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


Gene ID

Results: 1 - 11 of 11 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g10670 A02 4766026 C T missense_variant MODERATE c.2831G>A|p.Arg944Lys S160
2 BAA02g10670 A02 4766183 C T missense_variant MODERATE c.2674G>A|p.Gly892Arg S112
3 BAA02g10670 A02 4766642 C T synonymous_variant LOW c.2379G>A|p.Arg793Arg S152
4 BAA02g10670 A02 4767176 G A splice_region_variant&intron_variant LOW c.1933-4C>T| S85
5 BAA02g10670 A02 4767528 C T missense_variant MODERATE c.1649G>A|p.Ser550Asn S144
6 BAA02g10670 A02 4768009 C T missense_variant MODERATE c.1168G>A|p.Gly390Arg S8
7 BAA02g10670 A02 4768284 C T missense_variant MODERATE c.893G>A|p.Gly298Asp S55
8 BAA02g10670 A02 4768416 C T missense_variant MODERATE c.761G>A|p.Arg254Lys S46
9 BAA02g10670 A02 4769272 G A synonymous_variant LOW c.261C>T|p.Phe87Phe S43
10 BAA02g10670 A02 4772631 G A upstream_gene_variant MODIFIER c.-2738C>T| S296
11 BAA02g10670 A02 4773719 G A upstream_gene_variant MODIFIER c.-3826C>T| S4