Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g02660 | A10 | 1277102 | G | A | missense_variant | MODERATE | c.434C>T|p.Ser145Phe |
S79 S84 |
2 | BAA10g02660 | A10 | 1278223 | C | T | synonymous_variant | LOW | c.192G>A|p.Gln64Gln |
S197 |
3 | BAA10g02660 | A10 | 1279889 | G | A | upstream_gene_variant | MODIFIER | c.-966C>T| |
S180 |
4 | BAA10g02660 | A10 | 1279958 | C | T | upstream_gene_variant | MODIFIER | c.-1035G>A| |
S270 |
5 | BAA10g02660 | A10 | 1280024 | G | A | upstream_gene_variant | MODIFIER | c.-1101C>T| |
S48 |
6 | BAA10g02660 | A10 | 1280719 | G | A | upstream_gene_variant | MODIFIER | c.-1796C>T| |
S53 |
7 | BAA10g02660 | A10 | 1281960 | C | T | upstream_gene_variant | MODIFIER | c.-3037G>A| |
S54 |