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


Gene ID

Results: 1 - 15 of 15 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g18000 A10 17068194 G A upstream_gene_variant MODIFIER c.-4456G>A| S283
2 BAA10g18000 A10 17068264 C T upstream_gene_variant MODIFIER c.-4386C>T| S162
3 BAA10g18000 A10 17068328 C T upstream_gene_variant MODIFIER c.-4322C>T| S37
4 BAA10g18000 A10 17069979 C T upstream_gene_variant MODIFIER c.-2671C>T| S2
5 BAA10g18000 A10 17070882 C T upstream_gene_variant MODIFIER c.-1768C>T| S68
6 BAA10g18000 A10 17071455 C T upstream_gene_variant MODIFIER c.-1195C>T| S47
7 BAA10g18000 A10 17071576 G A upstream_gene_variant MODIFIER c.-1074G>A| S234
8 BAA10g18000 A10 17071725 C T upstream_gene_variant MODIFIER c.-925C>T| S44
9 BAA10g18000 A10 17072388 G A upstream_gene_variant MODIFIER c.-262G>A| S94
10 BAA10g18000 A10 17073042 G A stop_gained HIGH c.393G>A|p.Trp131* S112
11 BAA10g18000 A10 17073258 G A synonymous_variant LOW c.609G>A|p.Lys203Lys S32
12 BAA10g18000 A10 17073544 C T missense_variant MODERATE c.895C>T|p.Leu299Phe S187
13 BAA10g18000 A10 17073922 G A missense_variant MODERATE c.1273G>A|p.Asp425Asn S280
14 BAA10g18000 A10 17073973 G A missense_variant MODERATE c.1324G>A|p.Ala442Thr S66
15 BAA10g18000 A10 17074304 G A missense_variant MODERATE c.1655G>A|p.Gly552Glu S261