Product Details

SNP ID
rs13447462
Assay Type
Functionally Tested
NCBI dbSNP Submissions
2
Location
Chr.1:91501931 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAAAAATAAGATTGAATCTTATAAA[A/G]TGAATTGTATGTTTCTATAGGACAG
Phenotype
MIM: 603311
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
CDC7 PubMed Links

Gene Details

Gene
CDC7
Gene Name
cell division cycle 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001134419.1 Intron NP_001127891.1
NM_001134420.1 Intron NP_001127892.1
NM_003503.3 Intron NP_003494.1
XM_005271241.2 Intron XP_005271298.1
XM_005271244.2 Intron XP_005271301.1
XM_017002425.1 Intron XP_016857914.1
XM_017002426.1 Intron XP_016857915.1
XM_017002427.1 Intron XP_016857916.1

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