Product Details

SNP ID
rs76716752
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.6:116462422 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCAGGCCAAGGCGTCGGACGTGCAG[C/G]ACCTCCTGAAGGATCTGAAGGCTCA
Phenotype
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
FAM26F PubMed Links

Gene Details

Gene
FAM26F
Gene Name
family with sequence similarity 26 member F
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001010919.2 895 Missense Mutation CAC,GAC H165D NP_001010919.1
NM_001276460.1 895 Intron NP_001263389.1
XM_005266999.3 895 Missense Mutation CAC,GAC H165D XP_005267056.1
XM_011535845.2 895 Missense Mutation CAC,GAC H165D XP_011534147.1

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