NM_001042631.3(SDHAF1):c.269G>C (p.Cys90Ser) AND Mitochondrial complex 2 deficiency, nuclear type 2

Germline classification:: Benign (1 submission)
Last evaluated:: Jul 15, 2021
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:: RCV001807109.2

Allele description [Variation Report for NM_001042631.3(SDHAF1):c.269G>C (p.Cys90Ser)]

NM_001042631.3(SDHAF1):c.269G>C (p.Cys90Ser)

Genes:

LOC130064281:ATAC-STARR-seq lymphoblastoid silent region 10546 [Gene]
SDHAF1:succinate dehydrogenase complex assembly factor 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

19q13.12

Genomic location:

Preferred name:

NM_001042631.3(SDHAF1):c.269G>C (p.Cys90Ser)

HGVS:

NC_000019.10:g.35995543G>C
NG_016869.1:g.5356=
NM_001042631.3:c.269G>CMANE SELECT
NP_001036096.2:p.Cys90Ser
NC_000019.9:g.36486445G>C

Protein change:

C90S

Links:

dbSNP: rs7249826

NCBI 1000 Genomes Browser:

rs7249826

Molecular consequence:

NM_001042631.3:c.269G>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Mitochondrial complex 2 deficiency, nuclear type 2
Synonyms:: MITOCHONDRIAL COMPLEX II DEFICIENCY, NUCLEAR TYPE 2
Identifiers:: MONDO: MONDO:0030935; MedGen: C5436933; OMIM: 619166

Recent activity

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galectin-9 isoform X3 [Homo sapiens]
galectin-9 isoform X3 [Homo sapiens]
gi|578830915|ref|XP_006721958.1|

Protein
ribosomal protein S8e, partial [Aristolochia howii]
ribosomal protein S8e, partial [Aristolochia howii]
gi|1805184998|gb|QHU23756.1|

Protein
ribosomal protein S8e, partial [Aristolochia fangchi]
ribosomal protein S8e, partial [Aristolochia fangchi]
gi|1805184816|gb|QHU23696.1|

Protein
MULTISPECIES: helix-turn-helix domain-containing protein [Streptomyces]
MULTISPECIES: helix-turn-helix domain-containing protein [Streptomyces]
gi|2820892800|ref|WP_382178592.1|

Protein
Lactiplantibacillus plantarum strain 30.2.14 16S ribosomal RNA gene, partial seq...
Lactiplantibacillus plantarum strain 30.2.14 16S ribosomal RNA gene, partial sequence
gi|1147527702|gb|KX649062.1|

Nucleotide

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002054685	Genome-Nilou Lab	criteria provided, single submitter (ACMG Guidelines, 2015)	Benign (Jul 15, 2021)	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

SCV002054685

Genome-Nilou Lab

criteria provided, single submitter

(ACMG Guidelines, 2015)

Benign
(Jul 15, 2021)

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	no	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 Genome-Nilou Lab, SCV002054685.1

#	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	no	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Sep 29, 2024

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