Product Details

SNP ID
rs138954293
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:88427609 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CACCCCAGCTACCAGGACCACCAAG[A/G]GTGCCAGGGAGGCTGGCGGCCAGGC
Phenotype
MIM: 612078
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
ZNF469 PubMed Links

Gene Details

Gene
ZNF469
Gene Name
zinc finger protein 469
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001127464.2 332 Missense Mutation AGT,GGT S47G NP_001120936.2
XM_017023784.1 332 Missense Mutation AGT,GGT S47G XP_016879273.1
XM_017023785.1 332 Missense Mutation AGT,GGT S47G XP_016879274.1

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