Product Details

SNP ID

rs192135733

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:49832550 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AACGTAAAGTAGAAGGTGATTGCCA[A/G]GAAATGGATCTGGAAAAGACTCGGA

Phenotype

MIM: 300287

Polymorphism

A/G, Transition 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	271	Silent Mutation	CAA,CAG	Q64Q	NP_001305806.1
NM_007003.4	271	Silent Mutation	CAA,CAG	Q64Q	NP_008934.1

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