Product Details

SNP ID

rs145623767

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:70206397 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGGTACAAGAGGTTCAGCAGGCCC[A/G]TGACCTCCAGAACAGGAGTGGGGCC

Phenotype

MIM: 602457

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FADD PubMed Links

Gene Details

Gene

FADD

Gene Name

Fas associated via death domain

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003824.3	848	Missense Mutation	CAT,CGT	H184R	NP_003815.1

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