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
16601 BAA01g12570 A01 5937419 G A upstream_gene_variant MODIFIER c.-2012G>A| S80
16602 BAA01g12560 A01 5937695 G A stop_gained HIGH c.322C>T|p.Gln108* S15
16603 BAA01g12560 A01 5937959 G A synonymous_variant LOW c.162C>T|p.Leu54Leu S296
16604 BAA01g12570 A01 5938400 C T upstream_gene_variant MODIFIER c.-1031C>T| S9
16605 BAA01g12570 A01 5938457 C T upstream_gene_variant MODIFIER c.-974C>T| S79
S84
16606 BAA01g12580 A01 5940511 C T missense_variant MODERATE c.1970G>A|p.Ser657Asn S244
16607 BAA01g12580 A01 5941027 G A missense_variant MODERATE c.1601C>T|p.Ser534Phe S45
16608 BAA01g12580 A01 5941430 C T missense_variant&splice_region_variant MODERATE c.1270G>A|p.Val424Ile S221
16609 BAA01g12560 A01 5943570 T C upstream_gene_variant MODIFIER c.-4752A>G| S92
16610 BAA01g12580 A01 5945418 G A upstream_gene_variant MODIFIER c.-2085C>T| S144
16611 BAA01g12590 A01 5945807 C T synonymous_variant LOW c.474G>A|p.Gln158Gln S208
S93
16612 BAA01g12590 A01 5946174 C T missense_variant MODERATE c.107G>A|p.Arg36His S200
S261
16613 BAA01g12580 A01 5947804 C T upstream_gene_variant MODIFIER c.-4471G>A| S111
16614 BAA01g12580 A01 5947834 C T upstream_gene_variant MODIFIER c.-4501G>A| S19
16615 BAA01g12580 A01 5947989 C T upstream_gene_variant MODIFIER c.-4656G>A| S296
16616 BAA01g12580 A01 5948232 G A upstream_gene_variant MODIFIER c.-4899C>T| S287
16617 BAA01g12600 A01 5948684 C T missense_variant MODERATE c.1117G>A|p.Asp373Asn S198
16618 BAA01g12590 A01 5951019 G A upstream_gene_variant MODIFIER c.-4739C>T| S202
16619 BAA01g12600 A01 5953420 C T upstream_gene_variant MODIFIER c.-2990G>A| S44
16620 BAA01g12610 A01 5954211 G A missense_variant MODERATE c.110G>A|p.Gly37Asp S131
16621 BAA01g12610 A01 5954223 C T missense_variant MODERATE c.122C>T|p.Ser41Phe S182
16622 BAA01g12610 A01 5954364 C T missense_variant MODERATE c.263C>T|p.Ser88Phe S100
16623 BAA01g12610 A01 5954396 C T missense_variant MODERATE c.295C>T|p.Leu99Phe S8
16624 BAA01g12610 A01 5954602 C T synonymous_variant LOW c.501C>T|p.Cys167Cys S166
S209
16625 BAA01g12610 A01 5955080 G A missense_variant MODERATE c.979G>A|p.Asp327Asn S138