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


Gene ID

Results: 1 - 14 of 14 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA06g10900 A06 5536547 C T upstream_gene_variant MODIFIER c.-4648C>T| S243
2 BAA06g10900 A06 5537002 A T upstream_gene_variant MODIFIER c.-4193A>T| S39
3 BAA06g10900 A06 5537139 C T upstream_gene_variant MODIFIER c.-4056C>T| S171
4 BAA06g10900 A06 5537224 C T upstream_gene_variant MODIFIER c.-3971C>T| S242
5 BAA06g10900 A06 5537288 C T upstream_gene_variant MODIFIER c.-3907C>T| S302
6 BAA06g10900 A06 5539862 G A upstream_gene_variant MODIFIER c.-1333G>A| S81
S85
7 BAA06g10900 A06 5539904 C T upstream_gene_variant MODIFIER c.-1291C>T| S280
8 BAA06g10900 A06 5540082 C T upstream_gene_variant MODIFIER c.-1113C>T| S176
9 BAA06g10900 A06 5541076 C T upstream_gene_variant MODIFIER c.-119C>T| S288
10 BAA06g10900 A06 5541742 G A missense_variant MODERATE c.475G>A|p.Gly159Ser S32
11 BAA06g10900 A06 5541780 G A synonymous_variant LOW c.513G>A|p.Pro171Pro S13
12 BAA06g10900 A06 5545306 C T downstream_gene_variant MODIFIER c.*2500C>T| S103
13 BAA06g10900 A06 5545862 G A downstream_gene_variant MODIFIER c.*3056G>A| S297
14 BAA06g10900 A06 5546659 C T downstream_gene_variant MODIFIER c.*3853C>T| S37