Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g42660 | A07 | 36896698 | C | T | missense_variant | MODERATE | c.2492G>A|p.Cys831Tyr |
S63 |
2 | BAA07g42660 | A07 | 36896762 | G | A | synonymous_variant | LOW | c.2428C>T|p.Leu810Leu |
S41 |
3 | BAA07g42660 | A07 | 36897604 | G | A | missense_variant | MODERATE | c.1724C>T|p.Thr575Ile |
S143 |
4 | BAA07g42660 | A07 | 36898071 | G | A | synonymous_variant | LOW | c.1257C>T|p.Leu419Leu |
S115 |
5 | BAA07g42660 | A07 | 36898545 | G | A | synonymous_variant | LOW | c.783C>T|p.Ile261Ile |
S216 |
6 | BAA07g42660 | A07 | 36899406 | C | T | missense_variant | MODERATE | c.326G>A|p.Gly109Glu |
S156 |
7 | BAA07g42660 | A07 | 36902368 | C | T | upstream_gene_variant | MODIFIER | c.-2637G>A| |
S60 |
8 | BAA07g42660 | A07 | 36902765 | C | T | upstream_gene_variant | MODIFIER | c.-3034G>A| |
S37 |
9 | BAA07g42660 | A07 | 36903000 | C | T | upstream_gene_variant | MODIFIER | c.-3269G>A| |
S177 |
10 | BAA07g42660 | A07 | 36903738 | C | T | upstream_gene_variant | MODIFIER | c.-4007G>A| |
S203 |