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
167951 BAA02g13460 A02 6191725 C T synonymous_variant LOW c.1479G>A|p.Gln493Gln S63
167952 BAA02g13460 A02 6193672 G A synonymous_variant LOW c.549C>T|p.Ser183Ser S165
167953 BAA02g13460 A02 6195823 C T upstream_gene_variant MODIFIER c.-1415G>A| S249
167954 BAA02g13460 A02 6197026 C T upstream_gene_variant MODIFIER c.-2618G>A| S66
167955 BAA02g13460 A02 6197348 C T upstream_gene_variant MODIFIER c.-2940G>A| S208
S219
167956 BAA02g13460 A02 6197487 G A upstream_gene_variant MODIFIER c.-3079C>T| S225
S73
167957 BAA02g13470 A02 6197714 C T missense_variant MODERATE c.1379G>A|p.Arg460Gln S153
167958 BAA02g13470 A02 6198172 C T synonymous_variant LOW c.921G>A|p.Gln307Gln S116
167959 BAA02g13470 A02 6198444 G A missense_variant MODERATE c.649C>T|p.Pro217Ser S190
167960 BAA02g13470 A02 6198449 G A missense_variant MODERATE c.644C>T|p.Ser215Phe S23
167961 BAA02g13470 A02 6198648 G A missense_variant MODERATE c.445C>T|p.Pro149Ser S228
167962 BAA02g13470 A02 6198703 C T synonymous_variant LOW c.390G>A|p.Leu130Leu S177
167963 BAA02g13470 A02 6198762 C T missense_variant MODERATE c.331G>A|p.Gly111Arg S201
167964 BAA02g13470 A02 6201146 G A upstream_gene_variant MODIFIER c.-2054C>T| S295
167965 BAA02g13470 A02 6201360 G A upstream_gene_variant MODIFIER c.-2268C>T| S146
167966 BAA02g13470 A02 6203258 C T upstream_gene_variant MODIFIER c.-4166G>A| S266
167967 BAA02g13480 A02 6204454 C T downstream_gene_variant MODIFIER c.*594G>A| S15
S3
167968 BAA02g13480 A02 6205253 C T missense_variant MODERATE c.1052G>A|p.Arg351Lys S199
167969 BAA02g13480 A02 6205536 G A missense_variant MODERATE c.910C>T|p.Pro304Ser S298
167970 BAA02g13480 A02 6206603 C T splice_region_variant&intron_variant LOW c.504-4G>A| S293
167971 BAA02g13480 A02 6207787 C T missense_variant MODERATE c.4G>A|p.Glu2Lys S46
167972 BAA02g13480 A02 6207840 C T upstream_gene_variant MODIFIER c.-50G>A| S39
167973 BAA02g13480 A02 6208713 C T upstream_gene_variant MODIFIER c.-923G>A| S211
S227
167974 BAA02g13490 A02 6209345 C T missense_variant MODERATE c.2005G>A|p.Ala669Thr S240
167975 BAA02g13490 A02 6210253 C T missense_variant MODERATE c.1097G>A|p.Arg366Lys S156