Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g14400 | A05 | 7593467 | G | A | upstream_gene_variant | MODIFIER | c.-2492G>A| |
S289 |
2 | BAA05g14400 | A05 | 7593485 | C | T | upstream_gene_variant | MODIFIER | c.-2474C>T| |
S221 |
3 | BAA05g14400 | A05 | 7594455 | G | A | upstream_gene_variant | MODIFIER | c.-1504G>A| |
S112 |
4 | BAA05g14400 | A05 | 7595060 | G | A | upstream_gene_variant | MODIFIER | c.-899G>A| |
S109 |
5 | BAA05g14400 | A05 | 7595220 | C | T | upstream_gene_variant | MODIFIER | c.-739C>T| |
S9 S98 |
6 | BAA05g14400 | A05 | 7595451 | G | A | upstream_gene_variant | MODIFIER | c.-508G>A| |
S75 S81 |
7 | BAA05g14400 | A05 | 7596376 | C | T | missense_variant | MODERATE | c.418C>T|p.Pro140Ser |
S157 |
8 | BAA05g14400 | A05 | 7596696 | C | T | synonymous_variant | LOW | c.738C>T|p.Ala246Ala |
S171 |
9 | BAA05g14400 | A05 | 7597422 | C | T | synonymous_variant | LOW | c.1464C>T|p.Ser488Ser |
S238 |
10 | BAA05g14400 | A05 | 7597670 | G | A | missense_variant | MODERATE | c.1712G>A|p.Arg571Lys |
S104 S52 |
11 | BAA05g14400 | A05 | 7597699 | C | T | missense_variant | MODERATE | c.1741C>T|p.Arg581Cys |
S50 |