Genetic Variant NM_001289104.2:c.948_968dupGGAGGAGGAGGAGGAGGAGGA (chr19-11447525-A-AGAGGAGGAGGAGGAGGAGGAG) – ACMG Classification: Likely_benign (-1 pts)

Variant summary

Our verdict is Likely benign. The variant received -1 ACMG points: 0P and 1B. BP3

The NM_001289104.2(PRKCSH):c.948_968dupGGAGGAGGAGGAGGAGGAGGA(p.Glu317_Glu323dup) variant causes a disruptive inframe insertion change involving the alteration of a non-conserved nucleotide. It is difficult to determine the true allele frequency of this variant because it is of type INS_BIG, and the frequency of such variant types in population databases may be underestimated and unreliable. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar. Synonymous variant affecting the same amino acid position (i.e. E323E) has been classified as Likely benign.

Frequency

Genomes: not found (cov: 0)

Exomes 𝑓: 7.0e-7 ( 0 hom. )

Consequence

PRKCSH
NM_001289104.2 disruptive_inframe_insertion

Scores

Not classified

Clinical Significance

Not reported in ClinVar

Conservation

PhyloP100: 2.52

Publications

0 publications found

Variant links:

Genes affected

PRKCSH (HGNC:9411): (PRKCSH beta subunit of glucosidase II) This gene encodes the beta-subunit of glucosidase II, an N-linked glycan-processing enzyme in the endoplasmic reticulum. The encoded protein is an acidic phosphoprotein known to be a substrate for protein kinase C. Mutations in this gene have been associated with the autosomal dominant polycystic liver disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]

PRKCSH Gene-Disease associations (from GenCC):

polycystic liver disease 1
Inheritance: AD Classification: DEFINITIVE, STRONG, SUPPORTIVE Submitted by: Labcorp Genetics (formerly Invitae), ClinGen, Ambry Genetics, Orphanet, Genomics England PanelApp

PRKCSH links:

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ACMG classification

Classification was made for transcript

Our verdict: Likely_benign. The variant received -1 ACMG points.

BP3

Nonframeshift variant in repetitive region in NM_001289104.2

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001289104.2. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein
PRKCSH	NM_001289104.2	MANE Select	c.948_968dupGGAGGAGGAGGAGGAGGAGGA	p.Glu317_Glu323dup	disruptive_inframe_insertion	Exon 11 of 18	NP_001276033.1
PRKCSH	NM_001289103.2		c.948_968dupGGAGGAGGAGGAGGAGGAGGA	p.Glu317_Glu323dup	disruptive_inframe_insertion	Exon 11 of 18	NP_001276032.1
PRKCSH	NM_001379608.1		c.948_968dupGGAGGAGGAGGAGGAGGAGGA	p.Glu317_Glu323dup	disruptive_inframe_insertion	Exon 11 of 18	NP_001366537.1

Ensembl Transcripts

Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein
PRKCSH	ENST00000677123.1	MANE Select	c.948_968dupGGAGGAGGAGGAGGAGGAGGA	p.Glu317_Glu323dup	disruptive_inframe_insertion	Exon 11 of 18	ENSP00000503163.1
PRKCSH	ENST00000592741.5	TSL:1	c.948_968dupGGAGGAGGAGGAGGAGGAGGA	p.Glu317_Glu323dup	disruptive_inframe_insertion	Exon 11 of 18	ENSP00000466134.1
PRKCSH	ENST00000589838.5	TSL:1	c.948_968dupGGAGGAGGAGGAGGAGGAGGA	p.Glu317_Glu323dup	disruptive_inframe_insertion	Exon 10 of 17	ENSP00000465461.1

Frequencies

GnomAD3 genomes

Cov.:

GnomAD4 exome

AF:

6.97e-7

AC:

AN:

1434310

Hom.:

Cov.:

AF XY:

0.00000140

AC XY:

AN XY:

712786

show subpopulations

⚠️ The allele balance in gnomAD version 4 Exomes is significantly skewed from the expected value of 0.5.

African (AFR)

AF:

0.00

AC:

AN:

32884

American (AMR)

AF:

0.00

AC:

AN:

42036

Ashkenazi Jewish (ASJ)

AF:

0.00

AC:

AN:

25668

East Asian (EAS)

AF:

0.00

AC:

AN:

39096

South Asian (SAS)

AF:

0.00

AC:

AN:

84056

European-Finnish (FIN)

AF:

0.00

AC:

AN:

51680

Middle Eastern (MID)

AF:

0.00

AC:

AN:

5546

European-Non Finnish (NFE)

AF:

9.14e-7

AC:

AN:

1094004

Other (OTH)

AF:

0.00

AC:

AN:

59340

⚠️ The allele balance in gnomAD4 Exomes is highly skewed from 0.5 (p-value = 0), which strongly suggests a high chance of mosaicism in these individuals.

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.275

Heterozygous variant carriers

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

GnomAD4 genome

Cov.:

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name

Calibrated prediction

Score

Prediction

PhyloP100

2.5

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

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Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

Publications

ACMG classification

Variant Effect in Transcripts

RefSeq Transcripts

Ensembl Transcripts

Frequencies

ClinVar

Computational scores

Splicing

Publications

Other links and lift over