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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA05g33050	A05	34938685	G	A	synonymous_variant	LOW	c.837C>T\|p.Phe279Phe	S279
2	BAA05g33050	A05	34940091	G	A	missense_variant	MODERATE	c.251C>T\|p.Pro84Leu	S13
3	BAA05g33050	A05	34940123	A	G	synonymous_variant	LOW	c.219T>C\|p.Pro73Pro	S147 S91
4	BAA05g33050	A05	34940128	C	A	missense_variant	MODERATE	c.214G>T\|p.Asp72Tyr	S147 S267 S91
5	BAA05g33050	A05	34940132	A	G	synonymous_variant	LOW	c.210T>C\|p.Leu70Leu	S147 S267 S91
6	BAA05g33050	A05	34940133	A	C	missense_variant	MODERATE	c.209T>G\|p.Leu70Arg	S147 S267 S91
7	BAA05g33050	A05	34940141	G	T	synonymous_variant	LOW	c.201C>A\|p.Gly67Gly	S147 S267 S91
8	BAA05g33050	A05	34940144	A	G	synonymous_variant	LOW	c.198T>C\|p.Tyr66Tyr	S147 S267 S91
9	BAA05g33050	A05	34940147	A	G	synonymous_variant	LOW	c.195T>C\|p.Pro65Pro	S147 S267 S91
10	BAA05g33050	A05	34940153	T	A	missense_variant	MODERATE	c.189A>T\|p.Gln63His	S147 S267 S91
11	BAA05g33050	A05	34940155	G	A	stop_gained	HIGH	c.187C>T\|p.Gln63*	S147 S267 S91
12	BAA05g33050	A05	34940166	G	A	missense_variant	MODERATE	c.176C>T\|p.Pro59Leu	S147 S267 S91
13	BAA05g33050	A05	34940170	T	C	missense_variant	MODERATE	c.172A>G\|p.Asn58Asp	S147 S267 S91
14	BAA05g33050	A05	34940175	T	C	missense_variant	MODERATE	c.167A>G\|p.Lys56Arg	S147 S267 S91
15	BAA05g33050	A05	34940179	T	G	missense_variant	MODERATE	c.163A>C\|p.Lys55Gln	S147 S267 S91
16	BAA05g33050	A05	34940183	T	G	synonymous_variant	LOW	c.159A>C\|p.Leu53Leu	S147 S267 S91
17	BAA05g33050	A05	34940190	G	A	missense_variant	MODERATE	c.152C>T\|p.Ala51Val	S147 S267 S91
18	BAA05g33050	A05	34940210	A	G	synonymous_variant	LOW	c.132T>C\|p.Tyr44Tyr	S147 S267 S91
19	BAA05g33050	A05	34944783	C	T	upstream_gene_variant	MODIFIER	c.-4442G>A\|	S112

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