Product Details

SNP ID

rs60906481

Assay Type

DME

NCBI dbSNP Submissions

3

Location

Chr.1:171319886 on Build GRCh38

Set Membership

DME Validated Inventoried

Context Sequence [VIC/FAM]

GAGTGGCCTCTCCTCCATCAAATGC[C/T]GTGTGGATGAGGACCTGGAGCCCAC

Phenotype

MIM: 136131

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FMO4 PubMed Links

Gene Details

Gene

FMO4

Gene Name

flavin containing monooxygenase 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002022.2	494	Missense Mutation	CGT,TGT	R21C	NP_002013.1
XM_005245045.3	494	Intron			XP_005245102.1
XM_005245046.3	494	Missense Mutation	CGT,TGT	R21C	XP_005245103.1
XM_005245048.3	494	Missense Mutation	CGT,TGT	R21C	XP_005245105.1
XM_006711243.3	494	Missense Mutation	CGT,TGT	R21C	XP_006711306.1
XM_011509347.2	494	Missense Mutation	CGT,TGT	R21C	XP_011507649.1
XM_011509348.2	494	Intron			XP_011507650.1
XM_011509349.2	494	Missense Mutation	CGT,TGT	R21C	XP_011507651.1

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