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
156901 BAA02g04780 A02 2077969 G A missense_variant MODERATE c.877G>A|p.Asp293Asn S81
S85
156902 BAA02g04780 A02 2078196 C T synonymous_variant LOW c.1104C>T|p.Phe368Phe S13
156903 BAA02g04780 A02 2078293 C T missense_variant MODERATE c.1201C>T|p.Pro401Ser S306
156904 BAA02g04780 A02 2078495 C T missense_variant MODERATE c.1403C>T|p.Ala468Val S82
S92
156905 BAA02g04780 A02 2079018 C T synonymous_variant LOW c.1926C>T|p.Phe642Phe S77
S82
156906 BAA02g04780 A02 2079656 G A missense_variant MODERATE c.2564G>A|p.Arg855Lys S237
156907 BAA02g04780 A02 2080601 G A synonymous_variant LOW c.3183G>A|p.Gln1061Gln S249
156908 BAA02g04790 A02 2082108 C T missense_variant MODERATE c.7G>A|p.Ala3Thr S287
156909 BAA02g04790 A02 2082645 C T upstream_gene_variant MODIFIER c.-531G>A| S37
156910 BAA02g04790 A02 2082992 G A upstream_gene_variant MODIFIER c.-878C>T| S7
156911 BAA02g04800 A02 2083866 G A missense_variant MODERATE c.782G>A|p.Ser261Asn S246
156912 BAA02g04800 A02 2084093 C T missense_variant MODERATE c.1009C>T|p.Pro337Ser S250
156913 BAA02g04800 A02 2084130 C T missense_variant MODERATE c.1046C>T|p.Pro349Leu S179
156914 BAA02g04800 A02 2084178 C T missense_variant MODERATE c.1094C>T|p.Thr365Ile S216
156915 BAA02g04800 A02 2084240 C T missense_variant MODERATE c.1156C>T|p.Pro386Ser S233
156916 BAA02g04790 A02 2084398 G A upstream_gene_variant MODIFIER c.-2284C>T| S60
156917 BAA02g04800 A02 2084524 G A missense_variant MODERATE c.1367G>A|p.Arg456Gln S107
156918 BAA02g04790 A02 2085128 G A upstream_gene_variant MODIFIER c.-3014C>T| S127
156919 BAA02g04800 A02 2085688 G A missense_variant MODERATE c.1964G>A|p.Ser655Asn S266
156920 BAA02g04800 A02 2086399 C T missense_variant MODERATE c.2675C>T|p.Ala892Val S157
156921 BAA02g04800 A02 2087034 C T missense_variant MODERATE c.3026C>T|p.Thr1009Met S46
156922 BAA02g04810 A02 2087581 C T downstream_gene_variant MODIFIER c.*3637G>A| S286
156923 BAA02g04800 A02 2088027 C T missense_variant MODERATE c.3616C>T|p.Leu1206Phe S138
156924 BAA02g04810 A02 2088358 G A downstream_gene_variant MODIFIER c.*2860C>T| S155
S211
156925 BAA02g04800 A02 2088744 C T missense_variant MODERATE c.4019C>T|p.Ala1340Val S278