NM_001613.4(ACTA2):c.1109C>G (p.Ser370Cys) AND not provided

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Aug 25, 2021
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:: RCV002223993.3

Allele description [Variation Report for NM_001613.4(ACTA2):c.1109C>G (p.Ser370Cys)]

NM_001613.4(ACTA2):c.1109C>G (p.Ser370Cys)

Genes:

ACTA2-AS1:ACTA2 antisense RNA 1 [Gene - HGNC]
ACTA2:actin alpha 2, smooth muscle [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

10q23.31

Genomic location:

Preferred name:

NM_001613.4(ACTA2):c.1109C>G (p.Ser370Cys)

HGVS:

NC_000010.11:g.88935248G>C
NG_011541.1:g.61143C>G
NM_001141945.3:c.1109C>G
NM_001320855.2:c.1109C>G
NM_001406462.1:c.1109C>G
NM_001406463.1:c.1109C>G
NM_001406464.1:c.1109C>G
NM_001406466.1:c.998C>G
NM_001406467.1:c.980C>G
NM_001406468.1:c.980C>G
NM_001406469.1:c.980C>G
NM_001406471.1:c.917C>G
NM_001613.4:c.1109C>GMANE SELECT
NP_001135417.1:p.Ser370Cys
NP_001135417.1:p.Ser370Cys
NP_001135417.1:p.Ser370Cys
NP_001307784.1:p.Ser370Cys
NP_001307784.1:p.Ser370Cys
NP_001393391.1:p.Ser370Cys
NP_001393392.1:p.Ser370Cys
NP_001393393.1:p.Ser370Cys
NP_001393395.1:p.Ser333Cys
NP_001393396.1:p.Ser327Cys
NP_001393397.1:p.Ser327Cys
NP_001393398.1:p.Ser327Cys
NP_001393400.1:p.Ser306Cys
NP_001604.1:p.Ser370Cys
NP_001604.1:p.Ser370Cys
LRG_781t1:c.1109C>G
LRG_781t2:c.1109C>G
LRG_781:g.61143C>G
LRG_781p1:p.Ser370Cys
LRG_781p2:p.Ser370Cys
NC_000010.10:g.90695005G>C
NC_000010.10:g.90695005G>C
NM_001141945.1:c.1109C>G
NM_001141945.2:c.1109C>G
NM_001320855.1:c.1109C>G
NM_001613.2:c.1109C>G
NM_001613.2:c.1109C>G
NM_001613.3:c.1109C>G
NR_125373.1:n.873G>C

Protein change:

S306C

Links:

dbSNP: rs749867078

NCBI 1000 Genomes Browser:

rs749867078

Molecular consequence:

NM_001141945.3:c.1109C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001320855.2:c.1109C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001406462.1:c.1109C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001406463.1:c.1109C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001406464.1:c.1109C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001406466.1:c.998C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001406467.1:c.980C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001406468.1:c.980C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001406469.1:c.980C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001406471.1:c.917C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001613.4:c.1109C>G - missense variant - [Sequence Ontology: SO:0001583]
NR_125373.1:n.873G>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Observations:

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002501941	AiLife Diagnostics, AiLife Diagnostics	criteria provided, single submitter (ACMG Guidelines, 2015)	Uncertain significance (Aug 25, 2021)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002501941

AiLife Diagnostics, AiLife Diagnostics

criteria provided, single submitter

(ACMG Guidelines, 2015)

Uncertain significance
(Aug 25, 2021)

germline

clinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	yes	1	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]

PMID:: 25741868
PMCID:: PMC4544753

Details of each submission

From AiLife Diagnostics, AiLife Diagnostics, SCV002501941.1

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

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

Last Updated: May 1, 2024

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