NM_024747.5(HPS6):c.632G>C (p.Gly211Ala) AND Hermansky-Pudlak syndrome 6

Clinical significance:Likely benign (Last evaluated: Apr 27, 2017)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000368931.2

Allele description [Variation Report for NM_024747.5(HPS6):c.632G>C (p.Gly211Ala)]

NM_024747.5(HPS6):c.632G>C (p.Gly211Ala)

Gene:
HPS6:HPS6 biogenesis of lysosomal organelles complex 2 subunit 3 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
10q24.32
Genomic location:
Preferred name:
NM_024747.5(HPS6):c.632G>C (p.Gly211Ala)
HGVS:
  • NC_000010.11:g.102066106G>C
  • NG_012029.1:g.5717G>C
  • NM_024747.5:c.632G>C
  • NP_079023.2:p.Gly211Ala
  • LRG_564t1:c.632G>C
  • LRG_564:g.5717G>C
  • LRG_564p1:p.Gly211Ala
  • NC_000010.10:g.103825863G>C
Protein change:
G211A
Links:
dbSNP: rs200584437
NCBI 1000 Genomes Browser:
rs200584437
Molecular consequence:
  • NM_024747.5:c.632G>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Hermansky-Pudlak syndrome 6 (HPS6)
Identifiers:
MONDO: MONDO:0013558; MedGen: C3888007; Orphanet: 231512; Orphanet: 79430; OMIM: 614075

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000360064Illumina Clinical Services Laboratory,Illuminacriteria provided, single submitter
Likely benign
(Apr 27, 2017)
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 Illumina Clinical Services Laboratory,Illumina, SCV000360064.3

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

This variant was observed as part of a predisposition screen in an ostensibly healthy population. A literature search was performed for the gene, cDNA change, and amino acid change (where applicable). No publications were found based on this search. Allele frequency data from public databases allowed determination this variant is unlikely to cause disease. Therefore, this variant is classified as likely benign.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Jun 23, 2021

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