Product Details

SNP ID
rs4150050
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:77158542 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GGTGTCTTTACTGCAGATGAAGGAT[G/T]TGGGGGCAGAGCACTTGGCAGGTCA
Phenotype
MIM: 603203
Polymorphism
G/T, 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_004354.2 453 Missense Mutation GTG,TTG V4L NP_004345.1
XM_011532398.1 453 Missense Mutation GTG,TTG V4L XP_011530700.1
XM_011532399.2 453 Missense Mutation GTG,TTG V4L XP_011530701.1

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