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


Gene ID

Results: 1 - 13 of 13 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA08g25660 A08 18425570 G A upstream_gene_variant MODIFIER c.-1778G>A| S238
2 BAA08g25660 A08 18425615 C T upstream_gene_variant MODIFIER c.-1733C>T| S51
3 BAA08g25660 A08 18428314 C T synonymous_variant LOW c.783C>T|p.Leu261Leu S50
4 BAA08g25660 A08 18428906 C T missense_variant MODERATE c.1375C>T|p.Leu459Phe S163
5 BAA08g25660 A08 18429225 C T missense_variant MODERATE c.1694C>T|p.Ser565Phe S276
6 BAA08g25660 A08 18429338 G A missense_variant MODERATE c.1807G>A|p.Glu603Lys S264
7 BAA08g25660 A08 18429356 C T stop_gained HIGH c.1825C>T|p.Gln609* S212
8 BAA08g25660 A08 18430073 G A missense_variant MODERATE c.2542G>A|p.Glu848Lys S260
9 BAA08g25660 A08 18431759 C T missense_variant MODERATE c.3797C>T|p.Ser1266Phe S73
10 BAA08g25660 A08 18431767 G A missense_variant MODERATE c.3805G>A|p.Glu1269Lys S100
11 BAA08g25660 A08 18431858 C T missense_variant MODERATE c.3896C>T|p.Thr1299Ile S299
12 BAA08g25660 A08 18432426 G A missense_variant MODERATE c.4378G>A|p.Glu1460Lys S308
13 BAA08g25660 A08 18433096 C T synonymous_variant LOW c.4849C>T|p.Leu1617Leu S189