Product Details

SNP ID

rs9628

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.3:53287613 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

TGTGGTTGTCTTTGTTCTTGGTCAG[A/C]ACCTGCAAGTAGACTTCATGAAGTG

Phenotype

MIM: 607010

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

DCP1A PubMed Links

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	1712	Silent Mutation	GTG,GTT	V534V	NP_001277133.1
NM_001290205.1	1712	Silent Mutation	GTG,GTT	V500V	NP_001277134.1
NM_001290206.1	1712	Silent Mutation	GTG,GTT	V451V	NP_001277135.1
NM_001290207.1	1712	Silent Mutation	GTG,GTT	V413V	NP_001277136.1
NM_018403.6	1712	Silent Mutation	GTG,GTT	V572V	NP_060873.4

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