Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g25990 | A06 | 17820636 | C | T | missense_variant | MODERATE | c.1132G>A|p.Asp378Asn |
S142 |
2 | BAA06g25990 | A06 | 17823611 | C | T | upstream_gene_variant | MODIFIER | c.-1222G>A| |
S247 |
3 | BAA06g25990 | A06 | 17824109 | G | A | upstream_gene_variant | MODIFIER | c.-1720C>T| |
S195 |
4 | BAA06g25990 | A06 | 17825934 | G | A | upstream_gene_variant | MODIFIER | c.-3545C>T| |
S33 |
5 | BAA06g25990 | A06 | 17825936 | G | A | upstream_gene_variant | MODIFIER | c.-3547C>T| |
S44 |
6 | BAA06g25990 | A06 | 17827366 | C | T | upstream_gene_variant | MODIFIER | c.-4977G>A| |
S164 |