Is ADA p.Val205del (c.613_615del) pathogenic?

ADA p.Val205del (c.613615del) is classified Uncertain significance in ADA (ClinVar, Single submitter, 1 submitter). Very rare (popmax 0.000254%, nfe); Associated with severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency.

How common is ADA p.Val205del (c.613_615del) in the general population?

ADA p.Val205del (c.613_615del) is very rare (popmax 0.000254%, nfe) (gnomAD).

ADA p.Val205del

Q: What condition is associated with ADA p.Val205del (c.613_615del)?

ADA p.Val205del (c.613_615del) is associated with severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency (ClinVar).

Q: How is Severe combined immunodeficiency due to adenosine deaminase deficiency inherited?

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

c.613_615del · rs773067514 · VCV2627487

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Rare

very rare (popmax 0.000254%, nfe)

Conditions

severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Splicing
SpliceAI	—	not assessed · substitutions only
Constraint at this position
Conservation	phyloP 1.5	GERP 1.5, phastCons 0.82

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.000254% European (non-Finnish) · 3/1,179,924 alleles

Filtering AF 6.8e-05% ClinGen BA1/BS1 input FAF95, joint · FAF99 1.9e-05%

Overall 0.000205% 3/1,461,724 alleles · very rare

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: ADA
Protein: p.Val205del
Coding: c.613_615del
MANE Select: NM_000022
dbSNP: rs773067514
Type: Deletion
Location: chr20:44623070 (GRCh38)
Gene constraint: LOEUF 1.184 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 96.81 · 2 PDB
Residue 205: an α-helix

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

Disease context

severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

For Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet):

Inheritance: Autosomal recessive
Onset: Infancy, Neonatal
Prevalence: 1-9 / 1 000 000 (Europe)

Similar variants

ADA p.Val177_Val178insTer Pathogenic ★★★ same condition
ADA c.976-1_979del Pathogenic/Likely pathogenic ★★ same condition
ADA p.Arg324fs Pathogenic ★★ same condition
ADA p.Asp123fs Pathogenic/Likely pathogenic ★★ same condition
ADA p.Glu319fs Pathogenic ★★ same condition
ADA p.Gly136fs Likely pathogenic ★★ same condition
ADA p.Leu137fs Likely pathogenic ★★ same condition
ADA p.Leu236fs 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/ada-p-val205del (accessed [today's date]).

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