Home

Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
143851	BAA10g28580	A10	21857068	C	T	upstream_gene_variant	MODIFIER	c.-3826G>A\|	S272
143852	BAA10g28600	A10	21857687	C	T	missense_variant	MODERATE	c.1463C>T\|p.Thr488Ile	S296
143853	BAA10g28610	A10	21859581	G	A	splice_region_variant&intron_variant	LOW	c.242+8C>T\|	S263 S81 S85
143854	BAA10g28610	A10	21860117	G	A	missense_variant	MODERATE	c.5C>T\|p.Ser2Phe	S35
143855	BAA10g28620	A10	21860976	C	T	synonymous_variant	LOW	c.186C>T\|p.Gly62Gly	S123
143856	BAA10g28610	A10	21861006	G	A	upstream_gene_variant	MODIFIER	c.-885C>T\|	S270
143857	BAA10g28620	A10	21861966	C	T	synonymous_variant	LOW	c.690C>T\|p.Tyr230Tyr	S48
143858	BAA10g28620	A10	21862477	G	A	synonymous_variant	LOW	c.1017G>A\|p.Leu339Leu	S57
143859	BAA10g28610	A10	21862694	C	T	upstream_gene_variant	MODIFIER	c.-2573G>A\|	S168
143860	BAA10g28610	A10	21863112	C	T	upstream_gene_variant	MODIFIER	c.-2991G>A\|	S8
143861	BAA10g28630	A10	21864243	G	A	missense_variant	MODERATE	c.527G>A\|p.Arg176Lys	S109
143862	BAA10g28630	A10	21865913	G	A	missense_variant	MODERATE	c.1195G>A\|p.Ala399Thr	S199
143863	BAA10g28630	A10	21866037	G	A	missense_variant	MODERATE	c.1238G>A\|p.Gly413Glu	S250
143864	BAA10g28640	A10	21867666	C	T	synonymous_variant	LOW	c.216G>A\|p.Glu72Glu	S152
143865	BAA10g28650	A10	21875306	G	A	upstream_gene_variant	MODIFIER	c.-1918C>T\|	S216
143866	BAA10g28650	A10	21875364	C	T	upstream_gene_variant	MODIFIER	c.-1976G>A\|	S168
143867	BAA10g28650	A10	21875961	C	T	upstream_gene_variant	MODIFIER	c.-2573G>A\|	S296
143868	BAA10g28650	A10	21876652	G	A	upstream_gene_variant	MODIFIER	c.-3264C>T\|	S240
143869	BAA10g28660	A10	21876777	C	T	missense_variant	MODERATE	c.100C>T\|p.His34Tyr	S148 S210 S30 S31
143870	BAA10g28660	A10	21876829	C	T	missense_variant	MODERATE	c.152C>T\|p.Ser51Phe	S155
143871	BAA10g28660	A10	21876920	G	A	synonymous_variant	LOW	c.243G>A\|p.Glu81Glu	S236
143872	BAA10g28660	A10	21877163	G	A	synonymous_variant	LOW	c.414G>A\|p.Gln138Gln	S15 S156 S3 S34 S4 S6
143873	BAA10g28660	A10	21877488	C	T	missense_variant	MODERATE	c.605C>T\|p.Pro202Leu	S123 S210 S225
143874	BAA10g28660	A10	21877688	C	T	missense_variant	MODERATE	c.730C>T\|p.Pro244Ser	S206 S26
143875	BAA10g28660	A10	21881012	G	A	downstream_gene_variant	MODIFIER	c.*2868G>A\|	S259

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