Product Details

SNP ID

rs77806389

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:149739657 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAAGGTGGACAAATAAAAACCCTTA[C/T]AGAGGTATTTTTTATCATATGTTTT

Phenotype

MIM: 616699

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

COMMD2 PubMed Links

Gene Details

Gene

COMMD2

Gene Name

COMM domain containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_016094.3	2519	UTR 3			NP_057178.2

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