Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g02880 | A10 | 1395532 | C | T | missense_variant | MODERATE | c.1553G>A|p.Arg518Lys |
S170 |
2 | BAA10g02880 | A10 | 1395673 | C | T | missense_variant | MODERATE | c.1412G>A|p.Arg471Lys |
S16 |
3 | BAA10g02880 | A10 | 1398110 | C | T | missense_variant | MODERATE | c.529G>A|p.Glu177Lys |
S174 |
4 | BAA10g02880 | A10 | 1398422 | G | A | missense_variant | MODERATE | c.217C>T|p.Leu73Phe |
S118 |
5 | BAA10g02880 | A10 | 1399946 | C | T | upstream_gene_variant | MODIFIER | c.-1308G>A| |
S23 |
6 | BAA10g02880 | A10 | 1400519 | G | A | upstream_gene_variant | MODIFIER | c.-1881C>T| |
S171 |
7 | BAA10g02880 | A10 | 1400643 | C | T | upstream_gene_variant | MODIFIER | c.-2005G>A| |
S305 |