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
65751 BAA01g34390 A01 23037311 C T upstream_gene_variant MODIFIER c.-720C>T| S142
65752 BAA01g34390 A01 23037858 G A upstream_gene_variant MODIFIER c.-173G>A| S267
65753 BAA01g34390 A01 23038020 C T upstream_gene_variant MODIFIER c.-11C>T| S282
65754 BAA01g34390 A01 23038204 C T synonymous_variant LOW c.174C>T|p.Ile58Ile S186
65755 BAA01g34390 A01 23038410 C T missense_variant MODERATE c.380C>T|p.Pro127Leu S85
65756 BAA01g34390 A01 23038625 G A missense_variant MODERATE c.595G>A|p.Glu199Lys S296
65757 BAA01g34390 A01 23038752 C T missense_variant MODERATE c.722C>T|p.Ala241Val S237
65758 BAA01g34410 A01 23039029 C T upstream_gene_variant MODIFIER c.-4579C>T| S146
65759 BAA01g34400 A01 23039891 C T missense_variant MODERATE c.1474G>A|p.Ala492Thr S114
S236
65760 BAA01g34400 A01 23040267 C T missense_variant MODERATE c.1098G>A|p.Met366Ile S286
65761 BAA01g34400 A01 23040400 G A missense_variant MODERATE c.965C>T|p.Ala322Val S95
65762 BAA01g34410 A01 23040507 G A upstream_gene_variant MODIFIER c.-3101G>A| S13
65763 BAA01g34400 A01 23040859 C T synonymous_variant LOW c.585G>A|p.Lys195Lys S156
65764 BAA01g34400 A01 23040887 A T missense_variant MODERATE c.557T>A|p.Val186Asp S98
65765 BAA01g34400 A01 23041197 C T missense_variant MODERATE c.247G>A|p.Ala83Thr S82
S92
65766 BAA01g34400 A01 23041437 C T missense_variant MODERATE c.7G>A|p.Ala3Thr S282
65767 BAA01g34400 A01 23041825 C T upstream_gene_variant MODIFIER c.-382G>A| S266
65768 BAA01g34400 A01 23042205 C T upstream_gene_variant MODIFIER c.-762G>A| S28
65769 BAA01g34400 A01 23042990 C A upstream_gene_variant MODIFIER c.-1547G>T| S139
65770 BAA01g34400 A01 23043289 C T upstream_gene_variant MODIFIER c.-1846G>A| S198
65771 BAA01g34400 A01 23044382 C T upstream_gene_variant MODIFIER c.-2939G>A| S295
65772 BAA01g34410 A01 23046293 G A missense_variant MODERATE c.1288G>A|p.Gly430Arg S72
65773 BAA01g34420 A01 23048342 C T missense_variant MODERATE c.637G>A|p.Val213Met S77
S82
65774 BAA01g34420 A01 23048704 G A missense_variant MODERATE c.275C>T|p.Thr92Ile S218
65775 BAA01g34430 A01 23049040 G A upstream_gene_variant MODIFIER c.-707G>A| S169