Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
8601 | BAA01g06940 | A01 | 3075363 | C | T | synonymous_variant | LOW | c.315C>T|p.Ile105Ile |
S8 |
8602 | BAA01g06930 | A01 | 3075609 | G | A | upstream_gene_variant | MODIFIER | c.-2107C>T| |
S217 |
8603 | BAA01g06930 | A01 | 3076597 | C | T | upstream_gene_variant | MODIFIER | c.-3095G>A| |
S71 |
8604 | BAA01g06930 | A01 | 3077968 | G | A | upstream_gene_variant | MODIFIER | c.-4466C>T| |
S85 |
8605 | BAA01g06930 | A01 | 3078267 | G | A | upstream_gene_variant | MODIFIER | c.-4765C>T| |
S286 |
8606 | BAA01g06950 | A01 | 3079180 | G | A | upstream_gene_variant | MODIFIER | c.-1377C>T| |
S174 S216 S27 S39 |
8607 | BAA01g06960 | A01 | 3079512 | C | T | missense_variant | MODERATE | c.1321G>A|p.Gly441Arg |
S135 |
8608 | BAA01g06960 | A01 | 3079701 | C | T | missense_variant | MODERATE | c.1229G>A|p.Gly410Asp |
S233 |
8609 | BAA01g06960 | A01 | 3080139 | C | T | synonymous_variant | LOW | c.957G>A|p.Thr319Thr |
S152 S275 |
8610 | BAA01g06950 | A01 | 3082098 | C | T | upstream_gene_variant | MODIFIER | c.-4295G>A| |
S231 |
8611 | BAA01g06960 | A01 | 3082387 | G | A | synonymous_variant | LOW | c.93C>T|p.Arg31Arg |
S153 |
8612 | BAA01g06950 | A01 | 3082555 | C | T | upstream_gene_variant | MODIFIER | c.-4752G>A| |
S249 |
8613 | BAA01g06950 | A01 | 3082771 | A | C | upstream_gene_variant | MODIFIER | c.-4968T>G| |
S103 S223 S244 S255 S54 |
8614 | BAA01g06960 | A01 | 3082842 | G | A | upstream_gene_variant | MODIFIER | c.-363C>T| |
S142 |
8615 | BAA01g06960 | A01 | 3083027 | G | A | upstream_gene_variant | MODIFIER | c.-548C>T| |
S140 |
8616 | BAA01g06960 | A01 | 3083090 | G | A | upstream_gene_variant | MODIFIER | c.-611C>T| |
S174 S27 |
8617 | BAA01g06960 | A01 | 3083166 | G | A | upstream_gene_variant | MODIFIER | c.-687C>T| |
S165 |
8618 | BAA01g06960 | A01 | 3084607 | G | A | upstream_gene_variant | MODIFIER | c.-2128C>T| |
S245 |
8619 | BAA01g06970 | A01 | 3084988 | C | T | missense_variant | MODERATE | c.113G>A|p.Gly38Asp |
S231 |
8620 | BAA01g06970 | A01 | 3085173 | C | T | missense_variant | MODERATE | c.13G>A|p.Val5Met |
S275 |
8621 | BAA01g06960 | A01 | 3085239 | G | A | upstream_gene_variant | MODIFIER | c.-2760C>T| |
S202 |
8622 | BAA01g06960 | A01 | 3085355 | C | T | upstream_gene_variant | MODIFIER | c.-2876G>A| |
S125 |
8623 | BAA01g06960 | A01 | 3085500 | G | A | upstream_gene_variant | MODIFIER | c.-3021C>T| |
S65 |
8624 | BAA01g06960 | A01 | 3087163 | C | T | upstream_gene_variant | MODIFIER | c.-4684G>A| |
S275 |
8625 | BAA01g06990 | A01 | 3088756 | C | T | synonymous_variant | LOW | c.786G>A|p.Gly262Gly |
S109 |