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
139951 BAA10g25110 A10 20440913 G A upstream_gene_variant MODIFIER c.-4457C>T| S192
139952 BAA10g25130 A10 20441260 C T synonymous_variant LOW c.123C>T|p.Ser41Ser S111
S42
139953 BAA10g25130 A10 20441759 G A missense_variant MODERATE c.343G>A|p.Gly115Arg S178
139954 BAA10g25120 A10 20442262 G A upstream_gene_variant MODIFIER c.-3619C>T| S80
139955 BAA10g25120 A10 20443129 G A upstream_gene_variant MODIFIER c.-4486C>T| S58
139956 BAA10g25140 A10 20444038 G A upstream_gene_variant MODIFIER c.-528G>A| S62
139957 BAA10g25140 A10 20444128 G A upstream_gene_variant MODIFIER c.-438G>A| S99
139958 BAA10g25140 A10 20444700 C T synonymous_variant LOW c.135C>T|p.Leu45Leu S185
139959 BAA10g25140 A10 20444726 C T missense_variant MODERATE c.161C>T|p.Pro54Leu S45
139960 BAA10g25140 A10 20445407 G A missense_variant MODERATE c.842G>A|p.Gly281Glu S143
139961 BAA10g25150 A10 20447314 C T missense_variant MODERATE c.903G>A|p.Met301Ile S265
S39
139962 BAA10g25150 A10 20447322 C T missense_variant MODERATE c.895G>A|p.Glu299Lys S165
139963 BAA10g25150 A10 20448758 C T upstream_gene_variant MODIFIER c.-274G>A| S142
139964 BAA10g25150 A10 20449206 G A upstream_gene_variant MODIFIER c.-722C>T| S245
139965 BAA10g25150 A10 20449656 C T upstream_gene_variant MODIFIER c.-1172G>A| S265
139966 BAA10g25150 A10 20449773 C T upstream_gene_variant MODIFIER c.-1289G>A| S250
139967 BAA10g25150 A10 20450515 G A upstream_gene_variant MODIFIER c.-2031C>T| S158
139968 BAA10g25150 A10 20450598 C T upstream_gene_variant MODIFIER c.-2114G>A| S2
139969 BAA10g25150 A10 20451039 G A upstream_gene_variant MODIFIER c.-2555C>T| S106
139970 BAA10g25150 A10 20451551 C T upstream_gene_variant MODIFIER c.-3067G>A| S45
139971 BAA10g25150 A10 20451710 C T upstream_gene_variant MODIFIER c.-3226G>A| S257
139972 BAA10g25160 A10 20452195 G A synonymous_variant LOW c.267G>A|p.Lys89Lys S122
139973 BAA10g25160 A10 20453243 G A synonymous_variant LOW c.963G>A|p.Glu321Glu S63
139974 BAA10g25160 A10 20453277 G A missense_variant MODERATE c.997G>A|p.Glu333Lys S183
139975 BAA10g25160 A10 20453598 C T missense_variant MODERATE c.1253C>T|p.Ser418Phe S297