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
58001 BAA01g31250 A01 20292714 C T upstream_gene_variant MODIFIER c.-1497G>A| S112
58002 BAA01g31250 A01 20293022 T C upstream_gene_variant MODIFIER c.-1805A>G| S42
58003 BAA01g31260 A01 20293655 G A missense_variant MODERATE c.151G>A|p.Asp51Asn S228
58004 BAA01g31260 A01 20293762 G A synonymous_variant LOW c.258G>A|p.Glu86Glu S274
58005 BAA01g31250 A01 20294259 G A upstream_gene_variant MODIFIER c.-3042C>T| S105
S106
58006 BAA01g31250 A01 20294445 C T upstream_gene_variant MODIFIER c.-3228G>A| S64
58007 BAA01g31260 A01 20294744 C T synonymous_variant LOW c.528C>T|p.Phe176Phe S128
58008 BAA01g31260 A01 20294838 G A missense_variant MODERATE c.622G>A|p.Ala208Thr S138
58009 BAA01g31260 A01 20295167 C T synonymous_variant LOW c.883C>T|p.Leu295Leu S239
58010 BAA01g31250 A01 20295266 C T upstream_gene_variant MODIFIER c.-4049G>A| S136
58011 BAA01g31260 A01 20295306 C T splice_region_variant&intron_variant LOW c.922-6C>T| S82
S92
58012 BAA01g31260 A01 20295867 G A missense_variant MODERATE c.1477G>A|p.Glu493Lys S160
58013 BAA01g31260 A01 20296190 C T synonymous_variant LOW c.1800C>T|p.Pro600Pro S273
58014 BAA01g31260 A01 20296418 G T missense_variant MODERATE c.2028G>T|p.Lys676Asn S71
58015 BAA01g31260 A01 20296433 G A downstream_gene_variant MODIFIER c.*12G>A| S35
58016 BAA01g31260 A01 20296615 C T downstream_gene_variant MODIFIER c.*194C>T| S267
58017 BAA01g31260 A01 20297225 G A downstream_gene_variant MODIFIER c.*804G>A| S296
58018 BAA01g31260 A01 20297481 C T downstream_gene_variant MODIFIER c.*1060C>T| S196
58019 BAA01g31260 A01 20298329 G A downstream_gene_variant MODIFIER c.*1908G>A| S72
S78
58020 BAA01g31260 A01 20298464 C T downstream_gene_variant MODIFIER c.*2043C>T| S88
58021 BAA01g31260 A01 20298556 G A downstream_gene_variant MODIFIER c.*2135G>A| S129
58022 BAA01g31260 A01 20299054 G A downstream_gene_variant MODIFIER c.*2633G>A| S281
S282
58023 BAA01g31260 A01 20299290 G A downstream_gene_variant MODIFIER c.*2869G>A| S236
58024 BAA01g31260 A01 20299545 G A downstream_gene_variant MODIFIER c.*3124G>A| S84
S93
58025 BAA01g31260 A01 20299795 A T downstream_gene_variant MODIFIER c.*3374A>T| S112