NM_015205.3(ATP11A):c.3075C>G (p.His1025Gln) AND Inborn genetic diseases

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Feb 6, 2023
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:: RCV003199455.2

Allele description [Variation Report for NM_015205.3(ATP11A):c.3075C>G (p.His1025Gln)]

NM_015205.3(ATP11A):c.3075C>G (p.His1025Gln)

Genes:

ATP11A:ATPase phospholipid transporting 11A [Gene - OMIM - HGNC]
LOC126861868:CDK7 strongly-dependent group 2 enhancer GRCh37_chr13:113526644-113527843 [Gene]

Variant type:

single nucleotide variant

Cytogenetic location:

13q34

Genomic location:

Preferred name:

NM_015205.3(ATP11A):c.3075C>G (p.His1025Gln)

HGVS:

NC_000013.11:g.112873590C>G
NG_086366.2:g.1361C>G
NM_001405661.1:c.3075C>G
NM_001405662.1:c.3075C>G
NM_001405663.1:c.3075C>G
NM_015205.3:c.3075C>GMANE SELECT
NM_032189.4:c.3075C>G
NP_001392590.1:p.His1025Gln
NP_001392591.1:p.His1025Gln
NP_001392592.1:p.His1025Gln
NP_056020.2:p.His1025Gln
NP_115565.3:p.His1025Gln
NC_000013.10:g.113527904C>G
NM_032189.3:c.3075C>G

Protein change:

H1025Q

Molecular consequence:

NM_001405661.1:c.3075C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001405662.1:c.3075C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001405663.1:c.3075C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_015205.3:c.3075C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_032189.4:c.3075C>G - 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
SCV003893605	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Feb 6, 2023)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003893605

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Feb 6, 2023)

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, SCV003893605.2

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

Description

The c.3075C>G (p.H1025Q) alteration is located in exon 27 (coding exon 27) of the ATP11A gene. This alteration results from a C to G substitution at nucleotide position 3075, causing the histidine (H) at amino acid position 1025 to be replaced by a glutamine (Q). 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: May 1, 2024

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