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NM_019032.6(ADAMTSL4):c.2270del (p.Gly757fs) AND Ectopia lentis 2, isolated, autosomal recessive

Germline classification:
Likely pathogenic (1 submission)
Last evaluated:
Apr 11, 2023
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:
RCV003339741.1

Allele description

NM_019032.6(ADAMTSL4):c.2270del (p.Gly757fs)

Gene:
ADAMTSL4:ADAMTS like 4 [Gene - OMIM - HGNC]
Variant type:
Deletion
Cytogenetic location:
1q21.2
Genomic location:
Preferred name:
NM_019032.6(ADAMTSL4):c.2270del (p.Gly757fs)
HGVS:
  • NC_000001.11:g.150558037del
  • NG_012172.1:g.13616del
  • NM_001288607.2:c.2153del
  • NM_001288608.2:c.2339del
  • NM_001378596.1:c.2270del
  • NM_019032.5:c.2270del
  • NM_019032.6:c.2270delMANE SELECT
  • NM_025008.5:c.2270del
  • NP_001275536.1:p.Gly718fs
  • NP_001275537.1:p.Gly780fs
  • NP_001365525.1:p.Gly757fs
  • NP_061905.2:p.Gly757fs
  • NP_079284.2:p.Gly757fs
  • NC_000001.10:g.150530506del
  • NC_000001.10:g.150530513del
  • NM_019032.4:c.2270del
  • NM_019032.5:c.2270delG
  • NM_019032.6:c.2270del
Protein change:
G718fs
Links:
dbSNP: rs747160538
NCBI 1000 Genomes Browser:
rs747160538
Molecular consequence:
  • NM_001288607.2:c.2153del - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001288608.2:c.2339del - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001378596.1:c.2270del - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_019032.6:c.2270del - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_025008.5:c.2270del - frameshift variant - [Sequence Ontology: SO:0001589]

Condition(s)

Name:
Ectopia lentis 2, isolated, autosomal recessive (ECTOL2)
Synonyms:
Ectopia lentis, isolated autosomal recessive
Identifiers:
MONDO: MONDO:0009152; MedGen: C3541474; Orphanet: 1885; OMIM: 225100

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV004049597Genome-Nilou Lab
criteria provided, single submitter

(ACMG Guidelines, 2015)		Likely pathogenic
(Apr 11, 2023) 		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, SCV004049597.1

#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: Oct 8, 2024