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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA02g00180	A02	125738	A	T	synonymous_variant	LOW	c.783T>A\|p.Thr261Thr	S201 S213 S267
2	BAA02g00180	A02	125741	A	T	synonymous_variant	LOW	c.780T>A\|p.Ala260Ala	S201 S213 S267
3	BAA02g00180	A02	125747	G	C	synonymous_variant	LOW	c.774C>G\|p.Ala258Ala	S201 S213 S267
4	BAA02g00180	A02	125756	A	C	synonymous_variant	LOW	c.765T>G\|p.Ala255Ala	S201 S213 S267
5	BAA02g00180	A02	125780	G	C	synonymous_variant	LOW	c.741C>G\|p.Ala247Ala	S201 S213 S267
6	BAA02g00180	A02	125789	A	T	synonymous_variant	LOW	c.732T>A\|p.Ala244Ala	S201 S213 S267
7	BAA02g00180	A02	125792	G	A	synonymous_variant	LOW	c.729C>T\|p.His243His	S201 S213 S267
8	BAA02g00180	A02	125816	C	T	synonymous_variant	LOW	c.705G>A\|p.Gln235Gln	S201 S213 S267
9	BAA02g00180	A02	125822	C	A	missense_variant	MODERATE	c.699G>T\|p.Met233Ile	S201 S213 S267
10	BAA02g00180	A02	125823	A	G	missense_variant	MODERATE	c.698T>C\|p.Met233Thr	S201 S213 S267
11	BAA02g00180	A02	125831	A	C	synonymous_variant	LOW	c.690T>G\|p.Pro230Pro	S201 S213 S267
12	BAA02g00180	A02	125839	A	C	missense_variant	MODERATE	c.682T>G\|p.Ser228Ala	S201 S213 S267
13	BAA02g00180	A02	125849	A	T	synonymous_variant	LOW	c.672T>A\|p.Leu224Leu	S201 S213 S267
14	BAA02g00180	A02	125858	G	A	synonymous_variant	LOW	c.663C>T\|p.Phe221Phe	S201 S213 S267
15	BAA02g00180	A02	125864	T	C	synonymous_variant	LOW	c.657A>G\|p.Lys219Lys	S147 S201 S213 S267
16	BAA02g00180	A02	125870	G	T	synonymous_variant	LOW	c.651C>A\|p.Gly217Gly	S147 S201 S213 S267
17	BAA02g00180	A02	125873	A	G	synonymous_variant	LOW	c.648T>C\|p.Pro216Pro	S147 S201 S213 S267
18	BAA02g00180	A02	125879	C	T	synonymous_variant	LOW	c.642G>A\|p.Leu214Leu	S147 S201 S213 S267
19	BAA02g00180	A02	125891	A	C	synonymous_variant	LOW	c.630T>G\|p.Ser210Ser	S147 S201 S213 S267
20	BAA02g00180	A02	125894	G	A	synonymous_variant	LOW	c.627C>T\|p.Asp209Asp	S147 S201 S213 S267
21	BAA02g00180	A02	125903	A	G	synonymous_variant	LOW	c.618T>C\|p.Ala206Ala	S147 S201 S213 S267
22	BAA02g00180	A02	125957	C	T	synonymous_variant	LOW	c.564G>A\|p.Thr188Thr	S201 S226 S239 S267 S91
23	BAA02g00180	A02	125966	G	C	synonymous_variant	LOW	c.555C>G\|p.Ser185Ser	S201 S226 S239 S267 S91
24	BAA02g00180	A02	125972	G	A	synonymous_variant	LOW	c.549C>T\|p.Pro183Pro	S201 S226 S239 S267 S91
25	BAA02g00180	A02	125977	G	A	synonymous_variant	LOW	c.544C>T\|p.Leu182Leu	S201 S226 S239 S267 S91

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