Product Details

SNP ID: rs145683027
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.20:45124107 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AGCCCTGGGAGGCAGGTCTCCTTAC[A/C]TTCTTCCAGTTCCTTCACAGGAATC
Phenotype: MIM: 609872 MIM: 605161
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: WFDC12 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_080869.1	256	Missense Mutation			NP_543145.1

There are no transcripts associated with this gene.