Product Details

SNP ID: rs3219145
Assay Type: Functionally tested
NCBI dbSNP Submissions: 34
Location: Chr.1:226363128 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GACACTGTGCTTGCCCTTGGGTAAC[C/T]TGCTGATATGTGAAGCGTGCTTCAG
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	2990	Missense Mutation			NP_001609.2