Product Details

SNP ID

rs3762739

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:195729690 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCCTCCTGCGGCTGAGTGTGGCTT[C/G]CCCGGAAGACCTCACTGACCCCAGA

Phenotype

MIM: 610360

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

MUC20 PubMed Links

Additional Information

For this assay, SNP(s) [rs115826755] 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

MUC20

Gene Name

mucin 20, cell surface associated

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001282506.1	2138	Missense Mutation	TCC,TGC	S671C	NP_001269435.1
NM_001291833.1	2138	Missense Mutation	TCC,TGC	S497C	NP_001278762.1
NM_020790.1	2138	Missense Mutation	TCC,TGC	S517C	NP_065841.1
NM_152673.3	2138	Missense Mutation	TCC,TGC	S500C	NP_689886.3

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