Product Details

SNP ID

rs777179916

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:129653594 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGAGCTGGCAGCCCCAGGAGACAT[C/T]GACACAGAGGACAGGCAGCCTGGGA

Phenotype

MIM: 300297

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

APLN PubMed Links

Gene Details

Gene

APLN

Gene Name

apelin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_017413.4		Intron			NP_059109.3

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