Product Details

SNP ID
rs11570583
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:47119017 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCAGCAAGTTATGTTCTAAGCTTAG[C/G]TTTCTCCAGGCTTTATAACGCAGAA
Phenotype
MIM: 116946
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
CDC27 PubMed Links

Gene Details

Gene
CDC27
Gene Name
cell division cycle 27
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001114091.2 4474 Intron NP_001107563.1
NM_001256.4 4474 Intron NP_001247.3
NM_001293089.1 4474 Intron NP_001280018.1
NM_001293091.1 4474 Intron NP_001280020.1
XM_011525546.2 4474 UTR 3 XP_011523848.1
XM_011525547.2 4474 UTR 3 XP_011523849.1
XM_011525548.2 4474 UTR 3 XP_011523850.1
XM_011525549.2 4474 UTR 3 XP_011523851.1
XM_011525550.2 4474 UTR 3 XP_011523852.1
XM_017025481.1 4474 Intron XP_016880970.1
XM_017025482.1 4474 UTR 3 XP_016880971.1
XM_017025483.1 4474 UTR 3 XP_016880972.1
XM_017025484.1 4474 UTR 3 XP_016880973.1
XM_017025485.1 4474 UTR 3 XP_016880974.1
XM_017025486.1 4474 UTR 3 XP_016880975.1
XM_017025487.1 4474 UTR 3 XP_016880976.1
XM_017025488.1 4474 UTR 3 XP_016880977.1

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