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
125851 BAA10g14850 A10 15437879 G A upstream_gene_variant MODIFIER c.-3862G>A| S53
125852 BAA10g14840 A10 15439023 C T synonymous_variant LOW c.1023C>T|p.Leu341Leu S48
125853 BAA10g14840 A10 15439075 G A splice_donor_variant&intron_variant HIGH c.1074+1G>A| S284
125854 BAA10g14850 A10 15439099 G A upstream_gene_variant MODIFIER c.-2642G>A| S34
125855 BAA10g14840 A10 15439696 G A missense_variant MODERATE c.1438G>A|p.Gly480Arg S109
125856 BAA10g14840 A10 15439835 C T missense_variant MODERATE c.1577C>T|p.Thr526Ile S115
125857 BAA10g14850 A10 15440492 G A upstream_gene_variant MODIFIER c.-1249G>A| S303
125858 BAA10g14850 A10 15440538 G A upstream_gene_variant MODIFIER c.-1203G>A| S138
125859 BAA10g14850 A10 15440643 C T upstream_gene_variant MODIFIER c.-1098C>T| S20
125860 BAA10g14850 A10 15441601 G A upstream_gene_variant MODIFIER c.-140G>A| S265
125861 BAA10g14850 A10 15443171 C T synonymous_variant LOW c.705C>T|p.Asp235Asp S56
125862 BAA10g14860 A10 15445676 C T missense_variant MODERATE c.571G>A|p.Glu191Lys S84
S93
125863 BAA10g14860 A10 15446053 C T missense_variant MODERATE c.274G>A|p.Glu92Lys S169
125864 BAA10g14860 A10 15446093 G A synonymous_variant LOW c.234C>T|p.His78His S205
125865 BAA10g14860 A10 15446325 G A missense_variant MODERATE c.71C>T|p.Pro24Leu S292
125866 BAA10g14870 A10 15446440 T A upstream_gene_variant MODIFIER c.-3778T>A| S63
125867 BAA10g14860 A10 15447876 G A upstream_gene_variant MODIFIER c.-1238C>T| S176
125868 BAA10g14860 A10 15448155 G A upstream_gene_variant MODIFIER c.-1517C>T| S221
125869 BAA10g14860 A10 15449471 G A upstream_gene_variant MODIFIER c.-2833C>T| S155
S211
125870 BAA10g14870 A10 15450690 C T missense_variant MODERATE c.473C>T|p.Ser158Leu S202
125871 BAA10g14870 A10 15451365 C T missense_variant MODERATE c.877C>T|p.Arg293Cys S302
125872 BAA10g14890 A10 15452701 C T upstream_gene_variant MODIFIER c.-1253C>T| S249
125873 BAA10g14890 A10 15452718 G A upstream_gene_variant MODIFIER c.-1236G>A| S209
125874 BAA10g14880 A10 15452963 G A missense_variant&splice_region_variant MODERATE c.205C>T|p.His69Tyr S203
125875 BAA10g14880 A10 15453530 C T upstream_gene_variant MODIFIER c.-363G>A| S282