Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g00840 | A07 | 580586 | C | T | synonymous_variant | LOW | c.153C>T|p.Phe51Phe |
S152 |
2 | BAA07g00840 | A07 | 580832 | G | A | synonymous_variant | LOW | c.318G>A|p.Leu106Leu |
S187 |
3 | BAA07g00840 | A07 | 581325 | G | A | splice_donor_variant&intron_variant | HIGH | c.582+1G>A| |
S179 |
4 | BAA07g00840 | A07 | 582285 | G | A | missense_variant&splice_region_variant | MODERATE | c.1045G>A|p.Asp349Asn |
S125 |
5 | BAA07g00840 | A07 | 582701 | G | A | missense_variant | MODERATE | c.1292G>A|p.Arg431Lys |
S108 |
6 | BAA07g00840 | A07 | 583127 | G | A | missense_variant | MODERATE | c.1569G>A|p.Met523Ile |
S234 |
7 | BAA07g00840 | A07 | 583247 | C | T | synonymous_variant | LOW | c.1689C>T|p.Leu563Leu |
S232 |
8 | BAA07g00840 | A07 | 583270 | G | A | missense_variant | MODERATE | c.1712G>A|p.Gly571Glu |
S46 |
9 | BAA07g00840 | A07 | 583720 | C | T | missense_variant | MODERATE | c.2002C>T|p.Pro668Ser |
S150 |
10 | BAA07g00840 | A07 | 583900 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.2106-1G>A| |
S6 |
11 | BAA07g00840 | A07 | 584137 | C | T | missense_variant | MODERATE | c.2342C>T|p.Ser781Phe |
S239 S33 |
12 | BAA07g00840 | A07 | 586404 | C | T | downstream_gene_variant | MODIFIER | c.*1649C>T| |
S272 |