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NM_001737.5(C9):c.1184_1185del (p.Ser395fs) AND C9-related disorder

Germline classification:
Likely pathogenic (1 submission)
Last evaluated:
Oct 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:
RCV003408011.4

Allele description [Variation Report for NM_001737.5(C9):c.1184_1185del (p.Ser395fs)]

NM_001737.5(C9):c.1184_1185del (p.Ser395fs)

Gene:
C9:complement C9 [Gene - OMIM - HGNC]
Variant type:
Microsatellite
Cytogenetic location:
5p13.1
Genomic location:
Preferred name:
NM_001737.5(C9):c.1184_1185del (p.Ser395fs)
HGVS:
  • NC_000005.10:g.39308286GA[1]
  • NG_009894.1:g.61266CT[1]
  • NM_001737.5:c.1184_1185delMANE SELECT
  • NP_001728.1:p.Ser395fs
  • LRG_32:g.61266CT[1]
  • NC_000005.9:g.39308387_39308388del
  • NC_000005.9:g.39308388GA[1]
  • NM_001737.4:c.1184_1185delCT
Protein change:
S395fs
Links:
dbSNP: rs752437276
NCBI 1000 Genomes Browser:
rs752437276
Molecular consequence:
  • NM_001737.5:c.1184_1185del - frameshift variant - [Sequence Ontology: SO:0001589]

Condition(s)

Name:
C9-related disorder
Synonyms:
C9-related condition
Identifiers:

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV004106579PreventionGenetics, part of Exact Sciences
criteria provided, single submitter

(ACMG Guidelines, 2015)		Likely pathogenic
(Oct 6, 2022) 		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 PreventionGenetics, part of Exact Sciences, SCV004106579.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)

Description

The C9 c.1184_1185delCT variant is predicted to result in a frameshift and premature protein termination (p.Ser395Cysfs*4). To our knowledge, this variant has not been reported in the literature, but has been reported in 0.0047% of alleles in individuals of European (Non-Finnish) descent in gnomAD (http://gnomad.broadinstitute.org/variant/5-39308386-CAG-C). Truncating variants in C9 are expected to be pathogenic. This variant is interpreted as likely pathogenic.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 29, 2024