NM_000709.4(BCKDHA):c.1317A>G (p.Pro439=) AND Maple syrup urine disease type 1A

Germline classification:: Likely benign (1 submission)
Last evaluated:: Jun 26, 2021
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

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:: RCV001830856.1

Allele description [Variation Report for NM_000709.4(BCKDHA):c.1317A>G (p.Pro439=)]

NM_000709.4(BCKDHA):c.1317A>G (p.Pro439=)

Gene:

BCKDHA:branched chain keto acid dehydrogenase E1 subunit alpha [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

19q13.2

Genomic location:

Preferred name:

NM_000709.4(BCKDHA):c.1317A>G (p.Pro439=)

HGVS:

NC_000019.10:g.41424587A>G
NG_013004.1:g.31799A>G
NM_000709.4:c.1317A>GMANE SELECT
NM_001164783.2:c.1314A>G
NP_000700.1:p.Pro439=
NP_001158255.1:p.Pro438=
NC_000019.9:g.41930492A>G
NM_000709.3:c.1317A>G

Links:

dbSNP: rs749795206

NCBI 1000 Genomes Browser:

rs749795206

Molecular consequence:

NM_000709.4:c.1317A>G - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001164783.2:c.1314A>G - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Name:: Maple syrup urine disease type 1A (MSUD1A)
Synonyms:: MSUD type 1A
Identifiers:: MONDO: MONDO:0023691; MedGen: C1855369; OMIM: 248600

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Help

Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002088182	Natera, Inc.	no assertion criteria provided	Likely benign (Jun 26, 2021)	germline	clinical testing

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002088182

Natera, Inc.

no assertion criteria provided

Likely benign
(Jun 26, 2021)

germline

clinical testing

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 Natera, Inc., SCV002088182.1

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

Last Updated: Sep 29, 2024

ClinVar

Relating variation to medicine