Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g07880 | A02 | 3391317 | C | T | missense_variant | MODERATE | c.2314G>A|p.Asp772Asn |
S287 |
2 | BAA02g07880 | A02 | 3392783 | C | T | missense_variant | MODERATE | c.1105G>A|p.Gly369Arg |
S46 |
3 | BAA02g07880 | A02 | 3393167 | G | A | missense_variant | MODERATE | c.721C>T|p.Leu241Phe |
S174 |
4 | BAA02g07880 | A02 | 3393236 | C | T | missense_variant | MODERATE | c.652G>A|p.Gly218Ser |
S15 S3 |
5 | BAA02g07880 | A02 | 3393280 | G | A | missense_variant | MODERATE | c.608C>T|p.Thr203Ile |
S50 |
6 | BAA02g07880 | A02 | 3393679 | G | A | synonymous_variant | LOW | c.444C>T|p.Ala148Ala |
S105 S106 |
7 | BAA02g07880 | A02 | 3393821 | G | A | missense_variant | MODERATE | c.302C>T|p.Pro101Leu |
S158 |
8 | BAA02g07880 | A02 | 3393889 | C | T | synonymous_variant | LOW | c.234G>A|p.Ser78Ser |
S206 |
9 | BAA02g07880 | A02 | 3394096 | C | T | synonymous_variant | LOW | c.27G>A|p.Arg9Arg |
S174 S216 S265 S39 |
10 | BAA02g07880 | A02 | 3395613 | G | A | upstream_gene_variant | MODIFIER | c.-1491C>T| |
S202 |
11 | BAA02g07880 | A02 | 3398112 | G | A | upstream_gene_variant | MODIFIER | c.-3990C>T| |
S244 |