Product Details

SNP ID

rs145420508

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:55953131 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAGCCTTCGGCAATCAAAATTATCT[G/T]CTGTGAAAGCTGAAAAAGAAAGTGC

Phenotype

MIM: 611423

Polymorphism

G/T, Transversion 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	428	Missense Mutation	GCT,TCT	A54S	NP_079285.2
XM_005265788.3	428	UTR 5			XP_005265845.1
XM_006714055.2	428	Missense Mutation	GCT,TCT	A54S	XP_006714118.1
XM_011534412.2	428	Intron			XP_011532714.1

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