Product Details

SNP ID

rs200651923

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:138495057 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTAATTTCTTTACTGCAGGTACAAT[A/G]GCATCCAAGTCATCAATTTCTGTAA

Phenotype

MIM: 614310

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CEP70 PubMed Links

Gene Details

Gene

CEP70

Gene Name

centrosomal protein 70

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001288964.1	2382	Silent Mutation	GCC,GCT	A566A	NP_001275893.1
NM_001288965.1	2382	Silent Mutation	GCC,GCT	A564A	NP_001275894.1
NM_001288966.1	2382	Intron			NP_001275895.1
NM_001288967.1	2382	Silent Mutation	GCC,GCT	A432A	NP_001275896.1
NM_001320598.1	2382	Silent Mutation	GCC,GCT	A584A	NP_001307527.1
NM_001320599.1	2382	Intron			NP_001307528.1
NM_001320600.1	2382	Intron			NP_001307529.1
NM_024491.3	2382	Silent Mutation	GCC,GCT	A584A	NP_077817.2
XM_005247805.3	2382	Intron			XP_005247862.1
XM_011513209.2	2382	Intron			XP_011511511.1
XM_017007270.1	2382	Intron			XP_016862759.1
XM_017007271.1	2382	Intron			XP_016862760.1
XM_017007272.1	2382	Intron			XP_016862761.1
XM_017007273.1	2382	Intron			XP_016862762.1
XM_017007274.1	2382	Intron			XP_016862763.1
XM_017007275.1	2382	Silent Mutation	GCC,GCT	A584A	XP_016862764.1
XM_017007276.1	2382	Intron			XP_016862765.1
XM_017007277.1	2382	Intron			XP_016862766.1
XM_017007278.1	2382	Intron			XP_016862767.1
XM_017007279.1	2382	Intron			XP_016862768.1
XM_017007280.1	2382	Intron			XP_016862769.1
XM_017007281.1	2382	Intron			XP_016862770.1
XM_017007282.1	2382	Silent Mutation	GCC,GCT	A325A	XP_016862771.1
XM_017007283.1	2382	Silent Mutation	GCC,GCT	A325A	XP_016862772.1
XM_017007284.1	2382	Silent Mutation	GCC,GCT	A325A	XP_016862773.1

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