Product Details

SNP ID

rs79218728

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:102655227 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGAGAACGCAGCGCAGGCGCTGCAC[C/T]TCGGGGAGCGCATGCAGGAGGCCAA

Phenotype

MIM: 606125

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

TRIM8 PubMed Links

Gene Details

Gene

TRIM8

Gene Name

tripartite motif containing 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_030912.2	937	Missense Mutation	CTC,TTC	L272F	NP_112174.2

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