NM_001204286.1(MUC1):c.407C>A (p.Ala136Asp) AND Inborn genetic diseases

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Mar 20, 2023
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:: RCV003290136.2

Allele description [Variation Report for NM_001204286.1(MUC1):c.407C>A (p.Ala136Asp)]

NM_001204286.1(MUC1):c.407C>A (p.Ala136Asp)

Gene:

MUC1:mucin 1, cell surface associated [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1q22

Genomic location:

Preferred name:

NM_001204286.1(MUC1):c.407C>A (p.Ala136Asp)

HGVS:

NC_000001.11:g.155191962G>T
NM_001018016.3:c.186+221C>A
NM_001018017.3:c.159+221C>A
NM_001044390.3:c.159+221C>A
NM_001044391.3:c.159+221C>A
NM_001044392.3:c.186+221C>A
NM_001044393.3:c.159+221C>A
NM_001204285.2:c.380C>A
NM_001204286.1:c.407C>A
NM_001204287.2:c.186+221C>A
NM_001204288.2:c.186+221C>A
NM_001204289.2:c.186+221C>A
NM_001204290.2:c.123+221C>A
NM_001204291.1:c.186+221C>A
NM_001204292.1:c.186+221C>A
NM_001204293.2:c.159+221C>A
NM_001204294.2:c.159+221C>A
NM_001204295.1:c.186+221C>A
NM_001204296.2:c.186+221C>A
NM_001204297.2:c.186+221C>A
NM_001371720.2:c.407C>A
NM_002456.6:c.159+221C>A
NP_001191214.1:p.Ala127Asp
NP_001191215.1:p.Ala136Asp
NP_001358649.1:p.Ala136Asp
NP_001358649.2:p.Ala136Asp
NC_000001.10:g.155161753G>T
NM_001371720.1:c.407C>A

Protein change:

A127D

Molecular consequence:

NM_001018016.3:c.186+221C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001018017.3:c.159+221C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001044390.3:c.159+221C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001044391.3:c.159+221C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001044392.3:c.186+221C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001044393.3:c.159+221C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001204287.2:c.186+221C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001204288.2:c.186+221C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001204289.2:c.186+221C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001204290.2:c.123+221C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001204291.1:c.186+221C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001204292.1:c.186+221C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001204293.2:c.159+221C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001204294.2:c.159+221C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001204295.1:c.186+221C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001204296.2:c.186+221C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001204297.2:c.186+221C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_002456.6:c.159+221C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001204285.2:c.380C>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001204286.1:c.407C>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001371720.2:c.407C>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Inborn genetic diseases
Identifiers:: MeSH: D030342; MedGen: C0950123

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003960649	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Mar 20, 2023)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003960649

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Mar 20, 2023)

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, SCV003960649.2

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

Description

The c.407C>A (p.A136D) alteration is located in exon 2 (coding exon 2) of the MUC1 gene. This alteration results from a C to A substitution at nucleotide position 407, causing the alanine (A) at amino acid position 136 to be replaced by an aspartic acid (D). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

#	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: May 1, 2024

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