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
132151 BAA10g19130 A10 17670359 C T upstream_gene_variant MODIFIER c.-3661C>T| S183
132152 BAA10g19130 A10 17672010 C T upstream_gene_variant MODIFIER c.-2010C>T| S210
S225
132153 BAA10g19130 A10 17674057 C T missense_variant MODERATE c.38C>T|p.Ser13Phe S249
132154 BAA10g19130 A10 17674714 G A missense_variant MODERATE c.197G>A|p.Arg66Lys S197
132155 BAA10g19130 A10 17674807 C T missense_variant MODERATE c.290C>T|p.Ser97Phe S286
132156 BAA10g19130 A10 17675141 C T synonymous_variant LOW c.504C>T|p.Val168Val S257
132157 BAA10g19140 A10 17677363 C T upstream_gene_variant MODIFIER c.-174C>T| S72
132158 BAA10g19140 A10 17677504 G A upstream_gene_variant MODIFIER c.-33G>A| S292
132159 BAA10g19140 A10 17677585 C T missense_variant MODERATE c.49C>T|p.Arg17Trp S283
132160 BAA10g19140 A10 17677593 C T synonymous_variant LOW c.57C>T|p.Ala19Ala S298
132161 BAA10g19150 A10 17681116 G A splice_region_variant&intron_variant LOW c.271-8G>A| S250
132162 BAA10g19160 A10 17681215 G A upstream_gene_variant MODIFIER c.-3950G>A| S128
132163 BAA10g19160 A10 17681223 C T upstream_gene_variant MODIFIER c.-3942C>T| S19
132164 BAA10g19150 A10 17681296 C T splice_region_variant&synonymous_variant LOW c.354C>T|p.Asp118Asp S225
S73
132165 BAA10g19160 A10 17682054 C T upstream_gene_variant MODIFIER c.-3111C>T| S46
132166 BAA10g19150 A10 17682340 G A synonymous_variant LOW c.984G>A|p.Lys328Lys S4
132167 BAA10g19150 A10 17682512 G A missense_variant MODERATE c.1156G>A|p.Asp386Asn S111
132168 BAA10g19160 A10 17683017 G A upstream_gene_variant MODIFIER c.-2148G>A| S105
S106
132169 BAA10g19160 A10 17683864 C T upstream_gene_variant MODIFIER c.-1301C>T| S2
132170 BAA10g19160 A10 17684935 C T upstream_gene_variant MODIFIER c.-230C>T| S235
132171 BAA10g19180 A10 17688478 C T upstream_gene_variant MODIFIER c.-909C>T| S81
S85
132172 BAA10g19180 A10 17688700 G A upstream_gene_variant MODIFIER c.-687G>A| S43
132173 BAA10g19180 A10 17689438 C T missense_variant MODERATE c.52C>T|p.Pro18Ser S176
132174 BAA10g19180 A10 17689873 G A missense_variant MODERATE c.344G>A|p.Gly115Glu S132
S137
S215
132175 BAA10g19160 A10 17690162 C T downstream_gene_variant MODIFIER c.*4367C>T| S11