Product Details

SNP ID

rs11186478

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:91166943 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACCATGGGAGCAGCTTAATCTCTCA[A/G]AAGTTTCAGTTTTTTCAATCGGAGA

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

PCGF5 PubMed Links

Gene Details

Gene

PCGF5

Gene Name

polycomb group ring finger 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001256549.1		Intron			NP_001243478.1
NM_001257101.1		Intron			NP_001244030.1
NM_032373.4		Intron			NP_115749.2
XM_006718030.1		Intron			XP_006718093.1
XM_011540271.2		Intron			XP_011538573.1
XM_011540272.2		Intron			XP_011538574.1
XM_017016776.1		Intron			XP_016872265.1
XM_017016777.1		Intron			XP_016872266.1
XM_017016778.1		Intron			XP_016872267.1

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