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
165951 BAA02g12090 A02 5459329 C T upstream_gene_variant MODIFIER c.-3606G>A| S167
165952 BAA02g12100 A02 5461540 A T upstream_gene_variant MODIFIER c.-3290T>A| S176
165953 BAA02g12100 A02 5462879 G A upstream_gene_variant MODIFIER c.-4629C>T| S56
165954 BAA02g12110 A02 5463505 C T upstream_gene_variant MODIFIER c.-2942G>A| S13
165955 BAA02g12110 A02 5464591 C T upstream_gene_variant MODIFIER c.-4028G>A| S73
S91
165956 BAA02g12120 A02 5466234 C T upstream_gene_variant MODIFIER c.-837C>T| S246
165957 BAA02g12120 A02 5467408 G A missense_variant MODERATE c.338G>A|p.Gly113Glu S205
165958 BAA02g12120 A02 5467736 C T synonymous_variant LOW c.666C>T|p.Cys222Cys S65
165959 BAA02g12120 A02 5467861 G A missense_variant MODERATE c.791G>A|p.Gly264Asp S173
S176
165960 BAA02g12120 A02 5468084 G A stop_gained HIGH c.1014G>A|p.Trp338* S206
S26
165961 BAA02g12120 A02 5468410 G A stop_gained HIGH c.1340G>A|p.Trp447* S17
165962 BAA02g12120 A02 5468642 G A missense_variant MODERATE c.1486G>A|p.Gly496Arg S176
165963 BAA02g12120 A02 5470425 G A intron_variant MODIFIER c.2230+162G>A| S2
165964 BAA02g12120 A02 5471977 G A intron_variant MODIFIER c.2812+285G>A| S188
165965 BAA02g12130 A02 5474070 G A upstream_gene_variant MODIFIER c.-2992G>A| S52
165966 BAA02g12130 A02 5474876 C T upstream_gene_variant MODIFIER c.-2186C>T| S274
165967 BAA02g12130 A02 5475106 G A upstream_gene_variant MODIFIER c.-1956G>A| S161
165968 BAA02g12130 A02 5475480 C T upstream_gene_variant MODIFIER c.-1582C>T| S234
165969 BAA02g12130 A02 5475616 C T upstream_gene_variant MODIFIER c.-1446C>T| S181
165970 BAA02g12130 A02 5475723 C T upstream_gene_variant MODIFIER c.-1339C>T| S144
165971 BAA02g12130 A02 5477399 C T missense_variant MODERATE c.250C>T|p.Arg84Cys S299
165972 BAA02g12130 A02 5477889 C T missense_variant MODERATE c.506C>T|p.Thr169Ile S216
165973 BAA02g12130 A02 5478513 C T missense_variant MODERATE c.911C>T|p.Thr304Ile S224
165974 BAA02g12150 A02 5478821 C T upstream_gene_variant MODIFIER c.-3066C>T| S32
165975 BAA02g12150 A02 5479476 C T upstream_gene_variant MODIFIER c.-2411C>T| S99