Product Details

SNP ID
rs10901270
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.9:130670191 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CCCACTTCTCTGCTCCCCTTGGGGT[G/T]GGGCTAGGGCTTGGTGGAGATTTTT
Phenotype
MIM: 616458
Polymorphism
G/T, Transversion 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 Intron NP_067632.2

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