Product Details

SNP ID
rs687532
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.13:77046925 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CCCCACCAGTGGGTGGGGGAGAGTG[C/G]GCAGGATGGGGACACTCAATGGCAG
Phenotype
MIM: 610392
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
MYCBP2 PubMed Links

Gene Details

Gene
MYCBP2
Gene Name
MYC binding protein 2, E3 ubiquitin protein ligase
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_015057.4 Intron NP_055872.4
XM_005266299.2 Intron XP_005266356.1
XM_006719779.2 Intron XP_006719842.1
XM_006719780.2 Intron XP_006719843.1
XM_006719781.2 Intron XP_006719844.1
XM_006719782.2 Intron XP_006719845.1
XM_006719783.2 Intron XP_006719846.1
XM_006719784.2 Intron XP_006719847.1
XM_006719785.2 Intron XP_006719848.1
XM_006719786.2 Intron XP_006719849.1
XM_006719787.2 Intron XP_006719850.1
XM_006719788.2 Intron XP_006719851.1
XM_006719789.2 Intron XP_006719852.1
XM_011535004.2 Intron XP_011533306.1
XM_011535005.2 Intron XP_011533307.1
XM_017020454.1 Intron XP_016875943.1
XM_017020455.1 Intron XP_016875944.1
XM_017020456.1 Intron XP_016875945.1
XM_017020457.1 Intron XP_016875946.1
XM_017020458.1 Intron XP_016875947.1
XM_017020459.1 Intron XP_016875948.1
XM_017020460.1 Intron XP_016875949.1
XM_017020461.1 Intron XP_016875950.1
XM_017020462.1 Intron XP_016875951.1
XM_017020463.1 Intron XP_016875952.1
XM_017020464.1 Intron XP_016875953.1
XM_017020465.1 Intron XP_016875954.1
XM_017020466.1 Intron XP_016875955.1
XM_017020467.1 Intron XP_016875956.1
XM_017020468.1 Intron XP_016875957.1

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