NM_080615.1:c.1078G>A AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jun 17, 2024
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:: RCV004626787.1

Allele description [Variation Report for NM_080615.1:c.1078G>A]

NM_080615.1:c.1078G>A

Gene:: GCNT7:glucosaminyl (N-acetyl) transferase family member 7 [Gene - HGNC]
Variant type:: single nucleotide variant
Preferred name:: NM_080615.1:c.1078G>A
HGVS:: NM_080615.1:c.1078G>A
This HGVS expression did not pass validation

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

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PREDICTED: Homo sapiens cilia and flagella associated protein 410 (CFAP410), tra...
PREDICTED: Homo sapiens cilia and flagella associated protein 410 (CFAP410), transcript variant X9, mRNA
gi|2462583264|ref|XM_054324850.1|

Nucleotide
RecName: Full=Multiple C2 and transmembrane domain-containing protein 1
RecName: Full=Multiple C2 and transmembrane domain-containing protein 1
gi|300669650|sp|Q6DN14.2|MCTP1_HUMA

Protein
Xenopus laevis inhibin subunit beta C L homeolog (inhbc.1.L), mRNA
Xenopus laevis inhibin subunit beta C L homeolog (inhbc.1.L), mRNA
gi|148228928|ref|NM_001085864.1|

Nucleotide

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV005123727	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Jun 17, 2024)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV005123727

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Jun 17, 2024)

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, SCV005123727.1

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

Description

The c.1078G>A (p.E360K) alteration is located in exon 7 (coding exon 3) of the GCNT7 gene. This alteration results from a G to A substitution at nucleotide position 1078, causing the glutamic acid (E) at amino acid position 360 to be replaced by a lysine (K). 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: Aug 11, 2024

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