Product Details

SNP ID

rs2841225

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:104869373 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTGCAGGGAGCTGCCCTGCCCACTC[A/G]GACGTTGCCTCCTGGATGCAACGTG

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CEP170B PubMed Links

Gene Details

Gene

CEP170B

Gene Name

centrosomal protein 170B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001112726.2	807	Intron			NP_001106197.1
NM_015005.2	807	Intron			NP_055820.2
XM_005267550.3	807	Intron			XP_005267607.1
XM_011536665.2	807	Intron			XP_011534967.1
XM_011536666.2	807	Intron			XP_011534968.1
XM_011536667.2	807	Intron			XP_011534969.1
XM_017021227.1	807	Silent Mutation	TCA,TCG	S20S	XP_016876716.1
XM_017021228.1	807	Silent Mutation	TCA,TCG	S20S	XP_016876717.1
XM_017021229.1	807	Silent Mutation	TCA,TCG	S20S	XP_016876718.1
XM_017021230.1	807	Silent Mutation	TCA,TCG	S20S	XP_016876719.1

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