Product Details

SNP ID

rs199897213

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:49694135 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GATGCTCCCTCATCCTCTCTCTCTT[C/G]AGCAGGTGTAGAATCCTGACTTTGA

Phenotype

MIM: 300288

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

PAGE1 PubMed Links

Gene Details

Gene

PAGE1

Gene Name

PAGE family member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003785.3		Intron			NP_003776.2
XM_011543998.2		Intron			XP_011542300.1

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