Is NPHP4 p.Asp169His (c.505G>C) pathogenic?

NPHP4 p.Asp169His (c.505G>C) is classified Uncertain significance in NPHP4 (ClinVar, Single submitter, 1 submitter; last evaluated 2022-06-20). AlphaMissense: ambiguous (0.4537); Very rare (popmax 0.00341%, amr); Associated with nephronophthisis.

What condition is associated with NPHP4 p.Asp169His (c.505G>C)?

NPHP4 p.Asp169His (c.505G>C) is associated with nephronophthisis (ClinVar).

How common is NPHP4 p.Asp169His (c.505G>C) in the general population?

NPHP4 p.Asp169His (c.505G>C) is very rare (popmax 0.00341%, amr) (gnomAD).

How is Nephronophthisis inherited?

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

What do computational predictors say about NPHP4 p.Asp169His (c.505G>C)?

AlphaMissense predicts ambiguous (score 0.4537) — an in-silico prediction, not a clinical call.

NPHP4 p.Asp169His

c.505G>C · rs1237544876 · VCV1056447

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

ambiguous

0.4537 · ACMG-weighted

gnomAD v4.1

Rare

very rare (popmax 0.00341%, amr)

Conditions

nephronophthisis

Computational evidence

Protein change
AlphaMissense	0.4537	ambiguous
REVEL	0.606	indeterminate
SaProt	LLR -5.97	tolerated
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 7.5	GERP 2.1, phastCons 1
Regional constraint	o/e 1.02	unconstrained · MANE · 123 kb · p 0.49 · regional, not allelic
Overall
CADD	26.4	PHRED · no single calibrated threshold — expert panels disagree

AlphaMissense carries the ACMG weight for missense; REVEL and SaProt are independent agreement signals.

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.00341% Admixed American · 2/58,716 alleles

Filtering AF 0.000565% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.000211%

Overall 0.000125% 2/1,604,776 alleles · very rare exomes 1/1,452,564 · genomes 1/152,212 · joint denominator

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: NPHP4
Protein: p.Asp169His
Coding: c.505G>C
MANE Select: NM_015102
dbSNP: rs1237544876
Type: single nucleotide variant
Location: chr1:5967311 (GRCh38)
Gene constraint: LOEUF 1.183 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 72.44

Full NPHP4 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

nephronophthisis — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

For Nephronophthisis (Orphanet):

Inheritance: Autosomal recessive
Onset: Adolescent, Adult, Antenatal, Childhood, Infancy, Neonatal
Prevalence: 1-9 / 100 000 (Finland)

Similar variants

NPHP4 c.2304+1G>A Pathogenic ★★ same condition
NPHP4 c.2611+1G>A Pathogenic/Likely pathogenic ★★ same condition
NPHP4 c.2611+1G>C Pathogenic ★★ same condition
NPHP4 c.3644+1G>A Pathogenic/Likely pathogenic ★★ same condition
NPHP4 c.3644+1G>T Pathogenic/Likely pathogenic ★★ same condition
NPHP4 c.518-2A>G Likely pathogenic ★★ same condition
NPHP4 c.992+2T>C Likely pathogenic ★★ same condition
NPHP4 p.Arg1109Ter Pathogenic/Likely 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/nphp4-p-asp169his (accessed [today's date]).

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