VCV001793338.2 - ClinVar

NM_000535.7(PMS2):c.2579C>T (p.Ser860Phe)

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.

(1)

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.

Uncertain significance

criteria provided, single submitter

Somatic

No data submitted for somatic clinical impact

Somatic

No data submitted for oncogenicity

Variant Details

Identifiers

NM_000535.7(PMS2):c.2579C>T (p.Ser860Phe)

Variation ID: 1793338 Accession: VCV001793338.2

Type and length

single nucleotide variant, 1 bp

Location

Cytogenetic: 7p22.1 7: 5973409 (GRCh38) [ NCBI UCSC ] 7: 6013040 (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	Nov 29, 2022	May 1, 2024	Oct 12, 2022

HGVS

Nucleotide	Protein	Molecular consequence
NM_000535.7:c.2579C>T MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.	NP_000526.2:p.Ser860Phe	missense
NM_001018040.1:c.2174C>T	NP_001018050.1:p.Ser725Phe	missense
NM_001322003.2:c.2174C>T	NP_001308932.1:p.Ser725Phe	missense
NM_001322004.2:c.2174C>T	NP_001308933.1:p.Ser725Phe	missense
NM_001322005.2:c.2174C>T	NP_001308934.1:p.Ser725Phe	missense
NM_001322006.2:c.2423C>T	NP_001308935.1:p.Ser808Phe	missense
NM_001322007.2:c.2261C>T	NP_001308936.1:p.Ser754Phe	missense
NM_001322008.2:c.2261C>T	NP_001308937.1:p.Ser754Phe	missense
NM_001322009.2:c.2207C>T	NP_001308938.1:p.Ser736Phe	missense
NM_001322010.2:c.2018C>T	NP_001308939.1:p.Ser673Phe	missense
NM_001322011.2:c.1646C>T	NP_001308940.1:p.Ser549Phe	missense
NM_001322012.2:c.1646C>T	NP_001308941.1:p.Ser549Phe	missense
NM_001322013.2:c.2006C>T	NP_001308942.1:p.Ser669Phe	missense
NM_001322014.2:c.2612C>T	NP_001308943.1:p.Ser871Phe	missense
NM_001322015.2:c.2270C>T	NP_001308944.1:p.Ser757Phe	missense
NM_001406866.1:c.2765C>T	NP_001393795.1:p.Ser922Phe	missense
NM_001406868.1:c.2603C>T	NP_001393797.1:p.Ser868Phe	missense
NM_001406869.1:c.2471C>T	NP_001393798.1:p.Ser824Phe	missense
NM_001406870.1:c.2456C>T	NP_001393799.1:p.Ser819Phe	missense
NM_001406871.1:c.2435C>T	NP_001393800.1:p.Ser812Phe	missense
NM_001406872.1:c.2411C>T	NP_001393801.1:p.Ser804Phe	missense
NM_001406873.1:c.2381C>T	NP_001393802.1:p.Ser794Phe	missense
NM_001406874.1:c.2411C>T	NP_001393803.1:p.Ser804Phe	missense
NM_001406875.1:c.2303C>T	NP_001393804.1:p.Ser768Phe	missense
NM_001406876.1:c.2294C>T	NP_001393805.1:p.Ser765Phe	missense
NM_001406877.1:c.2270C>T	NP_001393806.1:p.Ser757Phe	missense
NM_001406878.1:c.2270C>T	NP_001393807.1:p.Ser757Phe	missense
NM_001406879.1:c.2270C>T	NP_001393808.1:p.Ser757Phe	missense
NM_001406880.1:c.2270C>T	NP_001393809.1:p.Ser757Phe	missense
NM_001406881.1:c.2270C>T	NP_001393810.1:p.Ser757Phe	missense
NM_001406882.1:c.2270C>T	NP_001393811.1:p.Ser757Phe	missense
NM_001406883.1:c.2261C>T	NP_001393812.1:p.Ser754Phe	missense
NM_001406884.1:c.2255C>T	NP_001393813.1:p.Ser752Phe	missense
NM_001406885.1:c.2243C>T	NP_001393814.1:p.Ser748Phe	missense
NM_001406886.1:c.2213C>T	NP_001393815.1:p.Ser738Phe	missense
NM_001406887.1:c.2207C>T	NP_001393816.1:p.Ser736Phe	missense
NM_001406888.1:c.2207C>T	NP_001393817.1:p.Ser736Phe	missense
NM_001406889.1:c.2174C>T	NP_001393818.1:p.Ser725Phe	missense
NM_001406890.1:c.2174C>T	NP_001393819.1:p.Ser725Phe	missense
NM_001406891.1:c.2174C>T	NP_001393820.1:p.Ser725Phe	missense
NM_001406892.1:c.2174C>T	NP_001393821.1:p.Ser725Phe	missense
NM_001406893.1:c.2174C>T	NP_001393822.1:p.Ser725Phe	missense
NM_001406894.1:c.2174C>T	NP_001393823.1:p.Ser725Phe	missense
NM_001406895.1:c.2174C>T	NP_001393824.1:p.Ser725Phe	missense
NM_001406896.1:c.2174C>T	NP_001393825.1:p.Ser725Phe	missense
NM_001406897.1:c.2174C>T	NP_001393826.1:p.Ser725Phe	missense
NM_001406898.1:c.2174C>T	NP_001393827.1:p.Ser725Phe	missense
NM_001406899.1:c.2174C>T	NP_001393828.1:p.Ser725Phe	missense
NM_001406900.1:c.2114C>T	NP_001393829.1:p.Ser705Phe	missense
NM_001406901.1:c.2105C>T	NP_001393830.1:p.Ser702Phe	missense
NM_001406902.1:c.2105C>T	NP_001393831.1:p.Ser702Phe	missense
NM_001406903.1:c.2093C>T	NP_001393832.1:p.Ser698Phe	missense
NM_001406904.1:c.2066C>T	NP_001393833.1:p.Ser689Phe	missense
NM_001406905.1:c.2066C>T	NP_001393834.1:p.Ser689Phe	missense
NM_001406906.1:c.2018C>T	NP_001393835.1:p.Ser673Phe	missense
NM_001406907.1:c.2018C>T	NP_001393836.1:p.Ser673Phe	missense
NM_001406908.1:c.2006C>T	NP_001393837.1:p.Ser669Phe	missense
NM_001406909.1:c.2006C>T	NP_001393838.1:p.Ser669Phe	missense
NM_001406910.1:c.1862C>T	NP_001393839.1:p.Ser621Phe	missense
NM_001406911.1:c.1808C>T	NP_001393840.1:p.Ser603Phe	missense
NM_001406912.1:c.1376C>T	NP_001393841.1:p.Ser459Phe	missense
NR_003085.2:n.2661C>T
NR_136154.1:n.2623C>T		non-coding transcript variant
NC_000007.14:g.5973409G>A
NC_000007.13:g.6013040G>A
NG_008466.1:g.40698C>T
LRG_161:g.40698C>T
LRG_161t1:c.2579C>T	LRG_161p1:p.Ser860Phe

... more HGVS ... less HGVS

Protein change

S669F, S725F, S736F, S748F, S754F, S768F, S794F, S812F, S824F, S871F, S868F, S459F, S603F, S673F, S689F, S698F, S738F, S752F, S804F, S819F, S922F, S549F, S621F, S702F, S705F, S757F, S765F, S808F, S860F

Other names

Canonical SPDI

NC_000007.14:5973408:G:A

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.
PMS2		Sufficient evidence for dosage pathogenicity	No evidence available	GRCh38 GRCh37	5252	5354

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	Uncertain significance (1)	criteria provided, single submitter	Oct 12, 2022	RCV002452819.2

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.
Uncertain significance (Oct 12, 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: SCV002738950.2 First in ClinVar: Nov 29, 2022 Last updated: May 01, 2024	Comment: The p.S860F variant (also known as c.2579C>T), located in coding exon 15 of the PMS2 gene, results from a C to T substitution at nucleotide … (more) The p.S860F variant (also known as c.2579C>T), located in coding exon 15 of the PMS2 gene, results from a C to T substitution at nucleotide position 2579. The serine at codon 860 is replaced by phenylalanine, an amino acid with highly dissimilar properties. This amino acid position is conserved. In addition, this alteration is predicted to be deleterious by in silico analysis. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear. (less)

Comment:

The p.S860F variant (also known as c.2579C>T), located in coding exon 15 of the PMS2 gene, results from a C to T substitution at nucleotide position 2579. The serine at codon 860 is replaced by phenylalanine, an amino acid with highly dissimilar properties. This amino acid position is conserved. In addition, this alteration is predicted to be deleterious by in silico analysis. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

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 May 01, 2024

ClinVar Genomic variation as it relates to human health

NM_000535.7(PMS2):c.2579C>T (p.Ser860Phe)

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for this variant ...