AHNAK2 p.Asp1801=
c.5403C>T · rs200413532 · VCV2644798
Benign
Single submitter
Classification
Benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
rare (popmax 0.198%, afr)
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 -0.89 | GERP -0.55, phastCons 0.004 |
| Overall | ||
| CADD | 0.064 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
0.198%
African / African-American · 140/70,784 alleles
Filtering AF
0.171%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 0.161%
Overall
0.0175%
277/1,583,168 alleles · rare
exomes 177/1,438,552 · genomes 100/144,616 · joint denominator
| Ancestry group | Frequency | 1 in |
|---|---|---|
| African / African-Americangrpmax | 0.198% | 506 |
| Admixed American | 0.089% | 1,124 |
| East Asian | 0.034% | 2,939 |
| Middle Eastern | 0.0333% | 3,005 |
| Remaining individualsnot grpmax-eligible | 0.0244% | 4,100 |
| South Asian | 0.0157% | 6,376 |
| Ashkenazi Jewishnot grpmax-eligible | 0.00687% | 14,565 |
| European (non-Finnish) | 0.00318% | 31,410 |
| Finnishnot grpmax-eligible | 0.00161% | 62,006 |
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
- AHNAK2
- Protein
- p.Asp1801=
- Coding
- c.5403C>T
- MANE Select
- NM_138420
- dbSNP
- rs200413532
- Type
- single nucleotide variant
- Location
- chr14:104950048 (GRCh38)
- Gene constraint
- LOEUF 0.917 · pLI <0.01 (gnomAD)
Similar variants
- AHNAK2 p.Asp1801Glu Likely benign ★ same residue
- AHNAK2 p.Glu3598Lys Uncertain significance ★★ ⚠ same type
- AHNAK2 p.Gly4376Ser Uncertain significance ★★ ⚠ same type
- AHNAK2 p.Lys2479Arg Uncertain significance ★★ ⚠ same type
- AHNAK2 p.Lys3309Asn Uncertain significance ★★ ⚠ same type
- AHNAK2 p.Val1351Met Uncertain significance ★★ ⚠ same type
- AHNAK2 p.Ala1115Val Benign/Likely benign ★★ same type
- AHNAK2 p.Ala1323Thr Likely benign ★★ same type
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/ahnak2-p-asp1801 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown