Product Details

SNP ID
hCV29573663
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:47977696 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCATGACAGTCACGAGCACTCTTGG[A/T]GATAATTGTTTTCTTGTCAGAAAAT
Phenotype
MIM: 314993
Polymorphism
A/T, Transversion substitution
Allele Nomenclature
Literature Links
ZNF182 PubMed Links

Gene Details

Gene
ZNF182
Gene Name
zinc finger protein 182
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001007088.1 643 Missense Mutation ACC,TCC T112S NP_001007089.1
NM_001178099.1 643 Missense Mutation ACC,TCC T131S NP_001171570.1
NM_006962.1 643 Missense Mutation ACC,TCC T131S NP_008893.1

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