Product Details

SNP ID

rs188691406

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.21:29007916 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TATAGATATGATGGCTGTAGATCCA[C/G]AGTCTCGTGAAGATGAGGTCAACTG

Phenotype

Polymorphism

C/G, Transversion 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	762	Silent Mutation	CTC,CTG	L161L	NP_001307653.1
NM_016940.2	762	Silent Mutation	CTC,CTG	L190L	NP_058636.1

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