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
169501 BAA02g14610 A02 6824876 C T synonymous_variant LOW c.300C>T|p.Ala100Ala S183
S198
169502 BAA02g14620 A02 6825879 C T missense_variant MODERATE c.397C>T|p.Pro133Ser S301
S304
169503 BAA02g14620 A02 6825930 G A missense_variant MODERATE c.448G>A|p.Val150Ile S244
169504 BAA02g14620 A02 6825978 G A missense_variant MODERATE c.496G>A|p.Glu166Lys S198
169505 BAA02g14610 A02 6826283 C T downstream_gene_variant MODIFIER c.*1053C>T| S201
169506 BAA02g14620 A02 6827060 G A missense_variant MODERATE c.1465G>A|p.Asp489Asn S192
169507 BAA02g14620 A02 6827210 C T stop_gained HIGH c.1615C>T|p.Arg539* S63
169508 BAA02g14610 A02 6827743 G A downstream_gene_variant MODIFIER c.*2513G>A| S37
169509 BAA02g14630 A02 6834831 G A upstream_gene_variant MODIFIER c.-1223G>A| S136
169510 BAA02g14630 A02 6835419 G A upstream_gene_variant MODIFIER c.-635G>A| S187
169511 BAA02g14630 A02 6835992 C T upstream_gene_variant MODIFIER c.-62C>T| S8
169512 BAA02g14630 A02 6836309 G A missense_variant MODERATE c.256G>A|p.Gly86Arg S244
169513 BAA02g14630 A02 6836707 G A synonymous_variant LOW c.654G>A|p.Pro218Pro S161
169514 BAA02g14640 A02 6841199 G A missense_variant MODERATE c.833C>T|p.Ser278Phe S95
169515 BAA02g14640 A02 6841727 G A synonymous_variant LOW c.519C>T|p.Ser173Ser S245
169516 BAA02g14650 A02 6842355 G A downstream_gene_variant MODIFIER c.*1782C>T| S207
169517 BAA02g14640 A02 6843001 G A synonymous_variant LOW c.111C>T|p.Ser37Ser S79
S91
169518 BAA02g14640 A02 6843572 G A upstream_gene_variant MODIFIER c.-398C>T| S67
169519 BAA02g14640 A02 6846111 G A upstream_gene_variant MODIFIER c.-2937C>T| S143
169520 BAA02g14640 A02 6846854 C T upstream_gene_variant MODIFIER c.-3680G>A| S18
169521 BAA02g14640 A02 6847998 G A upstream_gene_variant MODIFIER c.-4824C>T| S67
169522 BAA02g14660 A02 6849734 C T missense_variant MODERATE c.107G>A|p.Gly36Glu S182
169523 BAA02g14660 A02 6849750 G A missense_variant MODERATE c.91C>T|p.Leu31Phe S223
169524 BAA02g14660 A02 6851192 C T upstream_gene_variant MODIFIER c.-1352G>A| S73
169525 BAA02g14660 A02 6851230 C T upstream_gene_variant MODIFIER c.-1390G>A| S130