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 BAA09g45780 A09 50829572 C T missense_variant MODERATE c.2890G>A|p.Glu964Lys S28
2 BAA09g45780 A09 50829583 C T missense_variant MODERATE c.2879G>A|p.Cys960Tyr S32
3 BAA09g45780 A09 50830686 G A missense_variant MODERATE c.2354C>T|p.Ser785Phe S82
S92
4 BAA09g45780 A09 50831477 C T missense_variant MODERATE c.1933G>A|p.Asp645Asn S96
5 BAA09g45780 A09 50833125 C T splice_region_variant&intron_variant LOW c.1072+5G>A| S245
6 BAA09g45780 A09 50833790 C T missense_variant MODERATE c.614G>A|p.Arg205His S211
7 BAA09g45780 A09 50833887 G A synonymous_variant LOW c.517C>T|p.Leu173Leu S292
8 BAA09g45780 A09 50834584 G A missense_variant MODERATE c.220C>T|p.Pro74Ser S124
9 BAA09g45780 A09 50834741 C T synonymous_variant LOW c.63G>A|p.Arg21Arg S229
10 BAA09g45780 A09 50835704 G A upstream_gene_variant MODIFIER c.-901C>T| S162
11 BAA09g45780 A09 50837221 C T upstream_gene_variant MODIFIER c.-2418G>A| S286
12 BAA09g45780 A09 50838979 C T upstream_gene_variant MODIFIER c.-4176G>A| S286
13 BAA09g45780 A09 50839396 C T upstream_gene_variant MODIFIER c.-4593G>A| S198