Product Details

SNP ID
rs199507808
Assay Type
Functionally tested
NCBI dbSNP Submissions
8
Location
Chr.1:16250724 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGTTTGTTTTTGGATAGTACTTCAC[A/G]TTCTGTTTCTTGTCCATGAGTCCTC
Phenotype
MIM: 609109
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
FBXO42 PubMed Links

Gene Details

Gene
FBXO42
Gene Name
F-box protein 42
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_018994.2 2354 Silent Mutation AAC,AAT N700N NP_061867.1
XM_006710698.3 2354 Silent Mutation AAC,AAT N700N XP_006710761.1
XM_017001502.1 2354 Silent Mutation AAC,AAT N469N XP_016856991.1
XM_017001503.1 2354 Silent Mutation AAC,AAT N469N XP_016856992.1

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