Product Details

SNP ID
rs77985966
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.3:86942454 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGAGATCGTAAATGGTTGTGTTTTT[C/T]CCCCTTTTAATGCGGAAGATTTTTT
Phenotype
MIM: 609980
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
VGLL3 PubMed Links
Additional Information
For this assay, SNP(s) [rs77973813] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene
VGLL3
Gene Name
vestigial like family member 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001320493.1 5772 Intron NP_001307422.1
NM_001320494.1 5772 UTR 3 NP_001307423.1
NM_016206.3 5772 UTR 3 NP_057290.2
XM_006713138.3 5772 UTR 3 XP_006713201.1

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