Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19860 | A02 | 10438880 | G | A | intron_variant | MODIFIER | c.2194+98C>T| |
S59 |
2 | BAA02g19860 | A02 | 10439305 | C | T | missense_variant | MODERATE | c.1867G>A|p.Gly623Ser |
S171 |
3 | BAA02g19860 | A02 | 10439324 | G | A | synonymous_variant | LOW | c.1848C>T|p.Asn616Asn |
S296 |
4 | BAA02g19860 | A02 | 10440366 | G | A | intron_variant | MODIFIER | c.1690+19C>T| |
S11 |
5 | BAA02g19860 | A02 | 10440412 | C | T | missense_variant | MODERATE | c.1663G>A|p.Val555Ile |
S124 |
6 | BAA02g19860 | A02 | 10441592 | T | A | intron_variant | MODIFIER | c.755-92A>T| |
S172 S217 |
7 | BAA02g19860 | A02 | 10445299 | G | A | upstream_gene_variant | MODIFIER | c.-894C>T| |
S298 |
8 | BAA02g19860 | A02 | 10446008 | C | T | upstream_gene_variant | MODIFIER | c.-1603G>A| |
S262 |
9 | BAA02g19860 | A02 | 10448443 | G | A | upstream_gene_variant | MODIFIER | c.-4038C>T| |
S238 |
10 | BAA02g19860 | A02 | 10448567 | G | A | upstream_gene_variant | MODIFIER | c.-4162C>T| |
S189 S226 S250 S41 |
11 | BAA02g19860 | A02 | 10448625 | G | A | upstream_gene_variant | MODIFIER | c.-4220C>T| |
S303 |