Product Details

SNP ID: rs16984945
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.20:58153552 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GGAACTTTCTTTTTCAGGAAATACC[A/G]TCTGAAGGCTGAATCGGAAGCACGG
Phenotype
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: C20orf85 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_178456.2	115	Missense Mutation	CAT,CGT	H26R	NP_848551.1