Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 15 of 15 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g51880 A09 53968717 G A upstream_gene_variant MODIFIER c.-4688G>A| S178
2 BAA09g51880 A09 53968873 C T upstream_gene_variant MODIFIER c.-4532C>T| S133
3 BAA09g51880 A09 53969623 G A upstream_gene_variant MODIFIER c.-3782G>A| S76
4 BAA09g51880 A09 53969703 G A upstream_gene_variant MODIFIER c.-3702G>A| S39
5 BAA09g51880 A09 53970158 G A upstream_gene_variant MODIFIER c.-3247G>A| S216
6 BAA09g51880 A09 53972372 G A upstream_gene_variant MODIFIER c.-1033G>A| S13
7 BAA09g51880 A09 53972664 C T upstream_gene_variant MODIFIER c.-741C>T| S95
8 BAA09g51880 A09 53972681 G A upstream_gene_variant MODIFIER c.-724G>A| S221
9 BAA09g51880 A09 53972688 C T upstream_gene_variant MODIFIER c.-717C>T| S219
S72
10 BAA09g51880 A09 53973407 G A start_lost HIGH c.3G>A|p.Met1? S270
11 BAA09g51880 A09 53973446 G A synonymous_variant LOW c.42G>A|p.Arg14Arg S72
12 BAA09g51880 A09 53973771 C T missense_variant MODERATE c.367C>T|p.Leu123Phe S255
13 BAA09g51880 A09 53974049 C T synonymous_variant LOW c.645C>T|p.Ala215Ala S161
14 BAA09g51880 A09 53974220 G A synonymous_variant LOW c.816G>A|p.Thr272Thr S85
15 BAA09g51880 A09 53974286 G A synonymous_variant LOW c.882G>A|p.Glu294Glu S249