Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g39010 | A05 | 38216793 | C | T | synonymous_variant | LOW | c.1863G>A|p.Arg621Arg |
S255 |
2 | BAA05g39010 | A05 | 38217102 | C | T | splice_region_variant&intron_variant | LOW | c.1715+7G>A| |
S274 |
3 | BAA05g39010 | A05 | 38218157 | C | T | missense_variant | MODERATE | c.1064G>A|p.Gly355Glu |
S238 |
4 | BAA05g39010 | A05 | 38218176 | C | T | missense_variant | MODERATE | c.1045G>A|p.Glu349Lys |
S174 |
5 | BAA05g39010 | A05 | 38219876 | C | T | missense_variant | MODERATE | c.226G>A|p.Gly76Arg |
S298 |
6 | BAA05g39010 | A05 | 38220167 | G | A | synonymous_variant | LOW | c.15C>T|p.Thr5Thr |
S240 |
7 | BAA05g39010 | A05 | 38220496 | G | A | upstream_gene_variant | MODIFIER | c.-315C>T| |
S45 |
8 | BAA05g39010 | A05 | 38223029 | C | T | upstream_gene_variant | MODIFIER | c.-2848G>A| |
S236 |
9 | BAA05g39010 | A05 | 38223948 | C | T | upstream_gene_variant | MODIFIER | c.-3767G>A| |
S182 |
10 | BAA05g39010 | A05 | 38223966 | G | A | upstream_gene_variant | MODIFIER | c.-3785C>T| |
S239 |