NM_000179.3(MSH6):c.3622dup (p.Ser1208fs) AND Lynch syndrome 5

Germline classification:: Pathogenic (1 submission)
Last evaluated:: Aug 24, 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:: RCV003451257.1

Allele description [Variation Report for NM_000179.3(MSH6):c.3622dup (p.Ser1208fs)]

NM_000179.3(MSH6):c.3622dup (p.Ser1208fs)

Gene:

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

Variant type:

Duplication

Cytogenetic location:

2p16.3

Genomic location:

Preferred name:

NM_000179.3(MSH6):c.3622dup (p.Ser1208fs)

HGVS:

NC_000002.12:g.47805683dup
NG_007111.1:g.27537dup
NG_008397.1:g.104994dup
NM_000179.3:c.3622dupMANE SELECT
NM_001281492.2:c.3232dup
NM_001281493.2:c.2716dup
NM_001281494.2:c.2716dup
NP_000170.1:p.Ser1208fs
NP_001268421.1:p.Ser1078fs
NP_001268422.1:p.Ser906fs
NP_001268423.1:p.Ser906fs
LRG_219:g.27537dup
NC_000002.11:g.48032820_48032821insT
NC_000002.11:g.48032822dup
NM_000179.2:c.3622dupT

Protein change:

S1078fs

Links:

dbSNP: rs1553332733

NCBI 1000 Genomes Browser:

rs1553332733

Molecular consequence:

NM_000179.3:c.3622dup - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001281492.2:c.3232dup - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001281493.2:c.2716dup - frameshift variant - [Sequence Ontology: SO:0001589]
NM_001281494.2:c.2716dup - frameshift variant - [Sequence Ontology: SO:0001589]

Condition(s)

Name:: Lynch syndrome 5 (LYNCH5)
Synonyms:: Colorectal cancer, hereditary nonpolyposis, type 5; Hereditary non-polyposis colorectal cancer, type 5
Identifiers:: MONDO: MONDO:0013710; MedGen: C1833477; Orphanet: 144; OMIM: 614350

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004185676	Myriad Genetics, Inc.	criteria provided, single submitter (Myriad Autosomal Dominant, Autosomal Recessive and X-Linked Classification Criteria (2023))	Pathogenic (Aug 24, 2023)	unknown	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004185676

Myriad Genetics, Inc.

criteria provided, single submitter

(Myriad Autosomal Dominant, Autosomal Recessive and X-Linked Classification Criteria (2023))

Pathogenic
(Aug 24, 2023)

unknown

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	unknown	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Myriad Genetics, Inc., SCV004185676.1

#	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 considered pathogenic. This variant creates a frameshift predicted to result in premature protein truncation.

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	unknown	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Oct 8, 2024

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