NM_003002.4(SDHD):c.149A>G (p.His50Arg) AND Hereditary cancer-predisposing syndrome

This record was updated by the submitter. Please see the current version.

Germline classification:: Benign (2 submissions)
Last evaluated:: Aug 18, 2020
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:: RCV000129149.11

Allele description

NM_003002.4(SDHD):c.149A>G (p.His50Arg)

Gene:

SDHD:succinate dehydrogenase complex subunit D [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11q23.1

Genomic location:

Preferred name:

NM_003002.4(SDHD):c.149A>G (p.His50Arg)

Other names:

SDHD, HIS50ARG (rs11214077)

HGVS:

NC_000011.10:g.112087953A>G
NG_012337.3:g.6107A>G
NG_033145.1:g.3846T>C
NM_001276503.2:c.149A>G
NM_001276504.2:c.53-914A>G
NM_001276506.2:c.149A>G
NM_003002.4:c.149A>GMANE SELECT
NP_001263432.1:p.His50Arg
NP_001263435.1:p.His50Arg
NP_002993.1:p.His50Arg
LRG_9t1:c.149A>G
LRG_9:g.6107A>G
LRG_9p1:p.His50Arg
NC_000011.9:g.111958677A>G
NM_001276506.1:c.149A>G
NM_003002.2:c.149A>G
NM_003002.3:c.149A>G
NR_077060.2:n.184A>G
O14521:p.His50Arg
p.H50R

Protein change:

H50R; HIS50ARG

Links:

UniProtKB: O14521#VAR_017871; OMIM: 602690.0019; dbSNP: rs11214077

NCBI 1000 Genomes Browser:

rs11214077

Molecular consequence:

NM_001276504.2:c.53-914A>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001276503.2:c.149A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001276506.2:c.149A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_003002.4:c.149A>G - missense variant - [Sequence Ontology: SO:0001583]
NR_077060.2:n.184A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Observations:

Condition(s)

Name:: Hereditary cancer-predisposing syndrome
Synonyms:: Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000183872	Ambry Genetics	criteria provided, single submitter (Ambry General Variant Classification Scheme_2022)	Benign (Jun 29, 2014)	germline	clinical testing	Citation Link,
SCV002527118	Sema4, Sema4	criteria provided, single submitter (Sema4 Curation Guidelines)	Benign (Aug 18, 2020)	germline	curation	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000183872

Ambry Genetics

criteria provided, single submitter

(Ambry General Variant Classification Scheme_2022)

Benign
(Jun 29, 2014)

germline

clinical testing

Citation Link,

SCV002527118

Sema4, Sema4

criteria provided, single submitter

(Sema4 Curation Guidelines)

Benign
(Aug 18, 2020)

germline

curation

Citation Link

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	1	not provided	clinical testing, curation

Details of each submission

From Ambry Genetics, SCV000183872.8

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

Description

This alteration is classified as benign based on a combination of the following: population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

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

From Sema4, Sema4, SCV002527118.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	curation	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: Apr 20, 2024

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