Product Details

SNP ID

rs148700490

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:55263593 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGAATTGATGTATACAATGTGTTA[C/T]GAATAAGCAGGAGAAGGAAGCCATA

Phenotype

MIM: 300739

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

PAGE3 PubMed Links

Gene Details

Gene

PAGE3

Gene Name

PAGE family member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001017931.2		Intron			NP_001017931.2
NM_001171252.1		Intron			NP_001164723.1
NM_001303613.1		Intron			NP_001290542.1
XM_017029282.1		Intron			XP_016884771.1

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