NM_001048174.2(MUTYH):c.606+21C>A AND not provided

This record was updated by the submitter. Please see the current version.

Germline classification:: Likely benign (2 submissions)
Last evaluated:: Feb 1, 2024
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:: RCV001538427.11

Allele description

NM_001048174.2(MUTYH):c.606+21C>A

Gene:

MUTYH:mutY DNA glycosylase [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1p34.1

Genomic location:

Preferred name:

NM_001048174.2(MUTYH):c.606+21C>A

HGVS:

NC_000001.11:g.45332553G>T
NG_008189.1:g.12918C>A
NM_001048171.2:c.606+21C>A
NM_001048172.2:c.609+21C>A
NM_001048173.2:c.606+21C>A
NM_001048174.2:c.606+21C>AMANE SELECT
NM_001128425.2:c.690+21C>A
NM_001293190.2:c.651+21C>A
NM_001293191.2:c.639+21C>A
NM_001293192.2:c.330+21C>A
NM_001293195.2:c.606+21C>A
NM_001293196.2:c.330+21C>A
NM_001350650.2:c.261+21C>A
NM_001350651.2:c.261+21C>A
NM_012222.3:c.681+21C>A
LRG_220t1:c.690+21C>A
LRG_220:g.12918C>A
NC_000001.10:g.45798225G>T
NM_001128425.1:c.690+21C>A

Links:

dbSNP: rs148552450

NCBI 1000 Genomes Browser:

rs148552450

Molecular consequence:

NM_001048171.2:c.606+21C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001048172.2:c.609+21C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001048173.2:c.606+21C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001048174.2:c.606+21C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001128425.2:c.690+21C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001293190.2:c.651+21C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001293191.2:c.639+21C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001293192.2:c.330+21C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001293195.2:c.606+21C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001293196.2:c.330+21C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001350650.2:c.261+21C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001350651.2:c.261+21C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_012222.3:c.681+21C>A - intron variant - [Sequence Ontology: SO:0001627]

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
SCV001756077	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Likely benign (Jun 21, 2018)	germline	clinical testing	Citation Link,
SCV003916456	CeGaT Center for Human Genetics Tuebingen	criteria provided, single submitter (CeGaT Center For Human Genetics Tuebingen Variant Classification Criteria Version 2)	Likely benign (Feb 1, 2024)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001756077

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Likely benign
(Jun 21, 2018)

germline

clinical testing

Citation Link,

SCV003916456

CeGaT Center for Human Genetics Tuebingen

criteria provided, single submitter

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

Likely benign
(Feb 1, 2024)

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	16	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From GeneDx, SCV001756077.1

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

Description

This variant is associated with the following publications: (PMID: 27829682)

#	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 CeGaT Center for Human Genetics Tuebingen, SCV003916456.7

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	16	not provided	not provided	clinical testing	not provided

Description

MUTYH: BS2

#	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		16	not provided	not provided	not provided

Last Updated: Apr 15, 2024

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