Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g10640 | A08 | 9546073 | G | A | upstream_gene_variant | MODIFIER | c.-3990G>A| |
S139 |
2 | BAA08g10640 | A08 | 9546226 | G | A | upstream_gene_variant | MODIFIER | c.-3837G>A| |
S66 |
3 | BAA08g10640 | A08 | 9547077 | C | T | upstream_gene_variant | MODIFIER | c.-2986C>T| |
S189 |
4 | BAA08g10640 | A08 | 9548889 | G | A | upstream_gene_variant | MODIFIER | c.-1174G>A| |
S281 S282 |
5 | BAA08g10640 | A08 | 9550488 | C | T | synonymous_variant | LOW | c.426C>T|p.Ile142Ile |
S120 |
6 | BAA08g10640 | A08 | 9550753 | G | A | missense_variant | MODERATE | c.691G>A|p.Glu231Lys |
S32 |
7 | BAA08g10640 | A08 | 9550846 | C | T | missense_variant | MODERATE | c.784C>T|p.Arg262Cys |
S148 S210 S30 S31 |
8 | BAA08g10640 | A08 | 9551496 | G | A | missense_variant | MODERATE | c.1264G>A|p.Val422Ile |
S58 |
9 | BAA08g10640 | A08 | 9552866 | C | T | missense_variant | MODERATE | c.1835C>T|p.Thr612Ile |
S189 |
10 | BAA08g10640 | A08 | 9554668 | G | A | downstream_gene_variant | MODIFIER | c.*1227G>A| |
S128 |
11 | BAA08g10640 | A08 | 9556978 | G | A | downstream_gene_variant | MODIFIER | c.*3537G>A| |
S35 |