Product Details

SNP ID: rs6461275
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:16754509 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CTGGTGTGCCTCTGGGTTAGCTCTT[C/G]GTACCCTCGGGATTTTAATTGAGGC
Phenotype: MIM: 613139
Polymorphism: C/G, 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