_gene_variant | MODIFIER | c.-3334C>T| |
S261 |
3 | BAA01g26270 | A01 | 14589738 | G | A | upstream_gene_variant | MODIFIER | c.-3162G>A| |
S187 |
4 | BAA01g26270 | A01 | 14590555 | G | A | upstream_gene_variant | MODIFIER | c.-2345G>A| |
S83 |
5 | BAA01g26270 | A01 | 14591121 | C | T | upstream_gene_variant | MODIFIER | c.-1779C>T| |
S112 |
6 | BAA01g26270 | A01 | 14591725 | G | A | upstream_gene_variant | MODIFIER | c.-1175G>A| |
S70 |
7 | BAA01g26270 | A01 | 14594070 | G | A | splice_region_variant&synonymous_variant | LOW | c.507G>A|p.Gly169Gly |
S284 |
8 | BAA01g26270 | A01 | 14594587 | C | T | intron_variant | MODIFIER | c.745-42C>T| |
S67 |
9 | BAA01g26270 | A01 | 14594707 | C | T | missense_variant | MODERATE | c.823C>T|p.Arg275Trp |
S225 S73 |
10 | BAA01g26270 | A01 | 14595865 | G | A | downstream_gene_variant | MODIFIER | c.*901G>A| |
S202 |
11 | BAA01g26270 | A01 | 14596113 | C | T | downstream_gene_variant | MODIFIER | c.*1149C>T| |
S167 |
12 | BAA01g26270 | A01 | 14596861 | G | A | downstream_gene_variant | MODIFIER | c.*1897G>A| |
S121 |
13 | BAA01g26270 | A01 | 14597701 | C | T | downstream_gene_variant | MODIFIER | c.*2737C>T| |
S66 |
14 | BAA01g26270 | A01 | 14598333 | C | T | downstream_gene_variant | MODIFIER | c.*3369C>T| |
S1 S90 |
15 | BAA01g26270 | A01 | 14598445 | G | A | downstream_gene_variant | MODIFIER | c.*3481G>A| |
S172 S217 |
16 | BAA01g26270 | A01 | 14598849 | G | A | downstream_gene_variant | MODIFIER | c.*3885G>A| |
S60 |
17 | BAA01g26270 | A01 | 14598871 | C | T | downstream_gene_variant | MODIFIER | c.*3907C>T| |
S88 |
18 | BAA01g26270 | A01 | 14598946 | C | T | downstream_gene_variant | MODIFIER | c.*3982C>T| |
S113 |
19 | BAA01g26270 | A01 | 14599296 | C | T | downstream_gene_variant | MODIFIER | c.*4332C>T| |
S66 |