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SNP ID

rs4846864

Assay Type

Functionally tested

NCBI dbSNP Submissions

40

Location

Chr.1:230642745 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCTCTGCCCTGTGCCCTCTGTGGC[C/G]GTCTCTTCGGTCGGCTGCTCCTGCC

Phenotype

MIM: 606974

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

COG2 PubMed Links

Gene Details

Gene

COG2

Gene Name

component of oligomeric golgi complex 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145036.1		Intron			NP_001138508.1
NM_007357.2		Intron			NP_031383.1

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