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
85951 BAA01g45610 A01 30384519 G A synonymous_variant LOW c.1194G>A|p.Lys398Lys S10
85952 BAA01g45600 A01 30384904 G A downstream_gene_variant MODIFIER c.*3333G>A| S278
85953 BAA01g45600 A01 30385944 C T downstream_gene_variant MODIFIER c.*4373C>T| S305
85954 BAA01g45610 A01 30388129 G A downstream_gene_variant MODIFIER c.*3255G>A| S234
85955 BAA01g45630 A01 30389632 G A upstream_gene_variant MODIFIER c.-3553G>A| S15
S3
85956 BAA01g45630 A01 30389856 G A upstream_gene_variant MODIFIER c.-3329G>A| S169
85957 BAA01g45630 A01 30389938 C T upstream_gene_variant MODIFIER c.-3247C>T| S164
85958 BAA01g45620 A01 30390483 C T missense_variant MODERATE c.700G>A|p.Glu234Lys S85
85959 BAA01g45620 A01 30390489 G A synonymous_variant LOW c.694C>T|p.Leu232Leu S209
85960 BAA01g45620 A01 30391050 G A synonymous_variant LOW c.303C>T|p.Leu101Leu S34
85961 BAA01g45620 A01 30391229 G A missense_variant MODERATE c.124C>T|p.Pro42Ser S157
S163
85962 BAA01g45620 A01 30391455 G A upstream_gene_variant MODIFIER c.-103C>T| S172
S217
85963 BAA01g45630 A01 30393271 G A synonymous_variant LOW c.87G>A|p.Arg29Arg S48
85964 BAA01g45630 A01 30393547 C T missense_variant MODERATE c.229C>T|p.Pro77Ser S32
85965 BAA01g45630 A01 30394393 C T missense_variant MODERATE c.824C>T|p.Pro275Leu S267
85966 BAA01g45620 A01 30395067 G A upstream_gene_variant MODIFIER c.-3715C>T| S278
85967 BAA01g45640 A01 30401751 C T missense_variant MODERATE c.622C>T|p.Leu208Phe S166
85968 BAA01g45640 A01 30402003 G A missense_variant MODERATE c.874G>A|p.Glu292Lys S217
85969 BAA01g45640 A01 30402663 T G downstream_gene_variant MODIFIER c.*502T>G| S127
85970 BAA01g45640 A01 30404168 G A downstream_gene_variant MODIFIER c.*2007G>A| S80
85971 BAA01g45640 A01 30404661 G A downstream_gene_variant MODIFIER c.*2500G>A| S204
85972 BAA01g45640 A01 30405008 G A downstream_gene_variant MODIFIER c.*2847G>A| S5
85973 BAA01g45640 A01 30406647 C T downstream_gene_variant MODIFIER c.*4486C>T| S8
85974 BAA01g45640-BAA01g45650 A01 30407979 G A intergenic_region MODIFIER n.30407979G>A| S136
85975 BAA01g45640-BAA01g45650 A01 30410084 G A intergenic_region MODIFIER n.30410084G>A| S257