Product Details

SNP ID

rs6692555

Assay Type

Functionally tested

NCBI dbSNP Submissions

39

Location

Chr.1:15686162 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACTTTGTAAGTCAGGCTGTCACTTA[C/T]GAGTTAGGTGTGTTTGTTGAGGTGC

Phenotype

MIM: 609613

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

PLEKHM2 PubMed Links

Gene Details

Gene

PLEKHM2

Gene Name

pleckstrin homology and RUN domain containing M2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015164.2		Intron			NP_055979.2
XM_005245790.3		Intron			XP_005245847.1
XM_005245791.4		Intron			XP_005245848.1
XM_017000757.1		Intron			XP_016856246.1
XM_017000758.1		Intron			XP_016856247.1

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