Product Details

SNP ID

rs3785634

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.17:15650395 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

TCTAGCTTTAGGCAAAGAAAAACGA[C/G]TTGTTCTAGAAACAGTTTCCTTATC

Phenotype

MIM: 609505

Polymorphism

C/G, Transversion 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		Intron			NP_006461.3

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