Product Details

SNP ID
rs150229852
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:47119115 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CACCTTGTGCTTTGCCAATTAAAAA[A/G]ATAAAAGAATCTAAAATTAAATATT
Phenotype
MIM: 116946
Polymorphism
A/G, Transition 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 4376 Intron NP_001107563.1
NM_001256.4 4376 Intron NP_001247.3
NM_001293089.1 4376 Intron NP_001280018.1
NM_001293091.1 4376 Intron NP_001280020.1
XM_011525546.2 4376 UTR 3 XP_011523848.1
XM_011525547.2 4376 UTR 3 XP_011523849.1
XM_011525548.2 4376 UTR 3 XP_011523850.1
XM_011525549.2 4376 UTR 3 XP_011523851.1
XM_011525550.2 4376 UTR 3 XP_011523852.1
XM_017025481.1 4376 Intron XP_016880970.1
XM_017025482.1 4376 UTR 3 XP_016880971.1
XM_017025483.1 4376 UTR 3 XP_016880972.1
XM_017025484.1 4376 UTR 3 XP_016880973.1
XM_017025485.1 4376 UTR 3 XP_016880974.1
XM_017025486.1 4376 UTR 3 XP_016880975.1
XM_017025487.1 4376 UTR 3 XP_016880976.1
XM_017025488.1 4376 UTR 3 XP_016880977.1

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