Home

Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA01g10080	A01	4556784	G	A	synonymous_variant	LOW	c.5070C>T\|p.Val1690Val	S282
2	BAA01g10080	A01	4559793	G	A	synonymous_variant	LOW	c.3555C>T\|p.Tyr1185Tyr	S268
3	BAA01g10080	A01	4559995	G	A	missense_variant	MODERATE	c.3437C>T\|p.Pro1146Leu	S197
4	BAA01g10080	A01	4561921	G	A	stop_gained	HIGH	c.2230C>T\|p.Gln744*	S104 S52
5	BAA01g10080	A01	4564464	G	A	missense_variant	MODERATE	c.467C>T\|p.Ser156Leu	S32
6	BAA01g10080	A01	4565007	G	A	intron_variant	MODIFIER	c.156+28C>T\|	S142
7	BAA01g10080	A01	4565129	A	C	missense_variant	MODERATE	c.62T>G\|p.Val21Gly	S111 S178 S183 S193 S280 S34 S43 S61
8	BAA01g10080	A01	4566938	C	T	upstream_gene_variant	MODIFIER	c.-1748G>A\|	S287
9	BAA01g10080	A01	4567001	C	T	upstream_gene_variant	MODIFIER	c.-1811G>A\|	S200
10	BAA01g10080	A01	4567488	C	T	upstream_gene_variant	MODIFIER	c.-2298G>A\|	S113
11	BAA01g10080	A01	4567591	C	T	upstream_gene_variant	MODIFIER	c.-2401G>A\|	S130