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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA06g38120	A06	25001103	G	A	downstream_gene_variant	MODIFIER	c.*3738C>T\|	S229
2	BAA06g38120	A06	25005631	G	A	missense_variant	MODERATE	c.5489C>T\|p.Ala1830Val	S98
3	BAA06g38120	A06	25006190	G	A	synonymous_variant	LOW	c.4930C>T\|p.Leu1644Leu	S59
4	BAA06g38120	A06	25006724	C	T	missense_variant	MODERATE	c.4396G>A\|p.Gly1466Arg	S161
5	BAA06g38120	A06	25007170	C	T	synonymous_variant	LOW	c.4026G>A\|p.Leu1342Leu	S279
6	BAA06g38120	A06	25009270	T	C	synonymous_variant	LOW	c.2091A>G\|p.Ser697Ser	S151 S157 S166 S167 S257
7	BAA06g38120	A06	25009276	C	T	missense_variant	MODERATE	c.2085G>A\|p.Met695Ile	S69
8	BAA06g38120	A06	25009282	C	T	synonymous_variant	LOW	c.2079G>A\|p.Leu693Leu	S69
9	BAA06g38120	A06	25010046	C	T	missense_variant	MODERATE	c.1315G>A\|p.Glu439Lys	S174 S216 S241 S27
10	BAA06g38120	A06	25010553	C	T	missense_variant	MODERATE	c.808G>A\|p.Val270Ile	S128
11	BAA06g38120	A06	25010694	C	T	missense_variant	MODERATE	c.667G>A\|p.Gly223Arg	S274
12	BAA06g38120	A06	25010697	C	T	missense_variant	MODERATE	c.664G>A\|p.Val222Ile	S97
13	BAA06g38120	A06	25011281	G	A	missense_variant	MODERATE	c.80C>T\|p.Thr27Ile	S246
14	BAA06g38120	A06	25011298	G	A	synonymous_variant	LOW	c.63C>T\|p.Phe21Phe	S84 S93
15	BAA06g38120	A06	25011878	G	A	upstream_gene_variant	MODIFIER	c.-518C>T\|	S244 S289 S290
16	BAA06g38120	A06	25013332	G	A	upstream_gene_variant	MODIFIER	c.-1972C>T\|	S210 S225
17	BAA06g38120	A06	25013391	G	A	upstream_gene_variant	MODIFIER	c.-2031C>T\|	S59
18	BAA06g38120	A06	25013556	G	A	upstream_gene_variant	MODIFIER	c.-2196C>T\|	S152
19	BAA06g38120	A06	25014363	C	T	upstream_gene_variant	MODIFIER	c.-3003G>A\|	S108
20	BAA06g38120	A06	25015554	G	A	upstream_gene_variant	MODIFIER	c.-4194C>T\|	S32
21	BAA06g38120	A06	25016083	C	T	upstream_gene_variant	MODIFIER	c.-4723G>A\|	S109
22	BAA06g38120	A06	25016347	C	T	upstream_gene_variant	MODIFIER	c.-4987G>A\|	S252

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