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

Clinical significance:Conflicting interpretations of pathogenicity, Likely benign(2);Uncertain significance(1) (Last evaluated: Nov 15, 2020)

Review status:1 star out of maximum of 4 stars

criteria provided, conflicting interpretations

Based on:
3 submissions [Details]
Record status:
current
Accession:
RCV000725995.5

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:
4

Condition(s)

Identifiers:
MedGen: CN517202

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000341081EGL Genetic Diagnostics, Eurofins Clinical Diagnosticscriteria provided, single submitter
Uncertain significance
(May 15, 2018)
germlineclinical testing

Citation Link,

SCV001642362Invitaecriteria provided, single submitter
Likely benign
(Nov 15, 2020)
germlineclinical testing

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

SCV001817631GeneDxcriteria provided, single submitter
Likely benign
(Nov 9, 2020)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyesnot providednot providednot providednot providednot providedclinical testing
not providedgermlineunknown4not providednot providednot providednot providedclinical testing

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240-242.

PubMed [citation]
PMID:
28492532
PMCID:
PMC5632818

Details of each submission

From EGL Genetic Diagnostics, Eurofins Clinical Diagnostics, SCV000341081.4

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided4not providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot provided4not providednot providednot provided

From Invitae, SCV001642362.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

From GeneDx, SCV001817631.1

#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: Nov 27, 2021

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