Product Details

SNP ID
rs149485731
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:88428462 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCTACCCGCTGCCCACCCAGCCTG[C/T]GCCCTCACCCCTGCCCTGCTACCAG
Phenotype
MIM: 612078
Polymorphism
C/T, 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 1185 Missense Mutation GCG,GTG A331V NP_001120936.2
XM_017023784.1 1185 Missense Mutation GCG,GTG A331V XP_016879273.1
XM_017023785.1 1185 Missense Mutation GCG,GTG A331V XP_016879274.1

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