Product Details

SNP ID

rs11191650

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:103309482 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATGTTTTTGCCTTCAGCCATGATTG[C/G]AAGCTAAGCTGCTATGATTCCTGTA

Phenotype

MIM: 607816

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

PCGF6 PubMed Links

Gene Details

Gene

PCGF6

Gene Name

polycomb group ring finger 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001011663.1		Intron			NP_001011663.1
NM_032154.3		Intron			NP_115530.2

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