Product Details

SNP ID: rs373496
Assay Type: Validated
NCBI dbSNP Submissions: NA
Location: Chr.16:11966306 on Build GRCh38
Set Membership: HapMap Validated
Context Sequence [VIC/FAM]: CTAATGTTTTTGCTAAGGAAGATAA[A/G]CTCTGAACCATTAAAGGACGAGTTT
Phenotype: MIM: 109545
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: TNFRSF17 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001192.2	460	Missense Mutation	AAC,AGC	N81S	NP_001183.2