Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g09850 | A05 | 5021457 | C | T | upstream_gene_variant | MODIFIER | c.-4926C>T| |
S20 |
2 | BAA05g09850 | A05 | 5021791 | G | A | upstream_gene_variant | MODIFIER | c.-4592G>A| |
S247 |
3 | BAA05g09850 | A05 | 5021900 | G | A | upstream_gene_variant | MODIFIER | c.-4483G>A| |
S293 |
4 | BAA05g09850 | A05 | 5023295 | G | A | upstream_gene_variant | MODIFIER | c.-3088G>A| |
S301 S304 |
5 | BAA05g09850 | A05 | 5024986 | C | T | upstream_gene_variant | MODIFIER | c.-1397C>T| |
S12 S269 |
6 | BAA05g09850 | A05 | 5025397 | C | T | upstream_gene_variant | MODIFIER | c.-986C>T| |
S36 |
7 | BAA05g09850 | A05 | 5026074 | C | T | upstream_gene_variant | MODIFIER | c.-309C>T| |
S185 |
8 | BAA05g09850 | A05 | 5026618 | G | A | intron_variant | MODIFIER | c.175+61G>A| |
S62 |
9 | BAA05g09850 | A05 | 5027059 | C | T | missense_variant | MODERATE | c.241C>T|p.Pro81Ser |
S250 |
10 | BAA05g09850 | A05 | 5027461 | G | A | missense_variant | MODERATE | c.557G>A|p.Ser186Asn |
S76 |
11 | BAA05g09850 | A05 | 5027994 | G | A | synonymous_variant | LOW | c.930G>A|p.Glu310Glu |
S76 |
12 | BAA05g09850 | A05 | 5028321 | C | T | synonymous_variant | LOW | c.1161C>T|p.Val387Val |
S236 |
13 | BAA05g09850 | A05 | 5033476 | G | A | downstream_gene_variant | MODIFIER | c.*3825G>A| |
S173 |