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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA09g44380	A09	50080544	G	A	downstream_gene_variant	MODIFIER	c.*4609C>T\|	S266
2	BAA09g44380	A09	50081647	C	T	downstream_gene_variant	MODIFIER	c.*3506G>A\|	S208 S219
3	BAA09g44380	A09	50081668	G	A	downstream_gene_variant	MODIFIER	c.*3485C>T\|	S176
4	BAA09g44380	A09	50081835	C	T	downstream_gene_variant	MODIFIER	c.*3318G>A\|	S293
5	BAA09g44380	A09	50085460	G	T	synonymous_variant	LOW	c.151C>A\|p.Arg51Arg	S213 S238 S239 S267
6	BAA09g44380	A09	50085466	C	T	missense_variant	MODERATE	c.145G>A\|p.Val49Ile	S213 S238 S239 S267
7	BAA09g44380	A09	50085473	A	G	synonymous_variant	LOW	c.138T>C\|p.Gly46Gly	S213 S238 S239 S267
8	BAA09g44380	A09	50085484	G	A	synonymous_variant	LOW	c.127C>T\|p.Leu43Leu	S213 S238 S239 S267
9	BAA09g44380	A09	50085492	A	T	missense_variant	MODERATE	c.119T>A\|p.Ile40Asn	S213 S238 S239 S267
10	BAA09g44380	A09	50085493	T	A	missense_variant	MODERATE	c.118A>T\|p.Ile40Phe	S213 S238 S239 S267
11	BAA09g44380	A09	50085500	G	A	synonymous_variant	LOW	c.111C>T\|p.Gly37Gly	S213 S238 S239 S267
12	BAA09g44380	A09	50085507	T	C	missense_variant	MODERATE	c.104A>G\|p.Asn35Ser	S213 S238 S239 S267
13	BAA09g44380	A09	50085511	T	C	missense_variant	MODERATE	c.100A>G\|p.Ser34Gly	S213 S238 S239 S267
14	BAA09g44380	A09	50085514	C	T	missense_variant	MODERATE	c.97G>A\|p.Ala33Thr	S213 S238 S239 S267
15	BAA09g44380	A09	50085519	G	A	missense_variant	MODERATE	c.92C>T\|p.Ala31Val	S274
16	BAA09g44380	A09	50085527	A	C	synonymous_variant	LOW	c.84T>G\|p.Ser28Ser	S213 S239 S267
17	BAA09g44380	A09	50087380	C	T	upstream_gene_variant	MODIFIER	c.-1770G>A\|	S277