Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g15580 | A01 | 7542242 | C | T | missense_variant | MODERATE | c.2149G>A|p.Glu717Lys |
S177 |
2 | BAA01g15580 | A01 | 7542832 | G | A | missense_variant | MODERATE | c.1559C>T|p.Ser520Phe |
S294 |
3 | BAA01g15580 | A01 | 7542994 | G | A | missense_variant | MODERATE | c.1397C>T|p.Pro466Leu |
S202 |
4 | BAA01g15580 | A01 | 7543896 | C | T | missense_variant | MODERATE | c.698G>A|p.Gly233Asp |
S184 |
5 | BAA01g15580 | A01 | 7544010 | G | A | missense_variant | MODERATE | c.584C>T|p.Ser195Phe |
S180 |
6 | BAA01g15580 | A01 | 7544179 | C | T | missense_variant | MODERATE | c.415G>A|p.Gly139Ser |
S113 |
7 | BAA01g15580 | A01 | 7544206 | C | T | missense_variant | MODERATE | c.388G>A|p.Ala130Thr |
S226 |
8 | BAA01g15580 | A01 | 7544273 | G | A | synonymous_variant | LOW | c.321C>T|p.Leu107Leu |
S280 |
9 | BAA01g15580 | A01 | 7544459 | C | T | intron_variant | MODIFIER | c.193-58G>A| |
S185 |
10 | BAA01g15580 | A01 | 7545056 | G | A | intron_variant | MODIFIER | c.192+10C>T| |
S45 |
11 | BAA01g15580 | A01 | 7546786 | C | T | upstream_gene_variant | MODIFIER | c.-1529G>A| |
S100 |
12 | BAA01g15580 | A01 | 7547699 | G | A | upstream_gene_variant | MODIFIER | c.-2442C>T| |
S70 |