Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g14830 | A01 | 7030646 | G | A | upstream_gene_variant | MODIFIER | c.-2341G>A| |
S197 |
2 | BAA01g14830 | A01 | 7030686 | C | T | upstream_gene_variant | MODIFIER | c.-2301C>T| |
S61 |
3 | BAA01g14830 | A01 | 7030964 | C | T | upstream_gene_variant | MODIFIER | c.-2023C>T| |
S143 |
4 | BAA01g14830 | A01 | 7030981 | C | T | upstream_gene_variant | MODIFIER | c.-2006C>T| |
S99 |
5 | BAA01g14830 | A01 | 7032061 | G | A | upstream_gene_variant | MODIFIER | c.-926G>A| |
S209 |
6 | BAA01g14830 | A01 | 7032536 | C | T | upstream_gene_variant | MODIFIER | c.-451C>T| |
S63 |
7 | BAA01g14830 | A01 | 7032563 | C | T | upstream_gene_variant | MODIFIER | c.-424C>T| |
S4 |
8 | BAA01g14830 | A01 | 7033258 | C | T | missense_variant | MODERATE | c.272C>T|p.Ala91Val |
S51 |
9 | BAA01g14830 | A01 | 7033392 | G | A | missense_variant | MODERATE | c.406G>A|p.Asp136Asn |
S202 |