Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g13060 | A05 | 6756937 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1114-1G>A| |
S12 |
2 | BAA05g13060 | A05 | 6757410 | C | T | missense_variant&splice_region_variant | MODERATE | c.817G>A|p.Glu273Lys |
S15 S3 |
3 | BAA05g13060 | A05 | 6757500 | G | A | synonymous_variant | LOW | c.727C>T|p.Leu243Leu |
S1 S90 |
4 | BAA05g13060 | A05 | 6758676 | C | T | missense_variant | MODERATE | c.178G>A|p.Gly60Arg |
S247 |
5 | BAA05g13060 | A05 | 6758752 | G | A | synonymous_variant | LOW | c.102C>T|p.Asn34Asn |
S150 |
6 | BAA05g13060 | A05 | 6758993 | G | A | upstream_gene_variant | MODIFIER | c.-140C>T| |
S242 |
7 | BAA05g13060 | A05 | 6760133 | G | A | upstream_gene_variant | MODIFIER | c.-1280C>T| |
S289 |
8 | BAA05g13060 | A05 | 6762863 | A | T | upstream_gene_variant | MODIFIER | c.-4010T>A| |
S81 S85 |
9 | BAA05g13060 | A05 | 6762973 | C | T | upstream_gene_variant | MODIFIER | c.-4120G>A| |
S242 |
10 | BAA05g13060 | A05 | 6762979 | C | T | upstream_gene_variant | MODIFIER | c.-4126G>A| |
S250 |