Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g27230 | A10 | 21307270 | G | A | missense_variant | MODERATE | c.2755C>T|p.Pro919Ser |
S286 |
2 | BAA10g27230 | A10 | 21307672 | C | T | missense_variant | MODERATE | c.2353G>A|p.Asp785Asn |
S210 |
3 | BAA10g27230 | A10 | 21309352 | G | A | missense_variant | MODERATE | c.1850C>T|p.Thr617Ile |
S118 |
4 | BAA10g27230 | A10 | 21309704 | C | T | splice_donor_variant&intron_variant | HIGH | c.1728+1G>A| |
S282 |
5 | BAA10g27230 | A10 | 21315738 | G | A | upstream_gene_variant | MODIFIER | c.-2332C>T| |
S179 |
6 | BAA10g27230 | A10 | 21317221 | C | T | upstream_gene_variant | MODIFIER | c.-3815G>A| |
S140 |