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
90601 BAA10g00650 A10 320882 C T missense_variant MODERATE c.604G>A|p.Asp202Asn S142
90602 BAA10g00650 A10 321281 T C missense_variant MODERATE c.205A>G|p.Thr69Ala S240
90603 BAA10g00650 A10 321844 C T upstream_gene_variant MODIFIER c.-359G>A| S221
90604 BAA10g00650 A10 322066 C T upstream_gene_variant MODIFIER c.-581G>A| S72
90605 BAA10g00670 A10 326027 G A missense_variant MODERATE c.1394C>T|p.Ala465Val S140
90606 BAA10g00670 A10 326255 C T missense_variant MODERATE c.1166G>A|p.Gly389Glu S37
90607 BAA10g00670 A10 326579 C T missense_variant MODERATE c.842G>A|p.Gly281Asp S196
90608 BAA10g00670 A10 327012 C T missense_variant MODERATE c.409G>A|p.Asp137Asn S10
90609 BAA10g00660 A10 327525 G A upstream_gene_variant MODIFIER c.-2742C>T| S41
90610 BAA10g00660 A10 328093 C T upstream_gene_variant MODIFIER c.-3310G>A| S275
90611 BAA10g00660 A10 329321 G A upstream_gene_variant MODIFIER c.-4538C>T| S240
90612 BAA10g00670 A10 330395 C T upstream_gene_variant MODIFIER c.-2975G>A| S170
90613 BAA10g00670 A10 331712 G A upstream_gene_variant MODIFIER c.-4292C>T| S76
90614 BAA10g00670 A10 331741 G A upstream_gene_variant MODIFIER c.-4321C>T| S252
90615 BAA10g00680 A10 332999 G A downstream_gene_variant MODIFIER c.*584G>A| S107
90616 BAA10g00680 A10 333227 G A downstream_gene_variant MODIFIER c.*812G>A| S120
90617 BAA10g00690 A10 335125 G A missense_variant MODERATE c.586C>T|p.Pro196Ser S156
90618 BAA10g00690 A10 335297 G A synonymous_variant LOW c.414C>T|p.Asp138Asp S180
90619 BAA10g00690 A10 336213 G A upstream_gene_variant MODIFIER c.-503C>T| S16
90620 BAA10g00700 A10 338272 G A missense_variant MODERATE c.34C>T|p.Pro12Ser S41
90621 BAA10g00690 A10 338358 G A upstream_gene_variant MODIFIER c.-2648C>T| S158
90622 BAA10g00690 A10 339316 G A upstream_gene_variant MODIFIER c.-3606C>T| S134
90623 BAA10g00710 A10 339644 G A synonymous_variant LOW c.171G>A|p.Lys57Lys S167
90624 BAA10g00710 A10 340074 C T missense_variant MODERATE c.341C>T|p.Ser114Phe S72
S78
90625 BAA10g00710 A10 340188 C T missense_variant MODERATE c.455C>T|p.Thr152Met S123