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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA09g10240	A09	5635501	C	T	missense_variant	MODERATE	c.791G>A\|p.Arg264Lys	S68
2	BAA09g10240	A09	5635669	C	T	missense_variant	MODERATE	c.623G>A\|p.Arg208His	S302
3	BAA09g10240	A09	5636606	A	C	synonymous_variant	LOW	c.132T>G\|p.Ser44Ser	S213 S226 S267 S91
4	BAA09g10240	A09	5636618	T	G	synonymous_variant	LOW	c.120A>C\|p.Leu40Leu	S213 S226 S267 S91
5	BAA09g10240	A09	5636624	G	A	synonymous_variant	LOW	c.114C>T\|p.Phe38Phe	S213 S226 S267 S91
6	BAA09g10240	A09	5636627	T	A	synonymous_variant	LOW	c.111A>T\|p.Ser37Ser	S213 S226 S267 S91
7	BAA09g10240	A09	5636636	A	G	synonymous_variant	LOW	c.102T>C\|p.Val34Val	S213 S226 S267 S91
8	BAA09g10240	A09	5636641	T	C	missense_variant	MODERATE	c.97A>G\|p.Thr33Ala	S213 S226 S267 S91
9	BAA09g10240	A09	5636642	C	T	synonymous_variant	LOW	c.96G>A\|p.Gln32Gln	S213 S226 S267 S91
10	BAA09g10240	A09	5636651	C	T	synonymous_variant	LOW	c.87G>A\|p.Arg29Arg	S213 S226 S267 S91
11	BAA09g10240	A09	5636662	C	A	missense_variant	MODERATE	c.76G>T\|p.Ala26Ser	S213 S226 S267 S91
12	BAA09g10240	A09	5636666	C	T	synonymous_variant	LOW	c.72G>A\|p.Gly24Gly	S213 S226 S267 S91
13	BAA09g10240	A09	5636669	A	G	synonymous_variant	LOW	c.69T>C\|p.Arg23Arg	S213 S226 S267 S91
14	BAA09g10240	A09	5636686	A	C	missense_variant	MODERATE	c.52T>G\|p.Ser18Ala	S213 S226 S267
15	BAA09g10240	A09	5636711	G	A	synonymous_variant	LOW	c.27C>T\|p.Thr9Thr	S213 S226 S267 S91
16	BAA09g10240	A09	5636713	T	C	missense_variant	MODERATE	c.25A>G\|p.Thr9Ala	S213 S226 S267 S91
17	BAA09g10240	A09	5636716	C	T	missense_variant	MODERATE	c.22G>A\|p.Ala8Thr	S213 S226 S267
18	BAA09g10240	A09	5639995	C	T	upstream_gene_variant	MODIFIER	c.-3258G>A\|	S230
19	BAA09g10240	A09	5640313	G	A	upstream_gene_variant	MODIFIER	c.-3576C>T\|	S201
20	BAA09g10240	A09	5640373	G	A	upstream_gene_variant	MODIFIER	c.-3636C>T\|	S79 S84

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