Product Details

SNP ID: rs2395607
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.6:34805950 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TATTTCTCTGTCTCCTTTTTAAGCA[C/T]TTTGCACACCTAATTCTCTCTAATG
Phenotype
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: UHRF1BP1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_017754.3		Intron			NP_060224.3