Product Details

SNP ID

rs200643170

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:10681091 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCTGCTGGATGTGCTGGGTTCTTG[C/G]GGAAGGATGCTTGTCCATGGAGGCA

Phenotype

MIM: 600954

Polymorphism

C/G, Transversion 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	438	Silent Mutation	CCC,CCG	P77P	NP_001278892.1
NM_004394.2	438	Missense Mutation	CCA,GCA	P92A	NP_004385.1

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