Product Details

SNP ID

rs146856401

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.13:42786827 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATGAGGATTTACAACTCCAGGCCCC[A/G]GTGGGAGGCCCTGCAGACCCGCTAC

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FAM216B PubMed Links

Gene Details

Gene

FAM216B

Gene Name

family with sequence similarity 216 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001318932.1	287	Missense Mutation	CAG,CGG	Q55R	NP_001305861.1
NM_182508.2	287	Missense Mutation	CAG,CGG	Q55R	NP_872314.1

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