NM_003888.4(ALDH1A2):c.118-314T>C AND not provided

Germline classification:: Benign (2 submissions)
Last evaluated:: Jun 18, 2021
Review status:: 2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts

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:: RCV001609297.4

Allele description [Variation Report for NM_003888.4(ALDH1A2):c.118-314T>C]

NM_003888.4(ALDH1A2):c.118-314T>C

Gene:

ALDH1A2:aldehyde dehydrogenase 1 family member A2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

15q21.3

Genomic location:

Preferred name:

NM_003888.4(ALDH1A2):c.118-314T>C

HGVS:

NC_000015.10:g.58014595A>G
NG_012259.1:g.56114T>C
NM_001206897.2:c.55-314T>C
NM_003888.4:c.118-314T>CMANE SELECT
NM_170696.3:c.118-314T>C
NC_000015.9:g.58306793A>G

Links:

dbSNP: rs12903202

NCBI 1000 Genomes Browser:

rs12903202

Molecular consequence:

NM_001206897.2:c.55-314T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_003888.4:c.118-314T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_170696.3:c.118-314T>C - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001840475	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Benign (Jun 18, 2021)	germline	clinical testing	Citation Link,
SCV005289461	Breakthrough Genomics, Breakthrough Genomics	criteria provided, single submitter (ACMG Guidelines, 2015)	Benign	germline	not provided	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001840475

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Benign
(Jun 18, 2021)

germline

clinical testing

Citation Link,

SCV005289461

Breakthrough Genomics, Breakthrough Genomics

criteria provided, single submitter

(ACMG Guidelines, 2015)

Benign

germline

not provided

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	yes	not provided	not provided	not provided	not provided	not provided	clinical testing, not provided

Citations

PubMed

Nothing to display

Details of each submission

From GeneDx, SCV001840475.1

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

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	yes	not provided	not provided	not provided		not provided	not provided	not provided	not provided

From Breakthrough Genomics, Breakthrough Genomics, SCV005289461.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	not provided	PubMed (1)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	yes	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Sep 29, 2024

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