Product Details

SNP ID
rs200460352
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:30986309 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTGATCTCCAGTGGAGCCAGCACAG[C/T]CACCAACTCTGGGTCCAGTGTGACC
Phenotype
MIM: 616991
Polymorphism
C/T, Transition 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_001010909.3 361 Missense Mutation GCC,GTC A45V NP_001010909.2
NM_001322370.1 361 Missense Mutation NP_001309299.1
NM_001322371.1 361 Missense Mutation NP_001309300.1

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