Product Details

SNP ID
rs201818972
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.6:117268443 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTGAGCCAACCCAGCAGCTACTCT[C/G]CTAGCTGTACCAGCAGCAAAGCACC
Phenotype
MIM: 609979
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
VGLL2 PubMed Links

Gene Details

Gene
VGLL2
Gene Name
vestigial like family member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_153453.1 366 Missense Mutation CCT,GCT P115A NP_703154.1
NM_182645.3 366 Missense Mutation CCT,GCT P115A NP_872586.1
XM_005266883.2 366 Missense Mutation CCT,GCT P115A XP_005266940.1

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