Product Details

SNP ID

rs17314548

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:17515489 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTCCCTACTAATTTCATGAAACATA[C/T]GAAGTTCTTCAAGTACTAAGTCAAA

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

RAD51AP2 PubMed Links

Gene Details

Gene

RAD51AP2

Gene Name

RAD51 associated protein 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001099218.2	2951	Missense Mutation	CAT,CGT	H976R	NP_001092688.1
NM_001321233.1	2951	Missense Mutation	CAT,CGT	H967R	NP_001308162.1
XM_011533084.1	2951	Missense Mutation	CAT,CGT	H976R	XP_011531386.1

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