Product Details

SNP ID
rs17380212
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:17515790 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTTACTTCCTTACTTATTAATGAAA[C/G]TGACTGTACAGAAAACATGTCATCC
Phenotype
Polymorphism
C/G, Transversion 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 2650 Missense Mutation CTT,GTT L876V NP_001092688.1
NM_001321233.1 2650 Missense Mutation CTT,GTT L867V NP_001308162.1
XM_011533084.1 2650 Missense Mutation CTT,GTT L876V XP_011531386.1

View Full Product Details