Is DYNC1H1 p.Pro1907Ser (c.5719C>T) pathogenic?

DYNC1H1 p.Pro1907Ser (c.5719C>T) is classified Uncertain significance in DYNC1H1 (ClinVar, Single submitter, 1 submitter; last evaluated 2024-05-13). AlphaMissense: likely pathogenic (0.9926); Absent from gnomAD v4.1; Associated with Inborn genetic diseases.

What condition is associated with DYNC1H1 p.Pro1907Ser (c.5719C>T)?

DYNC1H1 p.Pro1907Ser (c.5719C>T) is associated with Inborn genetic diseases (ClinVar).

How common is DYNC1H1 p.Pro1907Ser (c.5719C>T) in the general population?

DYNC1H1 p.Pro1907Ser (c.5719C>T) is absent from gnomAD v4.1 (gnomAD).

What do computational predictors say about DYNC1H1 p.Pro1907Ser (c.5719C>T)?

AlphaMissense predicts likely pathogenic (score 0.9926) — an in-silico prediction, not a clinical call.

DYNC1H1 p.Pro1907Ser

c.5719C>T · VCV3274147

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely pathogenic

0.9926 · ACMG-weighted

gnomAD v4.1

Absent

absent from gnomAD v4.1

Conditions

Inborn genetic diseases

Computational evidence

Protein change
AlphaMissense	0.9926	likely pathogenic
REVEL	0.591	indeterminate
SaProt	—	not scored · why
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 7.6	GERP 2.5, phastCons 1
Regional constraint	o/e 0.20	constrained · MANE · 2,158 bp · p 6.3e-17 · regional, not allelic
Overall
CADD	24.8	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

Absent from gnomAD v4.1. Not observed in any sequenced alleles — a rarity signal (ACMG PM2-supporting), not evidence of pathogenicity on its own.

Variant & gene context

Gene: DYNC1H1
Protein: p.Pro1907Ser
Coding: c.5719C>T
MANE Select: NM_001376
Type: single nucleotide variant
Location: chr14:102007010 (GRCh38)
Gene constraint: LOEUF 0.117 · pLI 1.00 · ClinGen HI 0/3 (gnomAD)
Residue 1907: a β-strand; a binding site; the 'aaa 1' region

Full DYNC1H1 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

Similar variants

DYNC1H1 p.Pro1907= Likely benign ★ same residue
DYNC1H1 p.Arg1567Gln Pathogenic/Likely pathogenic ★★ same condition
DYNC1H1 p.Arg1962His Likely pathogenic ★★ same condition
DYNC1H1 p.Arg292Trp Pathogenic ★★ same condition
DYNC1H1 p.Gly2330Glu Pathogenic/Likely pathogenic ★★ same condition
DYNC1H1 p.Phe1093Ser Pathogenic ★★ same condition
DYNC1H1 c.3444+3G>A Uncertain significance ★★ same condition
DYNC1H1 c.4074+5A>G 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/dync1h1-p-pro1907ser (accessed [today's date]).

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