Product Details

SNP ID: rs747659
Assay Type: Functionally tested
NCBI dbSNP Submissions: 40
Location: Chr.1:226363040 on Build GRCh38
Set Membership: HapMap JSNP
Context Sequence [VIC/FAM]: CAGCCTTCTCAGGACAGCAAGCCCC[C/T]GGCTTCTGTGCTGTCCAGGGTGCCT
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