Product Details

SNP ID
rs4902734
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:69573164 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCGCTTCTCCTCGCGCATGATGCG[C/G]TCGCGCTCGGCCCGGCATTGCTGCA
Phenotype
Polymorphism
C/G, Transversion 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_001271507.1 829 Missense Mutation GAC,GAG D153E NP_001258436.1

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