Is CC2D2A p.Leu119= (c.355T>C) pathogenic?

CC2D2A p.Leu119= (c.355T>C) is classified Conflicting classifications of pathogenicity in CC2D2A (ClinVar, Conflicting submitters, 10 submitters; last evaluated 2026-02-03). Rare (popmax 0.108%, nfe); Associated with Meckel syndrome.

What condition is associated with CC2D2A p.Leu119= (c.355T>C)?

CC2D2A p.Leu119= (c.355T>C) is associated with Meckel syndrome, Meckel syndrome, type 6, Joubert syndrome 9 (ClinVar).

How common is CC2D2A p.Leu119= (c.355T>C) in the general population?

CC2D2A p.Leu119= (c.355T>C) is rare (popmax 0.108%, nfe) (gnomAD).

CC2D2A p.Leu119=

c.355T>C · rs202150325 · VCV198452

Conflicting classifications of pathogenicity Conflicting submitters

Classification

Conflicting classifications of pathogenicity

ClinVar

Review

Conflicting submitters ★☆☆☆

ClinVar · 10 submitters

gnomAD v4.1

Rare

rare (popmax 0.108%, nfe)

Conditions

Meckel syndrome

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP -0.26	GERP -3.7
Overall
CADD	6.144	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.108% European (non-Finnish) · 1,275/1,178,702 alleles

Filtering AF 0.103% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.101%

Overall 0.0835% 1,345/1,610,964 alleles · rare exomes 1,260/1,458,640 · genomes 85/152,324 · joint denominator

Ancestry group	Frequency	1 in
European (non-Finnish)grpmax	0.108%	924
Remaining individualsnot grpmax-eligible	0.0449%	2,229
African / African-American	0.0293%	3,407
Admixed American	0.0251%	3,976
Middle Eastern	0.0165%	6,058
Finnishnot grpmax-eligible	0.0047%	21,287
Ashkenazi Jewishnot grpmax-eligible	0.00339%	29,488

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: CC2D2A
Protein: p.Leu119=
Coding: c.355T>C
MANE Select: NM_001378615
dbSNP: rs202150325
Type: single nucleotide variant
Location: chr4:15502840 (GRCh38)
Gene constraint: LOEUF 0.854 · pLI <0.01 · ClinGen HI gene assoc. with recessive phenotype (gnomAD)
Structure: AlphaFold pLDDT 69.46
Residue 119: the 'disordered' region

Full CC2D2A gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

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

Also linked: Meckel syndrome, type 6 Joubert syndrome 9 Joubert syndrome

Similar variants

CC2D2A p.Leu119Ter Pathogenic ★ same residue
CC2D2A p.Leu119Phe Uncertain significance ★ ⚠ same residue
CC2D2A c.1017+1G>A Pathogenic/Likely pathogenic ★★ same condition
CC2D2A c.1149+1G>A Pathogenic/Likely pathogenic ★★ same condition
CC2D2A c.123+2T>G Likely pathogenic ★★ same condition
CC2D2A c.1359+1G>A Pathogenic/Likely pathogenic ★★ same condition
CC2D2A c.1359+1G>C Likely pathogenic ★★ same condition
CC2D2A c.1466+1G>A 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/cc2d2a-p-leu119 (accessed [today's date]).

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