Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g50000 | A09 | 53064413 | G | A | missense_variant | MODERATE | c.674G>A|p.Arg225Lys |
S1 S90 |
2 | BAA09g50000 | A09 | 53065612 | C | T | synonymous_variant | LOW | c.1434C>T|p.Ser478Ser |
S260 |
3 | BAA09g50000 | A09 | 53065775 | G | A | missense_variant | MODERATE | c.1597G>A|p.Asp533Asn |
S221 |
4 | BAA09g50000 | A09 | 53066073 | C | T | intron_variant | MODIFIER | c.1803+11C>T| |
S226 |
5 | BAA09g50000 | A09 | 53066392 | C | T | missense_variant | MODERATE | c.1970C>T|p.Pro657Leu |
S33 |
6 | BAA09g50000 | A09 | 53067835 | G | A | splice_donor_variant&intron_variant | HIGH | c.2781+1G>A| |
S15 S3 |
7 | BAA09g50000 | A09 | 53068938 | C | T | synonymous_variant | LOW | c.3637C>T|p.Leu1213Leu |
S100 |
8 | BAA09g50000 | A09 | 53069105 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.3715-1G>A| |
S278 |
9 | BAA09g50000 | A09 | 53070606 | G | A | downstream_gene_variant | MODIFIER | c.*121G>A| |
S132 S137 S215 |
10 | BAA09g50000 | A09 | 53072701 | G | A | downstream_gene_variant | MODIFIER | c.*2216G>A| |
S110 |
11 | BAA09g50000 | A09 | 53074745 | C | T | downstream_gene_variant | MODIFIER | c.*4260C>T| |
S146 |
12 | BAA09g50000 | A09 | 53074908 | G | A | downstream_gene_variant | MODIFIER | c.*4423G>A| |
S187 |