Product Details

SNP ID
rs34891389
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:24777289 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCAGAAACAAGAAGAAATCAAAGAG[A/C]ATATAAAGGTATGTGATTGAATAAC
Phenotype
MIM: 602842
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
GMNN PubMed Links

Gene Details

Gene
GMNN
Gene Name
geminin, DNA replication inhibitor
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001251989.1 174 Missense Mutation AAT,CAT N15H NP_001238918.1
NM_001251990.1 174 Missense Mutation AAT,CAT N15H NP_001238919.1
NM_001251991.1 174 Missense Mutation AAT,CAT N15H NP_001238920.1
NM_015895.4 174 Missense Mutation AAT,CAT N15H NP_056979.1
XM_005249159.1 174 Missense Mutation AAT,CAT N15H XP_005249216.1
XM_011514651.2 174 Intron XP_011512953.1

View Full Product Details