Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g57860 | A09 | 56903771 | G | A | stop_gained&splice_region_variant | HIGH | c.1198C>T|p.Arg400* |
S79 S91 |
2 | BAA09g57860 | A09 | 56903941 | G | A | missense_variant | MODERATE | c.1168C>T|p.Leu390Phe |
S173 |
3 | BAA09g57860 | A09 | 56904532 | C | T | missense_variant | MODERATE | c.697G>A|p.Val233Ile |
S67 |
4 | BAA09g57860 | A09 | 56906080 | G | A | missense_variant | MODERATE | c.22C>T|p.Leu8Phe |
S127 |
5 | BAA09g57860 | A09 | 56906990 | C | T | upstream_gene_variant | MODIFIER | c.-889G>A| |
S125 |
6 | BAA09g57860 | A09 | 56907763 | C | T | upstream_gene_variant | MODIFIER | c.-1662G>A| |
S100 |
7 | BAA09g57860 | A09 | 56908481 | C | T | upstream_gene_variant | MODIFIER | c.-2380G>A| |
S265 |
8 | BAA09g57860 | A09 | 56908930 | G | A | upstream_gene_variant | MODIFIER | c.-2829C>T| |
S280 |
9 | BAA09g57860 | A09 | 56909717 | C | T | upstream_gene_variant | MODIFIER | c.-3616G>A| |
S299 |