NM_004531.5(MOCS2):c.24del (p.Ser9fs) AND Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B

Germline classification:: Pathogenic (1 submission)
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:: RCV001619771.3

Allele description [Variation Report for NM_004531.5(MOCS2):c.24del (p.Ser9fs)]

NM_004531.5(MOCS2):c.24del (p.Ser9fs)

Gene:

MOCS2:molybdenum cofactor synthesis 2 [Gene - OMIM - HGNC]

Variant type:

Deletion

Cytogenetic location:

5q11.2

Genomic location:

Preferred name:

NM_004531.5(MOCS2):c.24del (p.Ser9fs)

HGVS:

NC_000005.10:g.53107152del
NG_008435.2:g.7618del
NM_004531.5:c.24delMANE SELECT
NM_176806.4:c.211del
NP_004522.1:p.Ser9fs
NP_789776.1:p.Leu71fs
NC_000005.9:g.52402982del
NM_004531.5:c.24delCMANE SELECT

Protein change:

L71fs

Links:

dbSNP: rs2112090886

NCBI 1000 Genomes Browser:

rs2112090886

Molecular consequence:

NM_004531.5:c.24del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_176806.4:c.211del - frameshift variant - [Sequence Ontology: SO:0001589]

Condition(s)

Name:: Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B
Synonyms:: Molybdenum cofactor deficiency, complementation group B; Molybdenum cofactor deficiency B
Identifiers:: MONDO: MONDO:0009644; MedGen: C1854989; Orphanet: 833; OMIM: 252160

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001847681	Suma Genomics	criteria provided, single submitter (ACMG Guidelines, 2015)	Pathogenic	inherited	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

SCV001847681

Suma Genomics

criteria provided, single submitter

(ACMG Guidelines, 2015)

Pathogenic

inherited

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	inherited	yes	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 Suma Genomics, SCV001847681.1

#	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	inherited	yes	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Nov 10, 2024

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