Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g08400 | A05 | 4175508 | G | A | synonymous_variant | LOW | c.1386C>T|p.Asn462Asn |
S138 |
2 | BAA05g08400 | A05 | 4175598 | C | T | synonymous_variant | LOW | c.1296G>A|p.Pro432Pro |
S198 |
3 | BAA05g08400 | A05 | 4175610 | C | T | synonymous_variant | LOW | c.1284G>A|p.Ser428Ser |
S1 S90 |
4 | BAA05g08400 | A05 | 4176256 | C | T | missense_variant | MODERATE | c.905G>A|p.Arg302Lys |
S193 |
5 | BAA05g08400 | A05 | 4177911 | C | T | splice_region_variant&intron_variant | LOW | c.109+5G>A| |
S36 |
6 | BAA05g08400 | A05 | 4180559 | G | A | upstream_gene_variant | MODIFIER | c.-2455C>T| |
S150 |
7 | BAA05g08400 | A05 | 4181663 | G | A | upstream_gene_variant | MODIFIER | c.-3559C>T| |
S40 S49 |
8 | BAA05g08400 | A05 | 4181718 | G | A | upstream_gene_variant | MODIFIER | c.-3614C>T| |
S274 |
9 | BAA05g08400 | A05 | 4181785 | C | T | upstream_gene_variant | MODIFIER | c.-3681G>A| |
S211 S227 |
10 | BAA05g08400 | A05 | 4182519 | C | T | upstream_gene_variant | MODIFIER | c.-4415G>A| |
S2 |
11 | BAA05g08400 | A05 | 4182977 | G | A | upstream_gene_variant | MODIFIER | c.-4873C>T| |
S179 |
12 | BAA05g08400 | A05 | 4182989 | C | T | upstream_gene_variant | MODIFIER | c.-4885G>A| |
S180 |