Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g69440 | A09 | 61964958 | G | A | intron_variant | MODIFIER | c.1260+40C>T| |
S46 |
2 | BAA09g69440 | A09 | 61965101 | C | T | intron_variant | MODIFIER | c.1186-29G>A| |
S9 |
3 | BAA09g69440 | A09 | 61965785 | G | A | synonymous_variant | LOW | c.822C>T|p.Phe274Phe |
S15 S3 |
4 | BAA09g69440 | A09 | 61966124 | G | A | synonymous_variant | LOW | c.651C>T|p.Tyr217Tyr |
S246 |
5 | BAA09g69440 | A09 | 61967828 | G | A | missense_variant | MODERATE | c.122C>T|p.Thr41Ile |
S28 |
6 | BAA09g69440 | A09 | 61968916 | G | A | upstream_gene_variant | MODIFIER | c.-967C>T| |
S263 |
7 | BAA09g69440 | A09 | 61970010 | G | A | upstream_gene_variant | MODIFIER | c.-2061C>T| |
S110 |
8 | BAA09g69440 | A09 | 61971409 | C | T | upstream_gene_variant | MODIFIER | c.-3460G>A| |
S250 |
9 | BAA09g69440 | A09 | 61971939 | G | A | upstream_gene_variant | MODIFIER | c.-3990C>T| |
S97 |