NM_001375978.1(CHRM3):c.1216G>A (p.Asp406Asn) AND not specified

Germline classification:: Likely benign (1 submission)
Last evaluated:: Jun 3, 2022
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:: RCV004239678.1

Allele description [Variation Report for NM_001375978.1(CHRM3):c.1216G>A (p.Asp406Asn)]

NM_001375978.1(CHRM3):c.1216G>A (p.Asp406Asn)

Gene:

CHRM3:cholinergic receptor muscarinic 3 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1q43

Genomic location:

Preferred name:

NM_001375978.1(CHRM3):c.1216G>A (p.Asp406Asn)

HGVS:

NC_000001.11:g.239908667G>A
NG_032046.2:g.526738G>A
NM_000740.4:c.1216G>A
NM_001347716.2:c.1216G>A
NM_001375978.1:c.1216G>AMANE SELECT
NM_001375979.1:c.1216G>A
NM_001375980.1:c.1216G>A
NM_001375981.1:c.1216G>A
NM_001375982.1:c.1216G>A
NM_001375983.1:c.1216G>A
NM_001375984.1:c.1216G>A
NM_001375985.1:c.1216G>A
NP_000731.1:p.Asp406Asn
NP_001334645.1:p.Asp406Asn
NP_001362907.1:p.Asp406Asn
NP_001362908.1:p.Asp406Asn
NP_001362909.1:p.Asp406Asn
NP_001362910.1:p.Asp406Asn
NP_001362911.1:p.Asp406Asn
NP_001362912.1:p.Asp406Asn
NP_001362913.1:p.Asp406Asn
NP_001362914.1:p.Asp406Asn
NC_000001.10:g.240071967G>A
NM_000740.2:c.1216G>A

Protein change:

D406N

Molecular consequence:

NM_000740.4:c.1216G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001347716.2:c.1216G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001375978.1:c.1216G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001375979.1:c.1216G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001375980.1:c.1216G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001375981.1:c.1216G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001375982.1:c.1216G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001375983.1:c.1216G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001375984.1:c.1216G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001375985.1:c.1216G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

Recent activity

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mitochondrial dicarboxylate carrier isoform 2 [Homo sapiens]
mitochondrial dicarboxylate carrier isoform 2 [Homo sapiens]
gi|20149598|ref|NP_036272.2|

Protein
Homo sapiens protein tyrosine phosphatase, non-receptor type 23, mRNA (cDNA clon...
Homo sapiens protein tyrosine phosphatase, non-receptor type 23, mRNA (cDNA clone IMAGE:4111514), partial cds
gi|39644963|gb|BC027711.2|

Nucleotide
Homo sapiens protein tyrosine phosphatase, non-receptor type 23, mRNA (cDNA clon...
Homo sapiens protein tyrosine phosphatase, non-receptor type 23, mRNA (cDNA clone IMAGE:3831058), partial cds
gi|39644458|gb|BC004881.2|

Nucleotide

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003754375	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Likely benign (Jun 3, 2022)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003754375

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Likely benign
(Jun 3, 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	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Ambry Genetics, SCV003754375.2

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

Description

This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

#	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: Oct 26, 2024

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