Product Details

SNP ID

rs143678497

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:10874406 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGCAGGGGCACCTGGTGGTGGAGT[C/T]GTGAGGTACCTGCAGGGAAGCTCTG

Phenotype

MIM: 603716

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

GCM2 PubMed Links

Gene Details

Gene

GCM2

Gene Name

glial cells missing homolog 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004752.3	1182	Silent Mutation	ACA,ACG	T370T	NP_004743.1

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