Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g14600 | A01 | 6936439 | G | A | intron_variant | MODIFIER | c.840+40C>T| |
S183 |
2 | BAA01g14600 | A01 | 6937674 | G | A | synonymous_variant | LOW | c.267C>T|p.Tyr89Tyr |
S263 |
3 | BAA01g14600 | A01 | 6937699 | G | A | missense_variant | MODERATE | c.242C>T|p.Ser81Phe |
S67 |
4 | BAA01g14600 | A01 | 6939023 | C | T | upstream_gene_variant | MODIFIER | c.-1083G>A| |
S51 |
5 | BAA01g14600 | A01 | 6940142 | C | T | upstream_gene_variant | MODIFIER | c.-2202G>A| |
S77 |
6 | BAA01g14600 | A01 | 6940348 | C | T | upstream_gene_variant | MODIFIER | c.-2408G>A| |
S260 |
7 | BAA01g14600 | A01 | 6940773 | G | A | upstream_gene_variant | MODIFIER | c.-2833C>T| |
S209 |
8 | BAA01g14600 | A01 | 6941770 | C | T | upstream_gene_variant | MODIFIER | c.-3830G>A| |
S166 |
9 | BAA01g14600 | A01 | 6942041 | C | T | upstream_gene_variant | MODIFIER | c.-4101G>A| |
S291 |