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SNP ID: rs3788441
Assay Type: Validated
NCBI dbSNP Submissions: NA
Location: Chr.22:31937797 on Build GRCh38
Set Membership: HapMap Validated
Context Sequence [VIC/FAM]: GACTCTCTGAAGGTCAGGGGCAGTG[C/G]TGGGAAGAATGGTGAAGATGGAGCA
Phenotype: MIM: 113508
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: C22orf24 PubMed Links

Gene Details

Gene: C22orf24
Gene Name: chromosome 22 open reading frame 24

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001302819.1		Intron			NP_001289748.1
NM_001302820.1		Intron			NP_001289749.1
NM_015372.2		Intron			NP_056187.1

Gene: YWHAH
Gene Name: tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein eta

There are no transcripts associated with this gene.

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