NM_206933.4(USH2A):c.11907A>T (p.Pro3969=) AND none provided

Clinical significance:Benign (Last evaluated: Oct 21, 2019)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV001282196.2

Allele description [Variation Report for NM_206933.4(USH2A):c.11907A>T (p.Pro3969=)]

NM_206933.4(USH2A):c.11907A>T (p.Pro3969=)

Gene:
USH2A:usherin [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
1q41
Genomic location:
Preferred name:
NM_206933.4(USH2A):c.11907A>T (p.Pro3969=)
Other names:
p.P3969P:CCA>CCT
HGVS:
  • NC_000001.11:g.215728189T>A
  • NG_009497.1:g.700208A>T
  • NG_009497.2:g.700260A>T
  • NM_206933.4:c.11907A>TMANE SELECT
  • NP_996816.3:p.Pro3969=
  • NC_000001.10:g.215901531T>A
  • NM_206933.2:c.11907A>T
  • NM_206933.3:c.11907A>T
  • c.11907A>T
  • p.Pro3969Pro
Links:
dbSNP: rs61635304
NCBI 1000 Genomes Browser:
rs61635304
Molecular consequence:
  • NM_206933.4:c.11907A>T - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Name:
none provided
Identifiers:
MedGen: CN235283

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV001156874ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratoriescriteria provided, single submitter
Benign
(Oct 21, 2019)
germlineclinical testing

Citation Link

Summary from all submissions

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

Details of each submission

From ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories, SCV001156874.2

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

Last Updated: Nov 27, 2021

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