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
180851 BAA02g20560 A02 10911342 C T stop_gained HIGH c.1057C>T|p.Gln353* S77
S82
180852 BAA02g20560 A02 10911488 G A missense_variant MODERATE c.1203G>A|p.Met401Ile S122
180853 BAA02g20560 A02 10912064 G A splice_region_variant&intron_variant LOW c.1458+6G>A| S43
180854 BAA02g20550 A02 10912245 C T downstream_gene_variant MODIFIER c.*4105C>T| S276
180855 BAA02g20570 A02 10913166 G A missense_variant MODERATE c.428C>T|p.Thr143Ile S86
180856 BAA02g20580 A02 10915816 G A synonymous_variant LOW c.816C>T|p.Ser272Ser S256
180857 BAA02g20580 A02 10916521 G A synonymous_variant LOW c.459C>T|p.Leu153Leu S294
180858 BAA02g20580 A02 10917208 G A synonymous_variant LOW c.112C>T|p.Leu38Leu S170
180859 BAA02g20570 A02 10917855 G A upstream_gene_variant MODIFIER c.-4009C>T| S298
180860 BAA02g20570 A02 10918041 G A upstream_gene_variant MODIFIER c.-4195C>T| S230
180861 BAA02g20590 A02 10918895 G A synonymous_variant LOW c.324G>A|p.Ser108Ser S191
180862 BAA02g20600 A02 10921004 C T missense_variant MODERATE c.566C>T|p.Ser189Phe S180
180863 BAA02g20580 A02 10921066 C T upstream_gene_variant MODIFIER c.-3491G>A| S289
S290
180864 BAA02g20610 A02 10922900 G A synonymous_variant LOW c.390G>A|p.Glu130Glu S261
S303
180865 BAA02g20610 A02 10922949 G A missense_variant MODERATE c.439G>A|p.Asp147Asn S62
180866 BAA02g20610 A02 10923069 G A synonymous_variant LOW c.483G>A|p.Arg161Arg S206
S26
180867 BAA02g20590 A02 10923945 G A downstream_gene_variant MODIFIER c.*4714G>A| S280
180868 BAA02g20590 A02 10924112 C T downstream_gene_variant MODIFIER c.*4881C>T| S71
180869 BAA02g20600 A02 10925356 C T downstream_gene_variant MODIFIER c.*3486C>T| S127
180870 BAA02g20600 A02 10925712 G A downstream_gene_variant MODIFIER c.*3842G>A| S156
180871 BAA02g20620 A02 10927824 C T missense_variant MODERATE c.1144G>A|p.Glu382Lys S160
180872 BAA02g20620 A02 10927966 C T stop_gained HIGH c.1002G>A|p.Trp334* S35
180873 BAA02g20630 A02 10928133 C T upstream_gene_variant MODIFIER c.-4445C>T| S124
180874 BAA02g20620 A02 10928439 G A missense_variant MODERATE c.695C>T|p.Ala232Val S10
S33
180875 BAA02g20620 A02 10929024 C T missense_variant MODERATE c.523G>A|p.Ala175Thr S51