Is FTCD p.Ala200= (c.600G>A) pathogenic?

FTCD p.Ala200= (c.600G>A) is classified Likely benign in FTCD (ClinVar, Single submitter, 2 submitters; last evaluated 2025-03-18). Rare (popmax 0.106%, sas); Associated with formiminoglutamic aciduria.

What condition is associated with FTCD p.Ala200= (c.600G>A)?

FTCD p.Ala200= (c.600G>A) is associated with formiminoglutamic aciduria (ClinVar).

How common is FTCD p.Ala200= (c.600G>A) in the general population?

FTCD p.Ala200= (c.600G>A) is rare (popmax 0.106%, sas) (gnomAD).

How is Formiminoglutamic aciduria inherited?

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

FTCD p.Ala200=

c.600G>A · rs147306849 · VCV2069773

Likely benign Single submitter

Classification

Likely benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 2 submitters

gnomAD v4.1

Rare

rare (popmax 0.106%, sas)

Conditions

formiminoglutamic aciduria

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 -0.025	GERP -2.4, phastCons 0.3
Overall
CADD	8.206	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.106% South Asian · 97/91,090 alleles

Filtering AF 0.0893% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.0829%

Overall 0.00893% 144/1,612,940 alleles · rare exomes 135/1,460,568 · genomes 9/152,372 · joint denominator

Ancestry group	Frequency	1 in
South Asiangrpmax	0.106%	939
Middle Eastern	0.033%	3,030
Admixed American	0.0233%	4,288
Remaining individualsnot grpmax-eligible	0.016%	6,249
European (non-Finnish)	0.00178%	56,187

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: FTCD
Protein: p.Ala200=
Coding: c.600G>A
MANE Select: NM_206965
dbSNP: rs147306849
Type: single nucleotide variant
Location: chr21:46151594 (GRCh38)
Gene constraint: LOEUF 1.61 · pLI <0.01 · ClinGen HI gene assoc. with recessive phenotype (gnomAD)
Structure: AlphaFold pLDDT 95.30
Residue 200: the 'formiminotransferase c-subdomain' region

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

Disease context

formiminoglutamic aciduria — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

For Formiminoglutamic aciduria (Orphanet):

Inheritance: Autosomal recessive
Onset: Childhood

Similar variants

FTCD p.Ala200Thr Uncertain significance ★ ⚠ same residue
FTCD p.Arg255Ter Pathogenic ★★ same condition
FTCD p.Arg71Ter Pathogenic/Likely pathogenic ★★ same condition
FTCD p.Leu536Ter Pathogenic/Likely pathogenic ★★ same condition
FTCD p.Ala108Thr Uncertain significance ★★ ⚠ same condition
FTCD p.Ala159Val Uncertain significance ★★ ⚠ same condition
FTCD p.Ala368Val Uncertain significance ★★ ⚠ same condition
FTCD p.Ala418Thr 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/ftcd-p-ala200 (accessed [today's date]).

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