Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g15990 | A09 | 9212686 | C | T | upstream_gene_variant | MODIFIER | c.-4737C>T| |
S174 S27 |
2 | BAA09g15990 | A09 | 9212769 | C | T | upstream_gene_variant | MODIFIER | c.-4654C>T| |
S249 |
3 | BAA09g15990 | A09 | 9213553 | C | T | upstream_gene_variant | MODIFIER | c.-3870C>T| |
S30 S31 |
4 | BAA09g15990 | A09 | 9215989 | G | A | upstream_gene_variant | MODIFIER | c.-1434G>A| |
S105 S106 |
5 | BAA09g15990 | A09 | 9216345 | G | A | upstream_gene_variant | MODIFIER | c.-1078G>A| |
S16 |
6 | BAA09g15990 | A09 | 9217148 | G | A | upstream_gene_variant | MODIFIER | c.-275G>A| |
S210 S225 |
7 | BAA09g15990 | A09 | 9217543 | G | A | missense_variant | MODERATE | c.121G>A|p.Gly41Arg |
S139 S94 |
8 | BAA09g15990 | A09 | 9217783 | C | T | missense_variant | MODERATE | c.361C>T|p.Pro121Ser |
S50 |
9 | BAA09g15990 | A09 | 9218515 | C | T | missense_variant | MODERATE | c.677C>T|p.Ser226Phe |
S107 |
10 | BAA09g15990 | A09 | 9218695 | G | A | missense_variant | MODERATE | c.755G>A|p.Ser252Asn |
S88 |
11 | BAA09g15990 | A09 | 9218717 | C | T | synonymous_variant | LOW | c.777C>T|p.Val259Val |
S294 |
12 | BAA09g15990 | A09 | 9219771 | G | A | downstream_gene_variant | MODIFIER | c.*632G>A| |
S259 |
13 | BAA09g15990 | A09 | 9219995 | G | A | downstream_gene_variant | MODIFIER | c.*856G>A| |
S181 |