Product Details

SNP ID

rs1366333

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:123347318 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTTGCTCCTAAACCTTTGTTGTTGT[A/T]TTGAACATATTTTTAAAAATTCATT

Phenotype

MIM: 613446

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

CEP120 PubMed Links

Gene Details

Gene

CEP120

Gene Name

centrosomal protein 120

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001166226.1		Intron			NP_001159698.1
NM_153223.3		Intron			NP_694955.2
XM_005271901.4		Intron			XP_005271958.1
XM_011543185.2		Intron			XP_011541487.1
XM_011543186.2		Intron			XP_011541488.1
XM_017009085.1		Intron			XP_016864574.1

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