Product Details

SNP ID

rs112068716

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:69572805 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGACGCCGACCCCGCTGGGCAGCTG[C/T]TCCTGGCCGAGGCCCGAGGCGGCCA

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CCDC177 PubMed Links

Gene Details

Gene

CCDC177

Gene Name

coiled-coil domain containing 177

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001271507.1	1188	Missense Mutation	AAC,AGC	N273S	NP_001258436.1

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