Product Details

SNP ID
rs140623300
Assay Type
Functionally tested
NCBI dbSNP Submissions
15
Location
Chr.1:100352985 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCGGAGTCAGGGGAACTAATCGGG[A/G]CTTGTGAGTTCATGAAAGGTGAGGA
Phenotype
MIM: 603504
Polymorphism
A/G, 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_001319210.1 519 Missense Mutation ACT,GCT T11A NP_001306139.1
NM_001319211.1 519 Intron NP_001306140.1
NM_001319212.1 519 UTR 5 NP_001306141.1
NM_003672.3 519 Missense Mutation ACT,GCT T11A NP_003663.2
NM_033312.2 519 Missense Mutation ACT,GCT T11A NP_201569.1
NM_033313.2 519 Missense Mutation ACT,GCT T11A NP_201570.1
XM_005271294.3 519 Intron XP_005271351.1
XM_005271296.3 519 Intron XP_005271353.1
XM_011542340.2 519 Intron XP_011540642.1
XM_011542341.2 519 Intron XP_011540643.1
XM_011542345.2 519 Intron XP_011540647.1
XM_011542346.2 519 Intron XP_011540648.1
XM_017002646.1 519 Intron XP_016858135.1
XM_017002647.1 519 Missense Mutation ACT,GCT T11A XP_016858136.1

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