Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g48740 | A09 | 52417689 | C | T | upstream_gene_variant | MODIFIER | c.-535C>T| |
S173 S176 |
2 | BAA09g48740 | A09 | 52419083 | G | A | missense_variant | MODERATE | c.860G>A|p.Gly287Glu |
S130 |
3 | BAA09g48740 | A09 | 52419235 | C | T | missense_variant | MODERATE | c.1012C>T|p.Pro338Ser |
S30 S31 |
4 | BAA09g48740 | A09 | 52419291 | G | A | synonymous_variant | LOW | c.1068G>A|p.Lys356Lys |
S167 |
5 | BAA09g48740 | A09 | 52419330 | C | T | synonymous_variant | LOW | c.1107C>T|p.Val369Val |
S33 |
6 | BAA09g48740 | A09 | 52419491 | C | T | missense_variant | MODERATE | c.1268C>T|p.Ser423Phe |
S232 |
7 | BAA09g48740 | A09 | 52420552 | C | T | missense_variant | MODERATE | c.2329C>T|p.Pro777Ser |
S33 |
8 | BAA09g48740 | A09 | 52420948 | G | A | missense_variant | MODERATE | c.2653G>A|p.Ala885Thr |
S221 |
9 | BAA09g48740 | A09 | 52422357 | C | T | downstream_gene_variant | MODIFIER | c.*1314C>T| |
S30 S31 |
10 | BAA09g48740 | A09 | 52422491 | G | A | downstream_gene_variant | MODIFIER | c.*1448G>A| |
S180 |