Product Details

SNP ID: rs142022446
Assay Type: Functionally Tested
NCBI dbSNP Submissions: 15
Location: Chr.1:159872983 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CTTTTTCCTCTTGATCTCATCGATG[A/C]GCTCACGGCGTTTCTGGGCCTCCTC
Phenotype: MIM: 605152
Polymorphism: A/C, Transversion Substitution
Allele Nomenclature
Literature Links: CFAP45 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_012337.2	1556	Missense Mutation			NP_036469.2