Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g32990 | A10 | 23560111 | C | T | missense_variant | MODERATE | c.1127G>A|p.Ser376Asn |
S169 |
2 | BAA10g32990 | A10 | 23560238 | C | T | missense_variant | MODERATE | c.1000G>A|p.Ala334Thr |
S20 |
3 | BAA10g32990 | A10 | 23564040 | G | A | upstream_gene_variant | MODIFIER | c.-190C>T| |
S240 |
4 | BAA10g32990 | A10 | 23564339 | C | T | upstream_gene_variant | MODIFIER | c.-489G>A| |
S119 |
5 | BAA10g32990 | A10 | 23566494 | G | A | upstream_gene_variant | MODIFIER | c.-2644C>T| |
S203 |