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
124001 BAA10g13740 A10 14723278 C T missense_variant MODERATE c.257G>A|p.Gly86Asp S202
124002 BAA10g13740 A10 14724248 C T upstream_gene_variant MODIFIER c.-714G>A| S202
124003 BAA10g13740 A10 14724704 C T upstream_gene_variant MODIFIER c.-1170G>A| S275
124004 BAA10g13740 A10 14725350 C T upstream_gene_variant MODIFIER c.-1816G>A| S116
124005 BAA10g13740 A10 14726123 C T upstream_gene_variant MODIFIER c.-2589G>A| S238
124006 BAA10g13750 A10 14726250 G A missense_variant&splice_region_variant MODERATE c.376G>A|p.Glu126Lys S174
S216
S241
S265
S39
124007 BAA10g13740 A10 14726767 G A upstream_gene_variant MODIFIER c.-3233C>T| S198
124008 BAA10g13750 A10 14726908 G A stop_gained HIGH c.597G>A|p.Trp199* S223
124009 BAA10g13740 A10 14727571 C T upstream_gene_variant MODIFIER c.-4037G>A| S44
124010 BAA10g13740 A10 14727667 C T upstream_gene_variant MODIFIER c.-4133G>A| S146
124011 BAA10g13760 A10 14729553 G A missense_variant MODERATE c.604G>A|p.Asp202Asn S169
124012 BAA10g13770 A10 14729749 C T upstream_gene_variant MODIFIER c.-4194C>T| S153
S213
124013 BAA10g13760 A10 14730181 C T synonymous_variant LOW c.921C>T|p.Phe307Phe S26
124014 BAA10g13760 A10 14730217 A G synonymous_variant LOW c.957A>G|p.Pro319Pro S57
124015 BAA10g13770 A10 14730288 G A upstream_gene_variant MODIFIER c.-3655G>A| S136
124016 BAA10g13760 A10 14730540 C T splice_region_variant&intron_variant LOW c.1099-3C>T| S135
124017 BAA10g13760 A10 14731394 G A missense_variant MODERATE c.1654G>A|p.Glu552Lys S290
124018 BAA10g13770 A10 14731982 G A upstream_gene_variant MODIFIER c.-1961G>A| S17
124019 BAA10g13770 A10 14733779 G A upstream_gene_variant MODIFIER c.-164G>A| S38
124020 BAA10g13770 A10 14733869 C T upstream_gene_variant MODIFIER c.-74C>T| S28
124021 BAA10g13770 A10 14734262 G A synonymous_variant LOW c.240G>A|p.Glu80Glu S61
124022 BAA10g13770 A10 14734292 C T synonymous_variant LOW c.270C>T|p.Pro90Pro S185
124023 BAA10g13770 A10 14734979 C T missense_variant MODERATE c.773C>T|p.Ala258Val S167
124024 BAA10g13770 A10 14734993 C T missense_variant MODERATE c.787C>T|p.Leu263Phe S298
124025 BAA10g13780 A10 14735567 C T upstream_gene_variant MODIFIER c.-896C>T| S146