Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g15700 | A04 | 20394565 | G | A | synonymous_variant | LOW | c.762C>T|p.His254His |
S245 |
2 | BAA04g15700 | A04 | 20395055 | C | T | missense_variant&splice_region_variant | MODERATE | c.521G>A|p.Gly174Asp |
S46 |
3 | BAA04g15700 | A04 | 20395127 | G | A | splice_region_variant&intron_variant | LOW | c.520+3C>T| |
S79 S91 |
4 | BAA04g15700 | A04 | 20395348 | C | T | missense_variant | MODERATE | c.406G>A|p.Glu136Lys |
S13 S270 |
5 | BAA04g15700 | A04 | 20395671 | C | T | missense_variant | MODERATE | c.259G>A|p.Ala87Thr |
S139 |
6 | BAA04g15700 | A04 | 20396372 | G | A | upstream_gene_variant | MODIFIER | c.-208C>T| |
S53 |
7 | BAA04g15700 | A04 | 20396834 | G | A | upstream_gene_variant | MODIFIER | c.-670C>T| |
S43 |
8 | BAA04g15700 | A04 | 20397733 | C | T | upstream_gene_variant | MODIFIER | c.-1569G>A| |
S42 |
9 | BAA04g15700 | A04 | 20398166 | G | A | upstream_gene_variant | MODIFIER | c.-2002C>T| |
S56 |
10 | BAA04g15700 | A04 | 20398282 | G | A | upstream_gene_variant | MODIFIER | c.-2118C>T| |
S263 |
11 | BAA04g15700 | A04 | 20398305 | C | T | upstream_gene_variant | MODIFIER | c.-2141G>A| |
S157 S163 |