U.S. flag

An official website of the United States government

NM_032634.4(PIGO):c.1960C>G (p.Leu654Val) AND Inborn genetic diseases

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Mar 19, 2024
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:
RCV004649202.1

Allele description [Variation Report for NM_032634.4(PIGO):c.1960C>G (p.Leu654Val)]

NM_032634.4(PIGO):c.1960C>G (p.Leu654Val)

Gene:
PIGO:phosphatidylinositol glycan anchor biosynthesis class O [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
9p13.3
Genomic location:
Preferred name:
NM_032634.4(PIGO):c.1960C>G (p.Leu654Val)
HGVS:
  • NC_000009.12:g.35091927G>C
  • NG_031990.1:g.9675C>G
  • NM_001201484.2:c.1344+616C>G
  • NM_032634.4:c.1960C>GMANE SELECT
  • NM_152850.4:c.1344+616C>G
  • NP_116023.2:p.Leu654Val
  • NC_000009.11:g.35091924G>C
  • NM_032634.3:c.1960C>G
Protein change:
L654V
Links:
dbSNP: rs766400679
NCBI 1000 Genomes Browser:
rs766400679
Molecular consequence:
  • NM_001201484.2:c.1344+616C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_152850.4:c.1344+616C>G - intron variant - [Sequence Ontology: SO:0001627]
  • NM_032634.4:c.1960C>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Inborn genetic diseases
Identifiers:
MeSH: D030342; MedGen: C0950123

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV005153605Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)
Uncertain significance
(Mar 19, 2024)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From Ambry Genetics, SCV005153605.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

The c.1960C>G (p.L654V) alteration is located in exon 7 (coding exon 6) of the PIGO gene. This alteration results from a C to G substitution at nucleotide position 1960, causing the leucine (L) at amino acid position 654 to be replaced by a valine (V). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 29, 2024