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
22901 BAA01g16560 A01 8059792 G A upstream_gene_variant MODIFIER c.-1937C>T| S27
22902 BAA01g16560 A01 8059981 G A upstream_gene_variant MODIFIER c.-2126C>T| S204
22903 BAA01g16560 A01 8060055 G A upstream_gene_variant MODIFIER c.-2200C>T| S85
22904 BAA01g16560 A01 8060928 C T upstream_gene_variant MODIFIER c.-3073G>A| S10
22905 BAA01g16560 A01 8061973 C T upstream_gene_variant MODIFIER c.-4118G>A| S198
22906 BAA01g16570 A01 8064632 G A intron_variant MODIFIER c.288-211C>T| S9
22907 BAA01g16570 A01 8066083 C T intron_variant MODIFIER c.288-1662G>A| S259
22908 BAA01g16580 A01 8068465 G A upstream_gene_variant MODIFIER c.-3802G>A| S172
S217
22909 BAA01g16570 A01 8068943 G A upstream_gene_variant MODIFIER c.-92C>T| S17
22910 BAA01g16570 A01 8069083 G A upstream_gene_variant MODIFIER c.-232C>T| S163
22911 BAA01g16570 A01 8069316 G A upstream_gene_variant MODIFIER c.-465C>T| S240
22912 BAA01g16570 A01 8070612 C T upstream_gene_variant MODIFIER c.-1761G>A| S18
22913 BAA01g16570 A01 8071714 C T upstream_gene_variant MODIFIER c.-2863G>A| S255
22914 BAA01g16570 A01 8071750 C T upstream_gene_variant MODIFIER c.-2899G>A| S291
22915 BAA01g16570 A01 8072247 G A upstream_gene_variant MODIFIER c.-3396C>T| S37
22916 BAA01g16570 A01 8072394 G A upstream_gene_variant MODIFIER c.-3543C>T| S298
22917 BAA01g16570 A01 8072708 C T upstream_gene_variant MODIFIER c.-3857G>A| S303
22918 BAA01g16570 A01 8073603 C T upstream_gene_variant MODIFIER c.-4752G>A| S218
22919 BAA01g16580 A01 8074421 C T synonymous_variant LOW c.948C>T|p.Gly316Gly S18
22920 BAA01g16580 A01 8075457 G A missense_variant MODERATE c.1903G>A|p.Asp635Asn S246
22921 BAA01g16580 A01 8075479 C T missense_variant MODERATE c.1925C>T|p.Pro642Leu S46
22922 BAA01g16580 A01 8075609 G A missense_variant MODERATE c.1978G>A|p.Glu660Lys S72
S78
22923 BAA01g16580 A01 8075921 C T missense_variant MODERATE c.2290C>T|p.Arg764Cys S284
22924 BAA01g16580 A01 8076017 G A missense_variant MODERATE c.2386G>A|p.Ala796Thr S191
22925 BAA01g16580 A01 8076138 G A missense_variant MODERATE c.2507G>A|p.Arg836Lys S152