VCV001791550.2 - ClinVar

NM_130839.5(UBE3A):c.2516C>T (p.Thr839Ile)

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_130839.5(UBE3A):c.2516C>T (p.Thr839Ile)

Variation ID: 1791550 Accession: VCV001791550.2

Type and length

single nucleotide variant, 1 bp

Location

Cytogenetic: 15q11.2 15: 25339240 (GRCh38) [ NCBI UCSC ] 15: 25584387 (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	Nov 15, 2017

HGVS

Nucleotide	Protein	Molecular consequence
NM_130839.5:c.2516C>T MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.	NP_570854.1:p.Thr839Ile	missense
NM_000462.5:c.2525C>T	NP_000453.2:p.Thr842Ile	missense
NM_001354505.1:c.2516C>T	NP_001341434.1:p.Thr839Ile	missense
NM_001354506.2:c.2456C>T	NP_001341435.1:p.Thr819Ile	missense
NM_001354507.2:c.2456C>T	NP_001341436.1:p.Thr819Ile	missense
NM_001354508.2:c.2456C>T	NP_001341437.1:p.Thr819Ile	missense
NM_001354509.2:c.2456C>T	NP_001341438.1:p.Thr819Ile	missense
NM_001354511.2:c.2456C>T	NP_001341440.1:p.Thr819Ile	missense
NM_001354512.2:c.2456C>T	NP_001341441.1:p.Thr819Ile	missense
NM_001354513.2:c.2456C>T	NP_001341442.1:p.Thr819Ile	missense
NM_001354523.2:c.2456C>T	NP_001341452.1:p.Thr819Ile	missense
NM_001354526.1:c.2456C>T	NP_001341455.1:p.Thr819Ile	missense
NM_001354538.2:c.2516C>T	NP_001341467.1:p.Thr839Ile	missense
NM_001354539.2:c.2456C>T	NP_001341468.1:p.Thr819Ile	missense
NM_001354540.2:c.2456C>T	NP_001341469.1:p.Thr819Ile	missense
NM_001354541.2:c.2456C>T	NP_001341470.1:p.Thr819Ile	missense
NM_001354542.2:c.2456C>T	NP_001341471.1:p.Thr819Ile	missense
NM_001354543.2:c.2456C>T	NP_001341472.1:p.Thr819Ile	missense
NM_001354544.2:c.2456C>T	NP_001341473.1:p.Thr819Ile	missense
NM_001354545.2:c.2360C>T	NP_001341474.1:p.Thr787Ile	missense
NM_001354546.2:c.2339C>T	NP_001341475.1:p.Thr780Ile	missense
NM_001354547.2:c.2300C>T	NP_001341476.1:p.Thr767Ile	missense
NM_001354548.2:c.2300C>T	NP_001341477.1:p.Thr767Ile	missense
NM_001354549.2:c.2291C>T	NP_001341478.1:p.Thr764Ile	missense
NM_001354550.2:c.1265C>T	NP_001341479.1:p.Thr422Ile	missense
NM_001354551.2:c.1205C>T	NP_001341480.1:p.Thr402Ile	missense
NM_001374461.1:c.2456C>T	NP_001361390.1:p.Thr819Ile	missense
NM_130838.4:c.2456C>T	NP_570853.1:p.Thr819Ile	missense
NR_148916.2:n.3028C>T		non-coding transcript variant
NC_000015.10:g.25339240G>A
NC_000015.9:g.25584387G>A
NG_009268.1:g.104742C>T
LRG_15:g.104742C>T
LRG_15t1:c.2456C>T	LRG_15p1:p.Thr819Ile

... more HGVS ... less HGVS

Protein change

T764I, T780I, T819I, T402I, T422I, T767I, T787I, T839I, T842I

Other names

Canonical SPDI

NC_000015.10:25339239: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.
UBE3A		Sufficient evidence for dosage pathogenicity	No evidence available	GRCh38 GRCh37	40	1234
SNHG14		-	-	GRCh38	4	1133

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.
Inborn genetic diseases	Uncertain significance (1)	criteria provided, single submitter	Nov 15, 2017	RCV002455455.2

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 (Nov 15, 2017)	criteria provided, single submitter (Ambry Variant Classification Scheme 2023) Method: clinical testing	Inborn genetic diseases Affected status: unknown Allele origin: germline	Ambry Genetics Accession: SCV002736851.2 First in ClinVar: Nov 29, 2022 Last updated: May 01, 2024	Comment: The p.T819I variant (also known as c.2456C>T), located in coding exon 10 of the UBE3A gene, results from a C to T substitution at nucleotide … (more) The p.T819I variant (also known as c.2456C>T), located in coding exon 10 of the UBE3A gene, results from a C to T substitution at nucleotide position 2456. The threonine at codon 819 is replaced by isoleucine, an amino acid with similar properties. This amino acid position is highly conserved in available vertebrate species. 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.T819I variant (also known as c.2456C>T), located in coding exon 10 of the UBE3A gene, results from a C to T substitution at nucleotide position 2456. The threonine at codon 819 is replaced by isoleucine, an amino acid with similar properties. This amino acid position is highly conserved in available vertebrate species. 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_130839.5(UBE3A):c.2516C>T (p.Thr839Ile)

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for this variant ...