NM_002627.5(PFKP):c.2141A>G (p.Asp714Gly) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Aug 2, 2021
Review status:: 1 star out of maximum of 4 stars
criteria provided, single submitter

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV004101396.1

Allele description [Variation Report for NM_002627.5(PFKP):c.2141A>G (p.Asp714Gly)]

NM_002627.5(PFKP):c.2141A>G (p.Asp714Gly)

Gene:

PFKP:phosphofructokinase, platelet [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

10p15.2

Genomic location:

Preferred name:

NM_002627.5(PFKP):c.2141A>G (p.Asp714Gly)

HGVS:

NC_000010.11:g.3135754A>G
NG_051598.1:g.73281A>G
NG_052908.1:g.42088T>C
NM_001242339.2:c.2117A>G
NM_001323067.2:c.2060A>G
NM_001323068.2:c.1988A>G
NM_001323069.2:c.1634A>G
NM_001323070.1:c.1340A>G
NM_001323071.2:c.2027A>G
NM_001323072.2:c.2027A>G
NM_001323073.1:c.1493A>G
NM_001323074.1:c.1493A>G
NM_001345944.1:c.2027A>G
NM_001410880.1:c.2294A>G
NM_002627.5:c.2141A>GMANE SELECT
NP_001229268.1:p.Asp706Gly
NP_001309996.1:p.Asp687Gly
NP_001309997.1:p.Asp663Gly
NP_001309998.1:p.Asp545Gly
NP_001309999.1:p.Asp447Gly
NP_001310000.1:p.Asp676Gly
NP_001310001.1:p.Asp676Gly
NP_001310002.1:p.Asp498Gly
NP_001310003.1:p.Asp498Gly
NP_001332873.1:p.Asp676Gly
NP_001397809.1:p.Asp765Gly
NP_002618.1:p.Asp714Gly
NC_000010.10:g.3177946A>G
NM_002627.4:c.2141A>G

Protein change:

D447G

Molecular consequence:

NM_001242339.2:c.2117A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001323067.2:c.2060A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001323068.2:c.1988A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001323069.2:c.1634A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001323070.1:c.1340A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001323071.2:c.2027A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001323072.2:c.2027A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001323073.1:c.1493A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001323074.1:c.1493A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001345944.1:c.2027A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001410880.1:c.2294A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_002627.5:c.2141A>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003569566	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Aug 2, 2021)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003569566

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Aug 2, 2021)

germline

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Ambry Genetics, SCV003569566.2

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

Description

The c.2141A>G (p.D714G) alteration is located in exon 21 (coding exon 21) of the PFKP gene. This alteration results from a A to G substitution at nucleotide position 2141, causing the aspartic acid (D) at amino acid position 714 to be replaced by a glycine (G). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Nov 24, 2024

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