Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g21800 | A01 | 10850096 | C | T | missense_variant | MODERATE | c.511G>A|p.Val171Ile |
S182 |
2 | BAA01g21800 | A01 | 10850324 | C | T | missense_variant | MODERATE | c.283G>A|p.Asp95Asn |
S111 |
3 | BAA01g21800 | A01 | 10850401 | G | A | missense_variant | MODERATE | c.206C>T|p.Ser69Phe |
S244 |
4 | BAA01g21800 | A01 | 10850503 | G | A | missense_variant | MODERATE | c.104C>T|p.Thr35Ile |
S34 |
5 | BAA01g21800 | A01 | 10851010 | G | A | upstream_gene_variant | MODIFIER | c.-404C>T| |
S239 |
6 | BAA01g21800 | A01 | 10853285 | C | T | upstream_gene_variant | MODIFIER | c.-2679G>A| |
S207 |
7 | BAA01g21800 | A01 | 10853573 | C | T | upstream_gene_variant | MODIFIER | c.-2967G>A| |
S20 |
8 | BAA01g21800 | A01 | 10853991 | G | A | upstream_gene_variant | MODIFIER | c.-3385C>T| |
S32 |
9 | BAA01g21800 | A01 | 10854016 | C | T | upstream_gene_variant | MODIFIER | c.-3410G>A| |
S148 S272 S30 S31 |