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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA08g02820	A08	1996346	C	T	synonymous_variant	LOW	c.3600G>A\|p.Arg1200Arg	S151 S153 S157 S167 S257 S262 S263
2	BAA08g02820	A08	1996469	C	T	synonymous_variant	LOW	c.3477G>A\|p.Leu1159Leu	S71
3	BAA08g02820	A08	1996610	C	T	synonymous_variant	LOW	c.3336G>A\|p.Arg1112Arg	S112
4	BAA08g02820	A08	1997764	C	T	intron_variant	MODIFIER	c.2840+509G>A\|	S175
5	BAA08g02820	A08	1998604	C	T	missense_variant	MODERATE	c.2509G>A\|p.Ala837Thr	S164
6	BAA08g02820	A08	1998615	G	A	missense_variant	MODERATE	c.2498C>T\|p.Ser833Phe	S257
7	BAA08g02820	A08	1998705	C	T	missense_variant	MODERATE	c.2408G>A\|p.Ser803Asn	S215
8	BAA08g02820	A08	1999929	T	G	missense_variant	MODERATE	c.1279A>C\|p.Ile427Leu	S61
9	BAA08g02820	A08	1999956	C	T	missense_variant	MODERATE	c.1252G>A\|p.Asp418Asn	S148 S30 S31
10	BAA08g02820	A08	2000133	C	T	missense_variant	MODERATE	c.1169G>A\|p.Ser390Asn	S34
11	BAA08g02820	A08	2000138	G	A	synonymous_variant	LOW	c.1164C>T\|p.Cys388Cys	S129
12	BAA08g02820	A08	2000254	G	A	missense_variant	MODERATE	c.1048C>T\|p.Pro350Ser	S240
13	BAA08g02820	A08	2000642	C	T	synonymous_variant	LOW	c.660G>A\|p.Pro220Pro	S142
14	BAA08g02820	A08	2000857	C	T	missense_variant	MODERATE	c.445G>A\|p.Val149Ile	S276
15	BAA08g02820	A08	2000969	C	T	synonymous_variant	LOW	c.333G>A\|p.Lys111Lys	S80
16	BAA08g02820	A08	2001403	G	A	upstream_gene_variant	MODIFIER	c.-102C>T\|	S124 S131 S190 S223 S284 S287 S57
17	BAA08g02820	A08	2001908	C	T	upstream_gene_variant	MODIFIER	c.-607G>A\|	S231
18	BAA08g02820	A08	2003390	G	A	upstream_gene_variant	MODIFIER	c.-2089C>T\|	S301 S304
19	BAA08g02820	A08	2004961	G	A	upstream_gene_variant	MODIFIER	c.-3660C>T\|	S260
20	BAA08g02820	A08	2005001	G	A	upstream_gene_variant	MODIFIER	c.-3700C>T\|	S157
21	BAA08g02820	A08	2005212	G	A	upstream_gene_variant	MODIFIER	c.-3911C>T\|	S197
22	BAA08g02820	A08	2005464	G	A	upstream_gene_variant	MODIFIER	c.-4163C>T\|	S103

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