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
10951 BAA01g08830 A01 3900159 G A upstream_gene_variant MODIFIER c.-988C>T| S15
S3
10952 BAA01g08830 A01 3900351 T A upstream_gene_variant MODIFIER c.-1180A>T| S255
10953 BAA01g08830 A01 3902136 C T upstream_gene_variant MODIFIER c.-2965G>A| S219
10954 BAA01g08830 A01 3902252 G A upstream_gene_variant MODIFIER c.-3081C>T| S189
10955 BAA01g08830 A01 3903704 C T upstream_gene_variant MODIFIER c.-4533G>A| S38
10956 BAA01g08840 A01 3905722 G A upstream_gene_variant MODIFIER c.-2066G>A| S173
10957 BAA01g08840 A01 3906392 C T upstream_gene_variant MODIFIER c.-1396C>T| S129
10958 BAA01g08840 A01 3907221 C A upstream_gene_variant MODIFIER c.-567C>A| S64
10959 BAA01g08840 A01 3908819 G A stop_gained HIGH c.702G>A|p.Trp234* S238
10960 BAA01g08850 A01 3910310 G A upstream_gene_variant MODIFIER c.-116C>T| S247
10961 BAA01g08860 A01 3911128 C T synonymous_variant LOW c.297G>A|p.Gln99Gln S36
10962 BAA01g08850 A01 3912022 C T upstream_gene_variant MODIFIER c.-1828G>A| S4
10963 BAA01g08870 A01 3912909 C T missense_variant MODERATE c.508C>T|p.Pro170Ser S263
10964 BAA01g08870 A01 3913271 G A missense_variant MODERATE c.683G>A|p.Gly228Asp S190
10965 BAA01g08870 A01 3913512 G A missense_variant MODERATE c.836G>A|p.Arg279Lys S274
10966 BAA01g08850 A01 3913649 C T upstream_gene_variant MODIFIER c.-3455G>A| S118
10967 BAA01g08880 A01 3913936 C T synonymous_variant LOW c.1107G>A|p.Lys369Lys S171
10968 BAA01g08880 A01 3914050 C T stop_gained HIGH c.993G>A|p.Trp331* S282
10969 BAA01g08880 A01 3914064 G A stop_gained HIGH c.979C>T|p.Arg327* S241
10970 BAA01g08880 A01 3914904 G A missense_variant MODERATE c.517C>T|p.Pro173Ser S108
10971 BAA01g08860 A01 3915548 C T upstream_gene_variant MODIFIER c.-3918G>A| S103
10972 BAA01g08860 A01 3916169 G A upstream_gene_variant MODIFIER c.-4539C>T| S80
10973 BAA01g08880 A01 3918322 C T upstream_gene_variant MODIFIER c.-2509G>A| S296
10974 BAA01g08890 A01 3919064 C T splice_region_variant&intron_variant LOW c.241-4G>A| S48
10975 BAA01g08890 A01 3919303 G A missense_variant MODERATE c.167C>T|p.Ala56Val S236