Is F9 p.Asn38= (c.114C>T) pathogenic?

F9 p.Asn38= (c.114C>T) is classified Benign in F9 (ClinVar, Single submitter, 2 submitters; last evaluated 2024-02-07). Ultra-rare (popmax 0.0592%, sas); Associated with thrombophilia, X-linked, due to factor 9 defect.

What condition is associated with F9 p.Asn38= (c.114C>T)?

F9 p.Asn38= (c.114C>T) is associated with thrombophilia, X-linked, due to factor 9 defect, hemophilia B (ClinVar).

How common is F9 p.Asn38= (c.114C>T) in the general population?

F9 p.Asn38= (c.114C>T) is ultra-rare (popmax 0.0592%, sas) (gnomAD).

F9 p.Asn38=

c.114C>T · rs745353370 · VCV700669

Benign Single submitter

Classification

Benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 2 submitters

gnomAD v4.1

Rare

ultra-rare (popmax 0.0592%, sas)

Conditions

thrombophilia, X-linked, due to factor 9 defect

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 1.1	GERP 0.75, phastCons 0.99
Overall
CADD	6.712	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.0592% South Asian · 33/55,698 alleles

Filtering AF 0.0433% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.0379%

Overall 0.0039% 47/1,206,508 alleles · ultra-rare exomes 45/1,094,313 · genomes 2/112,195 · joint denominator

Ancestry group	Frequency	1 in
South Asiangrpmax	0.0592%	1,688
Remaining individualsnot grpmax-eligible	0.0211%	4,748
Admixed American	0.00219%	45,581
European (non-Finnish)	0.000336%	297,793

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: F9
Protein: p.Asn38=
Coding: c.114C>T
MANE Select: NM_000133
dbSNP: rs745353370
Type: single nucleotide variant
Location: chrX:139537035 (GRCh38)
Structure: AlphaFold pLDDT 80.45 · 57 PDB

Full F9 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

thrombophilia, X-linked, due to factor 9 defect — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Also linked: hemophilia B

Similar variants

F9 c.520+13A>G Pathogenic ★★★ same condition
F9 c.88+1G>A Pathogenic ★★★ same condition
F9 c.88+5G>T Likely pathogenic ★★★ same condition
F9 p.Ala279Thr Pathogenic ★★★ ⚠ same condition
F9 p.Ala337Pro Likely pathogenic ★★★ same condition
F9 p.Ala337Thr Pathogenic ★★★ ⚠ same condition
F9 p.Ala337Val Pathogenic ★★★ ⚠ same condition
F9 p.Arg191His 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/f9-p-asn38 (accessed [today's date]).

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