NM_018036.7(ATG2B):c.5932C>T (p.Pro1978Ser) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Sep 19, 2022
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:: RCV004231114.1

Allele description [Variation Report for NM_018036.7(ATG2B):c.5932C>T (p.Pro1978Ser)]

NM_018036.7(ATG2B):c.5932C>T (p.Pro1978Ser)

Gene:

ATG2B:autophagy related 2B [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

14q32.2

Genomic location:

Preferred name:

NM_018036.7(ATG2B):c.5932C>T (p.Pro1978Ser)

HGVS:

NC_000014.9:g.96289730G>A
NG_051091.1:g.78672C>T
NG_051091.2:g.78611C>T
NM_018036.7:c.5932C>TMANE SELECT
NP_060506.6:p.Pro1978Ser
NC_000014.8:g.96756067G>A
NM_018036.5:c.5932C>T

Protein change:

P1978S

Molecular consequence:

NM_018036.7:c.5932C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

Recent activity

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PREDICTED: Salvia splendens tRNA (guanine(9)-N1)-methyltransferase-like (LOC1218...
PREDICTED: Salvia splendens tRNA (guanine(9)-N1)-methyltransferase-like (LOC121811690), mRNA
gi|2060341868|ref|XM_042212591.1|

Nucleotide
PREDICTED: Homo sapiens NIMA related kinase 7 (NEK7), transcript variant X9, mRN...
PREDICTED: Homo sapiens NIMA related kinase 7 (NEK7), transcript variant X9, mRNA
gi|2462504081|ref|XM_054334502.1|

Nucleotide

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003736352	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Sep 19, 2022)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003736352

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Sep 19, 2022)

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, SCV003736352.2

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

Description

The c.5932C>T (p.P1978S) alteration is located in exon 41 (coding exon 41) of the ATG2B gene. This alteration results from a C to T substitution at nucleotide position 5932, causing the proline (P) at amino acid position 1978 to be replaced by a serine (S). 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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