Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46820 | A02 | 37949853 | G | A | downstream_gene_variant | MODIFIER | c.*4672C>T| |
S223 |
2 | BAA02g46820 | A02 | 37950105 | C | T | downstream_gene_variant | MODIFIER | c.*4420G>A| |
S259 |
3 | BAA02g46820 | A02 | 37950360 | C | T | downstream_gene_variant | MODIFIER | c.*4165G>A| |
S183 S198 |
4 | BAA02g46820 | A02 | 37950591 | G | A | downstream_gene_variant | MODIFIER | c.*3934C>T| |
S209 |
5 | BAA02g46820 | A02 | 37951304 | C | T | downstream_gene_variant | MODIFIER | c.*3221G>A| |
S123 |
6 | BAA02g46820 | A02 | 37954962 | G | A | missense_variant | MODERATE | c.1331C>T|p.Thr444Ile |
S261 |
7 | BAA02g46820 | A02 | 37955290 | G | A | missense_variant | MODERATE | c.1003C>T|p.Pro335Ser |
S94 |
8 | BAA02g46820 | A02 | 37956251 | C | T | synonymous_variant | LOW | c.618G>A|p.Ser206Ser |
S15 S3 |
9 | BAA02g46820 | A02 | 37956353 | C | T | synonymous_variant | LOW | c.516G>A|p.Ala172Ala |
S183 S198 |
10 | BAA02g46820 | A02 | 37958612 | T | A | upstream_gene_variant | MODIFIER | c.-1744A>T| |
S224 |
11 | BAA02g46820 | A02 | 37959575 | C | T | upstream_gene_variant | MODIFIER | c.-2707G>A| |
S17 |
12 | BAA02g46820 | A02 | 37959782 | C | T | upstream_gene_variant | MODIFIER | c.-2914G>A| |
S262 |
13 | BAA02g46820 | A02 | 37960054 | C | T | upstream_gene_variant | MODIFIER | c.-3186G>A| |
S95 |