Home

Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA04g02020	A04	1173332	C	T	downstream_gene_variant	MODIFIER	c.*919G>A\|	S260
2	BAA04g02020	A04	1173708	C	T	downstream_gene_variant	MODIFIER	c.*543G>A\|	S7
3	BAA04g02020	A04	1173949	C	T	downstream_gene_variant	MODIFIER	c.*302G>A\|	S157 S163
4	BAA04g02020	A04	1174055	C	T	downstream_gene_variant	MODIFIER	c.*196G>A\|	S252
5	BAA04g02020	A04	1174436	G	A	synonymous_variant	LOW	c.1740C>T\|p.Cys580Cys	S272
6	BAA04g02020	A04	1174554	G	A	intron_variant	MODIFIER	c.1694+15C>T\|	S204
7	BAA04g02020	A04	1174873	G	A	missense_variant	MODERATE	c.1558C>T\|p.Leu520Phe	S151
8	BAA04g02020	A04	1175433	C	T	missense_variant	MODERATE	c.1303G>A\|p.Ala435Thr	S289 S290
9	BAA04g02020	A04	1175879	C	T	splice_region_variant&intron_variant	LOW	c.1101-4G>A\|	S208 S93
10	BAA04g02020	A04	1176956	C	T	missense_variant&splice_region_variant	MODERATE	c.706G>A\|p.Glu236Lys	S32
11	BAA04g02020	A04	1177962	G	A	intron_variant	MODIFIER	c.435-267C>T\|	S269
12	BAA04g02020	A04	1178688	C	T	intron_variant	MODIFIER	c.434+421G>A\|	S81 S85
13	BAA04g02020	A04	1178992	G	A	intron_variant	MODIFIER	c.434+117C>T\|	S36
14	BAA04g02020	A04	1179201	C	T	synonymous_variant	LOW	c.342G>A\|p.Lys114Lys	S187
15	BAA04g02020	A04	1179427	C	T	missense_variant	MODERATE	c.116G>A\|p.Arg39Lys	S159 S299
16	BAA04g02020	A04	1179438	C	T	synonymous_variant	LOW	c.105G>A\|p.Lys35Lys	S249
17	BAA04g02020	A04	1180556	C	T	upstream_gene_variant	MODIFIER	c.-1014G>A\|	S130
18	BAA04g02020	A04	1182382	C	T	upstream_gene_variant	MODIFIER	c.-2840G>A\|	S206 S26 S80 S84 S93 S98
19	BAA04g02020	A04	1182747	T	A	upstream_gene_variant	MODIFIER	c.-3205A>T\|	S37
20	BAA04g02020	A04	1182987	G	A	upstream_gene_variant	MODIFIER	c.-3445C>T\|	S66
21	BAA04g02020	A04	1183334	C	T	upstream_gene_variant	MODIFIER	c.-3792G>A\|	S95
22	BAA04g02020	A04	1183768	C	T	upstream_gene_variant	MODIFIER	c.-4226G>A\|	S163

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