Product Details

SNP ID

rs201621075

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:55952239 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTGTTTACCTTTGGTAGAAAAACTT[C/T]TCAGGTAAAGACAAAAATACAGTTT

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	377	Missense Mutation	CTC,TTC	L37F	NP_079285.2
XM_005265788.3	377	UTR 5			XP_005265845.1
XM_006714055.2	377	Missense Mutation	CTC,TTC	L37F	XP_006714118.1
XM_011534412.2	377	Intron			XP_011532714.1

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