Product Details

SNP ID: hCV27296660
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.17:20887557 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AGTATTCCCCAAGTACTGAGAACTA[G/C]TATATTCAGCATTTCACTTTATATT
Phenotype
Polymorphism: G/C, Transversion substitution
Allele Nomenclature
Literature Links: CCDC144NL PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001004306.2		Intron			NP_001004306.1

There are no transcripts associated with this gene.