Home

Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
147751	BAA10g32160	A10	23211933	G	A	missense_variant	MODERATE	c.1235G>A\|p.Arg412Lys	S308
147752	BAA10g32170	A10	23215034	G	A	upstream_gene_variant	MODIFIER	c.-519C>T\|	S223
147753	BAA10g32170	A10	23215785	C	T	upstream_gene_variant	MODIFIER	c.-1270G>A\|	S63
147754	BAA10g32190	A10	23216247	C	T	missense_variant	MODERATE	c.2365G>A\|p.Asp789Asn	S211 S227
147755	BAA10g32190	A10	23216956	C	T	synonymous_variant	LOW	c.1824G>A\|p.Glu608Glu	S282
147756	BAA10g32170	A10	23217150	G	A	upstream_gene_variant	MODIFIER	c.-2635C>T\|	S7
147757	BAA10g32170	A10	23217568	G	A	upstream_gene_variant	MODIFIER	c.-3053C>T\|	S178
147758	BAA10g32170	A10	23218589	C	T	upstream_gene_variant	MODIFIER	c.-4074G>A\|	S123
147759	BAA10g32170	A10	23219174	G	A	upstream_gene_variant	MODIFIER	c.-4659C>T\|	S183 S198
147760	BAA10g32190	A10	23219498	C	T	synonymous_variant	LOW	c.711G>A\|p.Lys237Lys	S155 S211
147761	BAA10g32180	A10	23220289	C	T	upstream_gene_variant	MODIFIER	c.-4704G>A\|	S204
147762	BAA10g32190	A10	23220348	C	T	missense_variant	MODERATE	c.256G>A\|p.Glu86Lys	S221
147763	BAA10g32200	A10	23221202	C	T	synonymous_variant	LOW	c.9C>T\|p.Val3Val	S72 S78
147764	BAA10g32200	A10	23222949	G	A	missense_variant&splice_region_variant	MODERATE	c.1141G>A\|p.Gly381Ser	S226
147765	BAA10g32200	A10	23223187	C	T	synonymous_variant	LOW	c.1293C>T\|p.Asp431Asp	S296
147766	BAA10g32190	A10	23223274	C	T	upstream_gene_variant	MODIFIER	c.-2587G>A\|	S190
147767	BAA10g32190	A10	23223856	C	T	upstream_gene_variant	MODIFIER	c.-3169G>A\|	S115
147768	BAA10g32210	A10	23224083	C	T	missense_variant	MODERATE	c.1639G>A\|p.Glu547Lys	S82 S92
147769	BAA10g32210	A10	23225294	C	T	missense_variant	MODERATE	c.428G>A\|p.Arg143Lys	S174 S216 S241 S27
147770	BAA10g32210	A10	23225820	C	T	synonymous_variant	LOW	c.57G>A\|p.Lys19Lys	S302
147771	BAA10g32210	A10	23225843	C	T	missense_variant	MODERATE	c.34G>A\|p.Val12Met	S116
147772	BAA10g32210	A10	23226084	G	A	upstream_gene_variant	MODIFIER	c.-208C>T\|	S35
147773	BAA10g32210	A10	23227854	C	T	upstream_gene_variant	MODIFIER	c.-1978G>A\|	S123
147774	BAA10g32210	A10	23229812	C	T	upstream_gene_variant	MODIFIER	c.-3936G>A\|	S266
147775	BAA10g32230	A10	23230166	C	T	missense_variant	MODERATE	c.1600G>A\|p.Asp534Asn	S78

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