Product Details

SNP ID
rs139598814
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.21:32576788 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTTTCCATCTTCAGACACCCCCCC[A/G]TCTCTCTGCACAGGGAGTTGGCCTT
Phenotype
MIM: 608365
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
TCP10L PubMed Links

Gene Details

Gene
TCP10L
Gene Name
t-complex 10-like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_144659.5 750 Missense Mutation CGG,TGG R212W NP_653260.1

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