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
90451 BAA10g00530 A10 267587 C T missense_variant MODERATE c.11G>A|p.Arg4Lys S266
90452 BAA10g00530 A10 267600 C T upstream_gene_variant MODIFIER c.-3G>A| S298
90453 BAA10g00530 A10 267672 G A upstream_gene_variant MODIFIER c.-75C>T| S20
90454 BAA10g00540 A10 268907 G A missense_variant MODERATE c.28G>A|p.Glu10Lys S191
90455 BAA10g00540 A10 269278 G A synonymous_variant LOW c.399G>A|p.Ala133Ala S262
90456 BAA10g00540 A10 269358 G A missense_variant MODERATE c.479G>A|p.Gly160Glu S172
S217
90457 BAA10g00530 A10 270024 C T upstream_gene_variant MODIFIER c.-2427G>A| S139
90458 BAA10g00530 A10 270782 C T upstream_gene_variant MODIFIER c.-3185G>A| S12
90459 BAA10g00530 A10 270906 C T upstream_gene_variant MODIFIER c.-3309G>A| S28
90460 BAA10g00530 A10 271309 G A upstream_gene_variant MODIFIER c.-3712C>T| S25
90461 BAA10g00550 A10 272098 C T synonymous_variant LOW c.315C>T|p.Tyr105Tyr S270
90462 BAA10g00550 A10 272814 G A missense_variant MODERATE c.1031G>A|p.Gly344Glu S278
90463 BAA10g00550 A10 272935 G A synonymous_variant LOW c.1152G>A|p.Ser384Ser S295
90464 BAA10g00550 A10 273509 G A synonymous_variant LOW c.1560G>A|p.Ser520Ser S119
90465 BAA10g00550 A10 273704 G A missense_variant MODERATE c.1655G>A|p.Arg552Lys S274
90466 BAA10g00570 A10 282947 G A upstream_gene_variant MODIFIER c.-2683G>A| S217
90467 BAA10g00570 A10 282949 G A upstream_gene_variant MODIFIER c.-2681G>A| S33
90468 BAA10g00570 A10 283361 C T upstream_gene_variant MODIFIER c.-2269C>T| S294
90469 BAA10g00570 A10 283980 A G upstream_gene_variant MODIFIER c.-1650A>G| S167
90470 BAA10g00570 A10 284038 G A upstream_gene_variant MODIFIER c.-1592G>A| S20
90471 BAA10g00570 A10 284157 G A upstream_gene_variant MODIFIER c.-1473G>A| S157
S163
90472 BAA10g00570 A10 284761 T A upstream_gene_variant MODIFIER c.-869T>A| S259
90473 BAA10g00570 A10 286102 C T synonymous_variant LOW c.399C>T|p.Thr133Thr S237
90474 BAA10g00570 A10 286261 G A missense_variant MODERATE c.558G>A|p.Met186Ile S283
90475 BAA10g00570 A10 286403 G A missense_variant MODERATE c.700G>A|p.Asp234Asn S48