Product Details

SNP ID

rs149679373

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:138495021 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAAATGATTTGATTTGTTTTCAGTA[G/T]GAAAGTACTTTTAATTTCTTTACTG

Phenotype

MIM: 614310

Polymorphism

G/T, Transversion 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	2418	Silent Mutation			NP_001275893.1
NM_001288965.1	2418	Silent Mutation			NP_001275894.1
NM_001288966.1	2418	Intron			NP_001275895.1
NM_001288967.1	2418	Silent Mutation			NP_001275896.1
NM_001320598.1	2418	Silent Mutation			NP_001307527.1
NM_001320599.1	2418	Intron			NP_001307528.1
NM_001320600.1	2418	Intron			NP_001307529.1
NM_024491.3	2418	Silent Mutation			NP_077817.2
XM_005247805.3	2418	Intron			XP_005247862.1
XM_011513209.2	2418	Intron			XP_011511511.1
XM_017007270.1	2418	Intron			XP_016862759.1
XM_017007271.1	2418	Intron			XP_016862760.1
XM_017007272.1	2418	Intron			XP_016862761.1
XM_017007273.1	2418	Intron			XP_016862762.1
XM_017007274.1	2418	Intron			XP_016862763.1
XM_017007275.1	2418	Silent Mutation			XP_016862764.1
XM_017007276.1	2418	Intron			XP_016862765.1
XM_017007277.1	2418	Intron			XP_016862766.1
XM_017007278.1	2418	Intron			XP_016862767.1
XM_017007279.1	2418	Intron			XP_016862768.1
XM_017007280.1	2418	Intron			XP_016862769.1
XM_017007281.1	2418	Intron			XP_016862770.1
XM_017007282.1	2418	Silent Mutation			XP_016862771.1
XM_017007283.1	2418	Silent Mutation			XP_016862772.1
XM_017007284.1	2418	Silent Mutation			XP_016862773.1

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