Product Details

SNP ID

rs111736215

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:55954326 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTTGGAGAAAGAGAGCAAAGCTAAG[A/G]ATGAAAGAATTCAACAACTTCAAGA

Phenotype

MIM: 611423

Polymorphism

A/G, 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	683	Missense Mutation	AAT,GAT	N139D	NP_079285.2
XM_005265788.3	683	UTR 5			XP_005265845.1
XM_006714055.2	683	Missense Mutation	AAT,GAT	N139D	XP_006714118.1
XM_011534412.2	683	Intron			XP_011532714.1

View Full Product Details