Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g04020 | A10 | 1962808 | C | T | splice_region_variant&intron_variant | LOW | c.1273-7G>A| |
S197 |
2 | BAA10g04020 | A10 | 1962905 | C | T | missense_variant | MODERATE | c.1262G>A|p.Gly421Glu |
S130 |
3 | BAA10g04020 | A10 | 1963254 | C | T | missense_variant | MODERATE | c.994G>A|p.Gly332Arg |
S212 S37 |
4 | BAA10g04020 | A10 | 1964037 | G | A | missense_variant | MODERATE | c.539C>T|p.Ala180Val |
S75 S81 |
5 | BAA10g04020 | A10 | 1964079 | C | T | missense_variant | MODERATE | c.497G>A|p.Gly166Glu |
S286 |
6 | BAA10g04020 | A10 | 1967011 | C | T | upstream_gene_variant | MODIFIER | c.-1671G>A| |
S256 |
7 | BAA10g04020 | A10 | 1967631 | C | T | upstream_gene_variant | MODIFIER | c.-2291G>A| |
S287 |
8 | BAA10g04020 | A10 | 1967737 | G | A | upstream_gene_variant | MODIFIER | c.-2397C>T| |
S134 |
9 | BAA10g04020 | A10 | 1969331 | G | A | upstream_gene_variant | MODIFIER | c.-3991C>T| |
S172 S217 |
10 | BAA10g04020 | A10 | 1969788 | G | A | upstream_gene_variant | MODIFIER | c.-4448C>T| |
S189 |