Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g02250 | A10 | 1074522 | G | A | missense_variant | MODERATE | c.1097C>T|p.Ser366Phe |
S242 |
2 | BAA10g02250 | A10 | 1075208 | C | T | synonymous_variant | LOW | c.411G>A|p.Lys137Lys |
S308 |
3 | BAA10g02250 | A10 | 1075524 | C | T | missense_variant | MODERATE | c.95G>A|p.Gly32Glu |
S119 |
4 | BAA10g02250 | A10 | 1078921 | G | A | upstream_gene_variant | MODIFIER | c.-3303C>T| |
S140 |
5 | BAA10g02250 | A10 | 1079665 | C | T | upstream_gene_variant | MODIFIER | c.-4047G>A| |
S275 |