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NM_002474.3(MYH11):c.4899C>T (p.Ala1633=) AND not provided

Germline classification:
Likely benign (1 submission)
Last evaluated:
Jan 26, 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:
RCV001697754.9

Allele description [Variation Report for NM_002474.3(MYH11):c.4899C>T (p.Ala1633=)]

NM_002474.3(MYH11):c.4899C>T (p.Ala1633=)

Genes:
MYH11:myosin heavy chain 11 [Gene - OMIM - HGNC]
NDE1:nudE neurodevelopment protein 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
16p13.11
Genomic location:
Preferred name:
NM_002474.3(MYH11):c.4899C>T (p.Ala1633=)
HGVS:
  • NC_000016.10:g.15720205G>A
  • NG_009299.1:g.141826C>T
  • NG_021210.1:g.81939G>A
  • NM_001040113.2:c.4920C>T
  • NM_001040114.2:c.4920C>T
  • NM_001143979.2:c.948-3986G>A
  • NM_002474.3:c.4899C>TMANE SELECT
  • NM_017668.3:c.948-3986G>AMANE SELECT
  • NM_022844.3:c.4899C>T
  • NP_001035202.1:p.Ala1640=
  • NP_001035203.1:p.Ala1640=
  • NP_002465.1:p.Ala1633=
  • NP_074035.1:p.Ala1633=
  • LRG_1401t1:c.4899C>T
  • LRG_1401t2:c.4920C>T
  • LRG_1401:g.141826C>T
  • LRG_1401p1:p.Ala1633=
  • LRG_1401p2:p.Ala1640=
  • NC_000016.9:g.15814062G>A
  • NM_001040113.1:c.4920C>T
  • NM_001143979.1:c.948-3986G>A
  • NM_002474.2:c.4899C>T
Links:
dbSNP: rs760584464
NCBI 1000 Genomes Browser:
rs760584464
Molecular consequence:
  • NM_001143979.2:c.948-3986G>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_017668.3:c.948-3986G>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001040113.2:c.4920C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001040114.2:c.4920C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_002474.3:c.4899C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_022844.3:c.4899C>T - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000720036GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)
Likely benign
(Jan 26, 2021)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyesnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From GeneDx, SCV000720036.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Jul 7, 2024