Product Details

SNP ID

rs201801259

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:15651146 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GACTATGGTGTGGCCACTGTGCTCC[C/T]GGCAACAGTCCTGGCAGATGCACTG

Phenotype

MIM: 609505

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

TRIM16 PubMed Links

Gene Details

Gene

TRIM16

Gene Name

tripartite motif containing 16

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006470.3	1021	Missense Mutation			NP_006461.3

View Full Product Details