Product Details

SNP ID

rs202076977

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:101088332 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCAGGCAGCTGCAGGGCTGCCCCTG[C/G]GCACCAGGCCCGGCCCCCTGCCTGC

Phenotype

MIM: 616996

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

TRIM56 PubMed Links

Gene Details

Gene

TRIM56

Gene Name

tripartite motif containing 56

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_030961.2	1317	Missense Mutation	TGC,TGG	C340W	NP_112223.1
XM_011516589.2	1317	Missense Mutation	TGC,TGG	C340W	XP_011514891.1

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