Product Details

SNP ID: rs11976749
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:16756412 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TTAAACCAGGATTGCATATGGGAAC[G/T]GCAGATGCCTGAAACATCATCATTG
Phenotype: MIM: 613139
Polymorphism: G/T, Transversion substitution
Allele Nomenclature
Literature Links: TSPAN13 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014399.3		Intron			NP_055214.1