rs1555568475

Variant names:

• chr17-15259189-C-T
• rs1555568475
• NM_000304.4:c.83G>A
• PMP22 p.Trp28*

GermlineCancer (beta)

Variant summary

Our verdict is Pathogenic.

+14 Pathogenic

-7

-6

-1

0

+5

+6

+9

+10

BenignB

Likely BenignLB

UncertainVUS

Likely PathogenicLP

PathogenicP

The variant received 14 classification points (ACMG Germline Pathogenicity v2019). PVS1PM2PP5_Strong

The NM_000304.4(PMP22):c.83G>A (p.Trp28*) variant causes a stop gained change involving the alteration of a non-conserved nucleotide. The variant is predicted to lead to nonsense-mediated mRNA decay (NMD). The variant is absent from the gnomAD population database at sites with sufficient sequencing coverage. In-silico predictor (BayesDel (noAF)) classifies this variant as likely damaging/oncogenic. Splicing prediction tools (SpliceAI) predict no significant impact on normal splicing. Variant has been reported in ClinVar as Pathogenic/Likely Pathogenic (★★).

• Frequency: Genomes: not found (cov: 31)
• Consequence: PMP22 NM_000304.4 stop_gained
• Clinical Significance: Pathogenic criteria provided, multiple submitters, no conflicts P:2
• Conservation: PhyloP100: 4.12
• Publications: 1 publications found

Genes affected

PMP22 (HGNC:9118): (peripheral myelin protein 22) This gene encodes an integral membrane protein that is a major component of myelin in the peripheral nervous system. Studies suggest two alternately used promoters drive tissue-specific expression. Various mutations of this gene are causes of Charcot-Marie-Tooth disease Type IA, Dejerine-Sottas syndrome, and hereditary neuropathy with liability to pressure palsies. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]

PMP22 Gene-Disease associations (from GenCC):

• Charcot-Marie-Tooth disease type 1A

  Inheritance: AD Classification: DEFINITIVE, STRONG, SUPPORTIVE Submitted by: Ambry Genetics, Orphanet, ClinGen, Laboratory for Molecular Medicine, Labcorp Genetics (formerly Invitae), PanelApp Australia
• hereditary neuropathy with liability to pressure palsies

  Inheritance: AD Classification: DEFINITIVE, STRONG, SUPPORTIVE Submitted by: Ambry Genetics, Labcorp Genetics (formerly Invitae), PanelApp Australia, ClinGen, Orphanet
• Charcot-Marie-Tooth disease type 1E

  Inheritance: AD Classification: STRONG, MODERATE, SUPPORTIVE Submitted by: Orphanet, Ambry Genetics, Labcorp Genetics (formerly Invitae), PanelApp Australia
• Charcot-Marie-Tooth disease type 3

  Inheritance: AD Classification: STRONG, SUPPORTIVE Submitted by: Orphanet, PanelApp Australia

Classification according to ACMG Germline Pathogenicity v2019

Classification was made for transcript:

Our verdict: Pathogenic. The variant received 14 points.

Apply	Criterion Code & Title / Strength	Strength	Rationale / Clinical Context
	PVS1Null variant in LOF gene		Frameshift/stop-gained, NMD predicted, LoF disease mechanism — very strong (PVS1); Stop-gained (exon 3 of 5) at amino acid 28 of 160, predicted to trigger nonsense-mediated mRNA decay. Loss of function is a known disease mechanism for this gene.
	PM2Absent/extremely low in population databases		Absent from gnomAD (AD/XL gene) — PM2; Absent from gnomAD at well-covered site (MOI: AD+AR) (threshold 0.0001) — PM2 moderate.
	PP5Reputable source reports pathogenic		ClinVar 2-star pathogenic — strong (PP5); ClinVar germline classification: Pathogenic/Likely Pathogenic, 2 star(s).

Variant Effect in Transcripts

Automated classification analysis was done for transcript: NM_000304.4. You can select a different transcript below to see updated classification assignments.

RefSeq Transcripts

Sel.	Gene / Transcript	Tags	HGVSc / HGVSp	Effect	Exon rank	Protein / UniProt
	PMP22 NM_000304.4	MANE Select	c.83G>A p.Trp28*	stop_gained	Exon 3 of 5	Prot: NP_000295.1 UniProt:
	PMP22 NM_001281455.2		c.83G>A p.Trp28*	stop_gained	Exon 3 of 5	Prot: NP_001268384.1 UniProt:
	PMP22 NM_001281456.2		c.83G>A p.Trp28*	stop_gained	Exon 3 of 5	Prot: NP_001268385.1 UniProt:

PMP22 NM_000304.4

MANE Select

HGVSc / HGVSpc.83G>Ap.Trp28*

Exon rankExon 3 of 5

stop_gained

Prot: NP_000295.1UniProt: Q01453Q6FH25

PMP22 NM_001281455.2

HGVSc / HGVSpc.83G>Ap.Trp28*

Exon rankExon 3 of 5

stop_gained

Prot: NP_001268384.1UniProt: Q6FH25Q01453

PMP22 NM_001281456.2

HGVSc / HGVSpc.83G>Ap.Trp28*

Exon rankExon 3 of 5

stop_gained

Prot: NP_001268385.1UniProt: Q01453Q6FH25

Ensembl Transcripts

Sel.	Gene / Transcript	Tags	HGVSc / HGVSp	Effect	Exon rank	Protein / UniProt
	PMP22 ENST00000312280.9	TSL:1MANE Select	c.83G>A p.Trp28*	stop_gained	Exon 3 of 5	Prot: ENSP00000308937.3 UniProt:
	PMP22 ENST00000395938.7	TSL:1	c.83G>A p.Trp28*	stop_gained	Exon 3 of 5	Prot: ENSP00000379269.3 UniProt:
	PMP22 ENST00000494511.7	TSL:1	c.-27+5965G>A	intron	Intron 1 of 2	Prot: ENSP00000462782.2 UniProt:

PMP22 ENST00000312280.9

TSL:1MANE Select

HGVSc / HGVSpc.83G>Ap.Trp28*

Exon rankExon 3 of 5

stop_gained

Prot: ENSP00000308937.3UniProt: Q01453

PMP22 ENST00000395938.7

TSL:1

HGVSc / HGVSpc.83G>Ap.Trp28*

Exon rankExon 3 of 5

stop_gained

Prot: ENSP00000379269.3UniProt: A0A6Q8PF08

PMP22 ENST00000494511.7

TSL:1

HGVSc / HGVSpc.-27+5965G>A

Exon rankIntron 1 of 2

intron

Prot: ENSP00000462782.2UniProt: J3KT36

Frequencies

Allele frequencies (AF), counts (AC/AN), homozygotes and coverage

Common (AF > 0.05 / Hom > 5)

Rare (AF ≤ 0.0001 / Hom ≤ 1)

Source / population	AF	AC	Hom	AN	Coverage
Global population databases 3 sources Large-scale international reference populations
GnomAD3 genomes	AF:	AC:	Hom:	AN:	Cov:31
GnomAD4 exome	AF:	AC:	Hom:	AN:	Cov:30
GnomAD4 genome	AF:	AC:	Hom:	AN:	Cov:31

Showing 3 sources

ClinVar

ClinVar submissions

Significance: Pathogenic

Revision: criteria provided, multiple submitters, no conflicts

Pathogenic	VUS	Benign	Condition
1	-	-	Charcot-Marie-Tooth disease, type I (1)
1	-	-	Hereditary liability to pressure palsies (1)

Computational Scores

Algorithm	Calibrated pred.	Score	Prediction
AlphaGenome AVI	Pathogenic	49
BayesDel_addAF	Pathogenic	0.63	D
BayesDel_noAF	Pathogenic	0.59
CADD	Pathogenic	42
DANN	Uncertain	1.0
Eigen	Pathogenic	0.81
Eigen_PC	Pathogenic	0.67
FATHMM_MKL	Uncertain	0.89	D
GPN-Star LLR	N/A	-9.9
GPN-Star score	N/A	9.9
Mutation Taster	N/A	4/196	disease causing (ClinVar)
PhyloP100	Uncertain	4.1
RBP_binding_hub_radar	N/A	0.0
RBP_regulation_power_radar	N/A	1.7

Showing 14 of 14 scores

Splicing Scores

Algorithm	Calibrated pred.	Score	Prediction
Pangolin (max)	Benign	0.090
SpliceAI score (max)	Benign	0.16	Details are displayed if max score is > 0.2

Showing 2 of 2 scores

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

MaxEntScan Visualizer can be used to analyze the impact of this mutation on the neighboring sequence.

MaveDB functional evidence

MaveDB is a public repository of laboratory assays that test the effect of thousands of variants at once — treat this as supporting research data and interpret it with great caution; it is not a clinical classification.

No MaveDB functional evidence found for this variant.

Other links and lift over

dbSNP: rs1555568475;

hg19: chr17-15162506;

ACMG debug oncogenicity

ACGS debug oncogenicity

ACMG debug germline

Submit to ClinVar