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


Gene ID

Results: 1 - 18 of 18 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA01g39720 A01 26369806 G A upstream_gene_variant MODIFIER c.-2469G>A| S238
2 BAA01g39720 A01 26371583 G A upstream_gene_variant MODIFIER c.-692G>A| S60
3 BAA01g39720 A01 26372169 C T upstream_gene_variant MODIFIER c.-106C>T| S157
4 BAA01g39720 A01 26372231 C T upstream_gene_variant MODIFIER c.-44C>T| S274
5 BAA01g39720 A01 26372232 G A upstream_gene_variant MODIFIER c.-43G>A| S70
6 BAA01g39720 A01 26372262 C T upstream_gene_variant MODIFIER c.-13C>T| S35
7 BAA01g39720 A01 26372305 C T missense_variant MODERATE c.31C>T|p.Arg11Trp S292
8 BAA01g39720 A01 26373169 G A missense_variant MODERATE c.386G>A|p.Arg129Lys S243
9 BAA01g39720 A01 26374093 G A missense_variant MODERATE c.730G>A|p.Ala244Thr S191
10 BAA01g39720 A01 26374096 G A missense_variant MODERATE c.733G>A|p.Asp245Asn S252
11 BAA01g39720 A01 26374911 G A missense_variant MODERATE c.1444G>A|p.Glu482Lys S132
12 BAA01g39720 A01 26375389 G A missense_variant&splice_region_variant MODERATE c.1831G>A|p.Glu611Lys S173
13 BAA01g39720 A01 26375720 C T synonymous_variant LOW c.2073C>T|p.Ser691Ser S68
14 BAA01g39720 A01 26376123 C T missense_variant MODERATE c.2386C>T|p.Pro796Ser S32
15 BAA01g39720 A01 26377013 C T downstream_gene_variant MODIFIER c.*660C>T| S55
16 BAA01g39720 A01 26377212 C T downstream_gene_variant MODIFIER c.*859C>T| S162
17 BAA01g39720 A01 26377393 C T downstream_gene_variant MODIFIER c.*1040C>T| S64
18 BAA01g39720 A01 26377789 G A downstream_gene_variant MODIFIER c.*1436G>A| S66