Product Details

SNP ID
rs148337492
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:148394787 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGAGACTGCACAACAATGGGGCCAC[A/G]AAAGAAAAGTGTGAAAACATGTATC
Phenotype
MIM: 608533
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
FBXO38 PubMed Links

Gene Details

Gene
FBXO38
Gene Name
F-box protein 38
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001271723.1 157 Missense Mutation CAA,CGA Q4R NP_001258652.1
NM_030793.4 157 Missense Mutation CAA,CGA Q4R NP_110420.3
XM_005268513.1 157 Missense Mutation CAA,CGA Q4R XP_005268570.1
XM_006714797.1 157 Missense Mutation CAA,CGA Q4R XP_006714860.1
XM_011537684.2 157 Intron XP_011535986.1
XM_017009899.1 157 UTR 5 XP_016865388.1
XM_017009900.1 157 Intron XP_016865389.1
XM_017009901.1 157 Intron XP_016865390.1
XM_017009902.1 157 Intron XP_016865391.1

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