Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19640 | A02 | 10211116 | G | A | upstream_gene_variant | MODIFIER | c.-3737G>A| |
S111 |
2 | BAA02g19640 | A02 | 10211402 | G | A | upstream_gene_variant | MODIFIER | c.-3451G>A| |
S257 |
3 | BAA02g19640 | A02 | 10211509 | C | T | upstream_gene_variant | MODIFIER | c.-3344C>T| |
S216 S241 S265 S39 |
4 | BAA02g19640 | A02 | 10211544 | C | T | upstream_gene_variant | MODIFIER | c.-3309C>T| |
S233 |
5 | BAA02g19640 | A02 | 10211566 | G | A | upstream_gene_variant | MODIFIER | c.-3287G>A| |
S134 |
6 | BAA02g19640 | A02 | 10215167 | G | A | synonymous_variant | LOW | c.315G>A|p.Lys105Lys |
S81 |
7 | BAA02g19640 | A02 | 10215583 | C | T | missense_variant | MODERATE | c.626C>T|p.Ala209Val |
S25 |
8 | BAA02g19640 | A02 | 10217125 | C | T | synonymous_variant | LOW | c.1803C>T|p.Ala601Ala |
S165 |
9 | BAA02g19640 | A02 | 10217177 | C | T | missense_variant | MODERATE | c.1855C>T|p.Pro619Ser |
S181 |
10 | BAA02g19640 | A02 | 10220916 | C | T | downstream_gene_variant | MODIFIER | c.*2539C>T| |
S302 |