Product Details

SNP ID
rs201996774
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:77133722 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTTGGAGCTCTCACTTCCGACATT[C/G]AACATGGGGACCAGCAGGCCCAGCA
Phenotype
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
ZDHHC22 PubMed Links

Gene Details

Gene
ZDHHC22
Gene Name
zinc finger DHHC-type containing 22
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_174976.2 956 Missense Mutation TTC,TTG F251L NP_777636.2
XM_006720119.3 956 Missense Mutation TTC,TTG F251L XP_006720182.1
XM_011536661.2 956 Missense Mutation TTC,TTG F251L XP_011534963.1

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