Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g16500 | A09 | 9622800 | G | A | upstream_gene_variant | MODIFIER | c.-4330G>A| |
S74 |
2 | BAA09g16500 | A09 | 9623880 | G | A | upstream_gene_variant | MODIFIER | c.-3250G>A| |
S249 |
3 | BAA09g16500 | A09 | 9623925 | C | T | upstream_gene_variant | MODIFIER | c.-3205C>T| |
S18 |
4 | BAA09g16500 | A09 | 9625114 | C | T | upstream_gene_variant | MODIFIER | c.-2016C>T| |
S5 |
5 | BAA09g16500 | A09 | 9625815 | C | T | upstream_gene_variant | MODIFIER | c.-1315C>T| |
S131 |
6 | BAA09g16500 | A09 | 9626135 | G | A | upstream_gene_variant | MODIFIER | c.-995G>A| |
S33 |
7 | BAA09g16500 | A09 | 9626639 | C | T | upstream_gene_variant | MODIFIER | c.-491C>T| |
S246 |
8 | BAA09g16500 | A09 | 9627265 | C | T | missense_variant | MODERATE | c.136C>T|p.Leu46Phe |
S80 |
9 | BAA09g16500 | A09 | 9628179 | C | T | synonymous_variant | LOW | c.886C>T|p.Leu296Leu |
S147 S96 |
10 | BAA09g16500 | A09 | 9628211 | G | A | synonymous_variant | LOW | c.918G>A|p.Glu306Glu |
S262 |
11 | BAA09g16500 | A09 | 9628350 | G | A | missense_variant | MODERATE | c.1057G>A|p.Val353Met |
S74 |
12 | BAA09g16500 | A09 | 9629323 | C | T | missense_variant | MODERATE | c.2030C>T|p.Pro677Leu |
S230 |