Product Details

SNP ID

rs12631328

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:53287612 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTGTGGTTGTCTTTGTTCTTGGTCA[A/G]AACCTGCAAGTAGACTTCATGAAGT

Phenotype

MIM: 607010

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

DCP1A PubMed Links

Additional Information

For this assay, SNP(s) [rs9628] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

DCP1A

Gene Name

decapping mRNA 1A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001290204.1	1713	Silent Mutation	CTG,TTG	L535L	NP_001277133.1
NM_001290205.1	1713	Silent Mutation	CTG,TTG	L501L	NP_001277134.1
NM_001290206.1	1713	Silent Mutation	CTG,TTG	L452L	NP_001277135.1
NM_001290207.1	1713	Silent Mutation	CTG,TTG	L414L	NP_001277136.1
NM_018403.6	1713	Silent Mutation	CTG,TTG	L573L	NP_060873.4

View Full Product Details