Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g38670 | A05 | 37993011 | C | T | missense_variant | MODERATE | c.325G>A|p.Asp109Asn |
S13 S278 S279 S64 |
2 | BAA05g38670 | A05 | 37993122 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.215-1G>A| |
S142 |
3 | BAA05g38670 | A05 | 37996249 | C | T | upstream_gene_variant | MODIFIER | c.-2834G>A| |
S80 |
4 | BAA05g38670 | A05 | 37997412 | G | A | upstream_gene_variant | MODIFIER | c.-3997C>T| |
S205 |
5 | BAA05g38670 | A05 | 37997707 | C | T | upstream_gene_variant | MODIFIER | c.-4292G>A| |
S193 |
6 | BAA05g38670 | A05 | 37997710 | G | A | upstream_gene_variant | MODIFIER | c.-4295C>T| |
S270 |
7 | BAA05g38670 | A05 | 37997711 | G | A | upstream_gene_variant | MODIFIER | c.-4296C>T| |
S156 |