Product Details

SNP ID

rs138966973

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:110201157 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGAAGCTGGGCAGCCTCTGGGATTC[C/T]GGTTCCTTGCTGAGTCATCTGATTG

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

C9orf152 PubMed Links

Gene Details

Gene

C9orf152

Gene Name

chromosome 9 open reading frame 152

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001012993.2	1065	Missense Mutation	AGA,GGA	R171G	NP_001013011.2

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