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
66601 BAA01g34870 A01 23312143 G A upstream_gene_variant MODIFIER c.-1397C>T| S55
66602 BAA01g34870 A01 23312159 G A upstream_gene_variant MODIFIER c.-1413C>T| S189
66603 BAA01g34870 A01 23312358 C T upstream_gene_variant MODIFIER c.-1612G>A| S88
66604 BAA01g34870 A01 23312521 G A upstream_gene_variant MODIFIER c.-1775C>T| S299
66605 BAA01g34870 A01 23313700 G A upstream_gene_variant MODIFIER c.-2954C>T| S32
66606 BAA01g34870 A01 23313774 G A upstream_gene_variant MODIFIER c.-3028C>T| S169
66607 BAA01g34870 A01 23314072 G A upstream_gene_variant MODIFIER c.-3326C>T| S109
66608 BAA01g34870 A01 23314523 G A upstream_gene_variant MODIFIER c.-3777C>T| S288
66609 BAA01g34870 A01 23315140 C T upstream_gene_variant MODIFIER c.-4394G>A| S98
66610 BAA01g34880 A01 23315877 G A missense_variant MODERATE c.170G>A|p.Arg57His S129
66611 BAA01g34880 A01 23315917 C T synonymous_variant LOW c.210C>T|p.Arg70Arg S149
66612 BAA01g34880 A01 23315949 C T missense_variant MODERATE c.242C>T|p.Thr81Met S134
S179
S193
66613 BAA01g34880 A01 23316873 C T missense_variant MODERATE c.766C>T|p.Pro256Ser S18
66614 BAA01g34880 A01 23317718 C T missense_variant MODERATE c.1093C>T|p.Pro365Ser S298
66615 BAA01g34880 A01 23317964 C T missense_variant MODERATE c.1339C>T|p.Pro447Ser S28
66616 BAA01g34880 A01 23318324 C T missense_variant MODERATE c.1699C>T|p.Pro567Ser S81
S85
66617 BAA01g34880 A01 23318423 C T missense_variant MODERATE c.1798C>T|p.Pro600Ser S115
66618 BAA01g34890 A01 23318723 G T upstream_gene_variant MODIFIER c.-417G>T| S206
66619 BAA01g34890 A01 23318738 G A upstream_gene_variant MODIFIER c.-402G>A| S9
66620 BAA01g34890 A01 23318920 G A upstream_gene_variant MODIFIER c.-220G>A| S15
S3
66621 BAA01g34890 A01 23319636 C T missense_variant MODERATE c.410C>T|p.Ser137Phe S11
66622 BAA01g34900 A01 23321511 G A synonymous_variant LOW c.45C>T|p.Phe15Phe S197
66623 BAA01g34900 A01 23322098 C T upstream_gene_variant MODIFIER c.-543G>A| S210
S225
66624 BAA01g34900 A01 23322172 G A upstream_gene_variant MODIFIER c.-617C>T| S125
66625 BAA01g34900 A01 23323222 G A upstream_gene_variant MODIFIER c.-1667C>T| S105
S106