Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g07660 | A08 | 6911302 | G | A | synonymous_variant | LOW | c.789C>T|p.Ile263Ile |
S122 |
2 | BAA08g07660 | A08 | 6911567 | C | T | missense_variant | MODERATE | c.674G>A|p.Gly225Glu |
S142 |
3 | BAA08g07660 | A08 | 6911777 | C | T | missense_variant | MODERATE | c.550G>A|p.Ala184Thr |
S162 |
4 | BAA08g07660 | A08 | 6912427 | C | T | synonymous_variant | LOW | c.387G>A|p.Glu129Glu |
S262 |
5 | BAA08g07660 | A08 | 6912802 | G | A | missense_variant | MODERATE | c.227C>T|p.Thr76Ile |
S249 |
6 | BAA08g07660 | A08 | 6916162 | C | T | upstream_gene_variant | MODIFIER | c.-2973G>A| |
S244 |
7 | BAA08g07660 | A08 | 6916662 | G | A | upstream_gene_variant | MODIFIER | c.-3473C>T| |
S249 |
8 | BAA08g07660 | A08 | 6916900 | C | T | upstream_gene_variant | MODIFIER | c.-3711G>A| |
S270 |
9 | BAA08g07660 | A08 | 6916919 | G | A | upstream_gene_variant | MODIFIER | c.-3730C>T| |
S35 |
10 | BAA08g07660 | A08 | 6917270 | G | A | upstream_gene_variant | MODIFIER | c.-4081C>T| |
S266 |