Product Details

SNP ID

rs139428854

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.21:29008038 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACCCACTCTGTGGCATTCAGTATAC[A/G]AACATCTCCATGACAATGTTTTTGC

Phenotype

Polymorphism

A/G, 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	640	Missense Mutation	CGT,TGT	R121C	NP_001307653.1
NM_016940.2	640	Missense Mutation	CGT,TGT	R150C	NP_058636.1

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