Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g44220 | A01 | 29303772 | C | T | missense_variant | MODERATE | c.367G>A|p.Glu123Lys |
S28 |
2 | BAA01g44220 | A01 | 29303778 | C | T | missense_variant | MODERATE | c.361G>A|p.Glu121Lys |
S128 |
3 | BAA01g44220 | A01 | 29303794 | C | T | synonymous_variant | LOW | c.345G>A|p.Arg115Arg |
S167 |
4 | BAA01g44220 | A01 | 29304316 | C | T | missense_variant | MODERATE | c.7G>A|p.Asp3Asn |
S289 S290 |
5 | BAA01g44220 | A01 | 29305754 | C | T | upstream_gene_variant | MODIFIER | c.-1432G>A| |
S192 |
6 | BAA01g44220 | A01 | 29305920 | G | A | upstream_gene_variant | MODIFIER | c.-1598C>T| |
S115 |
7 | BAA01g44220 | A01 | 29307558 | G | A | upstream_gene_variant | MODIFIER | c.-3236C>T| |
S67 |
8 | BAA01g44220 | A01 | 29308461 | G | A | upstream_gene_variant | MODIFIER | c.-4139C>T| |
S243 S299 |
9 | BAA01g44220 | A01 | 29308681 | G | A | upstream_gene_variant | MODIFIER | c.-4359C>T| |
S100 |
10 | BAA01g44220 | A01 | 29308728 | G | A | upstream_gene_variant | MODIFIER | c.-4406C>T| |
S172 S217 |
11 | BAA01g44220 | A01 | 29308904 | C | T | upstream_gene_variant | MODIFIER | c.-4582G>A| |
S57 |