Product Details

SNP ID
rs142033422
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:77158568 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGGGGCAGAGCACTTGGCAGGTCA[A/T]GAAGGGGTCCAACTTCTCGGGTTGT
Phenotype
MIM: 603203
Polymorphism
A/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_004354.2 479 Missense Mutation CAA,CAT Q12H NP_004345.1
XM_011532398.1 479 Missense Mutation CAA,CAT Q12H XP_011530700.1
XM_011532399.2 479 Missense Mutation CAA,CAT Q12H XP_011530701.1

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