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
11901 BAA01g09530 A01 4242746 C T upstream_gene_variant MODIFIER c.-2131C>T| S205
11902 BAA01g09530 A01 4242848 C T upstream_gene_variant MODIFIER c.-2029C>T| S210
11903 BAA01g09520 A01 4244440 G A synonymous_variant LOW c.105C>T|p.Arg35Arg S281
11904 BAA01g09530 A01 4244513 C T upstream_gene_variant MODIFIER c.-364C>T| S20
11905 BAA01g09530 A01 4245246 G A splice_acceptor_variant&intron_variant HIGH c.116-1G>A| S11
11906 BAA01g09540 A01 4246685 C T synonymous_variant LOW c.201G>A|p.Val67Val S221
11907 BAA01g09540 A01 4250410 G A upstream_gene_variant MODIFIER c.-3525C>T| S251
11908 BAA01g09540 A01 4250536 C T upstream_gene_variant MODIFIER c.-3651G>A| S246
11909 BAA01g09540 A01 4251235 G A upstream_gene_variant MODIFIER c.-4350C>T| S13
11910 BAA01g09560 A01 4251445 C T missense_variant MODERATE c.409G>A|p.Gly137Arg S132
S137
11911 BAA01g09560 A01 4251692 G A missense_variant MODERATE c.256C>T|p.Pro86Ser S274
11912 BAA01g09560 A01 4251877 C T missense_variant MODERATE c.71G>A|p.Gly24Glu S35
11913 BAA01g09570 A01 4253284 C T missense_variant&splice_region_variant MODERATE c.1882G>A|p.Glu628Lys S81
S85
11914 BAA01g09570 A01 4253787 C T missense_variant MODERATE c.1462G>A|p.Ala488Thr S247
11915 BAA01g09550 A01 4254134 G A upstream_gene_variant MODIFIER c.-4280C>T| S289
S290
11916 BAA01g09560 A01 4255133 G A upstream_gene_variant MODIFIER c.-3186C>T| S276
11917 BAA01g09560 A01 4255174 C T upstream_gene_variant MODIFIER c.-3227G>A| S155
S211
11918 BAA01g09560 A01 4256065 C T upstream_gene_variant MODIFIER c.-4118G>A| S43
11919 BAA01g09560 A01 4256623 A T upstream_gene_variant MODIFIER c.-4676T>A| S90
11920 BAA01g09560 A01 4256847 G A upstream_gene_variant MODIFIER c.-4900C>T| S274
11921 BAA01g09570 A01 4257865 C T intron_variant MODIFIER c.1086+2042G>A| S16
S270
11922 BAA01g09570 A01 4258300 C T intron_variant MODIFIER c.1086+1607G>A| S200
11923 BAA01g09570 A01 4259282 G A intron_variant MODIFIER c.1086+625C>T| S95
11924 BAA01g09570 A01 4259915 G A stop_gained HIGH c.1078C>T|p.Gln360* S40
S49
11925 BAA01g09570 A01 4260403 C T intron_variant MODIFIER c.736-146G>A| S148
S30
S31