NM_001289104.2(PRKCSH):c.939GGA[9] (p.Glu325del) AND Polycystic liver disease 1

Germline classification:: Benign (2 submissions)
Last evaluated:: Oct 25, 2021
Review status:: 2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV000377384.7

Allele description [Variation Report for NM_001289104.2(PRKCSH):c.939GGA[9] (p.Glu325del)]

NM_001289104.2(PRKCSH):c.939GGA[9] (p.Glu325del)

Gene:

PRKCSH:PRKCSH beta subunit of glucosidase II [Gene - OMIM - HGNC]

Variant type:

Microsatellite

Cytogenetic location:

19p13.2

Genomic location:

Preferred name:

NM_001289104.2(PRKCSH):c.939GGA[9] (p.Glu325del)

HGVS:

NC_000019.10:g.11447528GGA[9]
NG_009300.1:g.17075GGA[9]
NM_001001329.3:c.939GGA[9]
NM_001289102.2:c.939GGA[9]
NM_001289103.2:c.939GGA[9]
NM_001289104.2:c.939GGA[9]MANE SELECT
NM_001379608.1:c.939GGA[9]
NM_001379609.1:c.939GGA[9]
NM_002743.3:c.937_939del
NM_002743.3:c.939GGA[9]
NP_001001329.1:p.Glu325del
NP_001276031.1:p.Glu325del
NP_001276032.1:p.Glu325del
NP_001276033.1:p.Glu325del
NP_001366537.1:p.Glu325del
NP_001366538.1:p.Glu325del
NP_002734.2:p.Glu325del
NC_000019.9:g.11558341_11558343del
NC_000019.9:g.11558343GGA[9]
NM_001289104.2:c.939GGA[9]
NM_002743.2:c.966_968delGGA
NM_002743.3:c.937_939del
NM_002743.3:c.966_968delGGA

Protein change:

E325del

Links:

dbSNP: rs3217229

NCBI 1000 Genomes Browser:

rs3217229

Molecular consequence:

NM_001001329.3:c.939GGA[9] - inframe_deletion - [Sequence Ontology: SO:0001822]
NM_001289102.2:c.939GGA[9] - inframe_deletion - [Sequence Ontology: SO:0001822]
NM_001289103.2:c.939GGA[9] - inframe_deletion - [Sequence Ontology: SO:0001822]
NM_001289104.2:c.939GGA[9] - inframe_deletion - [Sequence Ontology: SO:0001822]
NM_001379608.1:c.939GGA[9] - inframe_deletion - [Sequence Ontology: SO:0001822]
NM_001379609.1:c.939GGA[9] - inframe_deletion - [Sequence Ontology: SO:0001822]
NM_002743.3:c.939GGA[9] - inframe_deletion - [Sequence Ontology: SO:0001822]

Condition(s)

Name:: Polycystic liver disease 1 (PCLD1)
Synonyms:: POLYCYSTIC LIVER DISEASE 1 WITH OR WITHOUT KIDNEY CYSTS
Identifiers:: MONDO: MONDO:0008265; MedGen: C0887850; Orphanet: 2924; OMIM: 174050

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000410688	Illumina Laboratory Services, Illumina	criteria provided, single submitter (ICSL Variant Classification 20161018)	Benign (Jun 14, 2016)	germline	clinical testing	ICSL_Variant_Classification_20161018.pdf, Citation Link,
SCV002031862	Genome-Nilou Lab	criteria provided, single submitter (ACMG Guidelines, 2015)	Benign (Oct 25, 2021)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000410688

Illumina Laboratory Services, Illumina

criteria provided, single submitter

(ICSL Variant Classification 20161018)

Benign
(Jun 14, 2016)

germline

clinical testing

ICSL_Variant_Classification_20161018.pdf,

Citation Link,

SCV002031862

Genome-Nilou Lab

criteria provided, single submitter

(ACMG Guidelines, 2015)

Benign
(Oct 25, 2021)

germline

clinical testing

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

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing
not provided	germline	no	not provided	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]

PMID:: 25741868
PMCID:: PMC4544753

Details of each submission

From Illumina Laboratory Services, Illumina, SCV000410688.2

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

From Genome-Nilou Lab, SCV002031862.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (1)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	no	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Sep 29, 2024

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