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SNP ID: rs12009522
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.X:71104072 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TCTGTTCCTAAAGGTCGGAGACTTG[C/T]GAGTGGACTTCTTTTTGTCTGATCG
Phenotype: MIM: 300033 MIM: 308380
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: CXorf65 PubMed Links

Gene Details

Gene: CXorf65
Gene Name: chromosome X open reading frame 65

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001025265.2	699	Missense Mutation	CAC,CGC	H156R	NP_001020436.1
XM_005262244.3	699	Missense Mutation	CAC,CGC	H133R	XP_005262301.1

Gene: FOXO4
Gene Name: forkhead box O4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001170931.1	699	Intron			NP_001164402.1
NM_005938.3	699	Intron			NP_005929.2
XM_011530957.2	699	Intron			XP_011529259.1

Gene: IL2RG
Gene Name: interleukin 2 receptor subunit gamma

There are no transcripts associated with this gene.

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