Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g44060 | A09 | 49909516 | C | T | missense_variant | MODERATE | c.2306G>A|p.Gly769Glu |
S136 |
2 | BAA09g44060 | A09 | 49909998 | G | A | synonymous_variant | LOW | c.1903C>T|p.Leu635Leu |
S162 |
3 | BAA09g44060 | A09 | 49910358 | G | A | missense_variant | MODERATE | c.1838C>T|p.Pro613Leu |
S190 |
4 | BAA09g44060 | A09 | 49910652 | G | A | synonymous_variant | LOW | c.1659C>T|p.Leu553Leu |
S156 S213 S34 S6 |
5 | BAA09g44060 | A09 | 49910743 | G | A | missense_variant | MODERATE | c.1568C>T|p.Ser523Phe |
S47 |
6 | BAA09g44060 | A09 | 49912878 | C | T | missense_variant | MODERATE | c.1021G>A|p.Val341Ile |
S118 |
7 | BAA09g44060 | A09 | 49912992 | C | T | missense_variant | MODERATE | c.907G>A|p.Asp303Asn |
S249 |
8 | BAA09g44060 | A09 | 49913666 | C | T | synonymous_variant | LOW | c.663G>A|p.Arg221Arg |
S208 S93 |
9 | BAA09g44060 | A09 | 49914270 | G | A | missense_variant | MODERATE | c.235C>T|p.Arg79Trp |
S164 |
10 | BAA09g44060 | A09 | 49915500 | C | T | upstream_gene_variant | MODIFIER | c.-996G>A| |
S37 |
11 | BAA09g44060 | A09 | 49916250 | C | T | upstream_gene_variant | MODIFIER | c.-1746G>A| |
S50 |
12 | BAA09g44060 | A09 | 49918112 | G | A | upstream_gene_variant | MODIFIER | c.-3608C>T| |
S268 |