Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g02000 | A01 | 930830 | C | T | synonymous_variant | LOW | c.2418G>A|p.Thr806Thr |
S166 |
2 | BAA01g02000 | A01 | 930846 | G | A | missense_variant | MODERATE | c.2402C>T|p.Ser801Phe |
S138 |
3 | BAA01g02000 | A01 | 931041 | A | G | missense_variant | MODERATE | c.2207T>C|p.Val736Ala |
S129 |
4 | BAA01g02000 | A01 | 931386 | C | T | missense_variant | MODERATE | c.1862G>A|p.Ser621Asn |
S225 S73 |
5 | BAA01g02000 | A01 | 931816 | G | A | missense_variant | MODERATE | c.1432C>T|p.Pro478Ser |
S156 |
6 | BAA01g02000 | A01 | 931858 | C | T | missense_variant | MODERATE | c.1390G>A|p.Glu464Lys |
S231 |
7 | BAA01g02000 | A01 | 932363 | C | T | synonymous_variant | LOW | c.885G>A|p.Arg295Arg |
S68 |
8 | BAA01g02000 | A01 | 932418 | G | A | missense_variant | MODERATE | c.830C>T|p.Pro277Leu |
S115 |
9 | BAA01g02000 | A01 | 932815 | G | A | missense_variant | MODERATE | c.433C>T|p.His145Tyr |
S23 |
10 | BAA01g02000 | A01 | 933003 | G | A | missense_variant | MODERATE | c.245C>T|p.Ser82Phe |
S256 |
11 | BAA01g02000 | A01 | 933356 | G | A | upstream_gene_variant | MODIFIER | c.-109C>T| |
S268 |
12 | BAA01g02000 | A01 | 933535 | C | T | upstream_gene_variant | MODIFIER | c.-288G>A| |
S25 |
13 | BAA01g02000 | A01 | 935292 | G | A | upstream_gene_variant | MODIFIER | c.-2045C>T| |
S169 |
14 | BAA01g02000 | A01 | 935311 | C | T | upstream_gene_variant | MODIFIER | c.-2064G>A| |
S8 |
15 | BAA01g02000 | A01 | 936353 | C | T | upstream_gene_variant | MODIFIER | c.-3106G>A| |
S278 |
16 | BAA01g02000 | A01 | 936718 | G | A | upstream_gene_variant | MODIFIER | c.-3471C>T| |
S5 |