Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g26980 | A05 | 31456100 | C | T | missense_variant | MODERATE | c.2222G>A|p.Gly741Glu |
S180 |
2 | BAA05g26980 | A05 | 31456638 | C | T | missense_variant | MODERATE | c.1984G>A|p.Glu662Lys |
S74 |
3 | BAA05g26980 | A05 | 31457180 | C | T | missense_variant | MODERATE | c.1531G>A|p.Val511Ile |
S274 |
4 | BAA05g26980 | A05 | 31458548 | G | A | synonymous_variant | LOW | c.372C>T|p.Phe124Phe |
S208 S219 |
5 | BAA05g26980 | A05 | 31458602 | C | T | synonymous_variant | LOW | c.318G>A|p.Gly106Gly |
S294 |
6 | BAA05g26980 | A05 | 31459213 | C | T | upstream_gene_variant | MODIFIER | c.-4G>A| |
S59 |
7 | BAA05g26980 | A05 | 31459808 | G | A | upstream_gene_variant | MODIFIER | c.-599C>T| |
S283 |
8 | BAA05g26980 | A05 | 31460825 | C | T | upstream_gene_variant | MODIFIER | c.-1616G>A| |
S135 |
9 | BAA05g26980 | A05 | 31462858 | A | C | upstream_gene_variant | MODIFIER | c.-3649T>G| |
S207 |
10 | BAA05g26980 | A05 | 31462861 | G | A | upstream_gene_variant | MODIFIER | c.-3652C>T| |
S159 |