NM_000338.3(SLC12A1):c.572T>A (p.Ile191Asn) AND Bartter disease type 1

Germline classification:: Likely pathogenic (1 submission)
Last evaluated:: Dec 12, 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:: RCV002287281.1

Allele description [Variation Report for NM_000338.3(SLC12A1):c.572T>A (p.Ile191Asn)]

NM_000338.3(SLC12A1):c.572T>A (p.Ile191Asn)

Genes:

CTXN2-AS1:CTXN2 antisense RNA 1 [Gene - HGNC]
SLC12A1:solute carrier family 12 member 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

15q21.1

Genomic location:

Preferred name:

NM_000338.3(SLC12A1):c.572T>A (p.Ile191Asn)

HGVS:

NC_000015.10:g.48220940T>A
NG_021301.1:g.19640T>A
NM_000338.3:c.572T>AMANE SELECT
NM_001184832.2:c.572T>A
NM_001384136.1:c.572T>A
NP_000329.2:p.Ile191Asn
NP_001171761.1:p.Ile191Asn
NP_001371065.1:p.Ile191Asn
NC_000015.9:g.48513137T>A

Protein change:

I191N

Molecular consequence:

NM_000338.3:c.572T>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001184832.2:c.572T>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001384136.1:c.572T>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Bartter disease type 1
Synonyms:: HYPOKALEMIC ALKALOSIS WITH HYPERCALCIURIA 1, ANTENATAL; Hyperprostaglandin E syndrome 1; Bartter syndrome, type 1, antenatal
Identifiers:: MONDO: MONDO:0100344; MedGen: C1866495; Orphanet: 112; OMIM: 601678

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002577529	Laboratory of Medical Genetics, National & Kapodistrian University of Athens	criteria provided, single submitter (ACMG Guidelines, 2015)	Likely pathogenic (Dec 12, 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

SCV002577529

Laboratory of Medical Genetics, National & Kapodistrian University of Athens

criteria provided, single submitter

(ACMG Guidelines, 2015)

Likely pathogenic
(Dec 12, 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	not provided	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 Laboratory of Medical Genetics, National & Kapodistrian University of Athens, SCV002577529.1

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

Description

PM2, PM3, PP2, PP3, PP5

#	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		not provided	not provided	not provided	not provided

Last Updated: Jan 15, 2023

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