Is DRC1 p.Lys171del (c.513_515del) pathogenic?

DRC1 p.Lys171del (c.513515del) is classified Uncertain significance in DRC1 (ClinVar, Single submitter, 1 submitter; last evaluated 2021-08-24). Very rare (popmax 0.000763%, nfe); Associated with primary ciliary dyskinesia.

What condition is associated with DRC1 p.Lys171del (c.513_515del)?

DRC1 p.Lys171del (c.513_515del) is associated with primary ciliary dyskinesia (ClinVar).

How common is DRC1 p.Lys171del (c.513_515del) in the general population?

DRC1 p.Lys171del (c.513_515del) is very rare (popmax 0.000763%, nfe) (gnomAD).

How is Primary ciliary dyskinesia inherited?

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

DRC1 p.Lys171del

c.513_515del · rs773138367 · VCV1498456

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Rare

very rare (popmax 0.000763%, nfe)

Conditions

primary ciliary dyskinesia

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Splicing
SpliceAI	—	not assessed · substitutions only
Constraint at this position
Conservation	phyloP -3.3	GERP -3.5
Overall
CADD	19.64	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.000763% European (non-Finnish) · 9/1,179,912 alleles

Filtering AF 0.000359% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.00026%

Overall 0.00062% 10/1,613,264 alleles · very rare

Ancestry group	Frequency	1 in
Remaining individualsnot grpmax-eligible	0.0016%	62,442
European (non-Finnish)grpmax	0.000763%	131,101

Remaining individuals shows a higher raw frequency than the grpmax group above it. gnomAD excludes bottlenecked groups — Finnish, Ashkenazi Jewish, Amish and “Remaining individuals” — from grpmax, because founder effects make their frequencies unrepresentative for filtering. The table is sorted by frequency, so an excluded group can sit above the grpmax row.

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: DRC1
Protein: p.Lys171del
Coding: c.513_515del
MANE Select: NM_145038
dbSNP: rs773138367
Type: Deletion
Location: chr2:26424425 (GRCh38)
Gene constraint: LOEUF 0.867 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 75.44 · 1 PDB
Residue 171: a UniProt-annotated variant site (in spgf80); a UniProt-annotated variant site (in cild21)

Full DRC1 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

primary ciliary dyskinesia — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

For Primary ciliary dyskinesia (Orphanet):

Inheritance: Autosomal dominant, Autosomal recessive, X-linked recessive
Onset: Neonatal
Prevalence: 1-5 / 10 000 (Pakistan)

Similar variants

DRC1 p.Ser659fs Pathogenic ★★ same condition
DRC1 p.Arg694fs Uncertain significance ★★ same condition
DRC1 p.Lys574_Glu578del Likely benign ★★ same condition
DRC1 p.Asn442fs Pathogenic ★ same condition
DRC1 p.Gln296fs Pathogenic ★ same condition
DRC1 p.Leu518fs Pathogenic ★ same condition
DRC1 p.Lys338fs Pathogenic ★ same condition
DRC1 p.Thr491fs Pathogenic ★ 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/drc1-p-lys171del (accessed [today's date]).

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