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
90751 BAA10g00810 A10 386343 G A downstream_gene_variant MODIFIER c.*3441G>A| S148
S30
90752 BAA10g00810 A10 386977 C T downstream_gene_variant MODIFIER c.*4075C>T| S79
S91
90753 BAA10g00830 A10 388322 G A missense_variant MODERATE c.665C>T|p.Ala222Val S69
90754 BAA10g00830 A10 388333 G A synonymous_variant LOW c.654C>T|p.Asp218Asp S83
S88
90755 BAA10g00830 A10 388951 C T missense_variant MODERATE c.323G>A|p.Arg108Lys S54
90756 BAA10g00830 A10 389048 C T missense_variant MODERATE c.226G>A|p.Asp76Asn S10
90757 BAA10g00820 A10 389103 G A downstream_gene_variant MODIFIER c.*4841G>A| S107
90758 BAA10g00840 A10 389379 C T downstream_gene_variant MODIFIER c.*3474G>A| S265
90759 BAA10g00830 A10 389760 C T upstream_gene_variant MODIFIER c.-44G>A| S175
90760 BAA10g00830 A10 390783 C T upstream_gene_variant MODIFIER c.-1067G>A| S266
90761 BAA10g00830 A10 391464 G A upstream_gene_variant MODIFIER c.-1748C>T| S159
S243
90762 BAA10g00830 A10 392016 C T upstream_gene_variant MODIFIER c.-2300G>A| S108
90763 BAA10g00830 A10 392168 G A upstream_gene_variant MODIFIER c.-2452C>T| S18
90764 BAA10g00830 A10 392703 T C upstream_gene_variant MODIFIER c.-2987A>G| S263
90765 BAA10g00830 A10 392801 G A upstream_gene_variant MODIFIER c.-3085C>T| S64
90766 BAA10g00840 A10 393083 C T missense_variant MODERATE c.862G>A|p.Gly288Ser S162
90767 BAA10g00840 A10 393246 G A synonymous_variant LOW c.699C>T|p.Asn233Asn S148
S30
90768 BAA10g00840 A10 393827 G A missense_variant MODERATE c.118C>T|p.Leu40Phe S81
S85
90769 BAA10g00840 A10 396884 C T upstream_gene_variant MODIFIER c.-2940G>A| S181
90770 BAA10g00840 A10 398103 G A upstream_gene_variant MODIFIER c.-4159C>T| S295
90771 BAA10g00840 A10 398296 C T upstream_gene_variant MODIFIER c.-4352G>A| S142
S247
90772 BAA10g00850 A10 399498 C T upstream_gene_variant MODIFIER c.-1961G>A| S233
90773 BAA10g00860 A10 403008 C T upstream_gene_variant MODIFIER c.-4725G>A| S37
90774 BAA10g00870 A10 404376 C T upstream_gene_variant MODIFIER c.-481C>T| S143
90775 BAA10g00870 A10 404887 G A missense_variant MODERATE c.31G>A|p.Glu11Lys S134
S193