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NM_000860.6(HPGD):c.584A>C (p.Glu195Ala) AND Inborn genetic diseases

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jun 11, 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:
RCV002642151.2

Allele description [Variation Report for NM_000860.6(HPGD):c.584A>C (p.Glu195Ala)]

NM_000860.6(HPGD):c.584A>C (p.Glu195Ala)

Gene:
HPGD:15-hydroxyprostaglandin dehydrogenase [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
4q34.1
Genomic location:
Preferred name:
NM_000860.6(HPGD):c.584A>C (p.Glu195Ala)
HGVS:
  • NC_000004.12:g.174493229T>G
  • NG_011689.1:g.34413A>C
  • NM_000860.4:c.584A>C
  • NM_000860.6:c.584A>CMANE SELECT
  • NM_001145816.3:c.499-1135A>C
  • NM_001256301.1:c.221A>C
  • NM_001256305.2:c.422-1135A>C
  • NM_001256306.2:c.380A>C
  • NM_001256307.2:c.221A>C
  • NP_000851.2:p.Glu195Ala
  • NP_001243230.1:p.Glu74Ala
  • NP_001243235.1:p.Glu127Ala
  • NP_001243236.1:p.Glu74Ala
  • NC_000004.11:g.175414380T>G
Protein change:
E127A
Links:
dbSNP: rs750778750
NCBI 1000 Genomes Browser:
rs750778750
Molecular consequence:
  • NM_001145816.3:c.499-1135A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001256305.2:c.422-1135A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_000860.6:c.584A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001256301.1:c.221A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001256306.2:c.380A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001256307.2:c.221A>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

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

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV003727095Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Jun 11, 2021) 		germlineclinical testing

Citation Link

Help

Summary from all submissions

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

Details of each submission

From Ambry Genetics, SCV003727095.2

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

Description

The c.584A>C (p.E195A) alteration is located in exon 6 (coding exon 6) of the HPGD gene. This alteration results from a A to C substitution at nucleotide position 584, causing the glutamic acid (E) at amino acid position 195 to be replaced by an alanine (A). 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