Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g20240 | A09 | 12487742 | G | A | missense_variant | MODERATE | c.127G>A|p.Val43Ile |
S95 |
2 | BAA09g20240 | A09 | 12488200 | G | A | synonymous_variant | LOW | c.273G>A|p.Val91Val |
S192 |
3 | BAA09g20240 | A09 | 12488681 | G | A | missense_variant | MODERATE | c.487G>A|p.Val163Ile |
S247 |
4 | BAA09g20240 | A09 | 12489006 | C | T | missense_variant | MODERATE | c.568C>T|p.Pro190Ser |
S85 |
5 | BAA09g20240 | A09 | 12489051 | C | T | stop_gained | HIGH | c.613C>T|p.Gln205* |
S108 |
6 | BAA09g20240 | A09 | 12489771 | G | A | missense_variant | MODERATE | c.1059G>A|p.Met353Ile |
S249 |
7 | BAA09g20240 | A09 | 12490063 | C | T | stop_gained | HIGH | c.1213C>T|p.Gln405* |
S15 S3 |
8 | BAA09g20240 | A09 | 12490405 | T | C | synonymous_variant | LOW | c.1473T>C|p.His491His |
S174 S216 |
9 | BAA09g20240 | A09 | 12494145 | C | T | downstream_gene_variant | MODIFIER | c.*2382C>T| |
S282 |