VCV003376240.1 - ClinVar

NM_001190737.2(NFIB):c.870C>G (p.Tyr290Ter)

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_001190737.2(NFIB):c.870C>G (p.Tyr290Ter)

Variation ID: 3376240 Accession: VCV003376240.1

Type and length

single nucleotide variant, 1 bp

Location

Cytogenetic: 9p23 9: 14146744 (GRCh38) [ NCBI UCSC ] 9: 14146743 (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 19, 2024	Nov 17, 2024	Oct 4, 2021

HGVS

Nucleotide	Protein	Molecular consequence
NM_001190737.2:c.870C>G MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.	NP_001177666.1:p.Tyr290Ter	nonsense
NM_001190738.2:c.948C>G	NP_001177667.1:p.Tyr316Ter	nonsense
NM_001282787.2:c.114C>G	NP_001269716.1:p.Tyr38Ter	nonsense
NM_001369458.1:c.936C>G	NP_001356387.1:p.Tyr312Ter	nonsense
NM_001369459.1:c.936C>G	NP_001356388.1:p.Tyr312Ter	nonsense
NM_001369460.1:c.858C>G	NP_001356389.1:p.Tyr286Ter	nonsense
NM_001369461.1:c.870C>G	NP_001356390.1:p.Tyr290Ter	nonsense
NM_001369462.1:c.936C>G	NP_001356391.1:p.Tyr312Ter	nonsense
NM_001369463.1:c.858C>G	NP_001356392.1:p.Tyr286Ter	nonsense
NM_001369464.1:c.870C>G	NP_001356393.1:p.Tyr290Ter	nonsense
NM_001369465.1:c.843C>G	NP_001356394.1:p.Tyr281Ter	nonsense
NM_001369466.1:c.858C>G	NP_001356395.1:p.Tyr286Ter	nonsense
NM_001369467.1:c.843C>G	NP_001356396.1:p.Tyr281Ter	nonsense
NM_001369468.1:c.936C>G	NP_001356397.1:p.Tyr312Ter	nonsense
NM_001369469.1:c.726C>G	NP_001356398.1:p.Tyr242Ter	nonsense
NM_001369470.1:c.633C>G	NP_001356399.1:p.Tyr211Ter	nonsense
NM_001369471.1:c.870C>G	NP_001356400.1:p.Tyr290Ter	nonsense
NM_001369472.1:c.858C>G	NP_001356401.1:p.Tyr286Ter	nonsense
NM_001369473.1:c.858C>G	NP_001356402.1:p.Tyr286Ter	nonsense
NM_001369474.1:c.855C>G	NP_001356403.1:p.Tyr285Ter	nonsense
NM_001369475.1:c.645C>G	NP_001356404.1:p.Tyr215Ter	nonsense
NM_001369476.1:c.843C>G	NP_001356405.1:p.Tyr281Ter	nonsense
NM_001369477.1:c.816C>G	NP_001356406.1:p.Tyr272Ter	nonsense
NM_001369478.1:c.633C>G	NP_001356407.1:p.Tyr211Ter	nonsense
NM_001369479.1:c.333C>G	NP_001356408.1:p.Tyr111Ter	nonsense
NM_001369480.1:c.333C>G	NP_001356409.1:p.Tyr111Ter	nonsense
NM_001429577.1:c.870C>G	NP_001416506.1:p.Tyr290Ter	nonsense
NM_005596.3:c.870C>G	NP_005587.2:p.Tyr290Ter	nonsense
NR_161382.1:n.404C>G		non-coding transcript variant
NR_161383.1:n.755C>G		non-coding transcript variant
NR_161384.1:n.402C>G		non-coding transcript variant
NR_161385.1:n.454C>G		non-coding transcript variant
NC_000009.12:g.14146744G>C
NC_000009.11:g.14146743G>C

... more HGVS ... less HGVS

Protein change

Y111*, Y211*, Y215*, Y242*, Y272*, Y281*, Y285*, Y286*, Y290*, Y312*, Y316*, Y38*

Other names

Canonical SPDI

NC_000009.12:14146743:G: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.
NFIB		-	-	GRCh38 GRCh37	132	259

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.
Macrocephaly, acquired, with impaired intellectual development	Pathogenic (1)	criteria provided, single submitter	Oct 4, 2021	RCV004784976.1

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.
Pathogenic (Oct 04, 2021)	criteria provided, single submitter (ACMG Guidelines, 2015) Method: clinical testing	Macrocephaly, acquired, with impaired intellectual development (Autosomal dominant inheritance) Affected status: yes Allele origin: germline	Pittsburgh Clinical Genomics Laboratory, University of Pittsburgh Medical Center Accession: SCV005397276.1 First in ClinVar: Nov 17, 2024 Last updated: Nov 17, 2024	Comment: This sequence variant is a single nucleotide substitution (C>G) which changes codon 290 of NFIB into an early termition codon. This variant is predicted to … (more) This sequence variant is a single nucleotide substitution (C>G) which changes codon 290 of NFIB into an early termition codon. This variant is predicted to generate a non-functiol allele through either the expression of a truncated protein or a loss of NFIB expression due to nonsense-mediated decay. This is novel variant which has not been reported in clinical genetics databases or observed in the medical literature in individuals with NFIB-related disease, to our knowledge. This variant is absent from the gnomAD control population dataset (0/~246000 alleles). Loss of function variants in NFIB are known to be pathogenic. Based on the available evidence, we consider this variant to be pathogenic. ACMG Criteria: PM2, PM6, PP3, PVS1 (less)

Comment:

This sequence variant is a single nucleotide substitution (C>G) which changes codon 290 of NFIB into an early termition codon. This variant is predicted to generate a non-functiol allele through either the expression of a truncated protein or a loss of NFIB expression due to nonsense-mediated decay. This is novel variant which has not been reported in clinical genetics databases or observed in the medical literature in individuals with NFIB-related disease, to our knowledge. This variant is absent from the gnomAD control population dataset (0/~246000 alleles). Loss of function variants in NFIB are known to be pathogenic. Based on the available evidence, we consider this variant to be pathogenic. ACMG Criteria: PM2, PM6, PP3, PVS1

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 Nov 19, 2024

ClinVar Genomic variation as it relates to human health

NM_001190737.2(NFIB):c.870C>G (p.Tyr290Ter)

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for this variant ...