Product Details

SNP ID

rs139563514

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:171868688 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAGGGAGAACGGGTCTCATTCTGGG[C/G]ACTGGGAGGCACATTTAAGAAATCC

Phenotype

MIM: 605651

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

FBXW11 PubMed Links

Gene Details

Gene

FBXW11

Gene Name

F-box and WD repeat domain containing 11

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_012300.2	1505	Missense Mutation	CCC,GCC	P526A	NP_036432.2
NM_033644.2	1505	Missense Mutation	CCC,GCC	P513A	NP_387448.2
NM_033645.2	1505	Missense Mutation	CCC,GCC	P492A	NP_387449.2
XM_005265855.4	1505	Missense Mutation	CCC,GCC	P547A	XP_005265912.1
XM_005265856.2	1505	Missense Mutation	CCC,GCC	P515A	XP_005265913.1
XM_005265857.2	1505	Missense Mutation	CCC,GCC	P499A	XP_005265914.1
XM_005265858.2	1505	Missense Mutation	CCC,GCC	P494A	XP_005265915.1
XM_017009279.1	1505	Missense Mutation	CCC,GCC	P526A	XP_016864768.1
XM_017009280.1	1505	Missense Mutation	CCC,GCC	P494A	XP_016864769.1
XM_017009281.1	1505	Missense Mutation	CCC,GCC	P494A	XP_016864770.1

View Full Product Details