Product Details

SNP ID

rs139844009

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:48372803 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GATTGCCTGACTTAGCTTTGAAGCG[A/G]ATCTTCTCTTTCCTGGACCTGTTCG

Phenotype

MIM: 609075

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FBXW12 PubMed Links

Gene Details

Gene

FBXW12

Gene Name

F-box and WD repeat domain containing 12

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001159927.1	235	Silent Mutation	CGA,CGG	R12R	NP_001153399.1
NM_001159929.1	235	Intron			NP_001153401.1
NM_207102.2	235	Silent Mutation	CGA,CGG	R12R	NP_996985.2
XM_017006224.1	235	Silent Mutation	CGA,CGG	R12R	XP_016861713.1

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