Product Details

SNP ID

rs201718359

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:65118799 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCATCCTTGGGGAACGAAGTTGCCT[C/T]TGGGATGATCGGATGGCACCAGGTA

Phenotype

MIM: 608138

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

PDCD7 PubMed Links

Gene Details

Gene

PDCD7

Gene Name

programmed cell death 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005707.1	1431	Missense Mutation	AAA,AGA	K459R	NP_005698.1

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