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DHDDS p.Pro200=

c.600T>C · rs2524686271 · VCV2100206

Likely benign Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Absent
absent from gnomAD v4.1
Conditions
1
retinitis pigmentosa 59

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Splicing
SpliceAI<0.2all four deltas below 0.2 · T>A here scores Δ0.42 · evaluated, not missing
Constraint at this position
ConservationphyloP -10GERP -4
Overall
CADD2.115PHRED · no single calibrated threshold — expert panels disagree

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
DHDDS
Protein
p.Pro200=
Coding
c.600T>C
MANE Select
NM_205861
dbSNP
rs2524686271
Type
single nucleotide variant
Location
chr1:26457848 (GRCh38)
Gene constraint
LOEUF 0.536 · pLI 0.91 (gnomAD)
Structure
AlphaFold pLDDT 95.01 · 9 PDB
Residue 200
a UniProt-annotated variant site (in rp59; in a patient with congenital disorder of glycosylation); an α-helix
Full DHDDS gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Similar variants

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/dhdds-p-pro200 (accessed [today's date]).

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