VCV002369067.2 - ClinVar

NM_001190737.2(NFIB):c.1026C>G (p.His342Gln)

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_001190737.2(NFIB):c.1026C>G (p.His342Gln)

Variation ID: 2369067 Accession: VCV002369067.2

Type and length

single nucleotide variant, 1 bp

Location

Cytogenetic: 9p23 9: 14125666 (GRCh38) [ NCBI UCSC ] 9: 14125665 (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	May 1, 2024	Dec 1, 2020

HGVS

Nucleotide	Protein	Molecular consequence
NM_001190737.2:c.1026C>G MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.	NP_001177666.1:p.His342Gln	missense
NM_001190738.2:c.1104C>G	NP_001177667.1:p.His368Gln	missense
NM_001282787.2:c.270C>G	NP_001269716.1:p.His90Gln	missense
NM_001369458.1:c.1092C>G	NP_001356387.1:p.His364Gln	missense
NM_001369459.1:c.1092C>G	NP_001356388.1:p.His364Gln	missense
NM_001369460.1:c.1014C>G	NP_001356389.1:p.His338Gln	missense
NM_001369461.1:c.1026C>G	NP_001356390.1:p.His342Gln	missense
NM_001369462.1:c.1092C>G	NP_001356391.1:p.His364Gln	missense
NM_001369463.1:c.1014C>G	NP_001356392.1:p.His338Gln	missense
NM_001369464.1:c.1026C>G	NP_001356393.1:p.His342Gln	missense
NM_001369465.1:c.999C>G	NP_001356394.1:p.His333Gln	missense
NM_001369466.1:c.1014C>G	NP_001356395.1:p.His338Gln	missense
NM_001369467.1:c.999C>G	NP_001356396.1:p.His333Gln	missense
NM_001369468.1:c.1092C>G	NP_001356397.1:p.His364Gln	missense
NM_001369469.1:c.882C>G	NP_001356398.1:p.His294Gln	missense
NM_001369470.1:c.789C>G	NP_001356399.1:p.His263Gln	missense
NM_001369471.1:c.1026C>G	NP_001356400.1:p.His342Gln	missense
NM_001369472.1:c.1014C>G	NP_001356401.1:p.His338Gln	missense
NM_001369473.1:c.1014C>G	NP_001356402.1:p.His338Gln	missense
NM_001369474.1:c.1011C>G	NP_001356403.1:p.His337Gln	missense
NM_001369475.1:c.801C>G	NP_001356404.1:p.His267Gln	missense
NM_001369476.1:c.999C>G	NP_001356405.1:p.His333Gln	missense
NM_001369477.1:c.972C>G	NP_001356406.1:p.His324Gln	missense
NM_001369478.1:c.789C>G	NP_001356407.1:p.His263Gln	missense
NM_001369479.1:c.489C>G	NP_001356408.1:p.His163Gln	missense
NM_001369480.1:c.489C>G	NP_001356409.1:p.His163Gln	missense
NM_005596.3:c.1026C>G	NP_005587.2:p.His342Gln	missense
NR_161382.1:n.560C>G		non-coding transcript variant
NR_161383.1:n.911C>G		non-coding transcript variant
NR_161384.1:n.558C>G		non-coding transcript variant
NR_161385.1:n.610C>G		non-coding transcript variant
NC_000009.12:g.14125666G>C
NC_000009.11:g.14125665G>C

... more HGVS ... less HGVS

Protein change

H338Q, H368Q, H324Q, H333Q, H90Q, H263Q, H267Q, H163Q, H294Q, H337Q, H342Q, H364Q

Other names

Canonical SPDI

NC_000009.12:14125665: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.
Inborn genetic diseases	Uncertain significance (1)	criteria provided, single submitter	Dec 1, 2020	RCV003000970.2

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 (Dec 01, 2020)	criteria provided, single submitter (Ambry Variant Classification Scheme 2023) Method: clinical testing	Inborn genetic diseases Affected status: unknown Allele origin: germline	Ambry Genetics Accession: SCV003707115.2 First in ClinVar: Feb 07, 2023 Last updated: May 01, 2024	Comment: The c.1026C>G (p.H342Q) alteration is located in coding exon 7 of the NFIB gene. This alteration results from a C to G substitution at nucleotide … (more) The c.1026C>G (p.H342Q) alteration is located in coding exon 7 of the NFIB gene. This alteration results from a C to G substitution at nucleotide position 1026, causing the histidine (H) at amino acid position 342 to be replaced by a glutamine (Q). Based on data from the Genome Aggregation Database (gnomAD) database, the NFIB c.1026C>G alteration was observed in 0.0008% (2/251254) of total alleles studied. The p.H342 amino acid is conserved in available higher vertebrate species. The p.H342Q alteration is predicted to be tolerated by in silico analysis. Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear. (less)

Comment:

The c.1026C>G (p.H342Q) alteration is located in coding exon 7 of the NFIB gene. This alteration results from a C to G substitution at nucleotide position 1026, causing the histidine (H) at amino acid position 342 to be replaced by a glutamine (Q). Based on data from the Genome Aggregation Database (gnomAD) database, the NFIB c.1026C>G alteration was observed in 0.0008% (2/251254) of total alleles studied. The p.H342 amino acid is conserved in available higher vertebrate species. The p.H342Q alteration is predicted to be tolerated by in silico analysis. Based on insufficient or conflicting evidence, 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_001190737.2(NFIB):c.1026C>G (p.His342Gln)

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for this variant ...