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
177651 BAA02g18900 A02 9773024 G A upstream_gene_variant MODIFIER c.-2494G>A| S79
S91
177652 BAA02g18900 A02 9773127 C T upstream_gene_variant MODIFIER c.-2391C>T| S90
177653 BAA02g18900 A02 9773964 C T upstream_gene_variant MODIFIER c.-1554C>T| S301
S304
177654 BAA02g18900 A02 9775937 C T downstream_gene_variant MODIFIER c.*144C>T| S80
177655 BAA02g18900 A02 9776274 C T downstream_gene_variant MODIFIER c.*481C>T| S216
S241
S265
S39
177656 BAA02g18910 A02 9776932 G A missense_variant MODERATE c.364C>T|p.Arg122Cys S7
177657 BAA02g18910 A02 9778513 G A upstream_gene_variant MODIFIER c.-1141C>T| S62
177658 BAA02g18910 A02 9779118 G A upstream_gene_variant MODIFIER c.-1746C>T| S132
S137
S215
S89
177659 BAA02g18910 A02 9779177 G A upstream_gene_variant MODIFIER c.-1805C>T| S247
177660 BAA02g18910 A02 9779237 G A upstream_gene_variant MODIFIER c.-1865C>T| S69
177661 BAA02g18920 A02 9779888 C T missense_variant MODERATE c.520G>A|p.Ala174Thr S165
177662 BAA02g18910 A02 9779964 G A upstream_gene_variant MODIFIER c.-2592C>T| S245
177663 BAA02g18920 A02 9780014 G A missense_variant&splice_region_variant MODERATE c.476C>T|p.Pro159Leu S236
177664 BAA02g18910 A02 9781017 C T upstream_gene_variant MODIFIER c.-3645G>A| S138
177665 BAA02g18910 A02 9781515 G A upstream_gene_variant MODIFIER c.-4143C>T| S228
177666 BAA02g18910 A02 9781666 C T upstream_gene_variant MODIFIER c.-4294G>A| S208
177667 BAA02g18910 A02 9781697 G A upstream_gene_variant MODIFIER c.-4325C>T| S155
177668 BAA02g18910 A02 9781701 C T upstream_gene_variant MODIFIER c.-4329G>A| S18
177669 BAA02g18930 A02 9783818 C T missense_variant MODERATE c.1129G>A|p.Asp377Asn S289
S290
177670 BAA02g18920 A02 9784042 C T upstream_gene_variant MODIFIER c.-1018G>A| S219
177671 BAA02g18930 A02 9784372 C T synonymous_variant LOW c.687G>A|p.Val229Val S123
177672 BAA02g18930 A02 9784738 C T missense_variant MODERATE c.391G>A|p.Asp131Asn S179
177673 BAA02g18930 A02 9784980 G A missense_variant MODERATE c.149C>T|p.Ser50Phe S110
177674 BAA02g18930 A02 9785070 G A missense_variant MODERATE c.59C>T|p.Ser20Phe S69
177675 BAA02g18920 A02 9785408 G A upstream_gene_variant MODIFIER c.-2384C>T| S173