Product Details

SNP ID: rs139645876
Assay Type: Functionally tested
NCBI dbSNP Submissions: 11
Location: Chr.1:152302701 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: ATTAATTCCTTTGCCATTAATTTCT[C/T]ACTCATAGTAATAGTATCTCTGTGA
Phenotype: MIM: 135940
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: FLG PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002016.1	12221	Silent Mutation	TAA,TGA	4062	NP_002007.1