Product Details

SNP ID: rs7717199
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:134911165 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: ATGTACCTGCTTGACTTATTTTCCC[C/T]GACTTTTTCTGGGCCGTTGGTAATT
Phenotype: MIM: 609836
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: PCBD2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032151.4		Intron			NP_115527.3

There are no transcripts associated with this gene.