Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g02550 | A10 | 1226493 | C | T | missense_variant | MODERATE | c.1397G>A|p.Gly466Asp |
S144 |
2 | BAA10g02550 | A10 | 1227802 | A | T | intron_variant | MODIFIER | c.542+60T>A| |
S20 |
3 | BAA10g02550 | A10 | 1228161 | C | T | synonymous_variant | LOW | c.243G>A|p.Gln81Gln |
S123 |
4 | BAA10g02550 | A10 | 1228298 | G | A | intron_variant | MODIFIER | c.146-40C>T| |
S198 |
5 | BAA10g02550 | A10 | 1230664 | G | A | upstream_gene_variant | MODIFIER | c.-2064C>T| |
S302 |
6 | BAA10g02550 | A10 | 1231176 | C | T | upstream_gene_variant | MODIFIER | c.-2576G>A| |
S144 |
7 | BAA10g02550 | A10 | 1232726 | G | A | upstream_gene_variant | MODIFIER | c.-4126C>T| |
S236 |
8 | BAA10g02550 | A10 | 1233505 | C | T | upstream_gene_variant | MODIFIER | c.-4905G>A| |
S44 |
9 | BAA10g02550 | A10 | 1233539 | C | T | upstream_gene_variant | MODIFIER | c.-4939G>A| |
S41 |