Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g18460 | A06 | 9442404 | G | A | missense_variant | MODERATE | c.22G>A|p.Gly8Arg |
S8 |
2 | BAA06g18460 | A06 | 9442413 | G | T | missense_variant | MODERATE | c.31G>T|p.Asp11Tyr |
S8 |
3 | BAA06g18460 | A06 | 9443205 | G | A | missense_variant | MODERATE | c.388G>A|p.Ala130Thr |
S109 |
4 | BAA06g18460 | A06 | 9443262 | G | A | missense_variant | MODERATE | c.445G>A|p.Val149Ile |
S105 S106 |
5 | BAA06g18460 | A06 | 9443313 | C | T | stop_gained | HIGH | c.496C>T|p.Gln166* |
S115 |
6 | BAA06g18460 | A06 | 9443358 | C | T | missense_variant | MODERATE | c.541C>T|p.Pro181Ser |
S70 |
7 | BAA06g18460 | A06 | 9445545 | G | A | missense_variant&splice_region_variant | MODERATE | c.1921G>A|p.Val641Ile |
S7 |
8 | BAA06g18460 | A06 | 9447456 | C | T | synonymous_variant | LOW | c.2883C>T|p.Val961Val |
S79 S91 |
9 | BAA06g18460 | A06 | 9447668 | C | T | missense_variant | MODERATE | c.3095C>T|p.Ala1032Val |
S167 |
10 | BAA06g18460 | A06 | 9449350 | C | T | downstream_gene_variant | MODIFIER | c.*1054C>T| |
S94 |