VCV002269889.2 - ClinVar

NM_001750.7(CAST):c.1852C>T (p.Leu618Phe)

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_001750.7(CAST):c.1852C>T (p.Leu618Phe)

Variation ID: 2269889 Accession: VCV002269889.2

Type and length

single nucleotide variant, 1 bp

Location

Cytogenetic: 5q15 5: 96762292 (GRCh38) [ NCBI UCSC ] 5: 96097996 (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	Jan 4, 2022

HGVS

Nucleotide	Protein	Molecular consequence
NM_001750.7:c.1852C>T MANE Select Help Transcripts from the Matched Annotation from the NCBI and EMBL-EBI (MANE) collaboration.	NP_001741.4:p.Leu618Phe	missense
NM_001042440.5:c.1729C>T	NP_001035905.1:p.Leu577Phe	missense
NM_001042441.3:c.1795C>T	NP_001035906.1:p.Leu599Phe	missense
NM_001042442.3:c.1786C>T	NP_001035907.1:p.Leu596Phe	missense
NM_001042443.3:c.1603C>T	NP_001035908.1:p.Leu535Phe	missense
NM_001042444.3:c.1480C>T	NP_001035909.1:p.Leu494Phe	missense
NM_001042445.3:c.1498C>T	NP_001035910.1:p.Leu500Phe	missense
NM_001042446.3:c.1441C>T	NP_001035911.1:p.Leu481Phe	missense
NM_001190442.2:c.1564C>T	NP_001177371.1:p.Leu522Phe	missense
NM_001284212.4:c.1480C>T	NP_001271141.1:p.Leu494Phe	missense
NM_001284213.4:c.1387C>T	NP_001271142.1:p.Leu463Phe	missense
NM_001330626.2:c.1756C>T	NP_001317555.1:p.Leu586Phe	missense
NM_001330627.2:c.1729C>T	NP_001317556.1:p.Leu577Phe	missense
NM_001330628.2:c.1684C>T	NP_001317557.1:p.Leu562Phe	missense
NM_001330629.2:c.1768C>T	NP_001317558.1:p.Leu590Phe	missense
NM_001330630.2:c.1441C>T	NP_001317559.1:p.Leu481Phe	missense
NM_001330631.2:c.1564C>T	NP_001317560.1:p.Leu522Phe	missense
NM_001330632.2:c.1537C>T	NP_001317561.1:p.Leu513Phe	missense
NM_001330633.2:c.1546C>T	NP_001317562.1:p.Leu516Phe	missense
NM_001330634.2:c.1507C>T	NP_001317563.1:p.Leu503Phe	missense
NM_001349244.2:c.*908G>A		3 prime UTR
NM_001375317.1:c.1741C>T	NP_001362246.1:p.Leu581Phe	missense
NM_001423250.1:c.1603C>T	NP_001410179.1:p.Leu535Phe	missense
NM_001423251.1:c.1564C>T	NP_001410180.1:p.Leu522Phe	missense
NM_001423252.1:c.1564C>T	NP_001410181.1:p.Leu522Phe	missense
NM_001423253.1:c.1537C>T	NP_001410182.1:p.Leu513Phe	missense
NM_001423254.1:c.1537C>T	NP_001410183.1:p.Leu513Phe	missense
NM_001423255.1:c.1498C>T	NP_001410184.1:p.Leu500Phe	missense
NM_001423256.1:c.1498C>T	NP_001410185.1:p.Leu500Phe	missense
NM_001423257.1:c.1498C>T	NP_001410186.1:p.Leu500Phe	missense
NM_001423258.1:c.1498C>T	NP_001410187.1:p.Leu500Phe	missense
NM_001423259.1:c.1498C>T	NP_001410188.1:p.Leu500Phe	missense
NM_001423260.1:c.1441C>T	NP_001410189.1:p.Leu481Phe	missense
NM_016442.5:c.*908G>A		3 prime UTR
NM_173060.5:c.1537C>T	NP_775083.1:p.Leu513Phe	missense
NR_104285.2:n.797C>T		non-coding transcript variant
NC_000005.10:g.96762292C>T
NC_000005.9:g.96097996C>T
NG_027839.2:g.178692G>A
NG_029490.2:g.105256C>T

... more HGVS ... less HGVS

Protein change

L463F, L481F, L513F, L535F, L500F, L503F, L522F, L590F, L596F, L618F, L562F, L581F, L599F, L494F, L516F, L577F, L586F

Other names

Canonical SPDI

NC_000005.10:96762291:C:T

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.
CAST		-	-	GRCh38 GRCh37	146	641
ERAP1		-	-	GRCh38 GRCh37	111	268

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	Jan 4, 2022	RCV002804360.9

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 04, 2022)	criteria provided, single submitter (Ambry Variant Classification Scheme 2023) Method: clinical testing	Inborn genetic diseases Affected status: unknown Allele origin: germline	Ambry Genetics Accession: SCV003605554.2 First in ClinVar: Feb 07, 2023 Last updated: May 01, 2024	Comment: The c.1729C>T (p.L577F) alteration is located in exon 23 (coding exon 23) of the CAST gene. This alteration results from a C to T substitution … (more) The c.1729C>T (p.L577F) alteration is located in exon 23 (coding exon 23) of the CAST gene. This alteration results from a C to T substitution at nucleotide position 1729, causing the leucine (L) at amino acid position 577 to be replaced by a phenylalanine (F). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear. (less)

Comment:

The c.1729C>T (p.L577F) alteration is located in exon 23 (coding exon 23) of the CAST gene. This alteration results from a C to T substitution at nucleotide position 1729, causing the leucine (L) at amino acid position 577 to be replaced by a phenylalanine (F). 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 Nov 03, 2024

ClinVar Genomic variation as it relates to human health

NM_001750.7(CAST):c.1852C>T (p.Leu618Phe)

Variant Details

Genes

Conditions - Germline

Submissions - Germline

Germline Functional Evidence

Citations for germline classification of this variant

Text-mined citations for this variant ...