VCV002138530.2 - ClinVar

NM_001034853.2(RPGR):c.3007_3008del (p.Gly1003fs)

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.

Pathogenic

criteria provided, single submitter

Somatic

No data submitted for somatic clinical impact

Somatic

No data submitted for oncogenicity

Variant Details

Identifiers

NM_001034853.2(RPGR):c.3007_3008del (p.Gly1003fs)

Variation ID: 2138530 Accession: VCV002138530.2

Type and length

Deletion, 2 bp

Location

Cytogenetic: Xp11.4 X: 38285991-38285992 (GRCh38) [ NCBI UCSC ] X: 38145244-38145245 (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	Feb 8, 2023	Feb 14, 2024	Jun 2, 2022

HGVS

Nucleotide	Protein	Molecular consequence
NM_001034853.2:c.3007_3008del MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.	NP_001030025.1:p.Gly1003fs	frameshift
NM_000328.3:c.1905+1102_1905+1103del		intron variant
NM_001367245.1:c.1902+1102_1902+1103del		intron variant
NM_001367246.1:c.1719+1102_1719+1103del		intron variant
NM_001367247.1:c.1572+4967_1572+4968del		intron variant
NM_001367248.1:c.1602+4967_1602+4968del		intron variant
NM_001367249.1:c.1569+4967_1569+4968del		intron variant
NM_001367250.1:c.1569+4967_1569+4968del		intron variant
NM_001367251.1:c.1386+4967_1386+4968del		intron variant
NC_000023.11:g.38285991_38285992del
NC_000023.10:g.38145244_38145245del
NG_009553.1:g.46544_46545del

... more HGVS ... less HGVS

Protein change

G1003fs

Other names

Canonical SPDI

NC_000023.11:38285990:CC:

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.
RPGR		-	-	GRCh38 GRCh37	1512	1685

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.
Primary ciliary dyskinesia	Pathogenic (1)	criteria provided, single submitter	Jun 2, 2022	RCV003050603.4

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.
Pathogenic (Jun 02, 2022)	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015)) Method: clinical testing	Primary ciliary dyskinesia Affected status: unknown Allele origin: germline	Labcorp Genetics (formerly Invitae), Labcorp Accession: SCV003445070.2 First in ClinVar: Feb 07, 2023 Last updated: Feb 14, 2024	Publications: PubMed (2) PubMed: 22264887‚ 12657579 Comment: This variant disrupts a region of the RPGR (ORF15) protein in which other variant(s) (p.Leu1130Lysfs13) have been determined to be pathogenic (PMID: 22264887). This suggests … (more) This variant disrupts a region of the RPGR (ORF15) protein in which other variant(s) (p.Leu1130Lysfs13) have been determined to be pathogenic (PMID: 22264887). This suggests that this is a clinically significant region of the protein, and that variants that disrupt it are likely to be disease-causing. For these reasons, this variant has been classified as Pathogenic. This variant is also known as g.ORF15+1254_1255delGG. This premature translational stop signal has been observed in individual(s) with retinitis pigmentosa (PMID: 12657579). This variant is not present in population databases (gnomAD no frequency). This sequence change creates a premature translational stop signal (p.Gly1003Argfs*75) in the RPGR (ORF15) gene. While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 150 amino acid(s) of the RPGR (ORF15) protein. (less)

Comment:

This variant disrupts a region of the RPGR (ORF15) protein in which other variant(s) (p.Leu1130Lysfs*13) have been determined to be pathogenic (PMID: 22264887). This suggests that this is a clinically significant region of the protein, and that variants that disrupt it are likely to be disease-causing. For these reasons, this variant has been classified as Pathogenic. This variant is also known as g.ORF15+1254_1255delGG. This premature translational stop signal has been observed in individual(s) with retinitis pigmentosa (PMID: 12657579). This variant is not present in population databases (gnomAD no frequency). This sequence change creates a premature translational stop signal (p.Gly1003Argfs*75) in the RPGR (ORF15) gene. While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 150 amino acid(s) of the RPGR (ORF15) protein.

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

Title	Author	Journal	Year	Link
Clinical course, genetic etiology, and visual outcome in cone and cone-rod dystrophy.	Thiadens AA	Ophthalmology	2012	PMID: 22264887
X-linked retinitis pigmentosa: RPGR mutations in most families with definite X linkage and clustering of mutations in a short sequence stretch of exon ORF15.	Bader I	Investigative ophthalmology & visual science	2003	PMID: 12657579

Text-mined citations for this variant ...

Record last updated Nov 03, 2024

ClinVar Genomic variation as it relates to human health

NM_001034853.2(RPGR):c.3007_3008del (p.Gly1003fs)

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for this variant ...