Product Details

SNP ID
rs145034037
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.6:10874299 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACAGCTCGAAAGGCTCTTCACCTCT[C/T]GCACACTGTCACTGTATTTCATAGC
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 1289 Missense Mutation CAA,CGA Q406R NP_004743.1

View Full Product Details