NM_000249.4(MLH1):c.636C>T (p.Thr212=) AND not provided

Germline classification:: Likely benign (3 submissions)
Last evaluated:: Aug 1, 2022
Review status:: 2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts

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:: RCV000233182.37

Allele description [Variation Report for NM_000249.4(MLH1):c.636C>T (p.Thr212=)]

NM_000249.4(MLH1):c.636C>T (p.Thr212=)

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.636C>T (p.Thr212=)

HGVS:

NC_000003.12:g.37012058C>T
NG_007109.2:g.23709C>T
NM_000249.4:c.636C>TMANE SELECT
NM_001167617.3:c.342C>T
NM_001167618.3:c.-88C>T
NM_001167619.3:c.-88C>T
NM_001258271.2:c.636C>T
NM_001258273.2:c.-88C>T
NM_001258274.3:c.-88C>T
NM_001354615.2:c.-88C>T
NM_001354616.2:c.-88C>T
NM_001354617.2:c.-88C>T
NM_001354618.2:c.-88C>T
NM_001354619.2:c.-88C>T
NM_001354620.2:c.342C>T
NM_001354621.2:c.-181C>T
NM_001354622.2:c.-294C>T
NM_001354623.2:c.-294C>T
NM_001354624.2:c.-191C>T
NM_001354625.2:c.-191C>T
NM_001354626.2:c.-191C>T
NM_001354627.2:c.-191C>T
NM_001354628.2:c.636C>T
NM_001354629.2:c.537C>T
NM_001354630.2:c.636C>T
NP_000240.1:p.Thr212=
NP_000240.1:p.Thr212=
NP_001161089.1:p.Thr114=
NP_001245200.1:p.Thr212=
NP_001341549.1:p.Thr114=
NP_001341557.1:p.Thr212=
NP_001341558.1:p.Thr179=
NP_001341559.1:p.Thr212=
LRG_216t1:c.636C>T
LRG_216:g.23709C>T
LRG_216p1:p.Thr212=
NC_000003.11:g.37053549C>T
NM_000249.3:c.636C>T
p.T212T

Links:

dbSNP: rs138735345

NCBI 1000 Genomes Browser:

rs138735345

Molecular consequence:

NM_001167618.3:c.-88C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001167619.3:c.-88C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001258273.2:c.-88C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001258274.3:c.-88C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001354615.2:c.-88C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001354616.2:c.-88C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001354617.2:c.-88C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001354618.2:c.-88C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001354619.2:c.-88C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001354621.2:c.-181C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001354622.2:c.-294C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001354623.2:c.-294C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001354624.2:c.-191C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001354625.2:c.-191C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001354626.2:c.-191C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001354627.2:c.-191C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_000249.4:c.636C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001167617.3:c.342C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001258271.2:c.636C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001354620.2:c.342C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001354628.2:c.636C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001354629.2:c.537C>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001354630.2:c.636C>T - synonymous variant - [Sequence Ontology: SO:0001819]

Observations:

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000518449	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Likely benign (Nov 30, 2020)	germline	clinical testing	Citation Link,
SCV001134319	Quest Diagnostics Nichols Institute San Juan Capistrano	criteria provided, single submitter (Quest Diagnostics criteria)	Likely benign (Jul 8, 2019)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]
SCV001248016	CeGaT Center for Human Genetics Tuebingen	criteria provided, single submitter (CeGaT Center For Human Genetics Tuebingen Variant Classification Criteria Version 2)	Likely benign (Aug 1, 2022)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000518449

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Likely benign
(Nov 30, 2020)

germline

clinical testing

Citation Link,

SCV001134319

Quest Diagnostics Nichols Institute San Juan Capistrano

criteria provided, single submitter

(Quest Diagnostics criteria)

Likely benign
(Jul 8, 2019)

germline

clinical testing

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

SCV001248016

CeGaT Center for Human Genetics Tuebingen

criteria provided, single submitter

(CeGaT Center For Human Genetics Tuebingen Variant Classification Criteria Version 2)

Likely benign
(Aug 1, 2022)

germline

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	yes	2	not provided	not provided	not provided	not provided	clinical testing
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

A Standardized DNA Variant Scoring System for Pathogenicity Assessments in Mendelian Disorders.

Karbassi I, Maston GA, Love A, DiVincenzo C, Braastad CD, Elzinga CD, Bright AR, Previte D, Zhang K, Rowland CM, McCarthy M, Lapierre JL, Dubois F, Medeiros KA, Batish SD, Jones J, Liaquat K, Hoffman CA, Jaremko M, Wang Z, Sun W, Buller-Burckle A, et al.

Hum Mutat. 2016 Jan;37(1):127-34. doi: 10.1002/humu.22918. Epub 2015 Oct 29.

PubMed [citation]

PMID:: 26467025
PMCID:: PMC4737317

Details of each submission

From GeneDx, SCV000518449.6

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

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

From Quest Diagnostics Nichols Institute San Juan Capistrano, SCV001134319.2

#	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

From CeGaT Center for Human Genetics Tuebingen, SCV001248016.26

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	2	not provided	not provided	clinical testing	not provided

Description

MLH1: BP4, BP7

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	yes	not provided	not provided	not provided		2	not provided	not provided	not provided

Last Updated: Oct 26, 2024

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