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NM_000249.4(MLH1):c.1517T>C (p.Val506Ala) AND not specified

Germline classification:
Likely pathogenic (1 submission)
Last evaluated:
Jun 6, 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:
RCV000259153.19

Allele description [Variation Report for NM_000249.4(MLH1):c.1517T>C (p.Val506Ala)]

NM_000249.4(MLH1):c.1517T>C (p.Val506Ala)

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.1517T>C (p.Val506Ala)
Other names:
p.V506A:GTT>GCT
HGVS:
  • NC_000003.12:g.37028891T>C
  • NG_007109.2:g.40542T>C
  • NM_000249.4:c.1517T>CMANE SELECT
  • NM_001167617.3:c.1223T>C
  • NM_001167618.3:c.794T>C
  • NM_001167619.3:c.794T>C
  • NM_001258271.2:c.1517T>C
  • NM_001258273.2:c.794T>C
  • NM_001258274.3:c.794T>C
  • NM_001354615.2:c.794T>C
  • NM_001354616.2:c.794T>C
  • NM_001354617.2:c.794T>C
  • NM_001354618.2:c.794T>C
  • NM_001354619.2:c.794T>C
  • NM_001354620.2:c.1223T>C
  • NM_001354621.2:c.494T>C
  • NM_001354622.2:c.494T>C
  • NM_001354623.2:c.494T>C
  • NM_001354624.2:c.443T>C
  • NM_001354625.2:c.443T>C
  • NM_001354626.2:c.443T>C
  • NM_001354627.2:c.443T>C
  • NM_001354628.2:c.1517T>C
  • NM_001354629.2:c.1418T>C
  • NM_001354630.2:c.1517T>C
  • NP_000240.1:p.Val506Ala
  • NP_000240.1:p.Val506Ala
  • NP_001161089.1:p.Val408Ala
  • NP_001161090.1:p.Val265Ala
  • NP_001161091.1:p.Val265Ala
  • NP_001245200.1:p.Val506Ala
  • NP_001245202.1:p.Val265Ala
  • NP_001245203.1:p.Val265Ala
  • NP_001341544.1:p.Val265Ala
  • NP_001341545.1:p.Val265Ala
  • NP_001341546.1:p.Val265Ala
  • NP_001341547.1:p.Val265Ala
  • NP_001341548.1:p.Val265Ala
  • NP_001341549.1:p.Val408Ala
  • NP_001341550.1:p.Val165Ala
  • NP_001341551.1:p.Val165Ala
  • NP_001341552.1:p.Val165Ala
  • NP_001341553.1:p.Val148Ala
  • NP_001341554.1:p.Val148Ala
  • NP_001341555.1:p.Val148Ala
  • NP_001341556.1:p.Val148Ala
  • NP_001341557.1:p.Val506Ala
  • NP_001341558.1:p.Val473Ala
  • NP_001341559.1:p.Val506Ala
  • LRG_216t1:c.1517T>C
  • LRG_216:g.40542T>C
  • LRG_216p1:p.Val506Ala
  • NC_000003.11:g.37070382T>C
  • NM_000249.3:c.1517T>C
  • NM_001167617.1:c.1223T>C
  • P40692:p.Val506Ala
  • p.V506A
Protein change:
V148A
Links:
UniProtKB: P40692#VAR_004456; dbSNP: rs63749909
NCBI 1000 Genomes Browser:
rs63749909
Molecular consequence:
  • NM_000249.4:c.1517T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001167617.3:c.1223T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001167618.3:c.794T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001167619.3:c.794T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001258271.2:c.1517T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001258273.2:c.794T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001258274.3:c.794T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354615.2:c.794T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354616.2:c.794T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354617.2:c.794T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354618.2:c.794T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354619.2:c.794T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354620.2:c.1223T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354621.2:c.494T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354622.2:c.494T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354623.2:c.494T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354624.2:c.443T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354625.2:c.443T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354626.2:c.443T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354627.2:c.443T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354628.2:c.1517T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354629.2:c.1418T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354630.2:c.1517T>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:
AllHighlyPenetrant
Identifiers:
MedGen: CN169374

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000885704ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories
criteria provided, single submitter

(ARUP Molecular Germline Variant Investigation Process)		Likely pathogenic
(Jun 6, 2019) 		germlineclinical testing

Citation Link

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Summary from all submissions

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

Details of each submission

From ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories, SCV000885704.2

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

Description

The MLH1 c.1517T>C; p.Val506Ala variant has been described in individuals and families that met diagnostic criteria for Lynch syndrome (Chao 2008, Liu 1996, Syngal 1999), and segregates with disease in several unrelated families (internal data, personal communication with GeneDx and Invitae). In vitro functional analyses demonstrate reduced protein expression, but close to wild-type mismatch repair activity (Hinrichsen 2013, Takahashi 2007). Additionally, yeast two hybrid assays have demonstrated reduced functional outputs (Kondo 2003, Shimodaira 1998). This variant is reported in ClinVar (Variation ID: 89757), and is only observed on one allele in the Genome Aggregation Database, indicating it is not a common polymorphism. The valine at codon 506 is moderately conserved, and computational analyses (SIFT, PolyPhen-2) predict that this variant is deleterious. Based on available information, this variant is considered to be likely pathogenic. References: Chao EC et al. Accurate classification of MLH1/MSH2 missense variants with multivariate analysis of protein polymorphisms-mismatch repair (MAPP-MMR). Hum Mutat. 2008 Jun;29(6):852-60. Hinrichsen I et al. Expression defect size among unclassified MLH1 variants determines pathogenicity in Lynch syndrome diagnosis. Clin Cancer Res. 2013 May 1;19(9):2432-41. Kondo E et al. A yeast two-hybrid assay provides a simple way to evaluate the vast majority of hMLH1 germ-line mutations. Cancer Res. 2003 Jun 15;63(12):3302-8. Liu B et al. Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients. Nat Med. 1996 Feb;2(2):169-74. Shimodaira H et al. Functional analysis of human MLH1 mutations in Saccharomyces cerevisiae. Nat Genet. 1998 Aug;19(4):384-9. Syngal S et al. Interpretation of genetic test results for hereditary nonpolyposis colorectal cancer: implications for clinical predisposition testing. JAMA. 1999 Jul 21;282(3):247-53. Takahashi M et al. Functional analysis of human MLH1 variants using yeast and in vitro mismatch repair assays. Cancer Res. 2007 May 15;67(10):4595-604.

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

Last Updated: Jun 29, 2024