U.S. flag

An official website of the United States government

NM_001001548.3(CD36):c.379_381dup (p.Ser127_Val128insSer) AND Platelet-type bleeding disorder 10

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Sep 9, 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:
RCV003144717.3

Allele description [Variation Report for NM_001001548.3(CD36):c.379_381dup (p.Ser127_Val128insSer)]

NM_001001548.3(CD36):c.379_381dup (p.Ser127_Val128insSer)

Gene:
CD36:CD36 molecule (CD36 blood group) [Gene - OMIM - HGNC]
Variant type:
Duplication
Cytogenetic location:
7q21.11
Genomic location:
Preferred name:
NM_001001548.3(CD36):c.379_381dup (p.Ser127_Val128insSer)
HGVS:
  • NC_000007.14:g.80661160_80661162dup
  • NG_008192.1:g.63973_63975dup
  • NM_000072.3:c.379_381dup
  • NM_001001547.3:c.379_381dup
  • NM_001001548.3:c.379_381dupMANE SELECT
  • NM_001127443.2:c.379_381dup
  • NM_001127444.2:c.379_381dup
  • NM_001289908.1:c.379_381dup
  • NM_001289909.1:c.379_381dup
  • NM_001289911.2:c.151_153dup
  • NM_001371074.1:c.379_381dup
  • NM_001371075.1:c.379_381dup
  • NM_001371077.1:c.379_381dup
  • NM_001371078.1:c.379_381dup
  • NM_001371079.1:c.277_279dup
  • NM_001371080.1:c.-87_-85dup
  • NM_001371081.1:c.-104_-102dup
  • NP_000063.2:p.Ser127_Val128insSer
  • NP_001001547.1:p.Ser127_Val128insSer
  • NP_001001548.1:p.Ser127_Val128insSer
  • NP_001120915.1:p.Ser127_Val128insSer
  • NP_001120916.1:p.Ser127_Val128insSer
  • NP_001276837.1:p.Ser127_Val128insSer
  • NP_001276838.1:p.Ser127_Val128insSer
  • NP_001276840.1:p.Ser51_Val52insSer
  • NP_001358003.1:p.Ser127_Val128insSer
  • NP_001358004.1:p.Ser127_Val128insSer
  • NP_001358006.1:p.Ser127_Val128insSer
  • NP_001358007.1:p.Ser127_Val128insSer
  • NP_001358008.1:p.Ser93_Val94insSer
  • NC_000007.13:g.80290476_80290478dup
  • NR_110501.1:n.558_560dup
Molecular consequence:
  • NM_001371080.1:c.-87_-85dup - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001371081.1:c.-104_-102dup - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_000072.3:c.379_381dup - inframe_insertion - [Sequence Ontology: SO:0001821]
  • NM_001001547.3:c.379_381dup - inframe_insertion - [Sequence Ontology: SO:0001821]
  • NM_001001548.3:c.379_381dup - inframe_insertion - [Sequence Ontology: SO:0001821]
  • NM_001127443.2:c.379_381dup - inframe_insertion - [Sequence Ontology: SO:0001821]
  • NM_001127444.2:c.379_381dup - inframe_insertion - [Sequence Ontology: SO:0001821]
  • NM_001289908.1:c.379_381dup - inframe_insertion - [Sequence Ontology: SO:0001821]
  • NM_001289909.1:c.379_381dup - inframe_insertion - [Sequence Ontology: SO:0001821]
  • NM_001289911.2:c.151_153dup - inframe_insertion - [Sequence Ontology: SO:0001821]
  • NM_001371074.1:c.379_381dup - inframe_insertion - [Sequence Ontology: SO:0001821]
  • NM_001371075.1:c.379_381dup - inframe_insertion - [Sequence Ontology: SO:0001821]
  • NM_001371077.1:c.379_381dup - inframe_insertion - [Sequence Ontology: SO:0001821]
  • NM_001371078.1:c.379_381dup - inframe_insertion - [Sequence Ontology: SO:0001821]
  • NM_001371079.1:c.277_279dup - inframe_insertion - [Sequence Ontology: SO:0001821]
  • NR_110501.1:n.558_560dup - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:
Platelet-type bleeding disorder 10
Synonyms:
CD36 DEFICIENCY; Platelet glycoprotein IV deficiency
Identifiers:
MONDO: MONDO:0012031; MedGen: C1842090; OMIM: 608404

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV003829382Revvity Omics, Revvity
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain significance
(Sep 9, 2021) 		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, SCV003829382.2

#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