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SNP ID

rs202219249

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:127197133 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTCTCCCACTCTGGGCGGGGCCACC[C/T]CCAGCCACTGTCCCCAGGTGGGATG

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

C3orf56 PubMed Links

Gene Details

Gene

C3orf56

Gene Name

chromosome 3 open reading frame 56

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001007534.2	688	Missense Mutation	CCC,TCC	P150S	NP_001007535.1

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