Product Details

SNP ID

rs200985291

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:98716279 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCAGGGAACAAAGCCGATGATCACA[C/T]GCCCATCAGTGAGCCAACTTGGTGA

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

C14orf177 PubMed Links

Gene Details

Gene

C14orf177

Gene Name

chromosome 14 open reading frame 177

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_182560.2	507	Missense Mutation	CGC,TGC	R30C	NP_872366.2

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