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NM_002473.6(MYH9):c.2838+10C>T AND multiple conditions

Germline classification:
Likely benign (1 submission)
Last evaluated:
Apr 1, 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:
RCV002498178.1

Allele description [Variation Report for NM_002473.6(MYH9):c.2838+10C>T]

NM_002473.6(MYH9):c.2838+10C>T

Genes:
LOC126863137:CDK7 strongly-dependent group 2 enhancer GRCh37_chr22:36696002-36697201 [Gene]
MYH9:myosin heavy chain 9 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
22q12.3
Genomic location:
Preferred name:
NM_002473.6(MYH9):c.2838+10C>T
HGVS:
  • NC_000022.11:g.36300841G>A
  • NG_011884.2:g.92178C>T
  • NM_002473.6:c.2838+10C>TMANE SELECT
  • LRG_567:g.92178C>T
  • NC_000022.10:g.36696887G>A
Links:
dbSNP: rs1027216058
NCBI 1000 Genomes Browser:
rs1027216058
Molecular consequence:
  • NM_002473.6:c.2838+10C>T - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:
Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss (MATINS)
Synonyms:
DOHLE LEUKOCYTE INCLUSIONS WITH GIANT PLATELETS; MACROTHROMBOCYTOPENIA WITH LEUKOCYTE INCLUSIONS; BLEEDING DISORDER, PLATELET-TYPE, 6; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0015912; MedGen: C5200934; Orphanet: 182050; OMIM: 155100
Name:
Autosomal dominant nonsyndromic hearing loss 17
Synonyms:
Deafness, autosomal dominant nonsyndromic sensorineural 17; Nonsyndromic hereditary deafness DFNA17; Late-onset progressive hereditary hearing impairment due to cochleosaccular degeneration; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0011350; MedGen: C1863659; Orphanet: 90635; OMIM: 603622

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002804562Fulgent Genetics, Fulgent Genetics
criteria provided, single submitter

(ACMG Guidelines, 2015)		Likely benign
(Apr 1, 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, SCV002804562.1

#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: Sep 29, 2024