U.S. flag

An official website of the United States government

NR_003051.3(RMRP):n.-21_-19dup AND multiple conditions

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
May 4, 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:
RCV002499149.8

Allele description [Variation Report for NR_003051.3(RMRP):n.-21_-19dup]

NR_003051.3(RMRP):n.-21_-19dup

Gene:
RMRP:RNA component of mitochondrial RNA processing endoribonuclease [Gene - OMIM - HGNC]
Variant type:
Microsatellite
Cytogenetic location:
9p13.3
Genomic location:
Preferred name:
NR_003051.3(RMRP):n.-21_-19dup
HGVS:
  • NC_000009.12:g.35658038GTA[3]
  • NG_017041.1:g.4977ACT[3]
  • NG_033120.1:g.4749GTA[3]
  • NG_116211.1:g.574GTA[3]
  • LRG_163t1:n.-21_-19dup
  • LRG_163:g.4977ACT[3]
  • NC_000009.11:g.35658033_35658034insAGT
  • NC_000009.11:g.35658035GTA[3]
  • NR_003051.3:n.-21_-19dup
Links:
dbSNP: rs1029136594
NCBI 1000 Genomes Browser:
rs1029136594

Condition(s)

Name:
Anauxetic dysplasia 1 (ANXD1)
Synonyms:
Spondylometaepiphyseal dysplasia Anauxetic type; Spondylometaepiphyseal dysplasia Menger type
Identifiers:
MONDO: MONDO:0054560; MedGen: C4551965; Orphanet: 93347; OMIM: 607095
Name:
Metaphyseal chondrodysplasia, McKusick type (CHH)
Synonyms:
Cartilage-Hair Hypoplasia
Identifiers:
MONDO: MONDO:0009595; MedGen: C0220748; Orphanet: 175; OMIM: 250250
Name:
Metaphyseal dysplasia without hypotrichosis
Synonyms:
Cartilage-hair hypoplasia-like skeletal dysplasia without hypotrichosis or immunodeficiency; Cartilage-hair hypoplasia variant, skeletal manifestations only
Identifiers:
MONDO: MONDO:0009601; MedGen: C1834821; OMIM: 250460

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
SCV002793547Fulgent Genetics, Fulgent Genetics
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain significance
(May 4, 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, SCV002793547.1

#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: Nov 3, 2024