Is SEC23B p.Ser577Phe (c.1730C>T) pathogenic?

SEC23B p.Ser577Phe (c.1730C>T) is classified Uncertain significance in SEC23B (ClinVar, Single submitter, 1 submitter; last evaluated 2023-09-04). AlphaMissense: ambiguous (0.4585); Ultra-rare (popmax 0.0168%, mid); Associated with congenital dyserythropoietic anemia type 2.

What condition is associated with SEC23B p.Ser577Phe (c.1730C>T)?

SEC23B p.Ser577Phe (c.1730C>T) is associated with congenital dyserythropoietic anemia type 2 (ClinVar).

How common is SEC23B p.Ser577Phe (c.1730C>T) in the general population?

SEC23B p.Ser577Phe (c.1730C>T) is ultra-rare (popmax 0.0168%, mid) (gnomAD).

How is Congenital dyserythropoietic anemia type II inherited?

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

What do computational predictors say about SEC23B p.Ser577Phe (c.1730C>T)?

AlphaMissense predicts ambiguous (score 0.4585) — an in-silico prediction, not a clinical call.

SEC23B p.Ser577Phe

c.1730C>T · rs1182198296 · VCV3236788

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

ambiguous

0.4585 · ACMG-weighted

gnomAD v4.1

Rare

ultra-rare (popmax 0.0168%, mid)

Missense predictors

2/2 damaging

REVEL, SaProt · AlphaMissense indeterminate

Conditions

congenital dyserythropoietic anemia type 2

Computational evidence

Protein change
AlphaMissense	0.4585	ambiguous
REVEL	0.75	pathogenic-leaning
SaProt	LLR -13.16	damaging
⇒ REVEL and SaProt both call this damaging; AlphaMissense is indeterminate.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 7.7	GERP 2.8, phastCons 1
Regional constraint	o/e 0.93	unconstrained · MANE · 50 kb · p 0.036 · regional, not allelic
Overall
CADD	28.1	PHRED · no single calibrated threshold — expert panels disagree

AlphaMissense carries the ACMG weight for missense; REVEL and SaProt are independent agreement signals.

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.0168% Middle Eastern · 1/5,936 alleles

Overall 0.00013% 2/1,539,626 alleles · ultra-rare exomes 2/1,387,344 · genomes 0/152,282 · joint denominator

Ancestry group	Frequency	1 in
Middle Easterngrpmax	0.0168%	5,936
European (non-Finnish)	8.99e-05%	1,112,132

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: SEC23B
Protein: p.Ser577Phe
Coding: c.1730C>T
MANE Select: NM_006363
dbSNP: rs1182198296
Type: single nucleotide variant
Location: chr20:18546020 (GRCh38)
Gene constraint: LOEUF 1.008 · pLI <0.01 · ClinGen HI gene assoc. with recessive phenotype (gnomAD)
Structure: AlphaFold pLDDT 92.41
Residue 577: a UniProt-annotated variant site (in cdan2)

Full SEC23B gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

congenital dyserythropoietic anemia type 2 — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

For Congenital dyserythropoietic anemia type II (Orphanet):

Inheritance: Autosomal recessive
Onset: Adolescent, Adult, Childhood, Elderly, Infancy, Neonatal
Prevalence: <1 / 1 000 000 (Europe)

Similar variants

SEC23B c.1314+1G>A Likely pathogenic ★★ same condition
SEC23B c.835-2A>G Pathogenic/Likely pathogenic ★★ same condition
SEC23B p.Ala524Val Pathogenic/Likely pathogenic ★★ same condition
SEC23B p.Arg14Trp Pathogenic/Likely pathogenic ★★ same condition
SEC23B p.Arg264Ter Pathogenic ★★ same condition
SEC23B p.Arg313His Pathogenic/Likely pathogenic ★★ same condition
SEC23B p.Arg324Ter Pathogenic/Likely pathogenic ★★ same condition
SEC23B p.Arg339Ter 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/sec23b-p-ser577phe (accessed [today's date]).

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