Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g68660 | A09 | 61647784 | C | T | missense_variant&splice_region_variant | MODERATE | c.1342G>A|p.Val448Ile |
S271 |
2 | BAA09g68660 | A09 | 61648020 | C | T | missense_variant | MODERATE | c.1282G>A|p.Glu428Lys |
S225 S73 |
3 | BAA09g68660 | A09 | 61648683 | G | A | synonymous_variant | LOW | c.777C>T|p.Ser259Ser |
S247 |
4 | BAA09g68660 | A09 | 61649962 | C | T | synonymous_variant | LOW | c.399G>A|p.Gly133Gly |
S185 |
5 | BAA09g68660 | A09 | 61650247 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.242-1G>A| |
S156 |
6 | BAA09g68660 | A09 | 61651231 | G | A | upstream_gene_variant | MODIFIER | c.-495C>T| |
S13 S283 |
7 | BAA09g68660 | A09 | 61651315 | C | T | upstream_gene_variant | MODIFIER | c.-579G>A| |
S18 |
8 | BAA09g68660 | A09 | 61651685 | C | T | upstream_gene_variant | MODIFIER | c.-949G>A| |
S146 |
9 | BAA09g68660 | A09 | 61651736 | G | A | upstream_gene_variant | MODIFIER | c.-1000C>T| |
S165 |
10 | BAA09g68660 | A09 | 61653956 | C | T | upstream_gene_variant | MODIFIER | c.-3220G>A| |
S156 |
11 | BAA09g68660 | A09 | 61655009 | C | T | upstream_gene_variant | MODIFIER | c.-4273G>A| |
S160 |
12 | BAA09g68660 | A09 | 61655577 | C | T | upstream_gene_variant | MODIFIER | c.-4841G>A| |
S192 |