Product Details

SNP ID

rs139146415

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:140678509 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTCAACTGCTACTACTATGAGAGC[C/T]GCTGCTGCCGCAATACCATCATCAC

Phenotype

Polymorphism

C/T, Transition 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	486	Missense Mutation	CGC,TGC	R94C	NP_689829.3
XM_011512740.2	486	Missense Mutation	CGC,TGC	R94C	XP_011511042.1

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