Product Details

SNP ID

rs138690504

Assay Type

Functionally tested

NCBI dbSNP Submissions

3

Location

Chr.1:214613794 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGAAGAATGGAAAGAAGGGCTGCCT[A/G]CAAGAGCTCTTCAGAAAATTCAAGA

Phenotype

MIM: 600236

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CENPF PubMed Links

Gene Details

Gene

CENPF

Gene Name

centromere protein F

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_016343.3	201	Missense Mutation	ACA,GCA	T14A	NP_057427.3
XM_011509082.2	201	Missense Mutation	ACA,GCA	T14A	XP_011507384.1
XM_017000086.1	201	Missense Mutation	ACA,GCA	T14A	XP_016855575.1

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