Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g11970 | A09 | 6757760 | C | T | missense_variant | MODERATE | c.1045G>A|p.Asp349Asn |
S302 |
2 | BAA09g11970 | A09 | 6757815 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.991-1G>A| |
S158 |
3 | BAA09g11970 | A09 | 6758438 | G | A | synonymous_variant | LOW | c.453C>T|p.Ile151Ile |
S198 |
4 | BAA09g11970 | A09 | 6758582 | G | A | synonymous_variant | LOW | c.309C>T|p.Arg103Arg |
S223 |
5 | BAA09g11970 | A09 | 6758676 | G | A | missense_variant | MODERATE | c.215C>T|p.Thr72Ile |
S163 |
6 | BAA09g11970 | A09 | 6762488 | C | T | upstream_gene_variant | MODIFIER | c.-3598G>A| |
S298 |
7 | BAA09g11970 | A09 | 6763601 | G | A | upstream_gene_variant | MODIFIER | c.-4711C>T| |
S207 |
8 | BAA09g11970 | A09 | 6763738 | G | A | upstream_gene_variant | MODIFIER | c.-4848C>T| |
S113 |
9 | BAA09g11970 | A09 | 6763857 | G | A | upstream_gene_variant | MODIFIER | c.-4967C>T| |
S298 |