NM_000179.3(MSH6):c.41C>G (p.Ser14Cys) AND Hereditary cancer-predisposing syndrome

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jun 14, 2021
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:: RCV002327852.2

Allele description [Variation Report for NM_000179.3(MSH6):c.41C>G (p.Ser14Cys)]

NM_000179.3(MSH6):c.41C>G (p.Ser14Cys)

Gene:

MSH6:mutS homolog 6 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

2p16.3

Genomic location:

Preferred name:

NM_000179.3(MSH6):c.41C>G (p.Ser14Cys)

HGVS:

NC_000002.12:g.47783274C>G
NG_007111.1:g.5128C>G
NM_000179.3:c.41C>GMANE SELECT
NM_001281492.2:c.41C>G
NM_001281493.2:c.-696C>G
NM_001406795.1:c.41C>G
NM_001406796.1:c.41C>G
NM_001406798.1:c.41C>G
NM_001406799.1:c.-288C>G
NM_001406800.1:c.41C>G
NM_001406802.1:c.41C>G
NM_001406803.1:c.41C>G
NM_001406804.1:c.-15C>G
NM_001406807.1:c.-888C>G
NM_001406808.1:c.41C>G
NM_001406809.1:c.41C>G
NM_001406811.1:c.-696C>G
NM_001406812.1:c.-543C>G
NM_001406813.1:c.41C>G
NM_001406814.1:c.-954C>G
NM_001406816.1:c.-499C>G
NM_001406817.1:c.41C>G
NM_001407362.1:c.41C>G
NP_000170.1:p.Ser14Cys
NP_000170.1:p.Ser14Cys
NP_001268421.1:p.Ser14Cys
NP_001393724.1:p.Ser14Cys
NP_001393725.1:p.Ser14Cys
NP_001393727.1:p.Ser14Cys
NP_001393729.1:p.Ser14Cys
NP_001393731.1:p.Ser14Cys
NP_001393732.1:p.Ser14Cys
NP_001393737.1:p.Ser14Cys
NP_001393738.1:p.Ser14Cys
NP_001393742.1:p.Ser14Cys
NP_001393746.1:p.Ser14Cys
NP_001394291.1:p.Ser14Cys
LRG_219t1:c.41C>G
LRG_219:g.5128C>G
LRG_219p1:p.Ser14Cys
NC_000002.11:g.48010413C>G
NM_000179.2:c.41C>G
NR_176256.1:n.130C>G
NR_176257.1:n.130C>G
NR_176258.1:n.130C>G
NR_176259.1:n.130C>G
NR_176260.1:n.130C>G
NR_176261.1:n.130C>G

Protein change:

S14C

Molecular consequence:

NM_001281493.2:c.-696C>G - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_000179.3:c.41C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001281492.2:c.41C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001406795.1:c.41C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001406796.1:c.41C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001406798.1:c.41C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001406800.1:c.41C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001406802.1:c.41C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001406803.1:c.41C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001406808.1:c.41C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001406809.1:c.41C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001406813.1:c.41C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001406817.1:c.41C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001407362.1:c.41C>G - missense variant - [Sequence Ontology: SO:0001583]

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

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002627290	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Jun 14, 2021)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002627290

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Jun 14, 2021)

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, SCV002627290.2

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

Description

The p.S14C variant (also known as c.41C>G), located in coding exon 1 of the MSH6 gene, results from a C to G substitution at nucleotide position 41. The serine at codon 14 is replaced by cysteine, an amino acid with dissimilar properties. This amino acid position is well conserved in available vertebrate species. In addition, the in silico prediction for this alteration is inconclusive. Since supporting evidence is limited at this time, 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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