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
90701 BAA10g00770 A10 366939 G A intron_variant MODIFIER c.253-323G>A| S95
90702 BAA10g00770 A10 367048 C T intron_variant MODIFIER c.253-214C>T| S159
S243
S299
90703 BAA10g00770 A10 367417 G A intron_variant MODIFIER c.325-73G>A| S15
S3
90704 BAA10g00770 A10 367907 C T missense_variant MODERATE c.526C>T|p.Leu176Phe S98
90705 BAA10g00780 A10 368083 G A upstream_gene_variant MODIFIER c.-4953G>A| S192
90706 BAA10g00770 A10 368448 G A splice_region_variant&intron_variant LOW c.783+5G>A| S158
90707 BAA10g00770 A10 368851 C T synonymous_variant LOW c.969C>T|p.Ile323Ile S157
90708 BAA10g00780 A10 370068 T C upstream_gene_variant MODIFIER c.-2968T>C| S189
90709 BAA10g00780 A10 372139 C T upstream_gene_variant MODIFIER c.-897C>T| S95
90710 BAA10g00780 A10 372395 G A upstream_gene_variant MODIFIER c.-641G>A| S148
S210
S30
90711 BAA10g00780 A10 373102 G A missense_variant MODERATE c.67G>A|p.Asp23Asn S69
90712 BAA10g00780 A10 374133 G A synonymous_variant LOW c.1098G>A|p.Glu366Glu S150
90713 BAA10g00780 A10 374244 G A synonymous_variant LOW c.1209G>A|p.Lys403Lys S276
90714 BAA10g00780 A10 374433 G A stop_gained HIGH c.1398G>A|p.Trp466* S20
90715 BAA10g00780 A10 375077 T C downstream_gene_variant MODIFIER c.*452T>C| S286
90716 BAA10g00780 A10 375114 C T downstream_gene_variant MODIFIER c.*489C>T| S171
90717 BAA10g00800 A10 375642 G A upstream_gene_variant MODIFIER c.-4562G>A| S13
90718 BAA10g00790 A10 376684 C T synonymous_variant LOW c.1356G>A|p.Arg452Arg S135
90719 BAA10g00790 A10 377082 C T missense_variant MODERATE c.958G>A|p.Asp320Asn S135
90720 BAA10g00790 A10 379273 C T upstream_gene_variant MODIFIER c.-589G>A| S269
90721 BAA10g00790 A10 379296 G A upstream_gene_variant MODIFIER c.-612C>T| S234
90722 BAA10g00800 A10 380604 C T missense_variant MODERATE c.214C>T|p.Pro72Ser S61
90723 BAA10g00800 A10 385024 C T downstream_gene_variant MODIFIER c.*4204C>T| S27
90724 BAA10g00810 A10 386161 C T downstream_gene_variant MODIFIER c.*3259C>T| S271
90725 BAA10g00810 A10 386267 G A downstream_gene_variant MODIFIER c.*3365G>A| S264