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
51651 BAA01g28560 A01 17905320 C T downstream_gene_variant MODIFIER c.*339G>A| S10
51652 BAA01g28560 A01 17905931 C T missense_variant MODERATE c.457G>A|p.Ala153Thr S277
51653 BAA01g28560 A01 17906281 C T missense_variant MODERATE c.233G>A|p.Ser78Asn S107
51654 BAA01g28560 A01 17907096 C T missense_variant MODERATE c.119G>A|p.Cys40Tyr S186
51655 BAA01g28560 A01 17907151 G A synonymous_variant LOW c.64C>T|p.Leu22Leu S181
51656 BAA01g28560 A01 17909067 G A upstream_gene_variant MODIFIER c.-1853C>T| S15
S3
51657 BAA01g28560 A01 17910301 G A upstream_gene_variant MODIFIER c.-3087C>T| S302
51658 BAA01g28560 A01 17911070 C T upstream_gene_variant MODIFIER c.-3856G>A| S282
51659 BAA01g28560 A01 17911809 C T upstream_gene_variant MODIFIER c.-4595G>A| S240
51660 BAA01g28570 A01 17912388 G A downstream_gene_variant MODIFIER c.*616C>T| S178
51661 BAA01g28570 A01 17912479 G A downstream_gene_variant MODIFIER c.*525C>T| S36
51662 BAA01g28570 A01 17914399 C T missense_variant MODERATE c.1918G>A|p.Gly640Arg S19
51663 BAA01g28570 A01 17915663 C T missense_variant MODERATE c.1186G>A|p.Ala396Thr S242
51664 BAA01g28570 A01 17917097 G A missense_variant MODERATE c.176C>T|p.Ser59Phe S308
51665 BAA01g28570 A01 17917946 C T upstream_gene_variant MODIFIER c.-674G>A| S11
51666 BAA01g28570 A01 17918913 G A upstream_gene_variant MODIFIER c.-1641C>T| S176
51667 BAA01g28580 A01 17919259 C T missense_variant MODERATE c.728C>T|p.Ala243Val S20
51668 BAA01g28580 A01 17919518 G C missense_variant MODERATE c.987G>C|p.Lys329Asn S216
51669 BAA01g28570 A01 17919662 G A upstream_gene_variant MODIFIER c.-2390C>T| S172
S217
51670 BAA01g28570 A01 17921165 G A upstream_gene_variant MODIFIER c.-3893C>T| S173
51671 BAA01g28600 A01 17922481 C T synonymous_variant LOW c.792C>T|p.Cys264Cys S111
51672 BAA01g28600 A01 17922527 C T missense_variant MODERATE c.838C>T|p.Pro280Ser S269
51673 BAA01g28590 A01 17925911 C T downstream_gene_variant MODIFIER c.*4824C>T| S41
51674 BAA01g28600 A01 17927087 C T intron_variant MODIFIER c.2569+27C>T| S282
51675 BAA01g28600 A01 17927779 C T intron_variant MODIFIER c.2811+54C>T| S13
S140
S168
S64