Product Details

SNP ID
rs143719119
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.6:126346253 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTTCATCGATTAGCAGAAGAGTCC[A/G]GGACAAACGCTTGTGCGAGTAAATG
Phenotype
MIM: 611264
Polymorphism
A/G, 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_001012507.3 713 Missense Mutation AGG,GGG R59G NP_001012525.1
NM_001286524.1 713 Missense Mutation AGG,GGG R74G NP_001273453.1
NM_001286525.1 713 Silent Mutation CCA,CCG P45P NP_001273454.1
XM_017010845.1 713 Silent Mutation CCA,CCG P45P XP_016866334.1

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