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
149401 BAA10g33540 A10 23843531 C T upstream_gene_variant MODIFIER c.-3621G>A| S16
149402 BAA10g33550 A10 23847642 G A intron_variant MODIFIER c.683-745G>A| S106
149403 BAA10g33550 A10 23848547 C T intron_variant MODIFIER c.794-27C>T| S161
149404 BAA10g33550 A10 23849447 G A missense_variant MODERATE c.1301G>A|p.Arg434Lys S294
149405 BAA10g33550 A10 23849790 G A missense_variant MODERATE c.1565G>A|p.Cys522Tyr S99
149406 BAA10g33550 A10 23850541 C T downstream_gene_variant MODIFIER c.*717C>T| S73
S91
149407 BAA10g33550 A10 23850670 C T downstream_gene_variant MODIFIER c.*846C>T| S54
149408 BAA10g33550 A10 23850978 C T downstream_gene_variant MODIFIER c.*1154C>T| S283
S98
149409 BAA10g33550 A10 23851803 G A downstream_gene_variant MODIFIER c.*1979G>A| S179
149410 BAA10g33550 A10 23853311 C T downstream_gene_variant MODIFIER c.*3487C>T| S63
149411 BAA10g33550 A10 23853493 G A downstream_gene_variant MODIFIER c.*3669G>A| S59
149412 BAA10g33560 A10 23854413 C T synonymous_variant LOW c.435G>A|p.Lys145Lys S124
149413 BAA10g33560 A10 23854679 C T missense_variant MODERATE c.367G>A|p.Asp123Asn S122
149414 BAA10g33560 A10 23855243 G A intron_variant MODIFIER c.14-14C>T| S185
149415 BAA10g33560 A10 23855859 G A upstream_gene_variant MODIFIER c.-505C>T| S171
149416 BAA10g33560 A10 23858115 G A upstream_gene_variant MODIFIER c.-2761C>T| S54
149417 BAA10g33560 A10 23858777 G A upstream_gene_variant MODIFIER c.-3423C>T| S38
149418 BAA10g33560 A10 23859083 C T upstream_gene_variant MODIFIER c.-3729G>A| S1
149419 BAA10g33560 A10 23859205 G A upstream_gene_variant MODIFIER c.-3851C>T| S1
S90
149420 BAA10g33570 A10 23860667 C T upstream_gene_variant MODIFIER c.-3053C>T| S67
149421 BAA10g33570 A10 23860982 G A upstream_gene_variant MODIFIER c.-2738G>A| S59
149422 BAA10g33570 A10 23861484 G A upstream_gene_variant MODIFIER c.-2236G>A| S265
149423 BAA10g33570 A10 23862106 G A upstream_gene_variant MODIFIER c.-1614G>A| S133
149424 BAA10g33570 A10 23862898 C T upstream_gene_variant MODIFIER c.-822C>T| S295
149425 BAA10g33570 A10 23862913 G A upstream_gene_variant MODIFIER c.-807G>A| S207