Product Details

SNP ID
rs139628790
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:77160775 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGTCTGTTCTTTTTTGCTGGCTGCT[A/G]GAATAGTTGAAGAAGACTGCAATAT
Phenotype
MIM: 603203
Polymorphism
A/G, Transition 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_004354.2 774 Missense Mutation AGA,GGA R111G NP_004345.1
XM_011532398.1 774 Missense Mutation AGA,GGA R111G XP_011530700.1
XM_011532399.2 774 Missense Mutation AGA,GGA R111G XP_011530701.1

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