Product Details

SNP ID

rs76665876

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:99892234 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCAACCAAAAAAATGGCCGGAGGC[A/G]TGAGACAGAAGAACAAGAAAAGGTG

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

TRIM4 PubMed Links

Gene Details

Gene

TRIM4

Gene Name

tripartite motif containing 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_033017.3	1553	Missense Mutation	CGC,TGC	R478C	NP_148977.2
NM_033091.2	1553	Missense Mutation	CGC,TGC	R452C	NP_149082.1

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