Product Details

SNP ID
rs149449772
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:130664780 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGCTTCCTGTACGGCCGCTGGCGC[A/G]ACGTGCTCGGGGAGCAGCTCTTCGA
Phenotype
MIM: 616458
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
PRDM12 PubMed Links

Gene Details

Gene
PRDM12
Gene Name
PR domain 12
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_021619.2 187 Missense Mutation AAC,GAC N43D NP_067632.2

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