Product Details

SNP ID

rs144908613

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:49830703 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TATTGTCTGCATATGTATGTTTTTA[A/C]GAGTCTGGAAATAGTCTTATGACTT

Phenotype

MIM: 300287

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

PAGE4 PubMed Links

Gene Details

Gene

PAGE4

Gene Name

PAGE family member 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001318877.1		Intron			NP_001305806.1
NM_007003.4		Intron			NP_008934.1

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