Product Details

SNP ID
rs72863863
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.10:132399986 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTGGAAAGGTCAGGGGACTGTCCT[C/T]TGTGAACCACACCCTAGGCCAGACA
Phenotype
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
PWWP2B PubMed Links

Gene Details

Gene
PWWP2B
Gene Name
PWWP domain containing 2B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001098637.1 Intron NP_001092107.1
NM_138499.3 Intron NP_612508.3
XM_006717659.3 Intron XP_006717722.1
XM_011539387.2 Intron XP_011537689.1

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