Product Details

SNP ID
rs148833429
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:30984019 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGTCTACTATTGCATTTAGAAGCT[G/T]GTGAGTGATTTTATTTAAAATCGGG
Phenotype
MIM: 616991
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
MUC21 PubMed Links

Gene Details

Gene
MUC21
Gene Name
mucin 21, cell surface associated
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001010909.3 288 Missense Mutation GCA,TCA A21S NP_001010909.2
NM_001322370.1 288 Missense Mutation NP_001309299.1
NM_001322371.1 288 Missense Mutation NP_001309300.1

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