Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g13970 | A02 | 6548691 | A | G | upstream_gene_variant | MODIFIER | c.-2858A>G| |
S223 |
2 | BAA02g13970 | A02 | 6548943 | G | A | upstream_gene_variant | MODIFIER | c.-2606G>A| |
S286 |
3 | BAA02g13970 | A02 | 6548955 | G | A | upstream_gene_variant | MODIFIER | c.-2594G>A| |
S202 |
4 | BAA02g13970 | A02 | 6549367 | G | A | upstream_gene_variant | MODIFIER | c.-2182G>A| |
S260 |
5 | BAA02g13970 | A02 | 6549689 | C | T | upstream_gene_variant | MODIFIER | c.-1860C>T| |
S131 |
6 | BAA02g13970 | A02 | 6551608 | C | T | synonymous_variant | LOW | c.60C>T|p.Phe20Phe |
S216 |
7 | BAA02g13970 | A02 | 6552115 | C | T | missense_variant | MODERATE | c.131C>T|p.Ala44Val |
S162 |
8 | BAA02g13970 | A02 | 6552344 | C | T | synonymous_variant | LOW | c.360C>T|p.Ser120Ser |
S301 S304 |
9 | BAA02g13970 | A02 | 6553108 | G | A | intron_variant | MODIFIER | c.1023+101G>A| |
S246 |
10 | BAA02g13970 | A02 | 6554533 | G | A | missense_variant | MODERATE | c.2047G>A|p.Asp683Asn |
S203 |
11 | BAA02g13970 | A02 | 6554985 | C | T | downstream_gene_variant | MODIFIER | c.*309C>T| |
S208 |
12 | BAA02g13970 | A02 | 6555044 | G | A | downstream_gene_variant | MODIFIER | c.*368G>A| |
S232 |
13 | BAA02g13970 | A02 | 6556041 | G | A | downstream_gene_variant | MODIFIER | c.*1365G>A| |
S302 |
14 | BAA02g13970 | A02 | 6557230 | C | T | downstream_gene_variant | MODIFIER | c.*2554C>T| |
S88 |
15 | BAA02g13970 | A02 | 6558301 | C | T | downstream_gene_variant | MODIFIER | c.*3625C>T| |
S5 |