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


Gene ID

Results: 1 - 489298 of 489298 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
177751 BAA02g18960 A02 9803424 C T downstream_gene_variant MODIFIER c.*4540C>T| S262
177752 BAA02g18970 A02 9807513 T A upstream_gene_variant MODIFIER c.-1258T>A| S83
S88
177753 BAA02g18970 A02 9808985 G A synonymous_variant LOW c.120G>A|p.Glu40Glu S157
177754 BAA02g18970 A02 9809256 G A downstream_gene_variant MODIFIER c.*220G>A| S17
177755 BAA02g18970 A02 9809502 G A downstream_gene_variant MODIFIER c.*466G>A| S265
177756 BAA02g18970 A02 9811688 G A downstream_gene_variant MODIFIER c.*2652G>A| S31
177757 BAA02g18970 A02 9811775 G A downstream_gene_variant MODIFIER c.*2739G>A| S272
177758 BAA02g18990 A02 9812980 G A upstream_gene_variant MODIFIER c.-4377G>A| S153
S213
177759 BAA02g18980 A02 9813373 C T missense_variant MODERATE c.989G>A|p.Gly330Glu S94
177760 BAA02g18980 A02 9814445 G A missense_variant MODERATE c.422C>T|p.Ser141Phe S47
177761 BAA02g18980 A02 9815077 G A upstream_gene_variant MODIFIER c.-211C>T| S70
177762 BAA02g18980 A02 9816086 C T upstream_gene_variant MODIFIER c.-1220G>A| S277
177763 BAA02g18980 A02 9816163 G A upstream_gene_variant MODIFIER c.-1297C>T| S92
177764 BAA02g18980 A02 9817068 C T upstream_gene_variant MODIFIER c.-2202G>A| S277
177765 BAA02g18980 A02 9817317 G A upstream_gene_variant MODIFIER c.-2451C>T| S168
177766 BAA02g18990 A02 9818151 G A missense_variant MODERATE c.352G>A|p.Glu118Lys S153
S213
177767 BAA02g18990 A02 9819132 G A missense_variant MODERATE c.1333G>A|p.Glu445Lys S272
177768 BAA02g18990 A02 9819258 G A missense_variant MODERATE c.1459G>A|p.Glu487Lys S247
177769 BAA02g18990 A02 9820210 G A missense_variant MODERATE c.1963G>A|p.Ala655Thr S34
177770 BAA02g18990 A02 9820514 G A missense_variant MODERATE c.2267G>A|p.Arg756Lys S229
177771 BAA02g18990 A02 9820521 G A synonymous_variant LOW c.2274G>A|p.Leu758Leu S207
S265
177772 BAA02g19000 A02 9821434 C T missense_variant MODERATE c.526G>A|p.Glu176Lys S166
177773 BAA02g19000 A02 9821857 G A missense_variant MODERATE c.103C>T|p.Pro35Ser S287
177774 BAA02g19000 A02 9821939 C T synonymous_variant LOW c.21G>A|p.Lys7Lys S34
177775 BAA02g19000 A02 9822206 C T upstream_gene_variant MODIFIER c.-166G>A| S299