U.S. flag

An official website of the United States government

NM_020297.4(ABCC9):c.406+38A>C AND Hypertrichotic osteochondrodysplasia Cantu type

Germline classification:
Benign (1 submission)
Last evaluated:
Jul 14, 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:
RCV001548919.2

Allele description [Variation Report for NM_020297.4(ABCC9):c.406+38A>C]

NM_020297.4(ABCC9):c.406+38A>C

Gene:
ABCC9:ATP binding cassette subfamily C member 9 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
12p12.1
Genomic location:
Preferred name:
NM_020297.4(ABCC9):c.406+38A>C
HGVS:
  • NC_000012.12:g.21925904T>G
  • NG_012819.1:g.15791A>C
  • NM_001377273.1:c.406+38A>C
  • NM_001377274.1:c.-49+38A>C
  • NM_005691.4:c.406+38A>C
  • NM_020297.4:c.406+38A>CMANE SELECT
  • LRG_377t1:c.406+38A>C
  • LRG_377:g.15791A>C
  • NC_000012.11:g.22078838T>G
  • NM_020297.2:c.406+38A>C
  • NM_020297.3:c.406+38A>C
Links:
dbSNP: rs2277405
NCBI 1000 Genomes Browser:
rs2277405
Molecular consequence:
  • NM_001377273.1:c.406+38A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001377274.1:c.-49+38A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_005691.4:c.406+38A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_020297.4:c.406+38A>C - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:
Hypertrichotic osteochondrodysplasia Cantu type
Synonyms:
Hypertrichotic osteochondrodysplasia; Cantu syndrome
Identifiers:
MONDO: MONDO:0009406; MedGen: C0795905; Orphanet: 1517; OMIM: 239850

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001768928Genome-Nilou Lab
criteria provided, single submitter

(ACMG Guidelines, 2015)		Benign
(Jul 14, 2021) 		germlineclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlinenonot 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 Genome-Nilou Lab, SCV001768928.1

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

Last Updated: Sep 29, 2024