Product Details

SNP ID: rs11555922
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:16753998 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TTGCGGGGGCTTCGCGTGTTCCAAG[A/G]ACTGCCTGTGCGCCCTCAACCTGCT
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	273	Missense Mutation	AAC,GAC	N11D	NP_055214.1