Product Details

SNP ID

rs200927296

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:55090036 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGTGGGAAATATGAGTGAGCTTCTA[A/G]GAGCAAGATCCCAATCCTCAGAAAG

Phenotype

MIM: 300738

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

PAGE2 PubMed Links

Gene Details

Gene

PAGE2

Gene Name

PAGE family member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_207339.3	76	Missense Mutation	AGA,GGA	R6G	NP_997222.1
XM_017029353.1	76	Missense Mutation	AGA,GGA	R6G	XP_016884842.1

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