Product Details

SNP ID: rs200421984
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.14:70459595 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TCTTTGTCTGTTTTGACTTTCCTGT[C/T]TACTGTCGGGCTTCTTATGTATCTA
Phenotype: MIM: 603713
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: ADAM20P1 PubMed Links

Gene Details

There are no transcripts associated with this gene.

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003813.3	2354	Missense Mutation	TCT,TTT	S699F	NP_003804.2