VCV002577600.1 - ClinVar

NM_001349999.2(RBFOX2):c.662A>G (p.Lys221Arg)

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_001349999.2(RBFOX2):c.662A>G (p.Lys221Arg)

Variation ID: 2577600 Accession: VCV002577600.1

Type and length

single nucleotide variant, 1 bp

Location

Cytogenetic: 22q12.3 22: 35778026 (GRCh38) [ NCBI UCSC ] 22: 36174073 (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	Sep 3, 2023	Sep 3, 2023	Jan 27, 2022

HGVS

Nucleotide	Protein	Molecular consequence
NM_001349999.2:c.662A>G MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.	NP_001336928.2:p.Lys221Arg	missense
NM_001031695.4:c.449A>G	NP_001026865.1:p.Lys150Arg	missense
NM_001082576.3:c.449A>G	NP_001076045.1:p.Lys150Arg	missense
NM_001082577.3:c.449A>G	NP_001076046.1:p.Lys150Arg	missense
NM_001082578.4:c.662A>G	NP_001076047.2:p.Lys221Arg	missense
NM_001082579.3:c.659A>G	NP_001076048.2:p.Lys220Arg	missense
NM_001349982.2:c.515A>G	NP_001336911.1:p.Lys172Arg	missense
NM_001349983.2:c.449A>G	NP_001336912.1:p.Lys150Arg	missense
NM_001349989.2:c.515A>G	NP_001336918.1:p.Lys172Arg	missense
NM_001349990.2:c.515A>G	NP_001336919.1:p.Lys172Arg	missense
NM_001349991.2:c.515A>G	NP_001336920.1:p.Lys172Arg	missense
NM_001349992.2:c.515A>G	NP_001336921.1:p.Lys172Arg	missense
NM_001349994.2:c.515A>G	NP_001336923.1:p.Lys172Arg	missense
NM_001349995.2:c.515A>G	NP_001336924.1:p.Lys172Arg	missense
NM_001349996.2:c.515A>G	NP_001336925.1:p.Lys172Arg	missense
NM_001349997.2:c.452A>G	NP_001336926.1:p.Lys151Arg	missense
NM_001349998.2:c.449A>G	NP_001336927.1:p.Lys150Arg	missense
NM_001394108.1:c.656A>G	NP_001381037.1:p.Lys219Arg	missense
NM_001394109.1:c.659A>G	NP_001381038.1:p.Lys220Arg	missense
NM_001394110.1:c.659A>G	NP_001381039.1:p.Lys220Arg	missense
NM_001394111.1:c.659A>G	NP_001381040.1:p.Lys220Arg	missense
NM_001394112.1:c.659A>G	NP_001381041.1:p.Lys220Arg	missense
NM_001394113.1:c.659A>G	NP_001381042.1:p.Lys220Arg	missense
NM_001394114.1:c.662A>G	NP_001381043.1:p.Lys221Arg	missense
NM_001394115.1:c.659A>G	NP_001381044.1:p.Lys220Arg	missense
NM_014309.4:c.452A>G	NP_055124.1:p.Lys151Arg	missense
NC_000022.11:g.35778026T>C
NC_000022.10:g.36174073T>C
NG_029628.1:g.255513A>G
NG_029628.2:g.255798A>G

... more HGVS ... less HGVS

Protein change

K150R, K151R, K172R, K219R, K220R, K221R

Other names

Canonical SPDI

NC_000022.11:35778025:T:C

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.
RBFOX2		-	-	GRCh38 GRCh38 GRCh37	73	95

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.
not provided	Uncertain significance (1)	criteria provided, single submitter	Jan 27, 2022	RCV003324937.1

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 (Jan 27, 2022)	criteria provided, single submitter (GeneDx Variant Classification Process June 2021) Method: clinical testing	Not Provided Affected status: yes Allele origin: germline	GeneDx Accession: SCV004030651.1 First in ClinVar: Sep 03, 2023 Last updated: Sep 03, 2023	Comment: Described as p.Lys150Arg using alternate nomenclature and identified as presumed de novo in published literature (Baker et al., 2019); however, clinical information was not provide … (more) Described as p.Lys150Arg using alternate nomenclature and identified as presumed de novo in published literature (Baker et al., 2019); however, clinical information was not provide on the proband; Described as p.K220R using alternate nomenclature and identified as de novo in proband with hypoplastic left heart syndrome in published literature (Edwards et al., 2020); Not observed at significant frequency in large population cohorts (gnomAD); In silico analysis supports that this missense variant has a deleterious effect on protein structure/function; Variants in candidate genes are classified as variants of uncertain significance in accordance with ACMG guidelines (Richards et al., 2015); This variant is associated with the following publications: (PMID: 30577886, 32368696) (less)

Comment:

Described as p.Lys150Arg using alternate nomenclature and identified as presumed de novo in published literature (Baker et al., 2019); however, clinical information was not provide on the proband; Described as p.K220R using alternate nomenclature and identified as de novo in proband with hypoplastic left heart syndrome in published literature (Edwards et al., 2020); Not observed at significant frequency in large population cohorts (gnomAD); In silico analysis supports that this missense variant has a deleterious effect on protein structure/function; Variants in candidate genes are classified as variants of uncertain significance in accordance with ACMG guidelines (Richards et al., 2015); This variant is associated with the following publications: (PMID: 30577886, 32368696)

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 03, 2023

ClinVar Genomic variation as it relates to human health

NM_001349999.2(RBFOX2):c.662A>G (p.Lys221Arg)

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for this variant ...