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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA10g33230	A10	23685500	C	T	missense_variant	MODERATE	c.4795G>A\|p.Asp1599Asn	S125
2	BAA10g33230	A10	23685548	C	T	missense_variant	MODERATE	c.4747G>A\|p.Glu1583Lys	S48
3	BAA10g33230	A10	23685995	C	T	splice_region_variant&intron_variant	LOW	c.4538+3G>A\|	S13 S219 S279 S72
4	BAA10g33230	A10	23686339	G	A	synonymous_variant	LOW	c.4287C>T\|p.Asp1429Asp	S298
5	BAA10g33230	A10	23687536	C	T	missense_variant	MODERATE	c.3542G>A\|p.Gly1181Glu	S204
6	BAA10g33230	A10	23687557	G	A	missense_variant	MODERATE	c.3521C>T\|p.Ala1174Val	S298
7	BAA10g33230	A10	23688070	C	T	missense_variant	MODERATE	c.3175G>A\|p.Asp1059Asn	S187
8	BAA10g33230	A10	23688095	G	A	synonymous_variant	LOW	c.3150C>T\|p.Val1050Val	S178
9	BAA10g33230	A10	23688480	C	T	missense_variant	MODERATE	c.2903G>A\|p.Arg968Lys	S36
10	BAA10g33230	A10	23689028	G	A	missense_variant	MODERATE	c.2594C>T\|p.Thr865Ile	S179
11	BAA10g33230	A10	23690705	G	A	missense_variant	MODERATE	c.1439C>T\|p.Pro480Leu	S125
12	BAA10g33230	A10	23691979	C	T	missense_variant	MODERATE	c.803G>A\|p.Gly268Glu	S11
13	BAA10g33230	A10	23692916	G	A	missense_variant	MODERATE	c.161C>T\|p.Ser54Phe	S132 S137 S138 S215 S89
14	BAA10g33230	A10	23693011	G	A	synonymous_variant	LOW	c.66C>T\|p.Leu22Leu	S130
15	BAA10g33230	A10	23693712	C	T	upstream_gene_variant	MODIFIER	c.-636G>A\|	S148 S210 S30 S31
16	BAA10g33230	A10	23695627	C	T	upstream_gene_variant	MODIFIER	c.-2551G>A\|	S92
17	BAA10g33230	A10	23696862	G	A	upstream_gene_variant	MODIFIER	c.-3786C>T\|	S172 S217
18	BAA10g33230	A10	23697122	G	A	upstream_gene_variant	MODIFIER	c.-4046C>T\|	S94
19	BAA10g33230	A10	23697491	G	A	upstream_gene_variant	MODIFIER	c.-4415C>T\|	S262

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