Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g21020 | A01 | 10341126 | G | A | upstream_gene_variant | MODIFIER | c.-3196G>A| |
S306 S308 |
2 | BAA01g21020 | A01 | 10344470 | C | T | missense_variant | MODERATE | c.149C>T|p.Ser50Phe |
S82 S92 |
3 | BAA01g21020 | A01 | 10344511 | C | T | stop_gained | HIGH | c.190C>T|p.Arg64* |
S36 |
4 | BAA01g21020 | A01 | 10344521 | C | T | missense_variant | MODERATE | c.200C>T|p.Pro67Leu |
S142 |
5 | BAA01g21020 | A01 | 10345068 | G | A | missense_variant | MODERATE | c.565G>A|p.Gly189Ser |
S175 S177 |
6 | BAA01g21020 | A01 | 10345380 | G | A | missense_variant | MODERATE | c.877G>A|p.Glu293Lys |
S202 |
7 | BAA01g21020 | A01 | 10347034 | G | A | missense_variant | MODERATE | c.1772G>A|p.Ser591Asn |
S251 |
8 | BAA01g21020 | A01 | 10347464 | G | A | missense_variant&splice_region_variant | MODERATE | c.2120G>A|p.Gly707Glu |
S180 |
9 | BAA01g21020 | A01 | 10348621 | G | A | missense_variant | MODERATE | c.2659G>A|p.Ala887Thr |
S5 |