Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g01840 | A09 | 1271519 | C | T | synonymous_variant | LOW | c.1266G>A|p.Lys422Lys |
S282 |
2 | BAA09g01840 | A09 | 1271589 | G | A | missense_variant | MODERATE | c.1196C>T|p.Pro399Leu |
S296 |
3 | BAA09g01840 | A09 | 1272112 | C | T | missense_variant | MODERATE | c.812G>A|p.Gly271Glu |
S161 |
4 | BAA09g01840 | A09 | 1272120 | G | A | synonymous_variant | LOW | c.804C>T|p.Leu268Leu |
S259 |
5 | BAA09g01840 | A09 | 1273723 | G | A | synonymous_variant | LOW | c.672C>T|p.Asn224Asn |
S199 |
6 | BAA09g01840 | A09 | 1273901 | C | T | missense_variant | MODERATE | c.494G>A|p.Arg165Lys |
S270 |
7 | BAA09g01840 | A09 | 1274125 | C | T | synonymous_variant | LOW | c.270G>A|p.Ala90Ala |
S104 S52 |
8 | BAA09g01840 | A09 | 1274333 | G | A | missense_variant | MODERATE | c.62C>T|p.Ala21Val |
S8 |
9 | BAA09g01840 | A09 | 1275784 | G | A | upstream_gene_variant | MODIFIER | c.-1390C>T| |
S223 |
10 | BAA09g01840 | A09 | 1275948 | C | T | upstream_gene_variant | MODIFIER | c.-1554G>A| |
S182 |