Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g22970 | A08 | 17114262 | C | T | upstream_gene_variant | MODIFIER | c.-2194C>T| |
S199 |
2 | BAA08g22970 | A08 | 17114791 | C | T | upstream_gene_variant | MODIFIER | c.-1665C>T| |
S142 |
3 | BAA08g22970 | A08 | 17114804 | C | T | upstream_gene_variant | MODIFIER | c.-1652C>T| |
S28 |
4 | BAA08g22970 | A08 | 17116552 | G | A | missense_variant | MODERATE | c.97G>A|p.Asp33Asn |
S242 |
5 | BAA08g22970 | A08 | 17116927 | C | T | missense_variant | MODERATE | c.472C>T|p.Leu158Phe |
S1 S90 |
6 | BAA08g22970 | A08 | 17117140 | C | T | missense_variant | MODERATE | c.685C>T|p.Pro229Ser |
S207 |
7 | BAA08g22970 | A08 | 17117938 | G | A | missense_variant | MODERATE | c.1483G>A|p.Glu495Lys |
S65 |
8 | BAA08g22970 | A08 | 17117961 | C | T | synonymous_variant | LOW | c.1506C>T|p.Asn502Asn |
S256 |
9 | BAA08g22970 | A08 | 17118194 | C | T | missense_variant | MODERATE | c.1739C>T|p.Ser580Phe |
S63 |