Product Details

SNP ID

rs143222398

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:147624991 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CATTTCCCTCCTTTATGTTGCTGTC[C/T]ACCATGGGCTATGGGAGAGTAAGTA

Phenotype

MIM: 613937

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

TMEM184C PubMed Links

Gene Details

Gene

TMEM184C

Gene Name

transmembrane protein 184C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_018241.2	1048	Missense Mutation	CCA,CTA	P160L	NP_060711.2

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