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
144701 BAA10g29350 A10 22130317 G A upstream_gene_variant MODIFIER c.-3968C>T| S28
144702 BAA10g29350 A10 22130339 G A upstream_gene_variant MODIFIER c.-3990C>T| S71
144703 BAA10g29350 A10 22130887 G A upstream_gene_variant MODIFIER c.-4538C>T| S134
144704 BAA10g29350 A10 22131303 G A upstream_gene_variant MODIFIER c.-4954C>T| S32
144705 BAA10g29360 A10 22131375 G A upstream_gene_variant MODIFIER c.-2627C>T| S274
144706 BAA10g29380 A10 22132459 G A missense_variant MODERATE c.722G>A|p.Cys241Tyr S126
144707 BAA10g29380 A10 22132471 G A stop_gained&splice_region_variant HIGH c.734G>A|p.Trp245* S125
144708 BAA10g29380 A10 22132635 C T missense_variant MODERATE c.794C>T|p.Ser265Phe S265
144709 BAA10g29360 A10 22133594 C T upstream_gene_variant MODIFIER c.-4846G>A| S204
144710 BAA10g29390 A10 22136785 G A missense_variant MODERATE c.155C>T|p.Pro52Leu S279
144711 BAA10g29390 A10 22136857 G A missense_variant MODERATE c.83C>T|p.Pro28Leu S136
144712 BAA10g29390 A10 22138209 G A upstream_gene_variant MODIFIER c.-1270C>T| S273
144713 BAA10g29400 A10 22138542 C T synonymous_variant LOW c.141C>T|p.Asn47Asn S87
144714 BAA10g29400 A10 22139225 G A synonymous_variant LOW c.561G>A|p.Gln187Gln S65
144715 BAA10g29400 A10 22139651 C T missense_variant MODERATE c.907C>T|p.Arg303Cys S82
S92
144716 BAA10g29400 A10 22139786 C T missense_variant MODERATE c.976C>T|p.Leu326Phe S269
144717 BAA10g29400 A10 22139848 C T synonymous_variant LOW c.1038C>T|p.Tyr346Tyr S114
144718 BAA10g29390 A10 22140799 C T upstream_gene_variant MODIFIER c.-3860G>A| S185
144719 BAA10g29410 A10 22141131 G A synonymous_variant LOW c.1869C>T|p.Phe623Phe S235
144720 BAA10g29390 A10 22141632 G A upstream_gene_variant MODIFIER c.-4693C>T| S273
144721 BAA10g29410 A10 22141758 C T splice_region_variant&intron_variant LOW c.1699+5G>A| S108
S72
144722 BAA10g29410 A10 22142553 G A missense_variant MODERATE c.1363C>T|p.Leu455Phe S132
S137
S138
S215
144723 BAA10g29410 A10 22142558 G A missense_variant MODERATE c.1358C>T|p.Pro453Leu S303
144724 BAA10g29410 A10 22142559 G A missense_variant MODERATE c.1357C>T|p.Pro453Ser S265
144725 BAA10g29410 A10 22143176 G A missense_variant MODERATE c.1052C>T|p.Thr351Ile S39