Product Details

SNP ID

rs183447127

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:16731242 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCAGAGCACTGCCTACCCTGAAGTG[C/T]CAGACCTTCTGCCAGAGGCACGGCT

Phenotype

MIM: 616250

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

NWD1 PubMed Links

Additional Information

For this assay, SNP(s) [rs8107776] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

NWD1

Gene Name

NACHT and WD repeat domain containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001007525.3	651	Silent Mutation	TGC,TGT	C15C	NP_001007526.3
NM_001290355.1	651	UTR 5			NP_001277284.1
XM_011527929.1	651	Silent Mutation	TGC,TGT	C15C	XP_011526231.1
XM_011527930.2	651	Silent Mutation	TGC,TGT	C15C	XP_011526232.1
XM_011527931.2	651	Silent Mutation	TGC,TGT	C15C	XP_011526233.1
XM_011527934.1	651	Intron			XP_011526236.1
XM_011527935.1	651	Silent Mutation	TGC,TGT	C15C	XP_011526237.1
XM_017026669.1	651	UTR 5			XP_016882158.1

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