Product Details

SNP ID

rs201579827

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:71096685 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTCCGAGCCGCCCGAGGTGGAGCCA[C/G]ATCTGGGGGAAAAGGTACACACGGA

Phenotype

MIM: 300033

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

CXorf65 PubMed Links

Gene Details

Gene

CXorf65

Gene Name

chromosome X open reading frame 65

There are no transcripts associated with this gene.

Gene

FOXO4

Gene Name

forkhead box O4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001170931.1	537	Missense Mutation	CAT,GAT	H53D	NP_001164402.1
NM_005938.3	537	Missense Mutation	CAT,GAT	H53D	NP_005929.2
XM_011530957.2	537	Intron			XP_011529259.1

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