NM_000249.4(MLH1):c.589-7T>C AND Hereditary cancer-predisposing syndrome

Germline classification:: Likely benign (1 submission)
Last evaluated:: Jun 6, 2016
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:: RCV000579995.10

Allele description [Variation Report for NM_000249.4(MLH1):c.589-7T>C]

NM_000249.4(MLH1):c.589-7T>C

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.589-7T>C

HGVS:

NC_000003.12:g.37012004T>C
NG_007109.2:g.23655T>C
NM_000249.4:c.589-7T>CMANE SELECT
NM_001167617.3:c.295-7T>C
NM_001167618.3:c.-135-7T>C
NM_001167619.3:c.-135-7T>C
NM_001258271.2:c.589-7T>C
NM_001258273.2:c.-135-7T>C
NM_001258274.3:c.-135-7T>C
NM_001354615.2:c.-135-7T>C
NM_001354616.2:c.-135-7T>C
NM_001354617.2:c.-135-7T>C
NM_001354618.2:c.-135-7T>C
NM_001354619.2:c.-135-7T>C
NM_001354620.2:c.295-7T>C
NM_001354621.2:c.-228-7T>C
NM_001354622.2:c.-341-7T>C
NM_001354623.2:c.-341-7T>C
NM_001354624.2:c.-238-7T>C
NM_001354625.2:c.-238-7T>C
NM_001354626.2:c.-238-7T>C
NM_001354627.2:c.-238-7T>C
NM_001354628.2:c.589-7T>C
NM_001354629.2:c.490-7T>C
NM_001354630.2:c.589-7T>C
LRG_216t1:c.589-7T>C
LRG_216:g.23655T>C
NC_000003.11:g.37053495T>C
NM_000249.3:c.589-7T>C

Links:

dbSNP: rs371767464

NCBI 1000 Genomes Browser:

rs371767464

Molecular consequence:

NM_000249.4:c.589-7T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001167617.3:c.295-7T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001167618.3:c.-135-7T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001167619.3:c.-135-7T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001258271.2:c.589-7T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001258273.2:c.-135-7T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001258274.3:c.-135-7T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001354615.2:c.-135-7T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001354616.2:c.-135-7T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001354617.2:c.-135-7T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001354618.2:c.-135-7T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001354619.2:c.-135-7T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001354620.2:c.295-7T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001354621.2:c.-228-7T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001354622.2:c.-341-7T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001354623.2:c.-341-7T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001354624.2:c.-238-7T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001354625.2:c.-238-7T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001354626.2:c.-238-7T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001354627.2:c.-238-7T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001354628.2:c.589-7T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001354629.2:c.490-7T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_001354630.2:c.589-7T>C - 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

Recent activity

Clear Turn Off Turn On

endothelin-converting enzyme 1 isoform 1 [Homo sapiens]
endothelin-converting enzyme 1 isoform 1 [Homo sapiens]
gi|4503443|ref|NP_001388.1|

Protein

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Help

Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000684847	Color Diagnostics, LLC DBA Color Health	criteria provided, single submitter (ACMG Guidelines, 2015)	Likely benign (Jun 6, 2016)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000684847

Color Diagnostics, LLC DBA Color Health

criteria provided, single submitter

(ACMG Guidelines, 2015)

Likely benign
(Jun 6, 2016)

germline

clinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical 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 Color Diagnostics, LLC DBA Color Health, SCV000684847.2

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (1)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Nov 3, 2024

ClinVar

Relating variation to medicine