Product Details

SNP ID

rs201886192

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:16939746 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCAGGGAAGCAGAAGCTGCAGGTC[G/T]CCACTGGCTCGGGGGATGTGCTCAC

Phenotype

MIM: 604907

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

TNFRSF13B PubMed Links

Gene Details

Gene

TNFRSF13B

Gene Name

TNF receptor superfamily member 13B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_012452.2	696	Missense Mutation	GAG,GCG	E228A	NP_036584.1

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