Product Details

SNP ID
rs779987797
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:44708796 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGGAGGCCTCTGAGGAAGGAGTACG[C/G]AGGCCGAGAAGGAGCCGGCATTTGA
Phenotype
MIM: 611661
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
DBF4B PubMed Links

Gene Details

Gene
DBF4B
Gene Name
DBF4 zinc finger B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_025104.3 162 UTR 5 NP_079380.2
NM_145663.2 162 UTR 5 NP_663696.1
XM_006722098.2 162 UTR 5 XP_006722161.1
XM_006722102.3 162 UTR 5 XP_006722165.1
XM_011525281.2 162 Intron XP_011523583.1
XM_017025145.1 162 UTR 5 XP_016880634.1
XM_017025146.1 162 Intron XP_016880635.1
XM_017025147.1 162 UTR 5 XP_016880636.1
XM_017025148.1 162 UTR 5 XP_016880637.1
XM_017025149.1 162 UTR 5 XP_016880638.1
XM_017025150.1 162 UTR 5 XP_016880639.1
XM_017025151.1 162 UTR 5 XP_016880640.1
XM_017025152.1 162 Intron XP_016880641.1
XM_017025153.1 162 Intron XP_016880642.1
XM_017025154.1 162 Intron XP_016880643.1
XM_017025155.1 162 UTR 5 XP_016880644.1
XM_017025156.1 162 UTR 5 XP_016880645.1

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