Product Details

SNP ID

rs5962279

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:104167904 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATACATATACAAAGGGCTGGGGGGG[G/T]GTGTGGTTAAGGCTCTAGGAGAGGG

Phenotype

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

FAM199X PubMed Links

Gene Details

Gene

FAM199X

Gene Name

family with sequence similarity 199, X-linked

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_207318.3		Intron			NP_997201.1
XM_005262079.2		Intron			XP_005262136.1
XM_017029270.1		Intron			XP_016884759.1

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