Product Details

SNP ID
hCV27338096
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:136826413 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TAGTGGCGATGGCTCGCTGCAGCTC[G/T]GGGACACTGCCAAAGCTGCAGGGCC
Phenotype
MIM: 601757
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
PEX7 PubMed Links

Gene Details

Gene
PEX7
Gene Name
peroxisomal biogenesis factor 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000288.3 385 Missense Mutation GGG,TGG G95W NP_000279.1

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