Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g21840 | A10 | 19076116 | G | A | upstream_gene_variant | MODIFIER | c.-3702G>A| |
S16 |
2 | BAA10g21840 | A10 | 19081107 | G | A | missense_variant | MODERATE | c.506G>A|p.Arg169Lys |
S286 |
3 | BAA10g21840 | A10 | 19081150 | G | A | synonymous_variant | LOW | c.549G>A|p.Glu183Glu |
S209 |
4 | BAA10g21840 | A10 | 19081357 | C | T | synonymous_variant | LOW | c.756C>T|p.Tyr252Tyr |
S234 |
5 | BAA10g21840 | A10 | 19081724 | G | A | missense_variant | MODERATE | c.1123G>A|p.Glu375Lys |
S94 |
6 | BAA10g21840 | A10 | 19081961 | G | A | missense_variant | MODERATE | c.1360G>A|p.Asp454Asn |
S75 S81 S90 |
7 | BAA10g21840 | A10 | 19081992 | C | T | missense_variant | MODERATE | c.1391C>T|p.Ser464Phe |
S84 S93 |
8 | BAA10g21840 | A10 | 19082088 | C | T | missense_variant | MODERATE | c.1487C>T|p.Thr496Ile |
S268 |