NM_000326.5(RLBP1):c.346+3_346+8del AND not provided

Clinical significance:Benign (Last evaluated: Dec 3, 2020)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000958695.3

Allele description [Variation Report for NM_000326.5(RLBP1):c.346+3_346+8del]

NM_000326.5(RLBP1):c.346+3_346+8del

Gene:
RLBP1:retinaldehyde binding protein 1 [Gene - OMIM - HGNC]
Variant type:
Deletion
Cytogenetic location:
15q26.1
Genomic location:
Preferred name:
NM_000326.5(RLBP1):c.346+3_346+8del
HGVS:
  • NC_000015.10:g.89217112_89217117del
  • NG_008116.1:g.9575_9580del
  • NM_000326.5:c.346+3_346+8delMANE SELECT
  • NC_000015.9:g.89760343_89760348del
  • NM_000326.4:c.346+3_346+8del
  • NM_000326.4:c.346+3_346+8delGAGGCC
Links:
dbSNP: rs56307321
NCBI 1000 Genomes Browser:
rs56307321
Molecular consequence:
  • NM_000326.5:c.346+3_346+8del - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Identifiers:
MedGen: CN517202

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV001105566Invitaecriteria provided, single submitter
Benign
(Dec 3, 2020)
germlineclinical testing

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

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot 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 Invitae, SCV001105566.3

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

Last Updated: Nov 27, 2021

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