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NM_000136.3(FANCC):c.2T>C (p.Met1Thr) AND Fanconi anemia complementation group C

Germline classification:
Likely pathogenic (1 submission)
Last evaluated:
Jun 28, 2019
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:
RCV001781081.4

Allele description [Variation Report for NM_000136.3(FANCC):c.2T>C (p.Met1Thr)]

NM_000136.3(FANCC):c.2T>C (p.Met1Thr)

Gene:
FANCC:FA complementation group C [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
9q22.32
Genomic location:
Preferred name:
NM_000136.3(FANCC):c.2T>C (p.Met1Thr)
HGVS:
  • NC_000009.12:g.95249290A>G
  • NG_011707.1:g.73420T>C
  • NM_000136.3:c.2T>CMANE SELECT
  • NM_001243743.2:c.2T>C
  • NM_001243744.2:c.2T>C
  • NP_000127.2:p.Met1Thr
  • NP_001230672.1:p.Met1Thr
  • NP_001230673.1:p.Met1Thr
  • LRG_497t1:c.2T>C
  • LRG_497:g.73420T>C
  • NC_000009.11:g.98011572A>G
  • NM_000136.2:c.2T>C
Protein change:
M1T
Links:
dbSNP: rs2136102345
NCBI 1000 Genomes Browser:
rs2136102345
Molecular consequence:
  • NM_000136.3:c.2T>C - initiator_codon_variant - [Sequence Ontology: SO:0001582]
  • NM_001243743.2:c.2T>C - initiator_codon_variant - [Sequence Ontology: SO:0001582]
  • NM_001243744.2:c.2T>C - initiator_codon_variant - [Sequence Ontology: SO:0001582]
  • NM_000136.3:c.2T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001243743.2:c.2T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001243744.2:c.2T>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Fanconi anemia complementation group C (FANCC)
Synonyms:
FANCONI PANCYTOPENIA, TYPE 3; FACC; Fanconi anemia, group C
Identifiers:
MONDO: MONDO:0009213; MedGen: C3468041; Orphanet: 84; OMIM: 227645

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002024578Revvity Omics, Revvity
criteria provided, single submitter

(ACMG Guidelines, 2015)		Likely pathogenic
(Jun 28, 2019) 		germlineclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot 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 Revvity Omics, Revvity, SCV002024578.4

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

Last Updated: Mar 16, 2024