Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g24110 | A06 | 15107636 | C | T | missense_variant | MODERATE | c.434C>T|p.Ala145Val |
S260 |
2 | BAA06g24110 | A06 | 15107836 | G | A | missense_variant | MODERATE | c.634G>A|p.Asp212Asn |
S237 |
3 | BAA06g24110 | A06 | 15108063 | G | A | synonymous_variant | LOW | c.861G>A|p.Lys287Lys |
S233 |
4 | BAA06g24110 | A06 | 15108403 | C | T | missense_variant | MODERATE | c.1201C>T|p.Pro401Ser |
S244 |
5 | BAA06g24110 | A06 | 15108429 | G | A | synonymous_variant | LOW | c.1227G>A|p.Thr409Thr |
S169 |
6 | BAA06g24110 | A06 | 15108902 | C | T | synonymous_variant | LOW | c.1620C>T|p.Ser540Ser |
S156 |
7 | BAA06g24110 | A06 | 15109086 | G | A | missense_variant | MODERATE | c.1804G>A|p.Gly602Arg |
S108 |
8 | BAA06g24110 | A06 | 15109265 | G | A | synonymous_variant | LOW | c.1983G>A|p.Leu661Leu |
S302 |
9 | BAA06g24110 | A06 | 15109534 | A | G | missense_variant | MODERATE | c.2252A>G|p.Gln751Arg |
S150 |
10 | BAA06g24110 | A06 | 15109740 | G | A | missense_variant | MODERATE | c.2458G>A|p.Glu820Lys |
S281 |
11 | BAA06g24110 | A06 | 15109876 | G | A | missense_variant | MODERATE | c.2594G>A|p.Gly865Glu |
S294 |
12 | BAA06g24110 | A06 | 15110774 | G | A | downstream_gene_variant | MODIFIER | c.*849G>A| |
S295 |
13 | BAA06g24110 | A06 | 15111581 | C | T | downstream_gene_variant | MODIFIER | c.*1656C>T| |
S111 |