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
168951 BAA02g14130 A02 6624084 G A upstream_gene_variant MODIFIER c.-4646G>A| S229
168952 BAA02g14130 A02 6624164 C T upstream_gene_variant MODIFIER c.-4566C>T| S130
168953 BAA02g14120 A02 6626473 G A upstream_gene_variant MODIFIER c.-20C>T| S113
S117
S23
S9
168954 BAA02g14120 A02 6628012 C T upstream_gene_variant MODIFIER c.-1559G>A| S252
168955 BAA02g14120 A02 6628647 C T upstream_gene_variant MODIFIER c.-2194G>A| S72
168956 BAA02g14130 A02 6629107 G A synonymous_variant LOW c.378G>A|p.Gln126Gln S228
168957 BAA02g14130 A02 6629342 C T missense_variant MODERATE c.542C>T|p.Pro181Leu S129
168958 BAA02g14120 A02 6629763 G A upstream_gene_variant MODIFIER c.-3310C>T| S291
168959 BAA02g14130 A02 6630171 C T missense_variant MODERATE c.976C>T|p.Pro326Ser S144
168960 BAA02g14130 A02 6630645 G A missense_variant MODERATE c.1159G>A|p.Asp387Asn S256
168961 BAA02g14130 A02 6630852 C T missense_variant MODERATE c.1222C>T|p.Pro408Ser S249
168962 BAA02g14120 A02 6631397 G A upstream_gene_variant MODIFIER c.-4944C>T| S38
168963 BAA02g14140 A02 6631610 C T downstream_gene_variant MODIFIER c.*1851G>A| S16
168964 BAA02g14130 A02 6632167 G A synonymous_variant LOW c.1917G>A|p.Lys639Lys S122
168965 BAA02g14130 A02 6632325 G A downstream_gene_variant MODIFIER c.*152G>A| S289
S290
168966 BAA02g14140 A02 6633745 C T missense_variant MODERATE c.1810G>A|p.Glu604Lys S241
168967 BAA02g14140 A02 6633959 C T synonymous_variant LOW c.1596G>A|p.Glu532Glu S129
168968 BAA02g14140 A02 6633989 C T synonymous_variant LOW c.1566G>A|p.Glu522Glu S139
168969 BAA02g14140 A02 6634468 G A missense_variant MODERATE c.1087C>T|p.Leu363Phe S198
168970 BAA02g14150 A02 6635502 C T upstream_gene_variant MODIFIER c.-3983C>T| S58
168971 BAA02g14140 A02 6635998 C T upstream_gene_variant MODIFIER c.-284G>A| S219
S72
168972 BAA02g14140 A02 6636705 C T upstream_gene_variant MODIFIER c.-991G>A| S47
168973 BAA02g14140 A02 6636945 G A upstream_gene_variant MODIFIER c.-1231C>T| S173
168974 BAA02g14140 A02 6637520 G A upstream_gene_variant MODIFIER c.-1806C>T| S67
168975 BAA02g14140 A02 6637868 C T upstream_gene_variant MODIFIER c.-2154G>A| S135