Product Details

SNP ID: rs6664761
Assay Type: Functionally tested
NCBI dbSNP Submissions: 41
Location: Chr.1:226362490 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GCTCTATCTTTCTTCAGATATAAAA[C/T]TAAGGCAATAAACCAAAGTTCCCAG
Phenotype: MIM: 173870
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: PARP1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001618.3		Intron			NP_001609.2