Home

Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
29301	BAA01g20640	A01	10196756	G	A	splice_region_variant&intron_variant	LOW	c.1751+4C>T\|	S173
29302	BAA01g20640	A01	10196892	G	A	missense_variant	MODERATE	c.1619C>T\|p.Pro540Leu	S245
29303	BAA01g20640	A01	10197169	C	T	synonymous_variant	LOW	c.1422G>A\|p.Lys474Lys	S10
29304	BAA01g20640	A01	10197425	C	T	missense_variant	MODERATE	c.1288G>A\|p.Val430Ile	S54
29305	BAA01g20640	A01	10197461	C	T	missense_variant	MODERATE	c.1252G>A\|p.Glu418Lys	S82 S92
29306	BAA01g20650	A01	10199510	G	A	upstream_gene_variant	MODIFIER	c.-2937G>A\|	S194
29307	BAA01g20640	A01	10200075	G	A	upstream_gene_variant	MODIFIER	c.-331C>T\|	S291
29308	BAA01g20640	A01	10201932	C	T	upstream_gene_variant	MODIFIER	c.-2188G>A\|	S295
29309	BAA01g20640	A01	10202223	C	T	upstream_gene_variant	MODIFIER	c.-2479G>A\|	S112
29310	BAA01g20650	A01	10202761	G	A	synonymous_variant	LOW	c.243G>A\|p.Glu81Glu	S60
29311	BAA01g20640	A01	10204472	G	A	upstream_gene_variant	MODIFIER	c.-4728C>T\|	S8
29312	BAA01g20650	A01	10204752	C	T	downstream_gene_variant	MODIFIER	c.*658C>T\|	S286
29313	BAA01g20660	A01	10207654	C	T	upstream_gene_variant	MODIFIER	c.-1449G>A\|	S168
29314	BAA01g20660	A01	10208305	G	A	upstream_gene_variant	MODIFIER	c.-2100C>T\|	S97
29315	BAA01g20660	A01	10208957	C	T	upstream_gene_variant	MODIFIER	c.-2752G>A\|	S143 S62
29316	BAA01g20660	A01	10209322	C	T	upstream_gene_variant	MODIFIER	c.-3117G>A\|	S20
29317	BAA01g20670	A01	10211250	G	A	synonymous_variant	LOW	c.234C>T\|p.Ser78Ser	S183
29318	BAA01g20670	A01	10212587	G	T	upstream_gene_variant	MODIFIER	c.-1104C>A\|	S73
29319	BAA01g20680	A01	10215791	C	T	synonymous_variant	LOW	c.219C>T\|p.Leu73Leu	S139
29320	BAA01g20680	A01	10217506	G	A	missense_variant	MODERATE	c.699G>A\|p.Met233Ile	S138
29321	BAA01g20680	A01	10217657	G	A	missense_variant	MODERATE	c.850G>A\|p.Asp284Asn	S249
29322	BAA01g20680	A01	10217829	G	A	missense_variant	MODERATE	c.1022G>A\|p.Gly341Glu	S132 S137 S138 S215 S288 S89
29323	BAA01g20680	A01	10218167	G	A	missense_variant	MODERATE	c.1360G>A\|p.Asp454Asn	S15 S3
29324	BAA01g20680	A01	10218766	C	T	missense_variant	MODERATE	c.1858C>T\|p.Leu620Phe	S286
29325	BAA01g20680	A01	10218843	G	A	synonymous_variant	LOW	c.1935G>A\|p.Lys645Lys	S240

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