Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g01100 | A09 | 794628 | C | T | upstream_gene_variant | MODIFIER | c.-259C>T| |
S286 |
2 | BAA09g01100 | A09 | 795821 | G | A | missense_variant | MODERATE | c.935G>A|p.Gly312Glu |
S223 |
3 | BAA09g01100 | A09 | 796525 | C | T | missense_variant | MODERATE | c.1562C>T|p.Ser521Phe |
S244 |
4 | BAA09g01100 | A09 | 796761 | C | T | missense_variant | MODERATE | c.1669C>T|p.Leu557Phe |
S119 |
5 | BAA09g01100 | A09 | 796829 | C | T | synonymous_variant | LOW | c.1737C>T|p.Ser579Ser |
S115 |
6 | BAA09g01100 | A09 | 797088 | G | A | missense_variant | MODERATE | c.1918G>A|p.Asp640Asn |
S232 |
7 | BAA09g01100 | A09 | 797266 | G | A | missense_variant | MODERATE | c.2017G>A|p.Glu673Lys |
S159 S243 |
8 | BAA09g01100 | A09 | 797978 | G | A | missense_variant | MODERATE | c.2653G>A|p.Gly885Arg |
S275 |
9 | BAA09g01100 | A09 | 800416 | G | A | intron_variant | MODIFIER | c.4002-21G>A| |
S233 |
10 | BAA09g01100 | A09 | 801356 | C | T | synonymous_variant | LOW | c.4476C>T|p.Leu1492Leu |
S181 |
11 | BAA09g01100 | A09 | 803612 | C | T | downstream_gene_variant | MODIFIER | c.*566C>T| |
S234 |