Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g40080 | A09 | 47415968 | G | A | upstream_gene_variant | MODIFIER | c.-4535G>A| |
S127 |
2 | BAA09g40080 | A09 | 47416439 | C | T | upstream_gene_variant | MODIFIER | c.-4064C>T| |
S278 |
3 | BAA09g40080 | A09 | 47417567 | C | T | upstream_gene_variant | MODIFIER | c.-2936C>T| |
S8 |
4 | BAA09g40080 | A09 | 47418400 | C | T | upstream_gene_variant | MODIFIER | c.-2103C>T| |
S5 |
5 | BAA09g40080 | A09 | 47419570 | C | T | upstream_gene_variant | MODIFIER | c.-933C>T| |
S144 |
6 | BAA09g40080 | A09 | 47420016 | C | T | upstream_gene_variant | MODIFIER | c.-487C>T| |
S135 |
7 | BAA09g40080 | A09 | 47422577 | G | A | synonymous_variant | LOW | c.513G>A|p.Glu171Glu |
S11 |
8 | BAA09g40080 | A09 | 47422645 | C | T | missense_variant | MODERATE | c.581C>T|p.Ala194Val |
S257 |
9 | BAA09g40080 | A09 | 47423289 | G | A | missense_variant&splice_region_variant | MODERATE | c.859G>A|p.Asp287Asn |
S178 |
10 | BAA09g40080 | A09 | 47423640 | C | T | synonymous_variant | LOW | c.1051C>T|p.Leu351Leu |
S182 |