Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g32340 | A10 | 23279885 | C | T | missense_variant | MODERATE | c.1520G>A|p.Gly507Asp |
S196 |
2 | BAA10g32340 | A10 | 23280269 | G | A | missense_variant | MODERATE | c.1372C>T|p.Leu458Phe |
S180 |
3 | BAA10g32340 | A10 | 23280464 | G | A | synonymous_variant | LOW | c.1288C>T|p.Leu430Leu |
S50 |
4 | BAA10g32340 | A10 | 23281123 | G | A | missense_variant | MODERATE | c.848C>T|p.Thr283Ile |
S68 |
5 | BAA10g32340 | A10 | 23281264 | G | A | missense_variant | MODERATE | c.707C>T|p.Thr236Ile |
S221 S294 |
6 | BAA10g32340 | A10 | 23282231 | G | A | missense_variant | MODERATE | c.260C>T|p.Ser87Phe |
S265 |
7 | BAA10g32340 | A10 | 23284367 | C | T | upstream_gene_variant | MODIFIER | c.-1661G>A| |
S153 S213 |
8 | BAA10g32340 | A10 | 23286876 | C | T | upstream_gene_variant | MODIFIER | c.-4170G>A| |
S268 |