Product Details

SNP ID

rs10761237

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:93578535 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCTGACCTGGCGAGCGCAGTCACTC[C/T]GCTACAGAACCTTCTGGGCACCTGT

Phenotype

MIM: 604351

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

PHF2 PubMed Links

Gene Details

Gene

PHF2

Gene Name

PHD finger protein 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005392.3		Intron			NP_005383.3
XM_005252051.2		Intron			XP_005252108.1
XM_006717143.2		Intron			XP_006717206.1

View Full Product Details