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
195951 BAA02g28810 A02 16228828 G A upstream_gene_variant MODIFIER c.-2019C>T| S302
195952 BAA02g28810 A02 16229613 C T upstream_gene_variant MODIFIER c.-2804G>A| S245
195953 BAA02g28810 A02 16229746 T A upstream_gene_variant MODIFIER c.-2937A>T| S6
195954 BAA02g28810 A02 16230201 G A upstream_gene_variant MODIFIER c.-3392C>T| S279
195955 BAA02g28810 A02 16230221 C T upstream_gene_variant MODIFIER c.-3412G>A| S284
195956 BAA02g28810 A02 16230800 G A upstream_gene_variant MODIFIER c.-3991C>T| S155
S211
195957 BAA02g28810 A02 16231323 G A upstream_gene_variant MODIFIER c.-4514C>T| S103
195958 BAA02g28820 A02 16231982 G A upstream_gene_variant MODIFIER c.-3561G>A| S148
S30
S31
195959 BAA02g28820 A02 16232063 C T upstream_gene_variant MODIFIER c.-3480C>T| S106
195960 BAA02g28820 A02 16234279 G A upstream_gene_variant MODIFIER c.-1264G>A| S13
195961 BAA02g28820 A02 16235716 G A stop_gained HIGH c.174G>A|p.Trp58* S45
195962 BAA02g28820 A02 16236014 G A missense_variant MODERATE c.373G>A|p.Val125Met S136
195963 BAA02g28840 A02 16236166 C T upstream_gene_variant MODIFIER c.-2455C>T| S16
195964 BAA02g28820 A02 16236210 C T splice_region_variant&intron_variant LOW c.479-7C>T| S283
195965 BAA02g28820 A02 16236237 C T missense_variant MODERATE c.499C>T|p.Arg167Trp S122
195966 BAA02g28820 A02 16237060 C T missense_variant MODERATE c.1039C>T|p.His347Tyr S63
195967 BAA02g28820 A02 16237462 C T synonymous_variant LOW c.1441C>T|p.Leu481Leu S292
195968 BAA02g28840 A02 16237600 G A upstream_gene_variant MODIFIER c.-1021G>A| S261
195969 BAA02g28830 A02 16238270 G A missense_variant MODERATE c.43C>T|p.Pro15Ser S72
S78
195970 BAA02g28840 A02 16240053 C T missense_variant MODERATE c.1433C>T|p.Pro478Leu S135
195971 BAA02g28840 A02 16240490 C T missense_variant MODERATE c.1870C>T|p.Pro624Ser S179
195972 BAA02g28840 A02 16240745 C T missense_variant MODERATE c.2125C>T|p.Pro709Ser S201
195973 BAA02g28840 A02 16240793 C T missense_variant MODERATE c.2173C>T|p.Pro725Ser S244
195974 BAA02g28840 A02 16240811 C T missense_variant MODERATE c.2191C>T|p.Pro731Ser S219
195975 BAA02g28830 A02 16241204 C T upstream_gene_variant MODIFIER c.-2892G>A| S42