Product Details

SNP ID

rs5745297

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:10680885 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTCCCCATAAACAAGGTTTGGGCTG[A/G]AGCTGTTTCTAGTTTTAAATATGGA

Phenotype

MIM: 600954

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

DAP PubMed Links

Gene Details

Gene

DAP

Gene Name

death associated protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001291963.1	644	Missense Mutation	TCC,TTC	S146F	NP_001278892.1
NM_004394.2	644	UTR 3			NP_004385.1

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