Product Details

SNP ID

rs563838

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:117331281 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCTTAGCTAGAGAATCCTAGGGTGT[C/T]CCCAGATGAGCAGAAGGCAGACTTG

Phenotype

MIM: 614848

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CEP164 PubMed Links

Gene Details

Gene

CEP164

Gene Name

centrosomal protein 164

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001271933.1		Intron			NP_001258862.1
NM_014956.4		Intron			NP_055771.4
XM_005271453.1		Intron			XP_005271510.1
XM_005271456.1		Intron			XP_005271513.1
XM_005271457.1		Intron			XP_005271514.1
XM_006718788.1		Intron			XP_006718851.1
XM_006718794.1		Intron			XP_006718857.1
XM_011542674.1		Intron			XP_011540976.1
XM_011542690.1		Intron			XP_011540992.1
XM_017017364.1		Intron			XP_016872853.1
XM_017017365.1		Intron			XP_016872854.1
XM_017017366.1		Intron			XP_016872855.1
XM_017017367.1		Intron			XP_016872856.1
XM_017017368.1		Intron			XP_016872857.1
XM_017017369.1		Intron			XP_016872858.1
XM_017017370.1		Intron			XP_016872859.1
XM_017017371.1		Intron			XP_016872860.1
XM_017017372.1		Intron			XP_016872861.1
XM_017017373.1		Intron			XP_016872862.1
XM_017017374.1		Intron			XP_016872863.1
XM_017017375.1		Intron			XP_016872864.1
XM_017017376.1		Intron			XP_016872865.1
XM_017017377.1		Intron			XP_016872866.1
XM_017017378.1		Intron			XP_016872867.1
XM_017017379.1		Intron			XP_016872868.1
XM_017017380.1		Intron			XP_016872869.1
XM_017017381.1		Intron			XP_016872870.1
XM_017017382.1		Intron			XP_016872871.1
XM_017017383.1		Intron			XP_016872872.1
XM_017017384.1		Intron			XP_016872873.1
XM_017017385.1		Intron			XP_016872874.1
XM_017017386.1		Intron			XP_016872875.1

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