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
59201 BAA01g31750 A01 20758655 A T upstream_gene_variant MODIFIER c.-2119T>A| S218
59202 BAA01g31750 A01 20760936 G A upstream_gene_variant MODIFIER c.-4400C>T| S196
59203 BAA01g31760 A01 20761292 G A missense_variant MODERATE c.28G>A|p.Glu10Lys S116
59204 BAA01g31760 A01 20761426 G A stop_gained&splice_region_variant HIGH c.162G>A|p.Trp54* S25
59205 BAA01g31760 A01 20764097 C T downstream_gene_variant MODIFIER c.*1816C>T| S117
59206 BAA01g31760 A01 20764269 C T downstream_gene_variant MODIFIER c.*1988C>T| S159
S243
59207 BAA01g31760 A01 20764499 G A downstream_gene_variant MODIFIER c.*2218G>A| S12
59208 BAA01g31760 A01 20764686 C T downstream_gene_variant MODIFIER c.*2405C>T| S255
59209 BAA01g31760 A01 20765254 G A downstream_gene_variant MODIFIER c.*2973G>A| S169
59210 BAA01g31760 A01 20765446 G A downstream_gene_variant MODIFIER c.*3165G>A| S174
59211 BAA01g31760 A01 20765486 G A downstream_gene_variant MODIFIER c.*3205G>A| S45
59212 BAA01g31760 A01 20765923 G A downstream_gene_variant MODIFIER c.*3642G>A| S70
59213 BAA01g31760 A01 20767189 C T downstream_gene_variant MODIFIER c.*4908C>T| S239
59214 BAA01g31770 A01 20767939 G A downstream_gene_variant MODIFIER c.*1312C>T| S176
59215 BAA01g31770 A01 20768023 G A downstream_gene_variant MODIFIER c.*1228C>T| S32
59216 BAA01g31770 A01 20768053 C T downstream_gene_variant MODIFIER c.*1198G>A| S213
59217 BAA01g31770 A01 20768104 C T downstream_gene_variant MODIFIER c.*1147G>A| S198
59218 BAA01g31770 A01 20768988 C T downstream_gene_variant MODIFIER c.*263G>A| S201
59219 BAA01g31770 A01 20769021 G A downstream_gene_variant MODIFIER c.*230C>T| S35
59220 BAA01g31770 A01 20770578 C T intron_variant MODIFIER c.244+97G>A| S178
59221 BAA01g31770 A01 20770630 G A intron_variant MODIFIER c.244+45C>T| S71
59222 BAA01g31770 A01 20771184 G A upstream_gene_variant MODIFIER c.-266C>T| S247
59223 BAA01g31770 A01 20771749 A T upstream_gene_variant MODIFIER c.-831T>A| S61
59224 BAA01g31770 A01 20772651 T C upstream_gene_variant MODIFIER c.-1733A>G| S174
S241
S27
S39
59225 BAA01g31770 A01 20773082 C T upstream_gene_variant MODIFIER c.-2164G>A| S249