NM_000179.3(MSH6):c.3592G>T (p.Ala1198Ser) AND Hereditary cancer-predisposing syndrome

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jul 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:: RCV003360811.2

Allele description [Variation Report for NM_000179.3(MSH6):c.3592G>T (p.Ala1198Ser)]

NM_000179.3(MSH6):c.3592G>T (p.Ala1198Ser)

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.3592G>T (p.Ala1198Ser)

HGVS:

NC_000002.12:g.47805653G>T
NG_007111.1:g.27507G>T
NG_008397.1:g.105023C>A
NM_000179.3:c.3592G>TMANE SELECT
NM_001281492.2:c.3202G>T
NM_001281493.2:c.2686G>T
NM_001281494.2:c.2686G>T
NM_001406795.1:c.3688G>T
NM_001406796.1:c.3592G>T
NM_001406797.1:c.3295G>T
NM_001406798.1:c.3418G>T
NM_001406799.1:c.3067G>T
NM_001406800.1:c.3592G>T
NM_001406801.1:c.3295G>T
NM_001406802.1:c.3688G>T
NM_001406803.1:c.2728G>T
NM_001406804.1:c.3514G>T
NM_001406805.1:c.3295G>T
NM_001406806.1:c.3067G>T
NM_001406807.1:c.3067G>T
NM_001406808.1:c.3592G>T
NM_001406809.1:c.3592G>T
NM_001406811.1:c.2686G>T
NM_001406812.1:c.2686G>T
NM_001406813.1:c.3598G>T
NM_001406814.1:c.2686G>T
NM_001406815.1:c.2686G>T
NM_001406816.1:c.2686G>T
NM_001406817.1:c.2026G>T
NM_001406818.1:c.3295G>T
NM_001406819.1:c.3295G>T
NM_001406820.1:c.3295G>T
NM_001406821.1:c.3295G>T
NM_001406822.1:c.3295G>T
NM_001406823.1:c.2686G>T
NM_001406824.1:c.3295G>T
NM_001406825.1:c.3295G>T
NM_001406826.1:c.3424G>T
NM_001406827.1:c.3295G>T
NM_001406828.1:c.3295G>T
NM_001406829.1:c.2686G>T
NM_001406830.1:c.3295G>T
NM_001406831.1:c.373G>T
NM_001406832.1:c.439G>T
NM_001407362.1:c.1537G>T
NP_000170.1:p.Ala1198Ser
NP_000170.1:p.Ala1198Ser
NP_001268421.1:p.Ala1068Ser
NP_001268422.1:p.Ala896Ser
NP_001268423.1:p.Ala896Ser
NP_001393724.1:p.Ala1230Ser
NP_001393725.1:p.Ala1198Ser
NP_001393726.1:p.Ala1099Ser
NP_001393727.1:p.Ala1140Ser
NP_001393728.1:p.Ala1023Ser
NP_001393729.1:p.Ala1198Ser
NP_001393730.1:p.Ala1099Ser
NP_001393731.1:p.Ala1230Ser
NP_001393732.1:p.Ala910Ser
NP_001393733.1:p.Ala1172Ser
NP_001393734.1:p.Ala1099Ser
NP_001393735.1:p.Ala1023Ser
NP_001393736.1:p.Ala1023Ser
NP_001393737.1:p.Ala1198Ser
NP_001393738.1:p.Ala1198Ser
NP_001393740.1:p.Ala896Ser
NP_001393741.1:p.Ala896Ser
NP_001393742.1:p.Ala1200Ser
NP_001393743.1:p.Ala896Ser
NP_001393744.1:p.Ala896Ser
NP_001393745.1:p.Ala896Ser
NP_001393746.1:p.Ala676Ser
NP_001393747.1:p.Ala1099Ser
NP_001393748.1:p.Ala1099Ser
NP_001393749.1:p.Ala1099Ser
NP_001393750.1:p.Ala1099Ser
NP_001393751.1:p.Ala1099Ser
NP_001393752.1:p.Ala896Ser
NP_001393753.1:p.Ala1099Ser
NP_001393754.1:p.Ala1099Ser
NP_001393755.1:p.Ala1142Ser
NP_001393756.1:p.Ala1099Ser
NP_001393757.1:p.Ala1099Ser
NP_001393758.1:p.Ala896Ser
NP_001393759.1:p.Ala1099Ser
NP_001393760.1:p.Ala125Ser
NP_001393761.1:p.Ala147Ser
NP_001394291.1:p.Ala513Ser
LRG_219t1:c.3592G>T
LRG_219:g.27507G>T
LRG_219p1:p.Ala1198Ser
NC_000002.11:g.48032792G>T
NM_000179.2:c.3592G>T
NR_176256.1:n.2522G>T
NR_176257.1:n.3853G>T
NR_176258.1:n.3782G>T
NR_176259.1:n.3681G>T
NR_176260.1:n.1626G>T
NR_176261.1:n.3563G>T

Protein change:

A1023S

Molecular consequence:

NM_000179.3:c.3592G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001281492.2:c.3202G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001281493.2:c.2686G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001281494.2:c.2686G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406795.1:c.3688G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406796.1:c.3592G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406797.1:c.3295G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406798.1:c.3418G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406799.1:c.3067G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406800.1:c.3592G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406801.1:c.3295G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406802.1:c.3688G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406803.1:c.2728G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406804.1:c.3514G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406805.1:c.3295G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406806.1:c.3067G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406807.1:c.3067G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406808.1:c.3592G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406809.1:c.3592G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406811.1:c.2686G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406812.1:c.2686G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406813.1:c.3598G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406814.1:c.2686G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406815.1:c.2686G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406816.1:c.2686G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406817.1:c.2026G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406818.1:c.3295G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406819.1:c.3295G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406820.1:c.3295G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406821.1:c.3295G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406822.1:c.3295G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406823.1:c.2686G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406824.1:c.3295G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406825.1:c.3295G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406826.1:c.3424G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406827.1:c.3295G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406828.1:c.3295G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406829.1:c.2686G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406830.1:c.3295G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406831.1:c.373G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001406832.1:c.439G>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001407362.1:c.1537G>T - missense variant - [Sequence Ontology: SO:0001583]
NR_176256.1:n.2522G>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_176257.1:n.3853G>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_176258.1:n.3782G>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_176259.1:n.3681G>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_176261.1:n.3563G>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]

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
SCV004057495	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Jul 20, 2023)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004057495

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Jul 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, SCV004057495.2

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

Description

The p.A1198S variant (also known as c.3592G>T), located in coding exon 7 of the MSH6 gene, results from a G to T substitution at nucleotide position 3592. The alanine at codon 1198 is replaced by serine, an amino acid with similar properties. This amino acid position is conserved. In addition, this alteration is predicted to be tolerated by in silico analysis. 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: Jun 17, 2024

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