Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g00150 | A01 | 62442 | G | A | synonymous_variant | LOW | c.663C>T|p.Ser221Ser |
S177 |
2 | BAA01g00150 | A01 | 62463 | G | A | synonymous_variant | LOW | c.642C>T|p.His214His |
S112 |
3 | BAA01g00150 | A01 | 62818 | C | T | missense_variant | MODERATE | c.287G>A|p.Gly96Asp |
S128 |
4 | BAA01g00150 | A01 | 62941 | C | T | missense_variant | MODERATE | c.164G>A|p.Arg55His |
S308 |
5 | BAA01g00150 | A01 | 65588 | G | A | upstream_gene_variant | MODIFIER | c.-2403C>T| |
S32 |
6 | BAA01g00150 | A01 | 66347 | C | T | upstream_gene_variant | MODIFIER | c.-3162G>A| |
S132 S137 S215 S89 |
7 | BAA01g00150 | A01 | 66513 | G | A | upstream_gene_variant | MODIFIER | c.-3328C>T| |
S175 |
8 | BAA01g00150 | A01 | 67455 | C | T | upstream_gene_variant | MODIFIER | c.-4270G>A| |
S25 |
9 | BAA01g00150 | A01 | 67969 | C | T | upstream_gene_variant | MODIFIER | c.-4784G>A| |
S208 S219 |
10 | BAA01g00150 | A01 | 68152 | C | T | upstream_gene_variant | MODIFIER | c.-4967G>A| |
S107 |