Product Details

SNP ID
rs2234929
Assay Type
Functionally Tested
NCBI dbSNP Submissions
9
Location
Chr.1:171635976 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAGTGACCATGTTCAAGTTGTCCCA[A/G]GCAAAGAGCTTCTTCTCCAGGGGGT
Phenotype
MIM: 601652
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
MYOC PubMed Links

Gene Details

Gene
MYOC
Gene Name
myocilin
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000261.1 1486 Silent Mutation NP_000252.1

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