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
100351 BAA10g06940 A10 3715877 G A downstream_gene_variant MODIFIER c.*4713C>T| S286
100352 BAA10g06940 A10 3716179 G A downstream_gene_variant MODIFIER c.*4411C>T| S280
100353 BAA10g06940 A10 3716233 G A downstream_gene_variant MODIFIER c.*4357C>T| S289
100354 BAA10g06950 A10 3719758 G A upstream_gene_variant MODIFIER c.-3673G>A| S129
100355 BAA10g06940 A10 3720794 C T upstream_gene_variant MODIFIER c.-34G>A| S130
100356 BAA10g06940 A10 3720830 C T upstream_gene_variant MODIFIER c.-70G>A| S210
100357 BAA10g06940 A10 3721162 G A upstream_gene_variant MODIFIER c.-402C>T| S293
100358 BAA10g06940 A10 3721483 G A upstream_gene_variant MODIFIER c.-723C>T| S268
100359 BAA10g06940 A10 3721816 C T upstream_gene_variant MODIFIER c.-1056G>A| S202
100360 BAA10g06940 A10 3723075 G A upstream_gene_variant MODIFIER c.-2315C>T| S1
S90
100361 BAA10g06950 A10 3723889 C T synonymous_variant LOW c.459C>T|p.Val153Val S15
100362 BAA10g06950 A10 3723958 C T synonymous_variant LOW c.528C>T|p.Phe176Phe S35
100363 BAA10g06950 A10 3724073 C T missense_variant MODERATE c.643C>T|p.Pro215Ser S233
100364 BAA10g06950 A10 3724714 C T synonymous_variant LOW c.1284C>T|p.Ser428Ser S185
100365 BAA10g06950 A10 3725030 G A missense_variant MODERATE c.1600G>A|p.Glu534Lys S303
100366 BAA10g06950 A10 3726227 C T downstream_gene_variant MODIFIER c.*1057C>T| S256
100367 BAA10g06960 A10 3727071 G A upstream_gene_variant MODIFIER c.-4413G>A| S279
100368 BAA10g06960 A10 3727077 G A upstream_gene_variant MODIFIER c.-4407G>A| S215
100369 BAA10g06960 A10 3727202 C T upstream_gene_variant MODIFIER c.-4282C>T| S143
100370 BAA10g06960 A10 3727824 G A upstream_gene_variant MODIFIER c.-3660G>A| S295
100371 BAA10g06960 A10 3728003 C T upstream_gene_variant MODIFIER c.-3481C>T| S143
100372 BAA10g06960 A10 3728604 G A upstream_gene_variant MODIFIER c.-2880G>A| S76
100373 BAA10g06960 A10 3729022 C T upstream_gene_variant MODIFIER c.-2462C>T| S56
100374 BAA10g06960 A10 3733072 G A intron_variant MODIFIER c.837+35G>A| S280
100375 BAA10g06960 A10 3733134 G A missense_variant MODERATE c.851G>A|p.Gly284Glu S85