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
158551 BAA02g06140 A02 2607825 C A stop_gained HIGH c.35C>A|p.Ser12* S63
158552 BAA02g06130 A02 2609567 G A upstream_gene_variant MODIFIER c.-2230C>T| S237
158553 BAA02g06130 A02 2610313 C T upstream_gene_variant MODIFIER c.-2976G>A| S207
158554 BAA02g06130 A02 2611078 G A upstream_gene_variant MODIFIER c.-3741C>T| S286
158555 BAA02g06130 A02 2611213 C T upstream_gene_variant MODIFIER c.-3876G>A| S263
158556 BAA02g06150 A02 2612636 G A missense_variant MODERATE c.2197C>T|p.Leu733Phe S187
158557 BAA02g06150 A02 2612858 C T missense_variant MODERATE c.1975G>A|p.Glu659Lys S218
158558 BAA02g06150 A02 2613741 C T synonymous_variant LOW c.1092G>A|p.Arg364Arg S42
158559 BAA02g06150 A02 2613935 G A stop_gained HIGH c.898C>T|p.Gln300* S257
158560 BAA02g06150 A02 2615234 G A synonymous_variant LOW c.213C>T|p.Leu71Leu S291
158561 BAA02g06150 A02 2615432 G A synonymous_variant LOW c.15C>T|p.Ser5Ser S297
158562 BAA02g06150 A02 2615743 G A upstream_gene_variant MODIFIER c.-297C>T| S305
158563 BAA02g06150 A02 2616141 G A upstream_gene_variant MODIFIER c.-695C>T| S294
158564 BAA02g06150 A02 2616509 G A upstream_gene_variant MODIFIER c.-1063C>T| S203
158565 BAA02g06160 A02 2616861 C T missense_variant MODERATE c.44C>T|p.Ser15Phe S274
158566 BAA02g06160 A02 2617022 C T synonymous_variant LOW c.123C>T|p.Ala41Ala S142
158567 BAA02g06160 A02 2617318 C T missense_variant MODERATE c.244C>T|p.Pro82Ser S181
158568 BAA02g06160 A02 2617859 C T splice_region_variant&intron_variant LOW c.401-3C>T| S1
S90
158569 BAA02g06160 A02 2618012 G A missense_variant&splice_region_variant MODERATE c.469G>A|p.Asp157Asn S173
158570 BAA02g06160 A02 2618186 C T missense_variant MODERATE c.553C>T|p.Arg185Cys S257
158571 BAA02g06160 A02 2618428 C T missense_variant MODERATE c.703C>T|p.Arg235Cys S200
158572 BAA02g06170 A02 2619776 C T synonymous_variant LOW c.282C>T|p.Ser94Ser S75
S81
158573 BAA02g06170 A02 2620808 G A missense_variant MODERATE c.436G>A|p.Glu146Lys S170
158574 BAA02g06170 A02 2620921 G A synonymous_variant LOW c.549G>A|p.Glu183Glu S149
158575 BAA02g06170 A02 2621198 G A missense_variant MODERATE c.709G>A|p.Glu237Lys S131