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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