Product Details

SNP ID: rs2270763
Assay Type: Validated
NCBI dbSNP Submissions: 82
Location: Chr.1:197905819 on Build GRCh38
Set Membership: HapMap JSNP Validated
Context Sequence [VIC/FAM]: AGGCTGGCCAGCTAAACTATGTGGA[C/T]CCAGCTACTGGCTATGTGGTGCTCA
Phenotype: MIM: 606066
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: C1orf53 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001024594.2	386	Silent Mutation	GAC,GAT	D96D	NP_001019765.1

There are no transcripts associated with this gene.