NM_001127222.2(CACNA1A):c.5051T>C (p.Phe1684Ser) AND Inborn genetic diseases

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jun 19, 2024
Review status:: 1 star out of maximum of 4 stars
criteria provided, single submitter

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV004605052.1

Allele description [Variation Report for NM_001127222.2(CACNA1A):c.5051T>C (p.Phe1684Ser)]

NM_001127222.2(CACNA1A):c.5051T>C (p.Phe1684Ser)

Gene:

CACNA1A:calcium voltage-gated channel subunit alpha1 A [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

19p13.13

Genomic location:

Preferred name:

NM_001127222.2(CACNA1A):c.5051T>C (p.Phe1684Ser)

HGVS:

NC_000019.10:g.13235630A>G
NG_011569.1:g.275831T>C
NM_000068.4:c.5069T>C
NM_001127221.2:c.5054T>C
NM_001127222.2:c.5051T>CMANE SELECT
NM_001174080.2:c.5060T>C
NM_023035.3:c.5069T>C
NP_000059.3:p.Phe1690Ser
NP_001120693.1:p.Phe1685Ser
NP_001120693.1:p.Phe1685Ser
NP_001120694.1:p.Phe1684Ser
NP_001167551.1:p.Phe1687Ser
NP_075461.2:p.Phe1690Ser
LRG_7t1:c.5054T>C
LRG_7:g.275831T>C
LRG_7p1:p.Phe1685Ser
NC_000019.9:g.13346444A>G
NM_001127221.1:c.5054T>C

Protein change:

F1684S

Molecular consequence:

NM_000068.4:c.5069T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001127221.2:c.5054T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001127222.2:c.5051T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001174080.2:c.5060T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_023035.3:c.5069T>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Inborn genetic diseases
Identifiers:: MeSH: D030342; MedGen: C0950123

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV005099570	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Jun 19, 2024)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV005099570

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Jun 19, 2024)

germline

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Ambry Genetics, SCV005099570.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

Description

The c.5054T>C (p.F1685S) alteration is located in exon 32 (coding exon 32) of the CACNA1A gene. This alteration results from a T to C substitution at nucleotide position 5054, causing the phenylalanine (F) at amino acid position 1685 to be replaced by a serine (S). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Sep 29, 2024

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Relating variation to medicine