Product Details

SNP ID
rs73391751
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:17367766 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAGAAGCAAGTCCAGAAAGCACCTC[C/G]TTCAGGTTACGTGACAATTCCGGGG
Phenotype
MIM: 607576
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
CECR2 PubMed Links

Gene Details

Gene
CECR2
Gene Name
CECR2, histone acetyl-lysine reader
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001290046.1 Intron NP_001276975.1
NM_001290047.1 Intron NP_001276976.1
XM_006724079.3 Intron XP_006724142.1
XM_011546128.2 Intron XP_011544430.1
XM_011546129.2 Intron XP_011544431.1
XM_011546132.2 Intron XP_011544434.1
XM_017028785.1 Intron XP_016884274.1

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