Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g11930 | A07 | 20457688 | G | A | missense_variant | MODERATE | c.2729C>T|p.Ala910Val |
S241 |
2 | BAA07g11930 | A07 | 20458223 | C | T | missense_variant | MODERATE | c.2194G>A|p.Glu732Lys |
S75 S81 |
3 | BAA07g11930 | A07 | 20458611 | C | T | synonymous_variant | LOW | c.1806G>A|p.Leu602Leu |
S274 |
4 | BAA07g11930 | A07 | 20460412 | C | T | synonymous_variant | LOW | c.609G>A|p.Arg203Arg |
S249 |
5 | BAA07g11930 | A07 | 20460642 | C | T | synonymous_variant | LOW | c.456G>A|p.Lys152Lys |
S174 |
6 | BAA07g11930 | A07 | 20461029 | C | T | stop_gained | HIGH | c.69G>A|p.Trp23* |
S303 |
7 | BAA07g11930 | A07 | 20461036 | C | T | missense_variant | MODERATE | c.62G>A|p.Cys21Tyr |
S168 |
8 | BAA07g11930 | A07 | 20462623 | C | T | upstream_gene_variant | MODIFIER | c.-1526G>A| |
S9 |
9 | BAA07g11930 | A07 | 20463164 | C | T | upstream_gene_variant | MODIFIER | c.-2067G>A| |
S205 S35 |
10 | BAA07g11930 | A07 | 20464465 | C | T | upstream_gene_variant | MODIFIER | c.-3368G>A| |
S181 |
11 | BAA07g11930 | A07 | 20465352 | C | T | upstream_gene_variant | MODIFIER | c.-4255G>A| |
S99 |