Product Details

SNP ID

rs201638083

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:55220640 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCGGTAATCGTGGCTGGGCTGGAA[C/G]GAGGGAGGAAGGTAGGCCGTGGAGG

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

PAGE5 PubMed Links

Gene Details

Gene

PAGE5

Gene Name

PAGE family member 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001013435.2	294	Intron			NP_001013453.1
NM_130467.4	294	Missense Mutation	ACG,AGG	T14R	NP_569734.2

View Full Product Details