Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g39120 | A09 | 46815127 | G | A | upstream_gene_variant | MODIFIER | c.-797G>A| |
S137 S215 |
2 | BAA09g39120 | A09 | 46815910 | G | A | upstream_gene_variant | MODIFIER | c.-14G>A| |
S190 |
3 | BAA09g39120 | A09 | 46816050 | C | T | missense_variant | MODERATE | c.127C>T|p.Leu43Phe |
S306 S308 |
4 | BAA09g39120 | A09 | 46816471 | G | A | splice_region_variant&stop_retained_variant | LOW | c.396G>A|p.Ter132Ter |
S4 |
5 | BAA09g39120 | A09 | 46820862 | A | T | downstream_gene_variant | MODIFIER | c.*4391A>T| |
S162 |
6 | BAA09g39120 | A09 | 46821050 | C | T | downstream_gene_variant | MODIFIER | c.*4579C>T| |
S241 S39 |
7 | BAA09g39120 | A09 | 46821169 | C | T | downstream_gene_variant | MODIFIER | c.*4698C>T| |
S64 |
8 | BAA09g39120 | A09 | 46821457 | C | T | downstream_gene_variant | MODIFIER | c.*4986C>T| |
S234 |