Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g12890 | A01 | 6115347 | C | T | upstream_gene_variant | MODIFIER | c.-2334C>T| |
S71 |
2 | BAA01g12890 | A01 | 6115461 | C | T | upstream_gene_variant | MODIFIER | c.-2220C>T| |
S108 |
3 | BAA01g12890 | A01 | 6115546 | G | A | upstream_gene_variant | MODIFIER | c.-2135G>A| |
S187 |
4 | BAA01g12890 | A01 | 6115656 | C | T | upstream_gene_variant | MODIFIER | c.-2025C>T| |
S111 |
5 | BAA01g12890 | A01 | 6116189 | G | A | upstream_gene_variant | MODIFIER | c.-1492G>A| |
S298 |
6 | BAA01g12890 | A01 | 6116242 | G | A | upstream_gene_variant | MODIFIER | c.-1439G>A| |
S251 |
7 | BAA01g12890 | A01 | 6116321 | G | A | upstream_gene_variant | MODIFIER | c.-1360G>A| |
S14 |
8 | BAA01g12890 | A01 | 6116490 | C | T | upstream_gene_variant | MODIFIER | c.-1191C>T| |
S211 S227 |
9 | BAA01g12890 | A01 | 6117846 | G | A | missense_variant | MODERATE | c.166G>A|p.Asp56Asn |
S292 |
10 | BAA01g12890 | A01 | 6118241 | C | T | synonymous_variant | LOW | c.561C>T|p.Asp187Asp |
S100 |
11 | BAA01g12890 | A01 | 6118318 | C | T | missense_variant | MODERATE | c.638C>T|p.Pro213Leu |
S139 |
12 | BAA01g12890 | A01 | 6120252 | G | A | missense_variant | MODERATE | c.2036G>A|p.Arg679Gln |
S173 |
13 | BAA01g12890 | A01 | 6123727 | G | A | downstream_gene_variant | MODIFIER | c.*3450G>A| |
S259 |