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NM_003001.5(SDHC):c.436C>A (p.Pro146Thr) AND multiple conditions

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Mar 6, 2022
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:
RCV002483272.2

Allele description [Variation Report for NM_003001.5(SDHC):c.436C>A (p.Pro146Thr)]

NM_003001.5(SDHC):c.436C>A (p.Pro146Thr)

Gene:
SDHC:succinate dehydrogenase complex subunit C [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
1q23.3
Genomic location:
Preferred name:
NM_003001.5(SDHC):c.436C>A (p.Pro146Thr)
HGVS:
  • NC_000001.11:g.161362359C>A
  • NG_012767.1:g.52984C>A
  • NM_001035511.3:c.272C>A
  • NM_001035512.3:c.334C>A
  • NM_001035513.3:c.277C>A
  • NM_001278172.3:c.170C>A
  • NM_001407115.1:c.556C>A
  • NM_001407116.1:c.379C>A
  • NM_001407117.1:c.373C>A
  • NM_001407118.1:c.328C>A
  • NM_001407119.1:c.325C>A
  • NM_001407120.1:c.325C>A
  • NM_001407121.1:c.215C>A
  • NM_003001.5:c.436C>AMANE SELECT
  • NP_001030588.1:p.Ser91Tyr
  • NP_001030588.1:p.Ser91Tyr
  • NP_001030589.1:p.Pro112Thr
  • NP_001030589.1:p.Pro112Thr
  • NP_001030590.1:p.Pro93Thr
  • NP_001030590.1:p.Pro93Thr
  • NP_001265101.1:p.Ser57Tyr
  • NP_001265101.1:p.Ser57Tyr
  • NP_001394044.1:p.Pro186Thr
  • NP_001394045.1:p.Pro127Thr
  • NP_001394046.1:p.Pro125Thr
  • NP_001394047.1:p.Pro110Thr
  • NP_001394048.1:p.Pro109Thr
  • NP_001394049.1:p.Pro109Thr
  • NP_001394050.1:p.Ser72Tyr
  • NP_002992.1:p.Pro146Thr
  • NP_002992.1:p.Pro146Thr
  • LRG_317t1:c.436C>A
  • LRG_317:g.52984C>A
  • LRG_317p1:p.Pro146Thr
  • NC_000001.10:g.161332149C>A
  • NM_001035511.2:c.272C>A
  • NM_001035512.2:c.334C>A
  • NM_001035513.2:c.277C>A
  • NM_001278172.2:c.170C>A
  • NM_003001.3:c.436C>A
  • NR_103459.2:n.488C>A
  • NR_103459.3:n.488C>A
  • p.P146T
Protein change:
P109T
Links:
dbSNP: rs541660851
NCBI 1000 Genomes Browser:
rs541660851
Molecular consequence:
  • NM_001035511.3:c.272C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001035512.3:c.334C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001035513.3:c.277C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001278172.3:c.170C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407115.1:c.556C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407116.1:c.379C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407117.1:c.373C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407118.1:c.328C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407119.1:c.325C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407120.1:c.325C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407121.1:c.215C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_003001.5:c.436C>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Gastrointestinal stromal tumor
Synonyms:
Gastrointestinal Stromal Sarcoma; Gastrointestinal stromal tumor, somatic; Gastrointestinal stroma tumor
Identifiers:
MONDO: MONDO:0011719; MeSH: D046152; MedGen: C0238198; Orphanet: 44890; OMIM: 606764; Human Phenotype Ontology: HP:0100723
Name:
Carney-Stratakis syndrome
Synonyms:
Paraganglioma and gastric stromal sarcoma; Paraganglioma and gastrointestinal stromal tumor; Paraganglioma and GIST; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0011740; MedGen: C1847319; Orphanet: 97286; OMIM: 606864
Name:
Paragangliomas 3 (PPGL3)
Synonyms:
Glomus tumors, familial, 3; SDHC-Related Hereditary Paraganglioma-Pheochromocytoma Syndrome (Paragangliomas 3); PHEOCHROMOCYTOMA/PARAGANGLIOMA SYNDROME 3
Identifiers:
MONDO: MONDO:0011544; MedGen: C1854336; Orphanet: 29072; OMIM: 605373

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002783358Fulgent Genetics, Fulgent Genetics
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain significance
(Mar 6, 2022) 		unknownclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedunknownunknownnot providednot providednot providednot providednot providedclinical 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 Fulgent Genetics, Fulgent Genetics, SCV002783358.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Oct 13, 2024