Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g30260 | A07 | 30561499 | C | T | missense_variant | MODERATE | c.568G>A|p.Asp190Asn |
S292 |
2 | BAA07g30260 | A07 | 30563527 | C | T | upstream_gene_variant | MODIFIER | c.-927G>A| |
S210 |
3 | BAA07g30260 | A07 | 30564758 | G | A | upstream_gene_variant | MODIFIER | c.-2158C>T| |
S134 |
4 | BAA07g30260 | A07 | 30564830 | G | A | upstream_gene_variant | MODIFIER | c.-2230C>T| |
S194 |
5 | BAA07g30260 | A07 | 30565780 | C | T | upstream_gene_variant | MODIFIER | c.-3180G>A| |
S276 |
6 | BAA07g30260 | A07 | 30565839 | G | A | upstream_gene_variant | MODIFIER | c.-3239C>T| |
S265 |
7 | BAA07g30260 | A07 | 30566586 | G | A | upstream_gene_variant | MODIFIER | c.-3986C>T| |
S138 |
8 | BAA07g30260 | A07 | 30566700 | G | A | upstream_gene_variant | MODIFIER | c.-4100C>T| |
S158 |
9 | BAA07g30260 | A07 | 30566939 | G | A | upstream_gene_variant | MODIFIER | c.-4339C>T| |
S263 |