Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g01900 | A07 | 1395899 | C | T | missense_variant | MODERATE | c.34C>T|p.Pro12Ser |
S38 |
2 | BAA07g01900 | A07 | 1396427 | G | A | synonymous_variant | LOW | c.378G>A|p.Glu126Glu |
S190 |
3 | BAA07g01900 | A07 | 1397870 | C | T | synonymous_variant | LOW | c.1299C>T|p.Ser433Ser |
S94 |
4 | BAA07g01900 | A07 | 1399457 | C | T | synonymous_variant | LOW | c.2328C>T|p.Asn776Asn |
S19 |
5 | BAA07g01900 | A07 | 1400772 | C | T | downstream_gene_variant | MODIFIER | c.*1240C>T| |
S38 |
6 | BAA07g01900 | A07 | 1401241 | G | A | downstream_gene_variant | MODIFIER | c.*1709G>A| |
S33 |
7 | BAA07g01900 | A07 | 1403447 | T | C | downstream_gene_variant | MODIFIER | c.*3915T>C| |
S200 |
8 | BAA07g01900 | A07 | 1404024 | G | A | downstream_gene_variant | MODIFIER | c.*4492G>A| |
S132 |