Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g06940 | A05 | 3386032 | C | T | upstream_gene_variant | MODIFIER | c.-2882C>T| |
S295 |
2 | BAA05g06940 | A05 | 3386676 | C | T | upstream_gene_variant | MODIFIER | c.-2238C>T| |
S180 |
3 | BAA05g06940 | A05 | 3386957 | C | T | upstream_gene_variant | MODIFIER | c.-1957C>T| |
S295 |
4 | BAA05g06940 | A05 | 3387399 | C | T | upstream_gene_variant | MODIFIER | c.-1515C>T| |
S251 |
5 | BAA05g06940 | A05 | 3389264 | C | T | synonymous_variant | LOW | c.351C>T|p.Leu117Leu |
S163 S211 |
6 | BAA05g06940 | A05 | 3389625 | G | A | missense_variant | MODERATE | c.712G>A|p.Gly238Ser |
S282 |
7 | BAA05g06940 | A05 | 3389676 | G | A | missense_variant | MODERATE | c.763G>A|p.Asp255Asn |
S126 S13 |
8 | BAA05g06940 | A05 | 3390375 | G | A | missense_variant | MODERATE | c.1462G>A|p.Glu488Lys |
S192 |
9 | BAA05g06940 | A05 | 3391096 | G | A | missense_variant | MODERATE | c.2183G>A|p.Arg728Lys |
S233 |
10 | BAA05g06940 | A05 | 3392204 | C | T | downstream_gene_variant | MODIFIER | c.*1056C>T| |
S2 |
11 | BAA05g06940 | A05 | 3392624 | C | T | downstream_gene_variant | MODIFIER | c.*1476C>T| |
S130 |
12 | BAA05g06940 | A05 | 3392716 | G | A | downstream_gene_variant | MODIFIER | c.*1568G>A| |
S186 |
13 | BAA05g06940 | A05 | 3393816 | G | A | downstream_gene_variant | MODIFIER | c.*2668G>A| |
S257 |
14 | BAA05g06940 | A05 | 3394091 | C | T | downstream_gene_variant | MODIFIER | c.*2943C>T| |
S206 S26 |