Product Details

SNP ID

rs61739670

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:171868665 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TAGAGATGTAAGTGTATGTTCTGGA[C/G]GGAGAACGGGTCTCATTCTGGGCAC

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	1528	Silent Mutation	CCC,CCG	P533P	NP_036432.2
NM_033644.2	1528	Silent Mutation	CCC,CCG	P520P	NP_387448.2
NM_033645.2	1528	Silent Mutation	CCC,CCG	P499P	NP_387449.2
XM_005265855.4	1528	Silent Mutation	CCC,CCG	P554P	XP_005265912.1
XM_005265856.2	1528	Silent Mutation	CCC,CCG	P522P	XP_005265913.1
XM_005265857.2	1528	Silent Mutation	CCC,CCG	P506P	XP_005265914.1
XM_005265858.2	1528	Silent Mutation	CCC,CCG	P501P	XP_005265915.1
XM_017009279.1	1528	Silent Mutation	CCC,CCG	P533P	XP_016864768.1
XM_017009280.1	1528	Silent Mutation	CCC,CCG	P501P	XP_016864769.1
XM_017009281.1	1528	Silent Mutation	CCC,CCG	P501P	XP_016864770.1

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