Product Details

SNP ID

rs142236639

Assay Type

Functionally tested

NCBI dbSNP Submissions

10

Location

Chr.1:151518558 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCAACATGGCTGAGCCCCGGGGCCC[C/T]GTAGACCATGGAGTCCAGATTCGCT

Phenotype

MIM: 609473

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CGN PubMed Links

Gene Details

Gene

CGN

Gene Name

cingulin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020770.2	183	Silent Mutation	CCC,CCT	P13P	NP_065821.1
XM_005245365.4	183	Silent Mutation	CCC,CCT	P13P	XP_005245422.1

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