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NM_000249.4(MLH1):c.588+3A>T AND Hereditary cancer-predisposing syndrome

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
May 1, 2019
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:
RCV004018432.1

Allele description [Variation Report for NM_000249.4(MLH1):c.588+3A>T]

NM_000249.4(MLH1):c.588+3A>T

Gene:
MLH1:mutL homolog 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
3p22.2
Genomic location:
Preferred name:
NM_000249.4(MLH1):c.588+3A>T
HGVS:
  • NC_000003.12:g.37011865A>T
  • NG_007109.2:g.23516A>T
  • NM_000249.4:c.588+3A>TMANE SELECT
  • NM_001167617.3:c.294+3A>T
  • NM_001167618.3:c.-136+3A>T
  • NM_001167619.3:c.-136+3A>T
  • NM_001258271.2:c.588+3A>T
  • NM_001258273.2:c.-136+3A>T
  • NM_001258274.3:c.-136+3A>T
  • NM_001354615.2:c.-136+3A>T
  • NM_001354616.2:c.-136+3A>T
  • NM_001354617.2:c.-136+3A>T
  • NM_001354618.2:c.-136+3A>T
  • NM_001354619.2:c.-136+3A>T
  • NM_001354620.2:c.294+3A>T
  • NM_001354621.2:c.-229+3A>T
  • NM_001354622.2:c.-342+3A>T
  • NM_001354623.2:c.-342+3A>T
  • NM_001354624.2:c.-239+3A>T
  • NM_001354625.2:c.-239+3A>T
  • NM_001354626.2:c.-239+3A>T
  • NM_001354627.2:c.-239+3A>T
  • NM_001354628.2:c.588+3A>T
  • NM_001354629.2:c.489+3A>T
  • NM_001354630.2:c.588+3A>T
  • LRG_216t1:c.588+3A>T
  • LRG_216:g.23516A>T
  • NC_000003.11:g.37053356A>T
  • NM_000249.3:c.588+3A>T
Molecular consequence:
  • NM_000249.4:c.588+3A>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001167617.3:c.294+3A>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001167618.3:c.-136+3A>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001167619.3:c.-136+3A>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001258271.2:c.588+3A>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001258273.2:c.-136+3A>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001258274.3:c.-136+3A>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354615.2:c.-136+3A>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354616.2:c.-136+3A>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354617.2:c.-136+3A>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354618.2:c.-136+3A>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354619.2:c.-136+3A>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354620.2:c.294+3A>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354621.2:c.-229+3A>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354622.2:c.-342+3A>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354623.2:c.-342+3A>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354624.2:c.-239+3A>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354625.2:c.-239+3A>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354626.2:c.-239+3A>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354627.2:c.-239+3A>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354628.2:c.588+3A>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354629.2:c.489+3A>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354630.2:c.588+3A>T - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:
Hereditary cancer-predisposing syndrome
Synonyms:
Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV004849073Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(May 1, 2019) 		germlineclinical testing

Citation Link

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From Ambry Genetics, SCV004849073.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

The c.588+3A>T intronic alteration consists of a A to T substitution nucleotides after coding exon 7 in the MLH1 gene. Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: May 1, 2024