Product Details

SNP ID
rs184759714
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:127435101 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTTGTTTTTTCAGGGATCCACATT[A/C]TTCAGCAGTGTGACGGTAGCTTTTG
Phenotype
MIM: 194552
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
ZNF79 PubMed Links

Gene Details

Gene
ZNF79
Gene Name
zinc finger protein 79
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001286696.1 638 Missense Mutation TTA,TTC L15F NP_001273625.1
NM_001286697.1 638 Missense Mutation TTA,TTC L15F NP_001273626.1
NM_001286698.1 638 Intron NP_001273627.1
NM_001322260.1 638 Missense Mutation TTA,TTC L15F NP_001309189.1
NM_007135.2 638 Missense Mutation TTA,TTC L39F NP_009066.2
XM_006717279.3 638 Missense Mutation TTA,TTC L15F XP_006717342.1

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