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
133151 BAA10g19730 A10 18009195 G A missense_variant MODERATE c.2030G>A|p.Gly677Glu S143
133152 BAA10g19730 A10 18009220 C T splice_region_variant&synonymous_variant LOW c.2055C>T|p.Phe685Phe S2
133153 BAA10g19730 A10 18010060 C T splice_region_variant&synonymous_variant LOW c.2484C>T|p.Val828Val S246
133154 BAA10g19740 A10 18011166 G A synonymous_variant LOW c.523C>T|p.Leu175Leu S245
133155 BAA10g19750 A10 18011631 G A upstream_gene_variant MODIFIER c.-2616G>A| S278
133156 BAA10g19740 A10 18012532 C T upstream_gene_variant MODIFIER c.-39G>A| S45
133157 BAA10g19740 A10 18012719 C T upstream_gene_variant MODIFIER c.-226G>A| S144
133158 BAA10g19740 A10 18013332 G A upstream_gene_variant MODIFIER c.-839C>T| S35
133159 BAA10g19740 A10 18013845 G A upstream_gene_variant MODIFIER c.-1352C>T| S273
133160 BAA10g19740 A10 18015756 C T upstream_gene_variant MODIFIER c.-3263G>A| S232
133161 BAA10g19760 A10 18018289 C T missense_variant MODERATE c.319G>A|p.Val107Met S26
133162 BAA10g19760 A10 18018416 G A synonymous_variant LOW c.192C>T|p.Arg64Arg S125
133163 BAA10g19760 A10 18018712 C T missense_variant MODERATE c.31G>A|p.Glu11Lys S246
133164 BAA10g19760 A10 18018920 C T upstream_gene_variant MODIFIER c.-178G>A| S183
133165 BAA10g19770 A10 18020435 C T synonymous_variant LOW c.3006G>A|p.Gln1002Gln S180
133166 BAA10g19770 A10 18020776 C T missense_variant MODERATE c.2665G>A|p.Ala889Thr S123
133167 BAA10g19770 A10 18023734 C T missense_variant MODERATE c.301G>A|p.Glu101Lys S200
133168 BAA10g19770 A10 18024863 G A upstream_gene_variant MODIFIER c.-748C>T| S267
133169 BAA10g19770 A10 18025544 C T upstream_gene_variant MODIFIER c.-1429G>A| S133
133170 BAA10g19780 A10 18025839 C T missense_variant MODERATE c.251C>T|p.Ser84Leu S84
133171 BAA10g19770 A10 18026572 C T upstream_gene_variant MODIFIER c.-2457G>A| S121
133172 BAA10g19790 A10 18027629 C T missense_variant MODERATE c.65C>T|p.Ala22Val S46
133173 BAA10g19780 A10 18029155 C T downstream_gene_variant MODIFIER c.*2987C>T| S89
133174 BAA10g19780 A10 18030537 C T downstream_gene_variant MODIFIER c.*4369C>T| S144
133175 BAA10g19790 A10 18031659 C T downstream_gene_variant MODIFIER c.*2945C>T| S189