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
183651 BAA02g22150 A02 11937099 G A synonymous_variant LOW c.321C>T|p.Asn107Asn S159
S243
183652 BAA02g22150 A02 11937658 G A upstream_gene_variant MODIFIER c.-154C>T| S230
183653 BAA02g22150 A02 11937668 G A upstream_gene_variant MODIFIER c.-164C>T| S237
183654 BAA02g22150 A02 11938354 G A upstream_gene_variant MODIFIER c.-850C>T| S50
183655 BAA02g22150 A02 11939627 C T upstream_gene_variant MODIFIER c.-2123G>A| S250
183656 BAA02g22160 A02 11939984 C T missense_variant MODERATE c.323C>T|p.Pro108Leu S164
183657 BAA02g22150 A02 11940530 G A upstream_gene_variant MODIFIER c.-3026C>T| S69
183658 BAA02g22150 A02 11940798 C T upstream_gene_variant MODIFIER c.-3294G>A| S112
183659 BAA02g22160 A02 11941103 G A missense_variant MODERATE c.785G>A|p.Arg262Lys S294
183660 BAA02g22150 A02 11941940 G A upstream_gene_variant MODIFIER c.-4436C>T| S156
183661 BAA02g22180 A02 11943972 C T missense_variant MODERATE c.556G>A|p.Gly186Arg S73
183662 BAA02g22180 A02 11945117 G A upstream_gene_variant MODIFIER c.-590C>T| S17
183663 BAA02g22180 A02 11945969 C T upstream_gene_variant MODIFIER c.-1442G>A| S181
183664 BAA02g22180 A02 11947979 C T upstream_gene_variant MODIFIER c.-3452G>A| S71
183665 BAA02g22180 A02 11948342 C T upstream_gene_variant MODIFIER c.-3815G>A| S209
183666 BAA02g22180 A02 11948451 T A upstream_gene_variant MODIFIER c.-3924A>T| S186
183667 BAA02g22180 A02 11949093 C T upstream_gene_variant MODIFIER c.-4566G>A| S178
183668 BAA02g22180 A02 11949228 C T upstream_gene_variant MODIFIER c.-4701G>A| S135
183669 BAA02g22190 A02 11950236 G A downstream_gene_variant MODIFIER c.*548C>T| S19
183670 BAA02g22190 A02 11954694 G A upstream_gene_variant MODIFIER c.-2131C>T| S34
183671 BAA02g22190 A02 11955164 C T upstream_gene_variant MODIFIER c.-2601G>A| S218
183672 BAA02g22200 A02 11955807 C T missense_variant MODERATE c.187C>T|p.Pro63Ser S296
183673 BAA02g22210 A02 11957835 C T missense_variant MODERATE c.674C>T|p.Thr225Ile S63
183674 BAA02g22210 A02 11958090 C T splice_region_variant&intron_variant LOW c.843+6C>T| S301
S304
183675 BAA02g22210 A02 11958670 C T missense_variant MODERATE c.1058C>T|p.Pro353Leu S206