Product Details

SNP ID

rs144663766

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:15651294 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGTTTGATGTTCACCTGATGCGGCT[A/G]CAAGTGCTCTTCACAGTAATTCACC

Phenotype

MIM: 609505

Polymorphism

A/G, 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	873	Nonsense Mutation			NP_006461.3

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