Product Details

SNP ID
rs594529
Assay Type
Functionally tested
NCBI dbSNP Submissions
55
Location
Chr.1:100352908 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GGGGAAGCCCCCGGGGGCGAGTGAC[C/T]TCAGCTGGCCACGACCCAGCCCTCC
Phenotype
MIM: 603504
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CDC14A PubMed Links

Gene Details

Gene
CDC14A
Gene Name
cell division cycle 14A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001319210.1 442 UTR 5 NP_001306139.1
NM_001319211.1 442 Intron NP_001306140.1
NM_001319212.1 442 UTR 5 NP_001306141.1
NM_003672.3 442 UTR 5 NP_003663.2
NM_033312.2 442 UTR 5 NP_201569.1
NM_033313.2 442 UTR 5 NP_201570.1
XM_005271294.3 442 Intron XP_005271351.1
XM_005271296.3 442 Intron XP_005271353.1
XM_011542340.2 442 Intron XP_011540642.1
XM_011542341.2 442 Intron XP_011540643.1
XM_011542345.2 442 Intron XP_011540647.1
XM_011542346.2 442 Intron XP_011540648.1
XM_017002646.1 442 Intron XP_016858135.1
XM_017002647.1 442 UTR 5 XP_016858136.1

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