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NM_000497.4(CYP11B1):c.1181del (p.Asn394fs) AND multiple conditions

Germline classification:
Pathogenic (1 submission)
Last evaluated:
Mar 5, 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:
RCV002481670.1

Allele description [Variation Report for NM_000497.4(CYP11B1):c.1181del (p.Asn394fs)]

NM_000497.4(CYP11B1):c.1181del (p.Asn394fs)

Genes:
LOC106799833:CYP11B1 recombination region [Gene]
CYP11B1:cytochrome P450 family 11 subfamily B member 1 [Gene - OMIM - HGNC]
Variant type:
Deletion
Cytogenetic location:
8q24.3
Genomic location:
Preferred name:
NM_000497.4(CYP11B1):c.1181del (p.Asn394fs)
HGVS:
  • NC_000008.11:g.142875254del
  • NG_007954.1:g.9568del
  • NG_046132.1:g.1121del
  • NM_000497.4:c.1181delMANE SELECT
  • NM_001026213.1:c.1181del
  • NP_000488.3:p.Asn394fs
  • NP_001021384.1:p.Asn394fs
  • NC_000008.10:g.143956669del
  • NC_000008.10:g.143956670del
  • NM_000497.3:c.1181delA
Protein change:
N394fs
Links:
dbSNP: rs1256580853
NCBI 1000 Genomes Browser:
rs1256580853
Molecular consequence:
  • NM_000497.4:c.1181del - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001026213.1:c.1181del - frameshift variant - [Sequence Ontology: SO:0001589]

Condition(s)

Name:
Deficiency of steroid 11-beta-monooxygenase (CYP11B1)
Synonyms:
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASE DEFICIENCY; 11-beta-hydroxylase deficiency; Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0008729; MedGen: C0268292; OMIM: 202010
Name:
Glucocorticoid-remediable aldosteronism
Synonyms:
ACTH-DEPENDENT HYPERALDOSTERONISM SYNDROME; ALDOSTERONISM, SENSITIVE TO DEXAMETHASONE; FH I; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0007080; MedGen: C3838731; Orphanet: 403; OMIM: 103900

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002801673Fulgent Genetics, Fulgent Genetics
criteria provided, single submitter

(ACMG Guidelines, 2015)		Pathogenic
(Mar 5, 2022) 		unknownclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedunknownunknownnot providednot providednot providednot providednot providedclinical 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 Fulgent Genetics, Fulgent Genetics, SCV002801673.1

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

Last Updated: Sep 29, 2024