Is PLCB1 p.Val38= (c.114T>C) pathogenic?

PLCB1 p.Val38= (c.114T>C) is classified Likely benign in PLCB1 (ClinVar, Multiple submitters, 2 submitters; last evaluated 2025-06-01). Ultra-rare (popmax 0.0165%, afr); Associated with developmental and epileptic encephalopathy, 12.

What condition is associated with PLCB1 p.Val38= (c.114T>C)?

PLCB1 p.Val38= (c.114T>C) is associated with developmental and epileptic encephalopathy, 12 (ClinVar).

How common is PLCB1 p.Val38= (c.114T>C) in the general population?

PLCB1 p.Val38= (c.114T>C) is ultra-rare (popmax 0.0165%, afr) (gnomAD).

PLCB1 p.Val38=

Q: How is Epilepsy of infancy with migrating focal seizures inherited?

Typically Autosomal dominant, Autosomal recessive (Orphanet). A genetic counselor can assess individual risk for a family.

c.114T>C · rs146304198 · VCV1099065

Likely benign Multiple submitters

Classification

Likely benign

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 2 submitters

gnomAD v4.1

Rare

ultra-rare (popmax 0.0165%, afr)

Conditions

developmental and epileptic encephalopathy, 12

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 0.052	GERP -2.6, phastCons 0.94
Overall
CADD	6.34	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.0165% African / African-American · 12/72,536 alleles

Filtering AF 0.00949% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.00744%

Overall 0.000859% 13/1,513,938 alleles · ultra-rare

Ancestry group	Frequency	1 in
African / African-Americangrpmax	0.0165%	6,045
Admixed American	0.00178%	56,166

Rarity supports pathogenicity (ACMG PM2); frequency above a disease-specific BA1/BS1 threshold argues against it. A variant frequent in one ancestry group can be near-absent in others, so a single global figure can mislead.

Variant & gene context

Gene: PLCB1
Protein: p.Val38=
Coding: c.114T>C
MANE Select: NM_015192
dbSNP: rs146304198
Type: single nucleotide variant
Location: chr20:8150308 (GRCh38)
Gene constraint: LOEUF 0.357 · pLI 1.00 (gnomAD)
Structure: AlphaFold pLDDT 84.55

Full PLCB1 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

developmental and epileptic encephalopathy, 12 — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

For Epilepsy of infancy with migrating focal seizures (Orphanet):

Inheritance: Autosomal dominant, Autosomal recessive, X-linked recessive
Onset: Infancy, Neonatal

Similar variants

PLCB1 p.Val38Ala Uncertain significance ★ ⚠ same residue
PLCB1 p.Arg222Ter Pathogenic/Likely pathogenic ★★ same condition
PLCB1 p.Arg815Ter Pathogenic/Likely pathogenic ★★ same condition
PLCB1 c.3336+3A>G Uncertain significance ★★ same condition
PLCB1 p.Ala1046Ser Uncertain significance ★★ ⚠ same condition
PLCB1 p.Ala1046Thr Uncertain significance ★★ ⚠ same condition
PLCB1 p.Ala1116Val Uncertain significance ★★ ⚠ same condition
PLCB1 p.Ala1182Val Uncertain significance ★★ ⚠ same condition

Built on 18 open, versioned datasets — ClinVar, gnomAD, AlphaMissense, REVEL, ClinGen & more — plus Sugi Variant's own cross-source analysis. Source data 2026-01–2026-10, ClinVar 2026-10. Full sources & versions →

Cite Sugi Variant

Gür T. Sugi Variant: A Deterministic Per-Variant Germline Reference from a Knowledge Graph for Humans and AI Agents. 2026. doi:10.5281/zenodo.21509445. This variant: https://sugi.bio/variant/plcb1-p-val38 (accessed [today's date]).

Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown