NM_001243177.4(ALDOA):c.226C>T (p.Arg76Cys) AND not provided

Germline classification:: Uncertain significance (2 submissions)
Last evaluated:: Dec 27, 2023
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:: RCV004696903.2

Allele description [Variation Report for NM_001243177.4(ALDOA):c.226C>T (p.Arg76Cys)]

NM_001243177.4(ALDOA):c.226C>T (p.Arg76Cys)

Genes:

ALDOA:aldolase, fructose-bisphosphate A [Gene - OMIM - HGNC]
LOC112694756:uncharaterized LOC112694756 [Gene]

Variant type:

single nucleotide variant

Cytogenetic location:

16p11.2

Genomic location:

Preferred name:

NM_001243177.4(ALDOA):c.226C>T (p.Arg76Cys)

Other names:

p.Arg22Cys

HGVS:

NC_000016.10:g.30067318C>T
NG_008010.1:g.19149C>T
NM_001127617.2:c.64C>T
NM_001243177.4:c.226C>TMANE SELECT
NM_001365304.2:c.*573C>TMANE SELECT
NM_001365305.2:c.*573C>T
NM_001365307.2:c.*573C>T
NM_184041.5:c.64C>T
NM_184043.2:c.64C>T
NP_001121089.1:p.Arg22Cys
NP_001230106.1:p.Arg76Cys
NP_908930.1:p.Arg22Cys
NP_908932.1:p.Arg22Cys
LRG_1180t1:c.64C>T
LRG_1180t2:c.226C>T
LRG_1180:g.19149C>T
LRG_1180p1:p.Arg22Cys
LRG_1180p2:p.Arg76Cys
NC_000016.9:g.30078639C>T
NM_184041.4:c.64C>T

Protein change:

R22C

Links:

dbSNP: rs145582724

Molecular consequence:

NM_001365304.2:c.*573C>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
NM_001365305.2:c.*573C>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
NM_001365307.2:c.*573C>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
NM_001127617.2:c.64C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001243177.4:c.226C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_184041.5:c.64C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_184043.2:c.64C>T - missense variant - [Sequence Ontology: SO:0001583]

Observations:

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
SCV005199513	Clinical Genetics Laboratory, Skane University Hospital Lund	criteria provided, single submitter (ACMG Guidelines, 2015)	Uncertain significance (Aug 23, 2022)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]
SCV005411287	Mayo Clinic Laboratories, Mayo Clinic	criteria provided, single submitter (ACMG Guidelines, 2015)	Uncertain significance (Dec 27, 2023)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV005199513

Clinical Genetics Laboratory, Skane University Hospital Lund

criteria provided, single submitter

(ACMG Guidelines, 2015)

Uncertain significance
(Aug 23, 2022)

germline

clinical testing

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

SCV005411287

Mayo Clinic Laboratories, Mayo Clinic

criteria provided, single submitter

(ACMG Guidelines, 2015)

Uncertain significance
(Dec 27, 2023)

germline

clinical testing

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	unknown	1	not provided	not provided	not provided	not provided	clinical testing
not provided	germline	yes	not provided	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee.

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]

PMID:: 25741868
PMCID:: PMC4544753

Details of each submission

From Clinical Genetics Laboratory, Skane University Hospital Lund, SCV005199513.1

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

From Mayo Clinic Laboratories, Mayo Clinic, SCV005411287.1

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

#	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		1	not provided	not provided	not provided

Last Updated: Aug 16, 2026

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