Product Details

SNP ID
rs77148910
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:77160721 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAGAAGCCTCTTGTTTTTTTCTCAG[C/G]TGAAACCTAAACATTTGTCTTGCAT
Phenotype
MIM: 603203
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
CCNG2 PubMed Links

Gene Details

Gene
CCNG2
Gene Name
cyclin G2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_004354.2 720 Missense Mutation CTG,GTG L93V NP_004345.1
XM_011532398.1 720 Missense Mutation CTG,GTG L93V XP_011530700.1
XM_011532399.2 720 Missense Mutation CTG,GTG L93V XP_011530701.1

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