NM_178009.5(DGKH):c.24C>G (p.His8Gln) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jul 5, 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:: RCV004353769.1

Allele description [Variation Report for NM_178009.5(DGKH):c.24C>G (p.His8Gln)]

NM_178009.5(DGKH):c.24C>G (p.His8Gln)

Genes:

LOC130009645:ATAC-STARR-seq lymphoblastoid silent region 5297 [Gene]
DGKH:diacylglycerol kinase eta [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

13q14.11

Genomic location:

Preferred name:

NM_178009.5(DGKH):c.24C>G (p.His8Gln)

HGVS:

NC_000013.11:g.42048797C>G
NG_029191.3:g.13762C>G
NG_189209.1:g.473C>G
NM_001204504.3:c.24C>G
NM_152910.6:c.24C>G
NM_178009.5:c.24C>GMANE SELECT
NP_001191433.1:p.His8Gln
NP_690874.2:p.His8Gln
NP_821077.1:p.His8Gln
NC_000013.10:g.42622933C>G
NM_178009.3:c.24C>G

Protein change:

H8Q

Molecular consequence:

NM_001204504.3:c.24C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_152910.6:c.24C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_178009.5:c.24C>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

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PREDICTED: Homo sapiens family with sequence similarity 110 member C (FAM110C), ...
PREDICTED: Homo sapiens family with sequence similarity 110 member C (FAM110C), transcript variant X8, mRNA
gi|2462575977|ref|XM_054343349.1|

Nucleotide
Homo sapiens TAF11 RNA polymerase II, TATA box binding protein (TBP)-associated ...
Homo sapiens TAF11 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 28kDa, mRNA (cDNA clone MGC:15243 IMAGE:3935882), complete cds
gi|33872155|gb|BC021972.2|

Nucleotide

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004083840	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Jul 5, 2023)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004083840

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Jul 5, 2023)

germline

clinical testing

Citation Link

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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, SCV004083840.2

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

Description

The c.24C>G (p.H8Q) alteration is located in exon 1 (coding exon 1) of the DGKH gene. This alteration results from a C to G substitution at nucleotide position 24, causing the histidine (H) at amino acid position 8 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: Nov 10, 2024

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