Product Details

SNP ID

rs147963916

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.22:31934369 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGTGATTGAAGAAAGGGAGAAATCC[A/G]GCTCTGTGGGCTAGGGCAGGTGCCC

Phenotype

Polymorphism

A/G, Transition 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	411	Missense Mutation	CGG,TGG	R145W	NP_001289748.1
NM_001302820.1	411	UTR 3			NP_001289749.1
NM_015372.2	411	Missense Mutation	CGG,TGG	R78W	NP_056187.1

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