Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g66150 | A09 | 60600379 | C | T | missense_variant | MODERATE | c.757G>A|p.Asp253Asn |
S142 |
2 | BAA09g66150 | A09 | 60600383 | G | A | synonymous_variant | LOW | c.753C>T|p.His251His |
S252 |
3 | BAA09g66150 | A09 | 60600554 | C | T | missense_variant | MODERATE | c.582G>A|p.Met194Ile |
S249 |
4 | BAA09g66150 | A09 | 60600633 | C | T | splice_region_variant&intron_variant | LOW | c.573+5G>A| |
S221 |
5 | BAA09g66150 | A09 | 60603846 | G | A | upstream_gene_variant | MODIFIER | c.-1821C>T| |
S246 |
6 | BAA09g66150 | A09 | 60604004 | G | A | upstream_gene_variant | MODIFIER | c.-1979C>T| |
S210 S225 |
7 | BAA09g66150 | A09 | 60605457 | C | T | upstream_gene_variant | MODIFIER | c.-3432G>A| |
S156 |
8 | BAA09g66150 | A09 | 60605993 | G | A | upstream_gene_variant | MODIFIER | c.-3968C>T| |
S277 |