Product Details

SNP ID

rs141960657

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:39025421 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAGGGTAGTGCTGGACTAGGACAGA[C/T]GGACTCGCACGATCACACTGGAGTT

Phenotype

MIM: 609099

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FBXO27 PubMed Links

Gene Details

Gene

FBXO27

Gene Name

F-box protein 27

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_178820.4	962	Missense Mutation	CAT,CGT	H281R	NP_849142.1
XM_017026290.1	962	Intron			XP_016881779.1

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