Home

Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
92151	BAA10g01960	A10	941865	G	A	missense_variant	MODERATE	c.1270G>A\|p.Glu424Lys	S273
92152	BAA10g01960	A10	942023	G	A	missense_variant	MODERATE	c.1327G>A\|p.Ala443Thr	S18
92153	BAA10g01960	A10	942223	G	A	missense_variant	MODERATE	c.1396G>A\|p.Val466Ile	S172 S217
92154	BAA10g01970	A10	943077	G	A	upstream_gene_variant	MODIFIER	c.-238G>A\|	S289
92155	BAA10g01970	A10	943803	C	T	missense_variant	MODERATE	c.206C>T\|p.Ala69Val	S294
92156	BAA10g01970	A10	944495	G	A	missense_variant	MODERATE	c.604G>A\|p.Val202Met	S112
92157	BAA10g01980	A10	944682	C	T	upstream_gene_variant	MODIFIER	c.-2249C>T\|	S63
92158	BAA10g01980	A10	944887	G	A	upstream_gene_variant	MODIFIER	c.-2044G>A\|	S211 S227
92159	BAA10g01970	A10	944998	C	T	synonymous_variant	LOW	c.765C>T\|p.Asp255Asp	S165
92160	BAA10g01970	A10	945318	G	A	synonymous_variant	LOW	c.906G>A\|p.Glu302Glu	S208 S219
92161	BAA10g01970	A10	945692	C	T	synonymous_variant	LOW	c.1153C>T\|p.Leu385Leu	S123
92162	BAA10g01970	A10	945854	G	A	missense_variant	MODERATE	c.1315G>A\|p.Ala439Thr	S80
92163	BAA10g01980	A10	947227	G	A	missense_variant&splice_region_variant	MODERATE	c.205G>A\|p.Val69Ile	S172 S217
92164	BAA10g01960	A10	947266	G	A	downstream_gene_variant	MODIFIER	c.*4945G>A\|	S43
92165	BAA10g01980	A10	947437	C	T	missense_variant	MODERATE	c.305C>T\|p.Ser102Leu	S221
92166	BAA10g01980	A10	947612	G	A	synonymous_variant	LOW	c.480G>A\|p.Lys160Lys	S280
92167	BAA10g01980	A10	947714	C	T	synonymous_variant	LOW	c.582C>T\|p.Val194Val	S12
92168	BAA10g01980	A10	947746	G	A	missense_variant	MODERATE	c.614G>A\|p.Gly205Asp	S237
92169	BAA10g01980	A10	947923	C	T	missense_variant	MODERATE	c.791C>T\|p.Ser264Leu	S25
92170	BAA10g01980	A10	948663	C	T	missense_variant	MODERATE	c.1304C>T\|p.Ser435Phe	S281
92171	BAA10g01970	A10	948736	C	T	downstream_gene_variant	MODIFIER	c.*2675C>T\|	S247
92172	BAA10g01980	A10	948766	G	A	missense_variant	MODERATE	c.1327G>A\|p.Asp443Asn	S83 S88
92173	BAA10g01970	A10	949543	G	A	downstream_gene_variant	MODIFIER	c.*3482G>A\|	S32
92174	BAA10g01970	A10	949555	G	A	downstream_gene_variant	MODIFIER	c.*3494G>A\|	S167
92175	BAA10g01970	A10	950831	G	T	downstream_gene_variant	MODIFIER	c.*4770G>T\|	S107 S142 S166 S168

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