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
137651 BAA10g23250 A10 19646761 G A upstream_gene_variant MODIFIER c.-3976C>T| S212
137652 BAA10g23270 A10 19648913 G A missense_variant MODERATE c.388C>T|p.Leu130Phe S262
137653 BAA10g23270 A10 19651128 C T upstream_gene_variant MODIFIER c.-711G>A| S122
137654 BAA10g23270 A10 19654362 C T upstream_gene_variant MODIFIER c.-3945G>A| S144
137655 BAA10g23290 A10 19656099 G A upstream_gene_variant MODIFIER c.-2022G>A| S74
137656 BAA10g23280 A10 19657010 G A missense_variant MODERATE c.881G>A|p.Arg294Lys S62
137657 BAA10g23280 A10 19657024 G A missense_variant MODERATE c.895G>A|p.Gly299Arg S245
137658 BAA10g23310 A10 19660077 C T upstream_gene_variant MODIFIER c.-3355C>T| S236
137659 BAA10g23300 A10 19660818 C T synonymous_variant LOW c.1125G>A|p.Glu375Glu S236
137660 BAA10g23300 A10 19661324 G A stop_gained HIGH c.619C>T|p.Gln207* S203
137661 BAA10g23300 A10 19661346 G A synonymous_variant LOW c.597C>T|p.Phe199Phe S289
S290
137662 BAA10g23310 A10 19661787 G A upstream_gene_variant MODIFIER c.-1645G>A| S136
137663 BAA10g23310 A10 19663469 G A missense_variant MODERATE c.38G>A|p.Ser13Asn S173
137664 BAA10g23300 A10 19663821 G A upstream_gene_variant MODIFIER c.-1107C>T| S16
137665 BAA10g23320 A10 19666710 G A missense_variant MODERATE c.445G>A|p.Glu149Lys S139
137666 BAA10g23320 A10 19667180 C T synonymous_variant LOW c.636C>T|p.Ser212Ser S34
137667 BAA10g23310 A10 19668166 C T downstream_gene_variant MODIFIER c.*3198C>T| S70
137668 BAA10g23320 A10 19669395 G A synonymous_variant LOW c.2040G>A|p.Glu680Glu S295
137669 BAA10g23320 A10 19669424 G A splice_region_variant&intron_variant LOW c.2064+5G>A| S120
137670 BAA10g23310 A10 19669463 C T downstream_gene_variant MODIFIER c.*4495C>T| S247
137671 BAA10g23320 A10 19670541 G A downstream_gene_variant MODIFIER c.*447G>A| S90
137672 BAA10g23330 A10 19671410 G A splice_region_variant&intron_variant LOW c.978-3C>T| S250
137673 BAA10g23330 A10 19672845 C T missense_variant MODERATE c.104G>A|p.Gly35Glu S142
137674 BAA10g23330 A10 19673220 C T upstream_gene_variant MODIFIER c.-272G>A| S155
S211
137675 BAA10g23330 A10 19673628 C T upstream_gene_variant MODIFIER c.-680G>A| S38