Product Details

SNP ID

rs184057154

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:101087745 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGCACCCGCCAGACCCACACCCAC[C/T]GCGTGGTGGACCTGGTGGGCTACAG

Phenotype

MIM: 616996

Polymorphism

C/T, Transition 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	730	Missense Mutation	CGC,TGC	R145C	NP_112223.1
XM_011516589.2	730	Missense Mutation	CGC,TGC	R145C	XP_011514891.1

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