NM_015922.3(NSDHL):c.387del (p.Ile129fs) AND Child syndrome

Germline classification:: Likely pathogenic (1 submission)
Last evaluated:: Oct 11, 2022
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:: RCV003148086.1

Allele description [Variation Report for NM_015922.3(NSDHL):c.387del (p.Ile129fs)]

NM_015922.3(NSDHL):c.387del (p.Ile129fs)

Gene:

NSDHL:NAD(P) dependent steroid dehydrogenase-like [Gene - OMIM - HGNC]

Variant type:

Deletion

Cytogenetic location:

Xq28

Genomic location:

Preferred name:

NM_015922.3(NSDHL):c.387del (p.Ile129fs)

HGVS:

NC_000023.11:g.152858889del
NG_009163.2:g.32923del
NM_001129765.2:c.387del
NM_015922.3:c.387delMANE SELECT
NP_001123237.1:p.Ile129fs
NP_057006.1:p.Ile129fs
NC_000023.10:g.152027433del

Protein change:

I129fs

Molecular consequence:

NM_001129765.2:c.387del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_015922.3:c.387del - frameshift variant - [Sequence Ontology: SO:0001589]

Condition(s)

Name:: Child syndrome
Synonyms:: Congenital Hemidysplasia with Ichthyosiform nevus and Limb Defects; Ichthyosis, CHILD syndrome
Identifiers:: MONDO: MONDO:0010621; MedGen: C0265267; Orphanet: 139; OMIM: 308050

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003835817	Baylor Genetics	criteria provided, single submitter (ACMG Guidelines, 2015)	Likely pathogenic (Oct 11, 2022)	unknown	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003835817

Baylor Genetics

criteria provided, single submitter

(ACMG Guidelines, 2015)

Likely pathogenic
(Oct 11, 2022)

unknown

clinical testing

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

Help

Summary from all submissions

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

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee.

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]

PMID:: 25741868
PMCID:: PMC4544753

Details of each submission

From Baylor Genetics, SCV003835817.1

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

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

Last Updated: Jul 29, 2023

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