Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g10000 | A05 | 5095792 | C | T | upstream_gene_variant | MODIFIER | c.-4851C>T| |
S182 |
2 | BAA05g10000 | A05 | 5095811 | C | T | upstream_gene_variant | MODIFIER | c.-4832C>T| |
S166 |
3 | BAA05g10000 | A05 | 5096220 | C | T | upstream_gene_variant | MODIFIER | c.-4423C>T| |
S165 |
4 | BAA05g10000 | A05 | 5096310 | C | T | upstream_gene_variant | MODIFIER | c.-4333C>T| |
S191 |
5 | BAA05g10000 | A05 | 5099691 | C | T | upstream_gene_variant | MODIFIER | c.-952C>T| |
S198 |
6 | BAA05g10000 | A05 | 5099938 | A | T | upstream_gene_variant | MODIFIER | c.-705A>T| |
S23 |
7 | BAA05g10000 | A05 | 5100638 | C | T | upstream_gene_variant | MODIFIER | c.-5C>T| |
S176 |
8 | BAA05g10000 | A05 | 5100929 | G | A | missense_variant | MODERATE | c.287G>A|p.Gly96Asp |
S192 |
9 | BAA05g10000 | A05 | 5100968 | G | A | missense_variant | MODERATE | c.326G>A|p.Arg109Gln |
S192 |
10 | BAA05g10000 | A05 | 5100973 | G | A | missense_variant | MODERATE | c.331G>A|p.Ala111Thr |
S155 |
11 | BAA05g10000 | A05 | 5101765 | G | A | missense_variant | MODERATE | c.728G>A|p.Ser243Asn |
S302 |
12 | BAA05g10000 | A05 | 5101896 | C | T | missense_variant | MODERATE | c.776C>T|p.Ser259Phe |
S121 |
13 | BAA05g10000 | A05 | 5101904 | G | A | missense_variant | MODERATE | c.784G>A|p.Glu262Lys |
S180 |