Product Details

SNP ID

rs189013609

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.13:102729737 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCTGATTTATGTTTGCTTTGGAAA[C/G]AATCCAATCTTTCTGACTCATAATC

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

CCDC168 PubMed Links

Gene Details

Gene

CCDC168

Gene Name

coiled-coil domain containing 168

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001146197.1	21100	Missense Mutation	TCT,TGT	S6987C	NP_001139669.1
XM_011521106.1	21100	Missense Mutation	TCT,TGT	S6947C	XP_011519408.1

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