Product Details

SNP ID
rs7876064
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.X:80355147 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCAAAAGGGGCTGCTGGCAAATTC[C/T]ACTGGCAGAGCAGTAGCTAGTCATG
Phenotype
MIM: 300976
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
FAM46D PubMed Links

Gene Details

Gene
FAM46D
Gene Name
family with sequence similarity 46 member D
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001170574.1 Intron NP_001164045.1
NM_152630.4 Intron NP_689843.1

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