Product Details

SNP ID

rs150527849

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:24370065 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTGCCCTCGCCCCGGGCCTCCCCT[C/T]GGCCATGGACCCCCGAAGATCCCTG

Phenotype

MIM: 602699

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

NFATC4 PubMed Links

Gene Details

Gene

NFATC4

Gene Name

nuclear factor of activated T-cells 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001136022.2	988	Missense Mutation	CGG,TGG	R286W	NP_001129494.1
NM_001198965.1	988	Missense Mutation	CGG,TGG	R223W	NP_001185894.1
NM_001198966.2	988	Missense Mutation	CGG,TGG	R153W	NP_001185895.1
NM_001198967.2	988	Missense Mutation	CGG,TGG	R286W	NP_001185896.1
NM_001288802.1	988	Missense Mutation	CGG,TGG	R211W	NP_001275731.1
NM_001320043.1	988	Missense Mutation	CGG,TGG	R286W	NP_001306972.1
NM_004554.4	988	Missense Mutation	CGG,TGG	R223W	NP_004545.2
XM_011536797.2	988	Missense Mutation	CGG,TGG	R211W	XP_011535099.1
XM_011536798.1	988	Missense Mutation	CGG,TGG	R200W	XP_011535100.1
XM_011536799.2	988	Missense Mutation	CGG,TGG	R211W	XP_011535101.1

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