Product Details

SNP ID

rs200202420

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:70206322 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACAGAGAAGGAGAACGCAACAGTGG[C/T]CCACCTGGTGGGGGCTCTCAGGTCC

Phenotype

MIM: 602457

Polymorphism

C/T, 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	773	Missense Mutation	GCC,GTC	A159V	NP_003815.1

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