Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g19750 | A09 | 12158366 | G | A | missense_variant | MODERATE | c.1772C>T|p.Thr591Ile |
S210 S225 |
2 | BAA09g19750 | A09 | 12158550 | C | T | missense_variant | MODERATE | c.1588G>A|p.Ala530Thr |
S11 |
3 | BAA09g19750 | A09 | 12158615 | C | T | missense_variant | MODERATE | c.1523G>A|p.Ser508Asn |
S169 |
4 | BAA09g19750 | A09 | 12158966 | C | T | missense_variant | MODERATE | c.1172G>A|p.Gly391Glu |
S231 |
5 | BAA09g19750 | A09 | 12159295 | C | T | stop_gained | HIGH | c.843G>A|p.Trp281* |
S148 S210 |
6 | BAA09g19750 | A09 | 12160531 | C | T | synonymous_variant | LOW | c.123G>A|p.Arg41Arg |
S208 S93 |
7 | BAA09g19750 | A09 | 12161828 | G | A | upstream_gene_variant | MODIFIER | c.-1175C>T| |
S178 |
8 | BAA09g19750 | A09 | 12162919 | G | A | upstream_gene_variant | MODIFIER | c.-2266C>T| |
S162 |
9 | BAA09g19750 | A09 | 12163227 | G | A | upstream_gene_variant | MODIFIER | c.-2574C>T| |
S51 S92 |
10 | BAA09g19750 | A09 | 12163658 | G | A | upstream_gene_variant | MODIFIER | c.-3005C>T| |
S280 |
11 | BAA09g19750 | A09 | 12164151 | G | A | upstream_gene_variant | MODIFIER | c.-3498C>T| |
S238 |
12 | BAA09g19750 | A09 | 12164324 | G | A | upstream_gene_variant | MODIFIER | c.-3671C>T| |
S149 |
13 | BAA09g19750 | A09 | 12165121 | G | A | upstream_gene_variant | MODIFIER | c.-4468C>T| |
S12 |