Product Details

SNP ID: rs10256794
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:16757815 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: AATTTATATTTTTATCACCTCTGAA[A/G]TTGGGATGCATTTTATTGTTTCTAT
Phenotype: MIM: 613139
Polymorphism: A/G, Transition 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