Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g40160 | A09 | 47450381 | G | A | upstream_gene_variant | MODIFIER | c.-3155G>A| |
S280 |
2 | BAA09g40160 | A09 | 47450755 | C | T | upstream_gene_variant | MODIFIER | c.-2781C>T| |
S245 |
3 | BAA09g40160 | A09 | 47451149 | C | T | upstream_gene_variant | MODIFIER | c.-2387C>T| |
S229 |
4 | BAA09g40160 | A09 | 47453745 | G | A | synonymous_variant | LOW | c.210G>A|p.Leu70Leu |
S73 S91 |
5 | BAA09g40160 | A09 | 47456646 | C | T | synonymous_variant | LOW | c.1039C>T|p.Leu347Leu |
S32 |
6 | BAA09g40160 | A09 | 47456660 | G | A | synonymous_variant | LOW | c.1053G>A|p.Lys351Lys |
S84 S93 |
7 | BAA09g40160 | A09 | 47456750 | G | A | missense_variant&splice_region_variant | MODERATE | c.1143G>A|p.Met381Ile |
S207 |
8 | BAA09g40160 | A09 | 47456981 | T | G | missense_variant | MODERATE | c.1204T>G|p.Ser402Ala |
S138 |
9 | BAA09g40160 | A09 | 47457009 | C | T | missense_variant | MODERATE | c.1232C>T|p.Pro411Leu |
S277 |