Product Details

SNP ID

rs2508665

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:117328073 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGACCCGAGGCACGCTCTCGAGCC[A/T]ACGAGCGTGATGCGCTCGAGTGTGG

Phenotype

MIM: 614848

Polymorphism

A/T, Transversion 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	140	Intron			NP_001258862.1
NM_014956.4	140	Intron			NP_055771.4
XM_005271453.1	140	UTR 5			XP_005271510.1
XM_005271456.1	140	UTR 5			XP_005271513.1
XM_005271457.1	140	UTR 5			XP_005271514.1
XM_006718788.1	140	UTR 5			XP_006718851.1
XM_006718794.1	140	UTR 5			XP_006718857.1
XM_011542674.1	140	UTR 5			XP_011540976.1
XM_011542690.1	140	UTR 5			XP_011540992.1
XM_017017364.1	140	Intron			XP_016872853.1
XM_017017365.1	140	Intron			XP_016872854.1
XM_017017366.1	140	Intron			XP_016872855.1
XM_017017367.1	140	UTR 5			XP_016872856.1
XM_017017368.1	140	UTR 5			XP_016872857.1
XM_017017369.1	140	UTR 5			XP_016872858.1
XM_017017370.1	140	UTR 5			XP_016872859.1
XM_017017371.1	140	UTR 5			XP_016872860.1
XM_017017372.1	140	UTR 5			XP_016872861.1
XM_017017373.1	140	UTR 5			XP_016872862.1
XM_017017374.1	140	Intron			XP_016872863.1
XM_017017375.1	140	UTR 5			XP_016872864.1
XM_017017376.1	140	UTR 5			XP_016872865.1
XM_017017377.1	140	UTR 5			XP_016872866.1
XM_017017378.1	140	UTR 5			XP_016872867.1
XM_017017379.1	140	UTR 5			XP_016872868.1
XM_017017380.1	140	Intron			XP_016872869.1
XM_017017381.1	140	UTR 5			XP_016872870.1
XM_017017382.1	140	Intron			XP_016872871.1
XM_017017383.1	140	UTR 5			XP_016872872.1
XM_017017384.1	140	Intron			XP_016872873.1
XM_017017385.1	140	Intron			XP_016872874.1
XM_017017386.1	140	UTR 5			XP_016872875.1

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