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
75951 BAA01g39980 A01 26555031 C T downstream_gene_variant MODIFIER c.*1188C>T| S282
75952 BAA01g39980 A01 26555095 C T downstream_gene_variant MODIFIER c.*1252C>T| S166
75953 BAA01g39980 A01 26555586 G A downstream_gene_variant MODIFIER c.*1743G>A| S229
75954 BAA01g39980 A01 26556727 G A downstream_gene_variant MODIFIER c.*2884G>A| S280
75955 BAA01g39980 A01 26557059 C T downstream_gene_variant MODIFIER c.*3216C>T| S198
75956 BAA01g39980 A01 26557496 G A downstream_gene_variant MODIFIER c.*3653G>A| S1
S90
75957 BAA01g39990 A01 26559272 C T downstream_gene_variant MODIFIER c.*2087G>A| S205
75958 BAA01g39990 A01 26559744 G A downstream_gene_variant MODIFIER c.*1615C>T| S105
S106
75959 BAA01g39990 A01 26560743 G A downstream_gene_variant MODIFIER c.*616C>T| S163
75960 BAA01g39990 A01 26561975 G A intron_variant MODIFIER c.1643-32C>T| S8
75961 BAA01g39990 A01 26562530 G A intron_variant MODIFIER c.1377-143C>T| S195
75962 BAA01g39990 A01 26563167 C T synonymous_variant LOW c.1026G>A|p.Lys342Lys S230
75963 BAA01g39990 A01 26563945 G T intron_variant MODIFIER c.651-10C>A| S149
75964 BAA01g39990 A01 26563946 A T intron_variant MODIFIER c.651-11T>A| S149
75965 BAA01g39990 A01 26564536 C T missense_variant&splice_region_variant MODERATE c.448G>A|p.Glu150Lys S198
75966 BAA01g39990 A01 26564759 C T intron_variant MODIFIER c.322-97G>A| S203
75967 BAA01g39990 A01 26564888 C T intron_variant MODIFIER c.321+218G>A| S139
75968 BAA01g39990 A01 26564958 C T intron_variant MODIFIER c.321+148G>A| S159
S243
75969 BAA01g39990 A01 26565274 C T synonymous_variant LOW c.153G>A|p.Lys51Lys S39
75970 BAA01g39990 A01 26565371 G A missense_variant MODERATE c.56C>T|p.Ala19Val S245
75971 BAA01g39990 A01 26568966 C T upstream_gene_variant MODIFIER c.-3540G>A| S148
S30
S31
75972 BAA01g39990 A01 26569060 C T upstream_gene_variant MODIFIER c.-3634G>A| S264
75973 BAA01g39990 A01 26570027 C T upstream_gene_variant MODIFIER c.-4601G>A| S206
S26
75974 BAA01g40000 A01 26571276 G A missense_variant MODERATE c.275C>T|p.Thr92Ile S181
75975 BAA01g40000 A01 26571365 C T synonymous_variant LOW c.186G>A|p.Arg62Arg S201