Is DYNC2I1 p.Ser292= (c.876C>T) pathogenic?

DYNC2I1 p.Ser292= (c.876C>T) is classified Likely benign in DYNC2I1 (ClinVar, Multiple submitters, 2 submitters; last evaluated 2025-05-21). Rare (popmax 0.116%, sas); Associated with short-rib thoracic dysplasia 8 with or without polydactyly.

What condition is associated with DYNC2I1 p.Ser292= (c.876C>T)?

DYNC2I1 p.Ser292= (c.876C>T) is associated with short-rib thoracic dysplasia 8 with or without polydactyly (ClinVar).

How common is DYNC2I1 p.Ser292= (c.876C>T) in the general population?

DYNC2I1 p.Ser292= (c.876C>T) is rare (popmax 0.116%, sas) (gnomAD).

DYNC2I1 p.Ser292=

c.876C>T · rs757328480 · VCV707022

Likely benign Multiple submitters

Classification

Likely benign

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 2 submitters

gnomAD v4.1

Rare

rare (popmax 0.116%, sas)

Conditions

short-rib thoracic dysplasia 8 with or without polydactyly

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Splicing
SpliceAI	<0.2	no splice effect predicted · four deltas, not one · how we know
Constraint at this position
Conservation	phyloP -3.5	GERP -2.1
Overall
CADD	3.241	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.116% South Asian · 101/86,806 alleles

Filtering AF 0.098% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.091%

Overall 0.0105% 166/1,587,964 alleles · rare exomes 159/1,435,842 · genomes 7/152,122 · joint denominator

Ancestry group	Frequency	1 in
South Asiangrpmax	0.116%	859
Ashkenazi Jewishnot grpmax-eligible	0.0784%	1,275
Middle Eastern	0.034%	2,944
Remaining individualsnot grpmax-eligible	0.0245%	4,078
Admixed American	0.00762%	13,124
European (non-Finnish)	0.00179%	55,791
African / African-American	0.00137%	72,936

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: DYNC2I1
Protein: p.Ser292=
Coding: c.876C>T
MANE Select: NM_018051
dbSNP: rs757328480
Type: single nucleotide variant
Location: chr7:158879986 (GRCh38)
Gene constraint: LOEUF 0.802 · pLI <0.01 · ClinGen HI gene assoc. with recessive phenotype (gnomAD)
Structure: AlphaFold pLDDT 62.87 · 4 PDB
Residue 292: the 'disordered' region

Full DYNC2I1 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

short-rib thoracic dysplasia 8 with or without polydactyly — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

DYNC2I1 p.Arg228Ter Pathogenic/Likely pathogenic ★★ same condition
DYNC2I1 p.Arg441Ter Pathogenic/Likely pathogenic ★★ same condition
DYNC2I1 p.Arg642Ter Pathogenic/Likely pathogenic ★★ same condition
DYNC2I1 p.Arg762Ter Pathogenic ★★ same condition
DYNC2I1 p.Ala157Val Uncertain significance ★★ ⚠ same condition
DYNC2I1 p.Ala609Val Uncertain significance ★★ ⚠ same condition
DYNC2I1 p.Ala800Thr Uncertain significance ★★ ⚠ same condition
DYNC2I1 p.Ala822Thr 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/dync2i1-p-ser292 (accessed [today's date]).

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