Product Details

SNP ID

rs150681316

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:55952194 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAAAAGGCTGGATCAGCTGGGATAC[C/T]GCCAGACTCTGACAGTGGAGTGTTT

Phenotype

MIM: 611423

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CEP135 PubMed Links

Gene Details

Gene

CEP135

Gene Name

centrosomal protein 135

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_025009.4	332	Missense Mutation	CGC,TGC	R22C	NP_079285.2
XM_005265788.3	332	UTR 5			XP_005265845.1
XM_006714055.2	332	Missense Mutation	CGC,TGC	R22C	XP_006714118.1
XM_011534412.2	332	Intron			XP_011532714.1

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