Product Details

SNP ID

rs17216678

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:56561578 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TATCCCCATTGCATTTGGGACTTCA[A/G]AATACTGATGCAACCTAAGTTTCCC

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CCDC66 PubMed Links

Gene Details

Gene

CCDC66

Gene Name

coiled-coil domain containing 66

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001012506.4		Intron			NP_001012524.4
NM_001141947.1		Intron			NP_001135419.1
XM_005265081.3		Intron			XP_005265138.1
XM_005265082.3		Intron			XP_005265139.1
XM_005265083.3		Intron			XP_005265140.1
XM_005265084.3		Intron			XP_005265141.1
XM_011533614.2		Intron			XP_011531916.1
XM_011533615.2		Intron			XP_011531917.1
XM_011533616.2		Intron			XP_011531918.1
XM_011533617.2		Intron			XP_011531919.1
XM_011533619.2		Intron			XP_011531921.1
XM_017006229.1		Intron			XP_016861718.1
XM_017006230.1		Intron			XP_016861719.1
XM_017006231.1		Intron			XP_016861720.1
XM_017006232.1		Intron			XP_016861721.1
XM_017006233.1		Intron			XP_016861722.1
XM_017006234.1		Intron			XP_016861723.1
XM_017006235.1		Intron			XP_016861724.1
XM_017006236.1		Intron			XP_016861725.1
XM_017006237.1		Intron			XP_016861726.1
XM_017006238.1		Intron			XP_016861727.1
XM_017006239.1		Intron			XP_016861728.1
XM_017006240.1		Intron			XP_016861729.1
XM_017006241.1		Intron			XP_016861730.1
XM_017006242.1		Intron			XP_016861731.1
XM_017006243.1		Intron			XP_016861732.1
XM_017006244.1		Intron			XP_016861733.1
XM_017006245.1		Intron			XP_016861734.1

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