NM_032119.4(ADGRV1):c.10563T>C (p.Leu3521=) AND not specified

Clinical significance:Likely benign (Last evaluated: Apr 25, 2017)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000179095.4

Allele description [Variation Report for NM_032119.4(ADGRV1):c.10563T>C (p.Leu3521=)]

NM_032119.4(ADGRV1):c.10563T>C (p.Leu3521=)

Gene:
ADGRV1:adhesion G protein-coupled receptor V1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
5q14.3
Genomic location:
Preferred name:
NM_032119.4(ADGRV1):c.10563T>C (p.Leu3521=)
HGVS:
  • NC_000005.10:g.90745059T>C
  • NG_007083.2:g.220716T>C
  • NM_032119.4:c.10563T>CMANE SELECT
  • NP_115495.3:p.Leu3521=
  • LRG_1095t1:c.10563T>C
  • LRG_1095:g.220716T>C
  • LRG_1095p1:p.Leu3521=
  • NC_000005.9:g.90040876T>C
  • NM_032119.3:c.10563T>C
  • NR_003149.2:n.10579T>C
  • p.Leu3521Leu
Links:
dbSNP: rs200946170
NCBI 1000 Genomes Browser:
rs200946170
Molecular consequence:
  • NR_003149.2:n.10579T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NM_032119.4:c.10563T>C - synonymous variant - [Sequence Ontology: SO:0001819]
Observations:
1

Condition(s)

Synonyms:
AllHighlyPenetrant
Identifiers:
MedGen: CN169374

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000711051Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicinecriteria provided, single submitter
Likely benign
(Apr 25, 2017)
germlineclinical testing

PubMed (1)
[See all records that cite this PMID]

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlinenot provided11not providednot providednot providedclinical testing

Citations

PubMed

A systematic approach to assessing the clinical significance of genetic variants.

Duzkale H, Shen J, McLaughlin H, Alfares A, Kelly MA, Pugh TJ, Funke BH, Rehm HL, Lebo MS.

Clin Genet. 2013 Nov;84(5):453-63. doi: 10.1111/cge.12257.

PubMed [citation]
PMID:
24033266
PMCID:
PMC3995020

Details of each submission

From Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine, SCV000711051.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testing PubMed (1)

Description

p.Leu3521Leu in exon 51 of GPR98: This variant is not expected to have clinical significance because it does not alter an amino acid residue, is not located wit hin the splice consensus sequence, and has been identified in 0.2% (57/24008) of African chromosomes by the Genome Aggregation Database (gnomAD, http://gnomad.b roadinstitute.org; dbSNP rs200946170).

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlinenot providednot providednot providednot provided1not provided1not provided

Last Updated: Jul 7, 2021

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