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NM_000414.4(HSD17B4):c.109G>A (p.Val37Ile) AND multiple conditions

Germline classification:
Likely benign (1 submission)
Last evaluated:
Jan 29, 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:
RCV002529309.2

Allele description

NM_000414.4(HSD17B4):c.109G>A (p.Val37Ile)

Gene:
HSD17B4:hydroxysteroid 17-beta dehydrogenase 4 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
5q23.1
Genomic location:
Preferred name:
NM_000414.4(HSD17B4):c.109G>A (p.Val37Ile)
HGVS:
  • NC_000005.10:g.119456365G>A
  • NG_008182.1:g.8913G>A
  • NM_000414.4:c.109G>AMANE SELECT
  • NM_001199291.3:c.119G>A
  • NM_001199292.2:c.58+3732G>A
  • NM_001292027.2:c.-29G>A
  • NM_001292028.2:c.-303G>A
  • NP_000405.1:p.Val37Ile
  • NP_001186220.1:p.Cys40Tyr
  • NC_000005.9:g.118792060G>A
  • NM_000414.3:c.109G>A
  • NM_001199291.1:c.119G>A
Protein change:
C40Y
Links:
dbSNP: rs747214551
NCBI 1000 Genomes Browser:
rs747214551
Molecular consequence:
  • NM_001292027.2:c.-29G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001292028.2:c.-303G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001199292.2:c.58+3732G>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_000414.4:c.109G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001199291.3:c.119G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Bifunctional peroxisomal enzyme deficiency (DBIF)
Synonyms:
D-bifunctional protein deficiency; DBP deficiency; D-bifunctional enzyme deficiency; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0009855; MedGen: C0342870; OMIM: 261515
Name:
Perrault syndrome
Synonyms:
Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance
Identifiers:
MONDO: MONDO:0017312; MedGen: C0685838; Orphanet: 2855; OMIM: PS233400

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV003452916Invitae
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Likely benign
(Jan 29, 2024) 		germlineclinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

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

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]
PMID:
28492532
PMCID:
PMC5632818

Details of each submission

From Invitae, SCV003452916.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Aug 11, 2024