NM_024677.6(NSUN7):c.1733C>G (p.Ala578Gly) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Feb 23, 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:: RCV004258224.1

Allele description [Variation Report for NM_024677.6(NSUN7):c.1733C>G (p.Ala578Gly)]

NM_024677.6(NSUN7):c.1733C>G (p.Ala578Gly)

Gene:

NSUN7:NOP2/Sun RNA methyltransferase family member 7 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

4p14

Genomic location:

Preferred name:

NM_024677.6(NSUN7):c.1733C>G (p.Ala578Gly)

HGVS:

NC_000004.12:g.40808515C>G
NG_013337.1:g.411104G>C
NM_001330648.3:c.*181C>G
NM_024677.6:c.1733C>GMANE SELECT
NP_078953.4:p.Ala578Gly
NC_000004.11:g.40810532C>G
NM_024677.4:c.1733C>G

Protein change:

A578G

Molecular consequence:

NM_001330648.3:c.*181C>G - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
NM_024677.6:c.1733C>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

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Human noggin (NOGGIN) gene, complete cds
Human noggin (NOGGIN) gene, complete cds
gi|1117816|gb|U31202.1|HSU31202

Nucleotide
PREDICTED: Homo sapiens zinc finger protein 518A (ZNF518A), transcript variant X...
PREDICTED: Homo sapiens zinc finger protein 518A (ZNF518A), transcript variant X3, mRNA
gi|2462522071|ref|XM_054367255.1|

Nucleotide

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003873792	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Feb 23, 2023)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003873792

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Feb 23, 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, SCV003873792.2

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

Description

The c.1733C>G (p.A578G) alteration is located in exon 12 (coding exon 11) of the NSUN7 gene. This alteration results from a C to G substitution at nucleotide position 1733, causing the alanine (A) at amino acid position 578 to be replaced by a glycine (G). 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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