Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g65920 | A09 | 60485520 | G | A | synonymous_variant | LOW | c.1699C>T|p.Leu567Leu |
S130 |
2 | BAA09g65920 | A09 | 60486157 | C | T | synonymous_variant | LOW | c.1365G>A|p.Lys455Lys |
S302 |
3 | BAA09g65920 | A09 | 60486462 | C | T | missense_variant | MODERATE | c.1150G>A|p.Glu384Lys |
S100 |
4 | BAA09g65920 | A09 | 60486854 | C | T | missense_variant | MODERATE | c.976G>A|p.Glu326Lys |
S133 |
5 | BAA09g65920 | A09 | 60487066 | C | T | synonymous_variant | LOW | c.852G>A|p.Glu284Glu |
S5 |
6 | BAA09g65920 | A09 | 60487439 | G | A | splice_region_variant&intron_variant | LOW | c.646-4C>T| |
S148 S210 S30 S31 |
7 | BAA09g65920 | A09 | 60489723 | G | A | upstream_gene_variant | MODIFIER | c.-321C>T| |
S107 |
8 | BAA09g65920 | A09 | 60491615 | C | T | upstream_gene_variant | MODIFIER | c.-2213G>A| |
S20 |
9 | BAA09g65920 | A09 | 60493533 | G | A | upstream_gene_variant | MODIFIER | c.-4131C>T| |
S4 |
10 | BAA09g65920 | A09 | 60493542 | C | T | upstream_gene_variant | MODIFIER | c.-4140G>A| |
S131 |