NM_000179.3(MSH6):c.3798_3801+9del AND Lynch syndrome 5

Germline classification:: Likely pathogenic (1 submission)
Last evaluated:: Aug 25, 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:: RCV003451305.1

Allele description [Variation Report for NM_000179.3(MSH6):c.3798_3801+9del]

NM_000179.3(MSH6):c.3798_3801+9del

Gene:

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

Variant type:

Deletion

Cytogenetic location:

2p16.3

Genomic location:

Preferred name:

NM_000179.3(MSH6):c.3798_3801+9del

HGVS:

NC_000002.12:g.47806355_47806367del
NG_007111.1:g.28209_28221del
NG_008397.1:g.104311_104323del
NM_000179.2:c.3798_3801+9del13
NM_000179.3:c.3798_3801+9delMANE SELECT
NM_001281492.2:c.3408_3411+9del
NM_001281493.2:c.2892_2895+9del
NM_001281494.2:c.2892_2895+9del
LRG_219t1:c.3798_3801+9del
LRG_219:g.28209_28221del
NC_000002.11:g.48033492_48033504del
NC_000002.11:g.48033494_48033506del
NM_000179.2:c.3798_3801+9del
NM_000179.2:c.3798_3801+9del13
NM_000179.2:c.3798_3801+9delTATGGTATGTGCA

Links:

dbSNP: rs1553333168

NCBI 1000 Genomes Browser:

rs1553333168

Molecular consequence:

NM_000179.3:c.3798_3801+9del - splice donor variant - [Sequence Ontology: SO:0001575]
NM_001281492.2:c.3408_3411+9del - splice donor variant - [Sequence Ontology: SO:0001575]
NM_001281493.2:c.2892_2895+9del - splice donor variant - [Sequence Ontology: SO:0001575]
NM_001281494.2:c.2892_2895+9del - splice donor variant - [Sequence Ontology: SO:0001575]

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
SCV004185541	Myriad Genetics, Inc.	criteria provided, single submitter (Myriad Autosomal Dominant, Autosomal Recessive and X-Linked Classification Criteria (2023))	Likely pathogenic (Aug 25, 2023)	unknown	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004185541

Myriad Genetics, Inc.

criteria provided, single submitter

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

Likely pathogenic
(Aug 25, 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., SCV004185541.1

#	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 likely pathogenic. This variant occurs within a consensus splice junction and is predicted to result in abnormal mRNA splicing of either an out-of-frame exon or an in-frame exon necessary for protein stability and/or normal function.

#	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 26, 2024

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