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
153951 BAA02g02310 A02 1038875 C T missense_variant MODERATE c.506G>A|p.Arg169Gln S100
153952 BAA02g02310 A02 1039171 C T synonymous_variant LOW c.210G>A|p.Arg70Arg S13
153953 BAA02g02320 A02 1039505 G A missense_variant MODERATE c.2353C>T|p.Pro785Ser S297
153954 BAA02g02320 A02 1039880 G A missense_variant MODERATE c.1978C>T|p.Pro660Ser S10
153955 BAA02g02320 A02 1040349 C T synonymous_variant LOW c.1509G>A|p.Glu503Glu S270
153956 BAA02g02310 A02 1041511 C T upstream_gene_variant MODIFIER c.-2131G>A| S280
153957 BAA02g02320 A02 1041609 G A synonymous_variant LOW c.552C>T|p.Ser184Ser S265
153958 BAA02g02320 A02 1041756 G A synonymous_variant LOW c.405C>T|p.Ser135Ser S10
153959 BAA02g02320 A02 1041888 G A synonymous_variant LOW c.273C>T|p.Leu91Leu S295
153960 BAA02g02320 A02 1041990 C T stop_gained HIGH c.171G>A|p.Trp57* S63
153961 BAA02g02330 A02 1042700 G A missense_variant MODERATE c.1495C>T|p.Leu499Phe S69
153962 BAA02g02330 A02 1044323 C T missense_variant MODERATE c.152G>A|p.Gly51Asp S13
153963 BAA02g02320 A02 1047152 C T upstream_gene_variant MODIFIER c.-4992G>A| S306
153964 BAA02g02340 A02 1047479 G A missense_variant MODERATE c.866C>T|p.Thr289Ile S202
153965 BAA02g02340 A02 1049594 G A upstream_gene_variant MODIFIER c.-1250C>T| S289
S290
153966 BAA02g02350 A02 1049933 C T splice_region_variant&synonymous_variant LOW c.69C>T|p.Tyr23Tyr S179
153967 BAA02g02350 A02 1050238 G A missense_variant MODERATE c.212G>A|p.Ser71Asn S44
153968 BAA02g02340 A02 1050634 C T upstream_gene_variant MODIFIER c.-2290G>A| S1
S90
153969 BAA02g02360 A02 1052598 C T missense_variant MODERATE c.52C>T|p.Pro18Ser S18
153970 BAA02g02360 A02 1052784 G A missense_variant MODERATE c.238G>A|p.Ala80Thr S263
153971 BAA02g02360 A02 1052849 C T synonymous_variant LOW c.303C>T|p.Arg101Arg S193
153972 BAA02g02380 A02 1053868 G A upstream_gene_variant MODIFIER c.-4629G>A| S225
S73
153973 BAA02g02370 A02 1054808 C T missense_variant MODERATE c.503G>A|p.Arg168Lys S61
153974 BAA02g02370 A02 1055290 C T synonymous_variant LOW c.21G>A|p.Lys7Lys S144
153975 BAA02g02370 A02 1056178 C T upstream_gene_variant MODIFIER c.-868G>A| S298