Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g15850 | A07 | 22911688 | C | T | missense_variant | MODERATE | c.515C>T|p.Ser172Phe |
S62 |
2 | BAA07g15850 | A07 | 22913616 | C | T | missense_variant | MODERATE | c.1480C>T|p.Pro494Ser |
S167 |
3 | BAA07g15850 | A07 | 22913848 | A | T | splice_acceptor_variant&intron_variant | HIGH | c.1634-2A>T| |
S262 |
4 | BAA07g15850 | A07 | 22914898 | G | A | missense_variant | MODERATE | c.2318G>A|p.Arg773Lys |
S132 |
5 | BAA07g15850 | A07 | 22914967 | G | A | missense_variant | MODERATE | c.2387G>A|p.Gly796Asp |
S135 |
6 | BAA07g15850 | A07 | 22915103 | G | A | synonymous_variant | LOW | c.2523G>A|p.Glu841Glu |
S269 |
7 | BAA07g15850 | A07 | 22920113 | G | A | downstream_gene_variant | MODIFIER | c.*4908G>A| |
S110 |