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
75651 BAA01g39830 A01 26455493 C T missense_variant MODERATE c.595G>A|p.Glu199Lys S11
75652 BAA01g39830 A01 26455502 G A missense_variant MODERATE c.586C>T|p.Leu196Phe S13
75653 BAA01g39830 A01 26455599 G A synonymous_variant LOW c.489C>T|p.Ala163Ala S246
75654 BAA01g39830 A01 26455790 C T missense_variant MODERATE c.298G>A|p.Glu100Lys S200
75655 BAA01g39840 A01 26456365 G A upstream_gene_variant MODIFIER c.-4943G>A| S207
75656 BAA01g39840 A01 26456817 G A upstream_gene_variant MODIFIER c.-4491G>A| S45
75657 BAA01g39840 A01 26456985 C T upstream_gene_variant MODIFIER c.-4323C>T| S9
75658 BAA01g39840 A01 26457071 C T upstream_gene_variant MODIFIER c.-4237C>T| S203
75659 BAA01g39830 A01 26458965 C T upstream_gene_variant MODIFIER c.-1177G>A| S182
75660 BAA01g39830 A01 26459364 C T upstream_gene_variant MODIFIER c.-1576G>A| S4
75661 BAA01g39840 A01 26463091 C T downstream_gene_variant MODIFIER c.*506C>T| S242
75662 BAA01g39840 A01 26463539 C T downstream_gene_variant MODIFIER c.*954C>T| S148
S210
S30
S31
75663 BAA01g39850 A01 26465160 C T missense_variant MODERATE c.2077G>A|p.Glu693Lys S41
75664 BAA01g39850 A01 26465688 C T missense_variant MODERATE c.1549G>A|p.Ala517Thr S98
75665 BAA01g39850 A01 26467129 G A synonymous_variant LOW c.108C>T|p.Phe36Phe S238
75666 BAA01g39850 A01 26467970 C T upstream_gene_variant MODIFIER c.-734G>A| S7
75667 BAA01g39850 A01 26469666 G A upstream_gene_variant MODIFIER c.-2430C>T| S244
75668 BAA01g39850 A01 26471210 G A upstream_gene_variant MODIFIER c.-3974C>T| S232
75669 BAA01g39850 A01 26471231 G A upstream_gene_variant MODIFIER c.-3995C>T| S186
75670 BAA01g39850 A01 26471500 G A upstream_gene_variant MODIFIER c.-4264C>T| S286
75671 BAA01g39850 A01 26471586 G A upstream_gene_variant MODIFIER c.-4350C>T| S61
75672 BAA01g39860 A01 26473335 G A downstream_gene_variant MODIFIER c.*2656C>T| S15
S3
75673 BAA01g39860 A01 26474191 G A downstream_gene_variant MODIFIER c.*1800C>T| S76
75674 BAA01g39860 A01 26474773 C T downstream_gene_variant MODIFIER c.*1218G>A| S204
75675 BAA01g39860 A01 26474789 G A downstream_gene_variant MODIFIER c.*1202C>T| S245