Is DYNC2H1 p.Ser2846Pro (c.8536T>C) pathogenic?

DYNC2H1 p.Ser2846Pro (c.8536T>C) is classified Conflicting classifications of pathogenicity in DYNC2H1 (ClinVar, Conflicting submitters, 3 submitters; last evaluated 2026-01-31). AlphaMissense: likely benign (0.0782); Ultra-rare (popmax 0.031%, eas); Associated with Inborn genetic diseases.

What condition is associated with DYNC2H1 p.Ser2846Pro (c.8536T>C)?

DYNC2H1 p.Ser2846Pro (c.8536T>C) is associated with Inborn genetic diseases, Jeune syndrome (ClinVar).

How common is DYNC2H1 p.Ser2846Pro (c.8536T>C) in the general population?

DYNC2H1 p.Ser2846Pro (c.8536T>C) is ultra-rare (popmax 0.031%, eas) (gnomAD).

What do computational predictors say about DYNC2H1 p.Ser2846Pro (c.8536T>C)?

AlphaMissense predicts likely benign (score 0.0782) — an in-silico prediction, not a clinical call.

DYNC2H1 p.Ser2846Pro

c.8536T>C · rs767717747 · VCV1318727

Conflicting classifications of pathogenicity Conflicting submitters

Classification

Conflicting classifications of pathogenicity

ClinVar

Review

Conflicting submitters ★☆☆☆

ClinVar · 3 submitters

AlphaMissense

likely benign

0.0782 · ACMG-weighted

gnomAD v4.1

Rare

ultra-rare (popmax 0.031%, eas)

Missense predictors

0/2 damaging

AlphaMissense, REVEL · SaProt no call

Conditions

Inborn genetic diseases

Computational evidence

Protein change
AlphaMissense	0.0782	likely benign
REVEL	0.072	moderately benign-leaning
SaProt	—	not scored · why
⇒ AlphaMissense and REVEL both call this tolerated; SaProt makes no call.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 0.64	GERP 1.2, phastCons 0.39
Regional constraint	o/e 0.98	unconstrained · MANE · 293 kb · p 0.28 · regional, not allelic
Overall
CADD	16.11	PHRED · no single calibrated threshold — expert panels disagree

AlphaMissense carries the ACMG weight for missense; REVEL is an independent agreement signal.

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.031% East Asian · 12/38,722 alleles

Filtering AF 0.0178% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.014%

Overall 0.00121% 18/1,483,344 alleles · ultra-rare exomes 13/1,331,412 · genomes 5/151,932 · joint denominator

Ancestry group	Frequency	1 in
East Asiangrpmax	0.031%	3,227
Remaining individualsnot grpmax-eligible	0.00698%	14,328
Admixed American	0.00248%	40,242
European (non-Finnish)	8.96e-05%	1,116,682

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: DYNC2H1
Protein: p.Ser2846Pro
Coding: c.8536T>C
MANE Select: NM_001377
dbSNP: rs767717747
Type: single nucleotide variant
Location: chr11:103209957 (GRCh38)
Gene constraint: LOEUF 0.859 · pLI <0.01 · ClinGen HI gene assoc. with recessive phenotype (gnomAD)
Residue 2846: the 'aaa 4' region

Full DYNC2H1 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

Inborn genetic diseases — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Also linked: Jeune syndrome

Similar variants

DYNC2H1 c.10042+2T>G Pathogenic/Likely pathogenic ★★ same condition
DYNC2H1 c.10462-2A>G Likely pathogenic ★★ same condition
DYNC2H1 c.10606-14A>G Pathogenic/Likely pathogenic ★★ same condition
DYNC2H1 c.10695+1G>A Likely pathogenic ★★ same condition
DYNC2H1 c.10813-2A>G Likely pathogenic ★★ same condition
DYNC2H1 c.11493+2T>A Likely pathogenic ★★ same condition
DYNC2H1 c.11650-1G>A Pathogenic/Likely pathogenic ★★ same condition
DYNC2H1 c.12457-1G>C 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/dync2h1-p-ser2846pro (accessed [today's date]).

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