Product Details

SNP ID

rs200336587

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:47453137 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTTCAATAGAATAAGGTTTTACTTC[A/G]CCATTTTCTTTTACATCTAGATGCA

Phenotype

MIM: 616656

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

COMMD8 PubMed Links

Gene Details

Gene

COMMD8

Gene Name

COMM domain containing 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_017008330.1	504	Silent Mutation	GGC,GGT	G151G	XP_016863819.1

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