Product Details

SNP ID

rs148678982

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:140678333 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCAAGTTCATCTTCACCTCAGAGC[G/T]GAACTGCACCTGCTTCCCCTGCCCT

Phenotype

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

TRIM42 PubMed Links

Gene Details

Gene

TRIM42

Gene Name

tripartite motif containing 42

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_152616.4	310	Missense Mutation	CAG,CGG	Q35R	NP_689829.3
XM_011512740.2	310	Missense Mutation	CAG,CGG	Q35R	XP_011511042.1

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