NM_032119.4(ADGRV1):c.1855T>G (p.Leu619Val) AND not specified

Clinical significance:Likely benign (Last evaluated: Apr 30, 2012)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000155099.3

Allele description [Variation Report for NM_032119.4(ADGRV1):c.1855T>G (p.Leu619Val)]

NM_032119.4(ADGRV1):c.1855T>G (p.Leu619Val)

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.1855T>G (p.Leu619Val)
HGVS:
  • NC_000005.10:g.90635129T>G
  • NG_007083.2:g.110786T>G
  • NM_032119.4:c.1855T>GMANE SELECT
  • NP_115495.3:p.Leu619Val
  • LRG_1095t1:c.1855T>G
  • LRG_1095:g.110786T>G
  • LRG_1095p1:p.Leu619Val
  • NC_000005.9:g.89930946T>G
  • NM_032119.3:c.1855T>G
  • NR_003149.2:n.1954T>G
Protein change:
L619V
Links:
dbSNP: rs202064612
NCBI 1000 Genomes Browser:
rs202064612
Molecular consequence:
  • NM_032119.4:c.1855T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NR_003149.2:n.1954T>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
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
SCV000204784Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicinecriteria provided, single submitter
Likely benign
(Apr 30, 2012)
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, SCV000204784.4

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

Description

Leu619Val in Exon 10 of GPR98: This variant is not expected to have clinical sig nificance because it has been identified in 0.4% (13/2896) of African American c hromosomes from a broad population by the NHLBI Exome Sequencing Project (http:/ /evs.gs.washington.edu/EVS).

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

Last Updated: Oct 30, 2021

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