NM_000020.3(ACVRL1):c.158T>C (p.Val53Ala) AND not provided

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jul 25, 2022
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:: RCV003481304.1

Allele description [Variation Report for NM_000020.3(ACVRL1):c.158T>C (p.Val53Ala)]

NM_000020.3(ACVRL1):c.158T>C (p.Val53Ala)

Gene:

ACVRL1:activin A receptor like type 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

12q13.13

Genomic location:

Preferred name:

NM_000020.3(ACVRL1):c.158T>C (p.Val53Ala)

Other names:

p.Val53Ala

HGVS:

NC_000012.12:g.51913195T>C
NG_009549.1:g.10778T>C
NM_000020.3:c.158T>CMANE SELECT
NM_001077401.2:c.158T>C
NM_001406487.1:c.158T>C
NM_001406488.1:c.158T>C
NM_001406489.1:c.158T>C
NM_001406490.1:c.158T>C
NM_001406491.1:c.158T>C
NM_001406492.1:c.158T>C
NM_001406493.1:c.158T>C
NM_001406494.1:c.158T>C
NP_000011.2:p.Val53Ala
NP_000011.2:p.Val53Ala
NP_001070869.1:p.Val53Ala
NP_001393416.1:p.Val53Ala
NP_001393417.1:p.Val53Ala
NP_001393418.1:p.Val53Ala
NP_001393419.1:p.Val53Ala
NP_001393420.1:p.Val53Ala
NP_001393421.1:p.Val53Ala
NP_001393422.1:p.Val53Ala
NP_001393423.1:p.Val53Ala
LRG_543t1:c.158T>C
LRG_543:g.10778T>C
LRG_543p1:p.Val53Ala
NC_000012.11:g.52306979T>C
NM_000020.2:c.158T>C

Protein change:

V53A

Molecular consequence:

NM_000020.3:c.158T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001077401.2:c.158T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001406487.1:c.158T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001406488.1:c.158T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001406489.1:c.158T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001406490.1:c.158T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001406491.1:c.158T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001406492.1:c.158T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001406493.1:c.158T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001406494.1:c.158T>C - missense variant - [Sequence Ontology: SO:0001583]

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
SCV004226343	Mayo Clinic Laboratories, Mayo Clinic	criteria provided, single submitter (ACMG Guidelines, 2015)	Uncertain significance (Jul 25, 2022)	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

SCV004226343

Mayo Clinic Laboratories, Mayo Clinic

criteria provided, single submitter

(ACMG Guidelines, 2015)

Uncertain significance
(Jul 25, 2022)

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	unknown	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 Mayo Clinic Laboratories, Mayo Clinic, SCV004226343.1

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

Description

PM2_supporting

#	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		1	not provided	not provided	not provided

Last Updated: May 1, 2024

ClinVar

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