Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g49730 | A09 | 52943783 | G | A | synonymous_variant | LOW | c.1131C>T|p.Val377Val |
S177 |
2 | BAA09g49730 | A09 | 52944228 | G | A | missense_variant | MODERATE | c.862C>T|p.Pro288Ser |
S78 |
3 | BAA09g49730 | A09 | 52945076 | C | T | splice_region_variant&intron_variant | LOW | c.413+5G>A| |
S30 S31 |
4 | BAA09g49730 | A09 | 52945878 | G | A | upstream_gene_variant | MODIFIER | c.-61C>T| |
S98 |
5 | BAA09g49730 | A09 | 52945957 | G | A | upstream_gene_variant | MODIFIER | c.-140C>T| |
S10 |
6 | BAA09g49730 | A09 | 52947573 | G | A | upstream_gene_variant | MODIFIER | c.-1756C>T| |
S130 |
7 | BAA09g49730 | A09 | 52948993 | C | T | upstream_gene_variant | MODIFIER | c.-3176G>A| |
S121 |