Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g22950 | A10 | 19522684 | C | T | intron_variant | MODIFIER | c.292-512G>A| |
S23 |
2 | BAA10g22950 | A10 | 19522770 | G | A | intron_variant | MODIFIER | c.292-598C>T| |
S161 |
3 | BAA10g22950 | A10 | 19526413 | G | A | missense_variant | MODERATE | c.236C>T|p.Ser79Phe |
S136 |
4 | BAA10g22950 | A10 | 19528523 | G | A | upstream_gene_variant | MODIFIER | c.-1791C>T| |
S16 |
5 | BAA10g22950 | A10 | 19529867 | G | A | upstream_gene_variant | MODIFIER | c.-3135C>T| |
S15 S3 |
6 | BAA10g22950 | A10 | 19530702 | C | A | upstream_gene_variant | MODIFIER | c.-3970G>T| |
S215 |