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
164101 BAA02g10670 A02 4766026 C T missense_variant MODERATE c.2831G>A|p.Arg944Lys S160
164102 BAA02g10670 A02 4766183 C T missense_variant MODERATE c.2674G>A|p.Gly892Arg S112
164103 BAA02g10660 A02 4766334 G A upstream_gene_variant MODIFIER c.-1374C>T| S133
164104 BAA02g10670 A02 4766642 C T synonymous_variant LOW c.2379G>A|p.Arg793Arg S152
164105 BAA02g10670 A02 4767176 G A splice_region_variant&intron_variant LOW c.1933-4C>T| S85
164106 BAA02g10670 A02 4767528 C T missense_variant MODERATE c.1649G>A|p.Ser550Asn S144
164107 BAA02g10670 A02 4768009 C T missense_variant MODERATE c.1168G>A|p.Gly390Arg S8
164108 BAA02g10670 A02 4768284 C T missense_variant MODERATE c.893G>A|p.Gly298Asp S55
164109 BAA02g10670 A02 4768416 C T missense_variant MODERATE c.761G>A|p.Arg254Lys S46
164110 BAA02g10670 A02 4769272 G A synonymous_variant LOW c.261C>T|p.Phe87Phe S43
164111 BAA02g10660 A02 4769667 G A upstream_gene_variant MODIFIER c.-4707C>T| S192
164112 BAA02g10680 A02 4772424 C T missense_variant MODERATE c.491C>T|p.Ser164Phe S186
S268
164113 BAA02g10670 A02 4772631 G A upstream_gene_variant MODIFIER c.-2738C>T| S296
164114 BAA02g10680 A02 4772756 G A splice_acceptor_variant&intron_variant HIGH c.637-1G>A| S166
164115 BAA02g10680 A02 4773248 G A synonymous_variant LOW c.1038G>A|p.Lys346Lys S191
164116 BAA02g10690 A02 4773694 C T missense_variant MODERATE c.1576G>A|p.Gly526Arg S116
164117 BAA02g10670 A02 4773719 G A upstream_gene_variant MODIFIER c.-3826C>T| S4
164118 BAA02g10690 A02 4775962 C T missense_variant MODERATE c.200G>A|p.Gly67Glu S255
164119 BAA02g10690 A02 4776683 C T upstream_gene_variant MODIFIER c.-381G>A| S97
164120 BAA02g10700 A02 4777086 C T missense_variant MODERATE c.1186G>A|p.Asp396Asn S54
164121 BAA02g10700 A02 4777855 C T synonymous_variant LOW c.585G>A|p.Arg195Arg S252
164122 BAA02g10700 A02 4778805 C T missense_variant MODERATE c.37G>A|p.Ala13Thr S292
164123 BAA02g10690 A02 4780890 C T upstream_gene_variant MODIFIER c.-4588G>A| S305
164124 BAA02g10710 A02 4783915 C T upstream_gene_variant MODIFIER c.-1292G>A| S181
164125 BAA02g10710 A02 4784588 C T upstream_gene_variant MODIFIER c.-1965G>A| S180