Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g68480 | A09 | 61573752 | C | T | missense_variant | MODERATE | c.1102G>A|p.Gly368Ser |
S80 |
2 | BAA09g68480 | A09 | 61573957 | C | T | synonymous_variant | LOW | c.975G>A|p.Arg325Arg |
S279 |
3 | BAA09g68480 | A09 | 61574512 | C | T | synonymous_variant | LOW | c.813G>A|p.Arg271Arg |
S53 |
4 | BAA09g68480 | A09 | 61574600 | C | T | missense_variant | MODERATE | c.725G>A|p.Arg242Lys |
S175 |
5 | BAA09g68480 | A09 | 61576082 | C | T | missense_variant | MODERATE | c.53G>A|p.Gly18Glu |
S146 |
6 | BAA09g68480 | A09 | 61577585 | G | A | upstream_gene_variant | MODIFIER | c.-1451C>T| |
S184 |
7 | BAA09g68480 | A09 | 61580575 | C | T | upstream_gene_variant | MODIFIER | c.-4441G>A| |
S179 |
8 | BAA09g68480 | A09 | 61580662 | G | A | upstream_gene_variant | MODIFIER | c.-4528C>T| |
S262 |
9 | BAA09g68480 | A09 | 61580705 | C | T | upstream_gene_variant | MODIFIER | c.-4571G>A| |
S249 |