Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g19950 | A01 | 9815792 | G | A | intron_variant | MODIFIER | c.498+39C>T| |
S197 |
2 | BAA01g19950 | A01 | 9816054 | G | A | missense_variant | MODERATE | c.275C>T|p.Ala92Val |
S249 |
3 | BAA01g19950 | A01 | 9816077 | C | T | synonymous_variant | LOW | c.252G>A|p.Pro84Pro |
S53 |
4 | BAA01g19950 | A01 | 9816428 | G | A | upstream_gene_variant | MODIFIER | c.-100C>T| |
S297 |
5 | BAA01g19950 | A01 | 9817029 | C | T | upstream_gene_variant | MODIFIER | c.-701G>A| |
S192 |
6 | BAA01g19950 | A01 | 9818884 | G | A | upstream_gene_variant | MODIFIER | c.-2556C>T| |
S138 |
7 | BAA01g19950 | A01 | 9819197 | C | T | upstream_gene_variant | MODIFIER | c.-2869G>A| |
S19 |
8 | BAA01g19950 | A01 | 9819432 | G | A | upstream_gene_variant | MODIFIER | c.-3104C>T| |
S251 |
9 | BAA01g19950 | A01 | 9820714 | C | T | upstream_gene_variant | MODIFIER | c.-4386G>A| |
S140 S168 S279 |
10 | BAA01g19950 | A01 | 9820971 | G | A | upstream_gene_variant | MODIFIER | c.-4643C>T| |
S299 |