Product Details

SNP ID
rs201019366
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.21:29007949 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGAAGATGAGGTCAACTGACTGGAC[C/T]GTGCTTCCTGTGGTGGGTGAAGATG
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
RWDD2B PubMed Links

Gene Details

Gene
RWDD2B
Gene Name
RWD domain containing 2B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001320724.1 729 Silent Mutation ACA,ACG T150T NP_001307653.1
NM_016940.2 729 Silent Mutation ACA,ACG T179T NP_058636.1

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