Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g08120 | A07 | 17246427 | C | T | missense_variant | MODERATE | c.1576G>A|p.Gly526Arg |
S148 S210 S30 S31 |
2 | BAA07g08120 | A07 | 17246439 | G | A | missense_variant | MODERATE | c.1564C>T|p.Pro522Ser |
S151 S52 |
3 | BAA07g08120 | A07 | 17247022 | C | T | synonymous_variant | LOW | c.981G>A|p.Lys327Lys |
S96 |
4 | BAA07g08120 | A07 | 17247499 | C | T | synonymous_variant | LOW | c.504G>A|p.Gln168Gln |
S301 S304 |
5 | BAA07g08120 | A07 | 17247691 | C | T | synonymous_variant | LOW | c.312G>A|p.Lys104Lys |
S165 |
6 | BAA07g08120 | A07 | 17247783 | C | T | missense_variant | MODERATE | c.220G>A|p.Glu74Lys |
S56 |
7 | BAA07g08120 | A07 | 17252604 | G | A | upstream_gene_variant | MODIFIER | c.-4602C>T| |
S133 |
8 | BAA07g08120 | A07 | 17252607 | C | T | upstream_gene_variant | MODIFIER | c.-4605G>A| |
S305 |
9 | BAA07g08120 | A07 | 17252717 | G | A | upstream_gene_variant | MODIFIER | c.-4715C>T| |
S146 |
10 | BAA07g08120 | A07 | 17252841 | G | A | upstream_gene_variant | MODIFIER | c.-4839C>T| |
S78 |