Product Details

SNP ID
rs142786698
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:126340296 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGATGGCGCTGTCGACCATAGTCT[C/T]CCAGAGGAAGCAGATAAAGCGGAAG
Phenotype
MIM: 611264
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CENPW PubMed Links

Gene Details

Gene
CENPW
Gene Name
centromere protein W
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001012507.3 601 Missense Mutation TCC,TTC S8F NP_001012525.1
NM_001286524.1 601 Missense Mutation TCC,TTC S8F NP_001273453.1
NM_001286525.1 601 Missense Mutation TCC,TTC S8F NP_001273454.1
XM_017010845.1 601 Missense Mutation TCC,TTC S8F XP_016866334.1

View Full Product Details