NM_138477.4(CDAN1):c.1787A>G (p.Gln596Arg) AND Anemia, congenital dyserythropoietic, type 1a

Germline classification:: Benign (1 submission)
Last evaluated:: Nov 29, 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:: RCV001801897.13

Allele description [Variation Report for NM_138477.4(CDAN1):c.1787A>G (p.Gln596Arg)]

NM_138477.4(CDAN1):c.1787A>G (p.Gln596Arg)

Gene:

CDAN1:codanin 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

15q15.2

Genomic location:

Preferred name:

NM_138477.4(CDAN1):c.1787A>G (p.Gln596Arg)

HGVS:

NC_000015.10:g.42731284T>C
NG_012491.1:g.10936A>G
NM_138477.4:c.1787A>GMANE SELECT
NP_612486.2:p.Gln596Arg
LRG_1164t1:c.1787A>G
LRG_1164:g.10936A>G
LRG_1164p1:p.Gln596Arg
NC_000015.9:g.43023482T>C
NM_138477.2:c.1787A>G
Q8IWY9:p.Gln596Arg

Protein change:

Q596R

Links:

UniProtKB: Q8IWY9#VAR_056785; dbSNP: rs12917189

NCBI 1000 Genomes Browser:

rs12917189

Molecular consequence:

NM_138477.4:c.1787A>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Anemia, congenital dyserythropoietic, type 1a (CDAN1A)
Synonyms:: DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE Ia
Identifiers:: MONDO: MONDO:0009135; MedGen: C5574667; OMIM: 224120

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001471888	ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories	criteria provided, single submitter (ARUP Molecular Germline Variant Investigation Process 2024)	Benign (Nov 29, 2024)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001471888

ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

criteria provided, single submitter

(ARUP Molecular Germline Variant Investigation Process 2024)

Benign
(Nov 29, 2024)

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 ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories, SCV001471888.8

#	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	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: May 16, 2025

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