Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g41550 | A02 | 34846405 | G | A | missense_variant | MODERATE | c.1559C>T|p.Ala520Val |
S67 |
2 | BAA02g41550 | A02 | 34846594 | C | T | missense_variant | MODERATE | c.1457G>A|p.Gly486Glu |
S120 |
3 | BAA02g41550 | A02 | 34848200 | G | A | synonymous_variant | LOW | c.270C>T|p.Ile90Ile |
S229 |
4 | BAA02g41550 | A02 | 34848209 | C | T | stop_gained&splice_region_variant | HIGH | c.261G>A|p.Trp87* |
S40 S49 |
5 | BAA02g41550 | A02 | 34849523 | C | T | upstream_gene_variant | MODIFIER | c.-897G>A| |
S15 |
6 | BAA02g41550 | A02 | 34851372 | C | T | upstream_gene_variant | MODIFIER | c.-2746G>A| |
S270 |
7 | BAA02g41550 | A02 | 34851738 | G | A | upstream_gene_variant | MODIFIER | c.-3112C>T| |
S282 |
8 | BAA02g41550 | A02 | 34851873 | G | A | upstream_gene_variant | MODIFIER | c.-3247C>T| |
S191 |
9 | BAA02g41550 | A02 | 34852071 | G | A | upstream_gene_variant | MODIFIER | c.-3445C>T| |
S247 |
10 | BAA02g41550 | A02 | 34852091 | G | A | upstream_gene_variant | MODIFIER | c.-3465C>T| |
S175 S177 |
11 | BAA02g41550 | A02 | 34852660 | G | A | upstream_gene_variant | MODIFIER | c.-4034C>T| |
S43 |