Product Details

SNP ID
rs143937615
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:531947 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGCCGCCGCCATGGCTCGGCCGCTA[A/G]TGCCCAGCTCGCAGAAGGCGCTGCT
Phenotype
MIM: 116948
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
CDC34 PubMed Links

Gene Details

Gene
CDC34
Gene Name
cell division cycle 34
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_004359.1 215 Missense Mutation ATG,GTG M6V NP_004350.1
XM_005259690.3 215 Missense Mutation ATG,GTG M6V XP_005259747.1
XM_006722952.2 215 Missense Mutation ATG,GTG M6V XP_006723015.1

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