Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g26550 | A01 | 14907558 | G | A | synonymous_variant | LOW | c.426C>T|p.Leu142Leu |
S108 |
2 | BAA01g26550 | A01 | 14907776 | C | T | missense_variant | MODERATE | c.208G>A|p.Asp70Asn |
S148 S30 S31 |
3 | BAA01g26550 | A01 | 14911269 | C | T | upstream_gene_variant | MODIFIER | c.-3192G>A| |
S237 |
4 | BAA01g26550 | A01 | 14911327 | G | A | upstream_gene_variant | MODIFIER | c.-3250C>T| |
S163 |
5 | BAA01g26550 | A01 | 14911353 | G | A | upstream_gene_variant | MODIFIER | c.-3276C>T| |
S96 |
6 | BAA01g26550 | A01 | 14911380 | C | T | upstream_gene_variant | MODIFIER | c.-3303G>A| |
S166 |
7 | BAA01g26550 | A01 | 14911773 | G | A | upstream_gene_variant | MODIFIER | c.-3696C>T| |
S287 |
8 | BAA01g26550 | A01 | 14912124 | C | T | upstream_gene_variant | MODIFIER | c.-4047G>A| |
S183 |
9 | BAA01g26550 | A01 | 14912467 | C | T | upstream_gene_variant | MODIFIER | c.-4390G>A| |
S36 |
10 | BAA01g26550 | A01 | 14912896 | G | A | upstream_gene_variant | MODIFIER | c.-4819C>T| |
S97 |