Product Details

SNP ID

rs11946612

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:67470253 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AATGGAGAGCCTTTGCTGAACCATA[C/T]GGGCTTTCAGTTTAGACAAAGAAAG

Phenotype

MIM: 117141

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CENPC PubMed Links

Gene Details

Gene

CENPC

Gene Name

centromere protein C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001812.2	5406	Intron			NP_001803.2
XM_006714064.2	5406	UTR 3			XP_006714127.1
XM_011531542.2	5406	Intron			XP_011529844.1

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