Product Details

SNP ID

rs144153566

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.13:102730310 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TAAATAAGAGTTGGCTTCCAGAAAC[A/G]CACATTCCTCACTCTCACTTACTTC

Phenotype

Polymorphism

A/G, Transition 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	20527	Missense Mutation	GCG,GTG	A6796V	NP_001139669.1
XM_011521106.1	20527	Missense Mutation	GCG,GTG	A6756V	XP_011519408.1

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