Product Details

SNP ID
rs200860973
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:84976418 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TAAATCGGAAGCCCACAAAGGGATT[C/G]ATCCAGAGGAGTGAGGGGGGCCCCC
Phenotype
MIM: 614604
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
ZDHHC7 PubMed Links

Gene Details

Gene
ZDHHC7
Gene Name
zinc finger DHHC-type containing 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001145548.1 716 Missense Mutation ATC,ATG I321M NP_001139020.1
NM_017740.2 716 Missense Mutation ATC,ATG I284M NP_060210.2
XM_011523222.1 716 Intron XP_011521524.1
XM_017023434.1 716 Missense Mutation ATC,ATG I167M XP_016878923.1
XM_017023435.1 716 Missense Mutation ATC,ATG I167M XP_016878924.1
XM_017023436.1 716 Missense Mutation ATC,ATG I167M XP_016878925.1

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