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Num	GeneID	Chromosome	Position	Ref.allele	Alt.allele	Mutant type	Impacts	Amino acid change	SampleID
1	BAA10g14040	A10	14891877	T	A	upstream_gene_variant	MODIFIER	c.-1226T>A\|	S1 S228 S244
2	BAA10g14040	A10	14891927	C	T	upstream_gene_variant	MODIFIER	c.-1176C>T\|	S191
3	BAA10g14040	A10	14892283	A	C	upstream_gene_variant	MODIFIER	c.-820A>C\|	S111 S131 S135 S172 S186 S204 S210 S218 S222 S223 S23 S247 S248 S252 S298 S36 S58 S61
4	BAA10g14040	A10	14893753	G	A	intron_variant	MODIFIER	c.382+59G>A\|	S176
5	BAA10g14040	A10	14895578	G	A	intron_variant	MODIFIER	c.949-23G>A\|	S278
6	BAA10g14040	A10	14895813	C	T	intron_variant	MODIFIER	c.1110+51C>T\|	S153 S296
7	BAA10g14040	A10	14896017	C	T	intron_variant	MODIFIER	c.1111-67C>T\|	S124
8	BAA10g14040	A10	14896284	C	T	intron_variant	MODIFIER	c.1292+19C>T\|	S38
9	BAA10g14040	A10	14897504	G	A	intron_variant	MODIFIER	c.1945-28G>A\|	S169
10	BAA10g14040	A10	14897548	C	T	missense_variant	MODERATE	c.1961C>T\|p.Pro654Leu	S177
11	BAA10g14040	A10	14897814	G	A	intron_variant	MODIFIER	c.2105+30G>A\|	S178
12	BAA10g14040	A10	14898753	G	A	downstream_gene_variant	MODIFIER	c.*806G>A\|	S139
13	BAA10g14040	A10	14899223	C	T	downstream_gene_variant	MODIFIER	c.*1276C>T\|	S306 S308
14	BAA10g14040	A10	14899392	G	A	downstream_gene_variant	MODIFIER	c.*1445G>A\|	S218
15	BAA10g14040	A10	14900142	C	T	downstream_gene_variant	MODIFIER	c.*2195C>T\|	S277
16	BAA10g14040	A10	14901119	G	A	downstream_gene_variant	MODIFIER	c.*3172G>A\|	S61
17	BAA10g14040	A10	14901347	C	T	downstream_gene_variant	MODIFIER	c.*3400C>T\|	S37
18	BAA10g14040	A10	14902108	G	A	downstream_gene_variant	MODIFIER	c.*4161G>A\|	S174 S216 S241 S265 S39