Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g20890 | A01 | 10292059 | C | T | missense_variant | MODERATE | c.431G>A|p.Cys144Tyr |
S275 |
2 | BAA01g20890 | A01 | 10292372 | G | A | missense_variant | MODERATE | c.118C>T|p.Leu40Phe |
S263 |
3 | BAA01g20890 | A01 | 10292399 | C | T | missense_variant | MODERATE | c.91G>A|p.Asp31Asn |
S95 |
4 | BAA01g20890 | A01 | 10293818 | C | T | upstream_gene_variant | MODIFIER | c.-1329G>A| |
S146 |
5 | BAA01g20890 | A01 | 10295163 | G | A | upstream_gene_variant | MODIFIER | c.-2674C>T| |
S268 |
6 | BAA01g20890 | A01 | 10295307 | G | A | upstream_gene_variant | MODIFIER | c.-2818C>T| |
S229 |
7 | BAA01g20890 | A01 | 10295954 | G | A | upstream_gene_variant | MODIFIER | c.-3465C>T| |
S149 |
8 | BAA01g20890 | A01 | 10296362 | C | T | upstream_gene_variant | MODIFIER | c.-3873G>A| |
S69 |
9 | BAA01g20890 | A01 | 10296397 | G | A | upstream_gene_variant | MODIFIER | c.-3908C>T| |
S294 |
10 | BAA01g20890 | A01 | 10296796 | G | A | upstream_gene_variant | MODIFIER | c.-4307C>T| |
S207 |