Home

Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
97951	BAA10g05710	A10	2922145	G	A	synonymous_variant	LOW	c.3003C>T\|p.Phe1001Phe	S105 S106
97952	BAA10g05710	A10	2922664	C	T	synonymous_variant	LOW	c.2568G>A\|p.Lys856Lys	S119
97953	BAA10g05710	A10	2922825	C	T	missense_variant	MODERATE	c.2407G>A\|p.Glu803Lys	S260
97954	BAA10g05710	A10	2923082	G	A	missense_variant	MODERATE	c.2150C>T\|p.Thr717Ile	S198
97955	BAA10g05710	A10	2924683	A	G	synonymous_variant	LOW	c.1245T>C\|p.Tyr415Tyr	S159 S243 S81
97956	BAA10g05710	A10	2924831	G	A	missense_variant	MODERATE	c.1166C>T\|p.Ala389Val	S157 S163
97957	BAA10g05700	A10	2925233	G	A	downstream_gene_variant	MODIFIER	c.*3966G>A\|	S242
97958	BAA10g05710	A10	2925713	G	A	splice_region_variant&intron_variant	LOW	c.840+6C>T\|	S136
97959	BAA10g05710	A10	2927391	C	T	upstream_gene_variant	MODIFIER	c.-491G>A\|	S70
97960	BAA10g05710	A10	2927394	G	A	upstream_gene_variant	MODIFIER	c.-494C>T\|	S242
97961	BAA10g05710	A10	2929781	G	A	upstream_gene_variant	MODIFIER	c.-2881C>T\|	S100
97962	BAA10g05720	A10	2937497	G	A	upstream_gene_variant	MODIFIER	c.-533C>T\|	S284
97963	BAA10g05720	A10	2938019	C	T	upstream_gene_variant	MODIFIER	c.-1055G>A\|	S294
97964	BAA10g05720	A10	2938667	G	A	upstream_gene_variant	MODIFIER	c.-1703C>T\|	S140
97965	BAA10g05720	A10	2939194	G	A	upstream_gene_variant	MODIFIER	c.-2230C>T\|	S303
97966	BAA10g05720	A10	2939450	C	T	upstream_gene_variant	MODIFIER	c.-2486G>A\|	S84 S93
97967	BAA10g05720	A10	2941339	C	T	upstream_gene_variant	MODIFIER	c.-4375G>A\|	S273
97968	BAA10g05720	A10	2941482	G	A	upstream_gene_variant	MODIFIER	c.-4518C>T\|	S198
97969	BAA10g05720	A10	2941920	C	T	upstream_gene_variant	MODIFIER	c.-4956G>A\|	S73 S91
97970	BAA10g05730	A10	2943050	A	G	upstream_gene_variant	MODIFIER	c.-767A>G\|	S169 S173 S225 S73
97971	BAA10g05730	A10	2943499	G	A	upstream_gene_variant	MODIFIER	c.-318G>A\|	S136
97972	BAA10g05730	A10	2943828	C	T	synonymous_variant	LOW	c.12C>T\|p.Pro4Pro	S89
97973	BAA10g05730	A10	2944115	C	T	missense_variant	MODERATE	c.299C>T\|p.Pro100Leu	S249
97974	BAA10g05730	A10	2944495	G	A	missense_variant	MODERATE	c.679G>A\|p.Val227Ile	S289
97975	BAA10g05730	A10	2944669	G	A	missense_variant	MODERATE	c.853G>A\|p.Asp285Asn	S207 S262

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