Home

Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA05g42350	A05	40173937	G	A	synonymous_variant	LOW	c.3183C>T\|p.Ile1061Ile	S198
2	BAA05g42350	A05	40174147	G	A	synonymous_variant	LOW	c.2973C>T\|p.Leu991Leu	S249
3	BAA05g42350	A05	40174424	C	T	missense_variant	MODERATE	c.2696G>A\|p.Cys899Tyr	S161
4	BAA05g42350	A05	40174557	C	T	missense_variant	MODERATE	c.2563G>A\|p.Glu855Lys	S136
5	BAA05g42350	A05	40174605	G	A	missense_variant	MODERATE	c.2515C>T\|p.Leu839Phe	S92
6	BAA05g42350	A05	40175480	C	T	synonymous_variant	LOW	c.1728G>A\|p.Lys576Lys	S280
7	BAA05g42350	A05	40175526	C	T	missense_variant	MODERATE	c.1682G>A\|p.Arg561Gln	S150
8	BAA05g42350	A05	40176571	C	T	synonymous_variant	LOW	c.717G>A\|p.Glu239Glu	S151 S153 S157 S166 S257 S263
9	BAA05g42350	A05	40179331	A	G	upstream_gene_variant	MODIFIER	c.-1778T>C\|	S62
10	BAA05g42350	A05	40179372	G	A	upstream_gene_variant	MODIFIER	c.-1819C>T\|	S71
11	BAA05g42350	A05	40180963	G	T	upstream_gene_variant	MODIFIER	c.-3410C>A\|	S189 S197 S205 S23 S256 S263 S284 S304 S38 S66 S72
12	BAA05g42350	A05	40181206	C	T	upstream_gene_variant	MODIFIER	c.-3653G>A\|	S162