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
22951 BAA01g16580 A01 8076666 G A missense_variant MODERATE c.3035G>A|p.Ser1012Asn S257
22952 BAA01g16580 A01 8076775 G A synonymous_variant LOW c.3144G>A|p.Leu1048Leu S32
22953 BAA01g16580 A01 8077403 C T missense_variant MODERATE c.3772C>T|p.Pro1258Ser S53
22954 BAA01g16580 A01 8077449 G A missense_variant MODERATE c.3818G>A|p.Gly1273Glu S114
22955 BAA01g16580 A01 8077716 C T missense_variant MODERATE c.4085C>T|p.Thr1362Ile S4
22956 BAA01g16580 A01 8077725 G A missense_variant MODERATE c.4094G>A|p.Gly1365Glu S83
S88
22957 BAA01g16590 A01 8078025 C T upstream_gene_variant MODIFIER c.-1349C>T| S71
22958 BAA01g16590 A01 8078832 C T upstream_gene_variant MODIFIER c.-542C>T| S169
22959 BAA01g16590 A01 8079204 C T upstream_gene_variant MODIFIER c.-170C>T| S221
22960 BAA01g16590 A01 8079265 C T upstream_gene_variant MODIFIER c.-109C>T| S47
22961 BAA01g16590 A01 8079840 C T synonymous_variant LOW c.159C>T|p.Phe53Phe S35
22962 BAA01g16590 A01 8080001 C T missense_variant MODERATE c.320C>T|p.Ser107Leu S20
22963 BAA01g16590 A01 8080937 C T missense_variant MODERATE c.1060C>T|p.His354Tyr S114
22964 BAA01g16590 A01 8081037 C T missense_variant MODERATE c.1160C>T|p.Ala387Val S68
22965 BAA01g16580 A01 8081182 C T downstream_gene_variant MODIFIER c.*3435C>T| S240
22966 BAA01g16580 A01 8081233 G A downstream_gene_variant MODIFIER c.*3486G>A| S28
22967 BAA01g16590 A01 8082063 G A missense_variant MODERATE c.1913G>A|p.Arg638Lys S273
22968 BAA01g16600 A01 8083416 G A upstream_gene_variant MODIFIER c.-200C>T| S197
22969 BAA01g16600 A01 8084768 C T upstream_gene_variant MODIFIER c.-1552G>A| S42
22970 BAA01g16610 A01 8089038 G A missense_variant MODERATE c.1384C>T|p.Leu462Phe S34
22971 BAA01g16620 A01 8090029 G A downstream_gene_variant MODIFIER c.*2851C>T| S23
22972 BAA01g16610 A01 8090111 C T missense_variant MODERATE c.880G>A|p.Glu294Lys S171
22973 BAA01g16620 A01 8091522 C T downstream_gene_variant MODIFIER c.*1358G>A| S246
22974 BAA01g16610 A01 8091828 C T splice_acceptor_variant&intron_variant HIGH c.230-1G>A| S76
22975 BAA01g16610 A01 8092193 C T upstream_gene_variant MODIFIER c.-61G>A| S294