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
125601 BAA10g14710 A10 15348168 G A upstream_gene_variant MODIFIER c.-689G>A| S250
125602 BAA10g14710 A10 15348369 G A upstream_gene_variant MODIFIER c.-488G>A| S72
125603 BAA10g14710 A10 15349865 G A missense_variant MODERATE c.383G>A|p.Ser128Asn S265
125604 BAA10g14710 A10 15350303 G A splice_acceptor_variant&intron_variant HIGH c.615-1G>A| S112
125605 BAA10g14710 A10 15350578 C T missense_variant MODERATE c.802C>T|p.Leu268Phe S44
125606 BAA10g14720 A10 15351111 G A upstream_gene_variant MODIFIER c.-1181G>A| S288
125607 BAA10g14720 A10 15351581 G A upstream_gene_variant MODIFIER c.-711G>A| S199
125608 BAA10g14720 A10 15352120 C T upstream_gene_variant MODIFIER c.-172C>T| S26
125609 BAA10g14720 A10 15352447 C T missense_variant MODERATE c.67C>T|p.Pro23Ser S163
125610 BAA10g14700 A10 15352548 G A downstream_gene_variant MODIFIER c.*4962G>A| S118
125611 BAA10g14710 A10 15352629 C T downstream_gene_variant MODIFIER c.*1157C>T| S274
125612 BAA10g14720 A10 15353555 G A splice_donor_variant&intron_variant HIGH c.405+1G>A| S118
125613 BAA10g14720 A10 15354291 G A missense_variant MODERATE c.563G>A|p.Gly188Glu S288
125614 BAA10g14720 A10 15354393 A T missense_variant MODERATE c.665A>T|p.Gln222Leu S267
125615 BAA10g14710 A10 15354475 G A downstream_gene_variant MODIFIER c.*3003G>A| S130
125616 BAA10g14710 A10 15354593 G A downstream_gene_variant MODIFIER c.*3121G>A| S279
125617 BAA10g14710 A10 15354676 G A downstream_gene_variant MODIFIER c.*3204G>A| S40
S49
125618 BAA10g14710 A10 15355171 G A downstream_gene_variant MODIFIER c.*3699G>A| S201
125619 BAA10g14710 A10 15355508 C T downstream_gene_variant MODIFIER c.*4036C>T| S6
125620 BAA10g14720 A10 15358077 C T downstream_gene_variant MODIFIER c.*3677C>T| S103
125621 BAA10g14730 A10 15359787 C T downstream_gene_variant MODIFIER c.*3722G>A| S48
125622 BAA10g14730 A10 15360095 C T downstream_gene_variant MODIFIER c.*3414G>A| S206
125623 BAA10g14730 A10 15363068 C T downstream_gene_variant MODIFIER c.*441G>A| S38
125624 BAA10g14730 A10 15363081 G A downstream_gene_variant MODIFIER c.*428C>T| S62
125625 BAA10g14730 A10 15363809 C T intron_variant MODIFIER c.1272-12G>A| S243