Product Details

SNP ID

rs202184327

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.21:29008002 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTATCTCTGCTGACATAGCCAGAGG[C/T]GTGTTCTCTAACCCACTCTGTGGCA

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	676	Missense Mutation	ACC,GCC	T133A	NP_001307653.1
NM_016940.2	676	Missense Mutation	ACC,GCC	T162A	NP_058636.1

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