VCV000920597.9 - ClinVar

NM_000249.4(MLH1):c.654_655inv (p.Ile219Val)

Germline

Classification

The aggregate germline classification for this variant, typically for a monogenic or Mendelian disorder as in the ACMG/AMP guidelines, or for response to a drug. This value is calculated by NCBI based on data from submitters. Read our rules for calculating the aggregate classification.

(3)

Stars represent the aggregate review status, or the level of review supporting the aggregate germline classification for this VCV record. This value is calculated by NCBI based on data from submitters. Read our rules for calculating the review status. The number of submissions which contribute to this review status is shown in parentheses.

Likely benign

criteria provided, multiple submitters, no conflicts

Somatic

No data submitted for somatic clinical impact

Somatic

No data submitted for oncogenicity

Variant Details

Identifiers

NM_000249.4(MLH1):c.654_655inv (p.Ile219Val)

Variation ID: 920597 Accession: VCV000920597.9

Type and length

Inversion, 2 bp

Location

Cytogenetic: 3p22.2 3: 37012076-37012077 (GRCh38) [ NCBI UCSC ] 3: 37053567-37053568 (GRCh37) [ NCBI UCSC ]

Timeline in ClinVar

	First in ClinVar Help The date this variant first appeared in ClinVar with each type of classification.	Last submission Help The date of the most recent submission for each type of classification for this variant.	Last evaluated Help The most recent date that a submitter evaluated this variant for each type of classification.
Germline	Jun 22, 2020	May 1, 2024	Dec 10, 2023

HGVS

Nucleotide	Protein	Molecular consequence
NM_000249.4:c.654_655delinsTG MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.
NM_000249.4:c.654_655inv MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.	NP_000240.1:p.Ile219Val	missense
NM_000249.3:c.654_655delCAinsTG
NM_001167617.3:c.360_361inv	NP_001161089.1:p.Ile121Val	missense
NM_001167618.3:c.-70_-69inv		5 prime UTR
NM_001167619.3:c.-70_-69inv		5 prime UTR
NM_001258271.2:c.654_655inv	NP_001245200.1:p.Ile219Val	missense
NM_001258273.2:c.-70_-69inv		5 prime UTR
NM_001258274.3:c.-70_-69inv		5 prime UTR
NM_001354615.2:c.-70_-69inv		5 prime UTR
NM_001354616.2:c.-70_-69inv		5 prime UTR
NM_001354617.2:c.-70_-69inv		5 prime UTR
NM_001354618.2:c.-70_-69inv		5 prime UTR
NM_001354619.2:c.-70_-69inv		5 prime UTR
NM_001354620.2:c.360_361inv	NP_001341549.1:p.Ile121Val	missense
NM_001354621.2:c.-163_-162inv		5 prime UTR
NM_001354622.2:c.-276_-275inv		5 prime UTR
NM_001354623.2:c.-276_-275inv		5 prime UTR
NM_001354624.2:c.-173_-172inv		5 prime UTR
NM_001354625.2:c.-173_-172inv		5 prime UTR
NM_001354626.2:c.-173_-172inv		5 prime UTR
NM_001354627.2:c.-173_-172inv		5 prime UTR
NM_001354628.2:c.654_655inv	NP_001341557.1:p.Ile219Val	missense
NM_001354629.2:c.555_556inv	NP_001341558.1:p.Ile186Val	missense
NM_001354630.2:c.654_655inv	NP_001341559.1:p.Ile219Val	missense
NC_000003.12:g.37012076_37012077inv
NC_000003.11:g.37053567_37053568inv
NG_007109.2:g.23727_23728inv
LRG_216:g.23727_23728inv
LRG_216t1:c.654_655delinsTG

... more HGVS ... less HGVS

Protein change

I121V, I186V, I219V

Other names

Canonical SPDI

NC_000003.12:37012075:CA:TG

Functional consequence Help The effect of the variant on RNA or protein function, based on experimental evidence from submitters.

Global minor allele frequency (GMAF) Help The global minor allele frequency calculated by the 1000 Genomes Project. The minor allele at this location is indicated in parentheses and may be different from the allele represented by this VCV record.

Allele frequency Help The frequency of the allele represented by this VCV record.

Links

VarSome

Genes

Gene	OMIM	ClinGen Gene Dosage Sensitivity Curation		Variation Viewer Help Links to Variation Viewer, a genome browser to view variation data from NCBI databases.	Related variants
Gene	OMIM	HI score Help The haploinsufficiency score for the gene, curated by ClinGen’s Dosage Sensitivity Curation task team.	TS score Help The triplosensitivity score for the gene, curated by ClinGen’s Dosage Sensitivity Curation task team.		Within gene Help The number of variants in ClinVar that are contained within this gene, with a link to view the list of variants.	All Help The number of variants in ClinVar for this gene, including smaller variants within the gene and larger CNVs that overlap or fully contain the gene.
MLH1		Sufficient evidence for dosage pathogenicity	No evidence available	GRCh38 GRCh37	5693	5754

Conditions - Germline

Condition Help The condition for this variant-condition (RCV) record in ClinVar.	Classification Help The aggregate germline classification for this variant-condition (RCV) record in ClinVar. The number of submissions that contribute to this aggregate classification is shown in parentheses. (# of submissions)	Review status Help The aggregate review status for this variant-condition (RCV) record in ClinVar. This value is calculated by NCBI based on data from submitters. Read our rules for calculating the review status.	Last evaluated Help The most recent date that a submitter evaluated this variant for the condition.	Variation/condition record Help The RCV accession number, with most recent version number, for the variant-condition record, with a link to the RCV web page.
Hereditary cancer-predisposing syndrome	Likely benign (2)	criteria provided, multiple submitters, no conflicts	Jun 16, 2022	RCV001179447.5
Hereditary nonpolyposis colorectal neoplasms	Likely benign (1)	criteria provided, single submitter	Dec 10, 2023	RCV001448370.6

Submissions - Germline

Classification Help The submitted germline classification for each SCV record. (Last evaluated)	Review status Help Stars represent the review status, or the level of review supporting the submitted (SCV) record. This value is calculated by NCBI based on data from the submitter. Read our rules for calculating the review status. This column also includes a link to the submitter’s assertion criteria if provided, and the collection method. (Assertion criteria)	Condition Help The condition for the classification, provided by the submitter for this submitted (SCV) record. This column also includes the affected status and allele origin of individuals observed with this variant.	Submitter Help The submitting organization for this submitted (SCV) record. This column also includes the SCV accession and version number, the date this SCV first appeared in ClinVar, and the date that this SCV was last updated in ClinVar.	More information Help This column includes more information supporting the classification, including citations, the comment on classification, and detailed evidence provided as observations of the variant by the submitter.
Likely benign (Dec 10, 2023)	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015)) Method: clinical testing	Hereditary nonpolyposis colorectal neoplasms Affected status: unknown Allele origin: germline	Labcorp Genetics (formerly Invitae), Labcorp Accession: SCV001651460.3 First in ClinVar: May 23, 2021 Last updated: Feb 14, 2024
Likely benign (Jan 03, 2022)	criteria provided, single submitter (ACMG Guidelines, 2015) Method: clinical testing	Hereditary cancer-predisposing syndrome Affected status: unknown Allele origin: germline	Color Diagnostics, LLC DBA Color Health Accession: SCV001344108.2 First in ClinVar: Jun 22, 2020 Last updated: Feb 14, 2024
Likely benign (Jun 16, 2022)	criteria provided, single submitter (Ambry Variant Classification Scheme 2023) Method: clinical testing	Hereditary cancer-predisposing syndrome Affected status: unknown Allele origin: germline	Ambry Genetics Accession: SCV002661259.2 First in ClinVar: Nov 29, 2022 Last updated: May 01, 2024	Comment: This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of … (more) This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity. (less)

Comment:

This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

Germline Functional Evidence

There is no functional evidence in ClinVar for this variation. If you have generated functional data for this variation, please consider submitting that data to ClinVar.

Comment:

Citations for germline classification of this variant

There are no citations for germline classification of this variant in ClinVar. If you know of citations for this variation, please consider submitting that information to ClinVar.

Text-mined citations for this variant ...

Record last updated Sep 29, 2024

ClinVar Genomic variation as it relates to human health

NM_000249.4(MLH1):c.654_655inv (p.Ile219Val)

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for this variant ...