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
28851 BAA01g20390 A01 10039743 C T upstream_gene_variant MODIFIER c.-2084G>A| S38
28852 BAA01g20390 A01 10041193 C T upstream_gene_variant MODIFIER c.-3534G>A| S230
28853 BAA01g20390 A01 10041523 C T upstream_gene_variant MODIFIER c.-3864G>A| S159
S243
28854 BAA01g20390 A01 10042289 C T upstream_gene_variant MODIFIER c.-4630G>A| S18
28855 BAA01g20400 A01 10042732 C T downstream_gene_variant MODIFIER c.*1986G>A| S42
28856 BAA01g20400 A01 10043788 C T downstream_gene_variant MODIFIER c.*930G>A| S128
28857 BAA01g20400 A01 10043926 C T downstream_gene_variant MODIFIER c.*792G>A| S176
28858 BAA01g20400 A01 10044185 G A downstream_gene_variant MODIFIER c.*533C>T| S245
28859 BAA01g20400 A01 10044444 C T downstream_gene_variant MODIFIER c.*274G>A| S247
28860 BAA01g20400 A01 10045572 C T intron_variant MODIFIER c.2614-771G>A| S279
28861 BAA01g20400 A01 10045586 G A intron_variant MODIFIER c.2614-785C>T| S74
28862 BAA01g20400 A01 10046310 G A intron_variant MODIFIER c.2613+449C>T| S103
28863 BAA01g20400 A01 10046524 C T intron_variant MODIFIER c.2613+235G>A| S245
28864 BAA01g20400 A01 10046572 C T intron_variant MODIFIER c.2613+187G>A| S70
28865 BAA01g20400 A01 10047115 G A synonymous_variant LOW c.2257C>T|p.Leu753Leu S209
28866 BAA01g20400 A01 10047623 C T synonymous_variant LOW c.1749G>A|p.Lys583Lys S213
28867 BAA01g20400 A01 10047816 C T missense_variant MODERATE c.1651G>A|p.Ala551Thr S27
28868 BAA01g20400 A01 10047867 T C missense_variant MODERATE c.1600A>G|p.Ile534Val S198
28869 BAA01g20400 A01 10048216 C T synonymous_variant LOW c.1251G>A|p.Ser417Ser S198
28870 BAA01g20400 A01 10048333 G A synonymous_variant LOW c.1134C>T|p.Asp378Asp S281
28871 BAA01g20400 A01 10049077 C T stop_gained HIGH c.390G>A|p.Trp130* S228
28872 BAA01g20400 A01 10049143 C T stop_gained HIGH c.324G>A|p.Trp108* S148
S30
S31
28873 BAA01g20400 A01 10049375 C T missense_variant MODERATE c.92G>A|p.Ser31Asn S228
28874 BAA01g20400 A01 10049414 G T missense_variant MODERATE c.53C>A|p.Thr18Asn S116
28875 BAA01g20400 A01 10049517 G A upstream_gene_variant MODIFIER c.-51C>T| S274