Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g67050 | A09 | 60959436 | C | T | missense_variant | MODERATE | c.1315G>A|p.Glu439Lys |
S182 |
2 | BAA09g67050 | A09 | 60961808 | G | A | missense_variant | MODERATE | c.227C>T|p.Ala76Val |
S262 |
3 | BAA09g67050 | A09 | 60961826 | G | A | missense_variant | MODERATE | c.209C>T|p.Pro70Leu |
S265 |
4 | BAA09g67050 | A09 | 60961954 | C | T | synonymous_variant | LOW | c.81G>A|p.Arg27Arg |
S100 |
5 | BAA09g67050 | A09 | 60962027 | G | A | splice_region_variant&intron_variant | LOW | c.11-3C>T| |
S190 |
6 | BAA09g67050 | A09 | 60965152 | G | A | upstream_gene_variant | MODIFIER | c.-3047C>T| |
S155 |
7 | BAA09g67050 | A09 | 60965582 | C | T | upstream_gene_variant | MODIFIER | c.-3477G>A| |
S296 |
8 | BAA09g67050 | A09 | 60965636 | C | T | upstream_gene_variant | MODIFIER | c.-3531G>A| |
S282 |
9 | BAA09g67050 | A09 | 60966787 | C | T | upstream_gene_variant | MODIFIER | c.-4682G>A| |
S158 |
10 | BAA09g67050 | A09 | 60967009 | C | T | upstream_gene_variant | MODIFIER | c.-4904G>A| |
S113 |