Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g01070 | A02 | 485189 | C | T | upstream_gene_variant | MODIFIER | c.-3354C>T| |
S281 |
2 | BAA02g01070 | A02 | 485332 | C | T | upstream_gene_variant | MODIFIER | c.-3211C>T| |
S15 S3 |
3 | BAA02g01070 | A02 | 486343 | C | T | upstream_gene_variant | MODIFIER | c.-2200C>T| |
S267 |
4 | BAA02g01070 | A02 | 486631 | G | A | upstream_gene_variant | MODIFIER | c.-1912G>A| |
S90 |
5 | BAA02g01070 | A02 | 489155 | G | A | missense_variant | MODERATE | c.355G>A|p.Asp119Asn |
S12 |
6 | BAA02g01070 | A02 | 489222 | G | A | missense_variant | MODERATE | c.422G>A|p.Gly141Glu |
S286 |
7 | BAA02g01070 | A02 | 489853 | G | A | missense_variant | MODERATE | c.784G>A|p.Asp262Asn |
S68 |
8 | BAA02g01070 | A02 | 490000 | C | T | missense_variant | MODERATE | c.931C>T|p.Pro311Ser |
S246 |
9 | BAA02g01070 | A02 | 490261 | G | A | missense_variant | MODERATE | c.1100G>A|p.Gly367Asp |
S5 |
10 | BAA02g01070 | A02 | 490292 | C | T | synonymous_variant | LOW | c.1131C>T|p.Asp377Asp |
S177 |
11 | BAA02g01070 | A02 | 490937 | C | T | synonymous_variant | LOW | c.1542C>T|p.Tyr514Tyr |
S2 |
12 | BAA02g01070 | A02 | 491446 | C | T | stop_gained | HIGH | c.1969C>T|p.Gln657* |
S19 |
13 | BAA02g01070 | A02 | 494322 | G | A | downstream_gene_variant | MODIFIER | c.*2577G>A| |
S50 |