Product Details

SNP ID

rs145737909

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:47453180 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TAGATGCAGGCTTAAAAGTGGCATT[C/T]GTAATGCAGCAATCTTGTCACTGGA

Phenotype

MIM: 616656

Polymorphism

C/T, 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	461	Missense Mutation	CAA,CGA	Q137R	XP_016863819.1

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