U.S. flag

An official website of the United States government

NM_000249.4(MLH1):c.17G>T (p.Gly6Val) AND Hereditary cancer-predisposing syndrome

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Nov 29, 2020
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:
RCV002407891.2

Allele description [Variation Report for NM_000249.4(MLH1):c.17G>T (p.Gly6Val)]

NM_000249.4(MLH1):c.17G>T (p.Gly6Val)

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.17G>T (p.Gly6Val)
HGVS:
  • NC_000003.12:g.36993564G>T
  • NG_007109.2:g.5215G>T
  • NG_008418.1:g.4741C>A
  • NM_000249.4:c.17G>TMANE SELECT
  • NM_001167617.3:c.-500G>T
  • NM_001167618.3:c.-929G>T
  • NM_001167619.3:c.-842G>T
  • NM_001258271.2:c.17G>T
  • NM_001258273.2:c.-616G>T
  • NM_001258274.3:c.-1079G>T
  • NM_001354615.2:c.-610G>T
  • NM_001354616.2:c.-610G>T
  • NM_001354617.2:c.-702G>T
  • NM_001354618.2:c.-934G>T
  • NM_001354619.2:c.-1058G>T
  • NM_001354620.2:c.-268G>T
  • NM_001354621.2:c.-1027G>T
  • NM_001354622.2:c.-1140G>T
  • NM_001354623.2:c.-1049G>T
  • NM_001354624.2:c.-810G>T
  • NM_001354625.2:c.-708G>T
  • NM_001354626.2:c.-805G>T
  • NM_001354627.2:c.-1037G>T
  • NM_001354628.2:c.17G>T
  • NM_001354629.2:c.17G>T
  • NM_001354630.2:c.17G>T
  • NP_000240.1:p.Gly6Val
  • NP_000240.1:p.Gly6Val
  • NP_001245200.1:p.Gly6Val
  • NP_001341557.1:p.Gly6Val
  • NP_001341558.1:p.Gly6Val
  • NP_001341559.1:p.Gly6Val
  • LRG_216t1:c.17G>T
  • LRG_216:g.5215G>T
  • LRG_216p1:p.Gly6Val
  • NC_000003.11:g.37035055G>T
  • NM_000249.3:c.17G>T
Protein change:
G6V
Molecular consequence:
  • NM_001167617.3:c.-500G>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001167618.3:c.-929G>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001167619.3:c.-842G>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001258273.2:c.-616G>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001258274.3:c.-1079G>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001354615.2:c.-610G>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001354616.2:c.-610G>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001354617.2:c.-702G>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001354618.2:c.-934G>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001354619.2:c.-1058G>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001354620.2:c.-268G>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001354621.2:c.-1027G>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001354622.2:c.-1140G>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001354623.2:c.-1049G>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001354624.2:c.-810G>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001354625.2:c.-708G>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001354626.2:c.-805G>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001354627.2:c.-1037G>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_000249.4:c.17G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001258271.2:c.17G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354628.2:c.17G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354629.2:c.17G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354630.2:c.17G>T - missense variant - [Sequence Ontology: SO:0001583]

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

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
SCV002710753Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Nov 29, 2020) 		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, SCV002710753.2

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

Description

The p.G6V variant (also known as c.17G>T), located in coding exon 1 of the MLH1 gene, results from a G to T substitution at nucleotide position 17. The glycine at codon 6 is replaced by valine, an amino acid with dissimilar properties. This amino acid position is highly conserved in available vertebrate species. In addition, this alteration is predicted to be deleterious by in silico analysis. Since supporting evidence is limited at this time, 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