Home

Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
142951	BAA10g27780	A10	21537062	C	T	upstream_gene_variant	MODIFIER	c.-3662C>T\|	S156
142952	BAA10g27760	A10	21538012	G	A	upstream_gene_variant	MODIFIER	c.-112C>T\|	S158
142953	BAA10g27770	A10	21538321	C	T	missense_variant	MODERATE	c.1162G>A\|p.Glu388Lys	S221
142954	BAA10g27770	A10	21538550	C	T	synonymous_variant	LOW	c.933G>A\|p.Arg311Arg	S243
142955	BAA10g27770	A10	21539830	C	T	missense_variant	MODERATE	c.157G>A\|p.Glu53Lys	S40 S49
142956	BAA10g27780	A10	21540827	G	A	missense_variant	MODERATE	c.104G>A\|p.Gly35Glu	S125
142957	BAA10g27770	A10	21543110	T	G	upstream_gene_variant	MODIFIER	c.-3124A>C\|	S159 S243 S276 S298
142958	BAA10g27790	A10	21543434	G	A	missense_variant	MODERATE	c.559G>A\|p.Val187Met	S149
142959	BAA10g27800	A10	21545659	C	T	missense_variant	MODERATE	c.782C>T\|p.Ser261Phe	S68
142960	BAA10g27800	A10	21545894	C	T	synonymous_variant	LOW	c.1017C>T\|p.Leu339Leu	S114
142961	BAA10g27820	A10	21548519	G	A	upstream_gene_variant	MODIFIER	c.-2554G>A\|	S282
142962	BAA10g27820	A10	21549375	G	A	upstream_gene_variant	MODIFIER	c.-1698G>A\|	S115
142963	BAA10g27820	A10	21551112	C	T	missense_variant	MODERATE	c.40C>T\|p.Leu14Phe	S152
142964	BAA10g27830	A10	21551264	G	A	upstream_gene_variant	MODIFIER	c.-2560G>A\|	S134
142965	BAA10g27820	A10	21552040	C	T	synonymous_variant	LOW	c.456C>T\|p.Asp152Asp	S146
142966	BAA10g27820	A10	21552381	C	T	synonymous_variant	LOW	c.720C>T\|p.Asn240Asn	S104 S52 S65
142967	BAA10g27820	A10	21552528	C	T	synonymous_variant	LOW	c.867C>T\|p.Leu289Leu	S238
142968	BAA10g27820	A10	21552683	T	G	missense_variant	MODERATE	c.1022T>G\|p.Ile341Ser	S106 S117 S142 S146 S176 S202 S208 S257 S265 S268 S301 S51 S81 S84
142969	BAA10g27830	A10	21553195	C	T	upstream_gene_variant	MODIFIER	c.-629C>T\|	S204
142970	BAA10g27830	A10	21554087	C	T	synonymous_variant	LOW	c.177C>T\|p.Thr59Thr	S148 S210 S30 S31
142971	BAA10g27830	A10	21554180	C	T	synonymous_variant	LOW	c.270C>T\|p.Leu90Leu	S133
142972	BAA10g27840	A10	21554492	C	T	upstream_gene_variant	MODIFIER	c.-1902C>T\|	S12
142973	BAA10g27840	A10	21554808	C	T	upstream_gene_variant	MODIFIER	c.-1586C>T\|	S36
142974	BAA10g27840	A10	21554963	C	T	upstream_gene_variant	MODIFIER	c.-1431C>T\|	S148 S210 S30 S31
142975	BAA10g27840	A10	21556293	G	A	upstream_gene_variant	MODIFIER	c.-101G>A\|	S183 S198

Users can query the SNP information according to the gene ID.