Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g41370 | A05 | 39534207 | G | A | upstream_gene_variant | MODIFIER | c.-6G>A| |
S149 |
2 | BAA05g41370 | A05 | 39534902 | G | A | splice_region_variant&intron_variant | LOW | c.18-4G>A| |
S294 |
3 | BAA05g41370 | A05 | 39535096 | C | T | missense_variant | MODERATE | c.208C>T|p.Pro70Ser |
S250 S265 |
4 | BAA05g41370 | A05 | 39535547 | G | A | missense_variant | MODERATE | c.571G>A|p.Glu191Lys |
S15 S2 S3 S34 |
5 | BAA05g41370 | A05 | 39535651 | G | A | synonymous_variant | LOW | c.675G>A|p.Glu225Glu |
S125 |
6 | BAA05g41370 | A05 | 39535794 | C | T | missense_variant | MODERATE | c.818C>T|p.Ala273Val |
S146 |
7 | BAA05g41370 | A05 | 39536961 | G | A | missense_variant | MODERATE | c.1985G>A|p.Ser662Asn |
S269 |
8 | BAA05g41370 | A05 | 39537924 | C | T | downstream_gene_variant | MODIFIER | c.*683C>T| |
S245 |
9 | BAA05g41370 | A05 | 39538144 | C | T | downstream_gene_variant | MODIFIER | c.*903C>T| |
S14 |