SRCAP p.Glu180fs
c.539_540del · VCV4077671
Likely pathogenic
Single submitter
Classification
Likely pathogenic
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
Consequence
frameshift
predicted LoF
gnomAD v4.1
Rare
Computational evidence
| Protein change | ||
| Missense predictors do not apply to this variant type; conservation carries the signal. | ||
| Consequence | frameshift | predicted loss-of-function in a haploinsufficient gene (ClinGen) |
|---|---|---|
| NMD | predicted | premature termination codon in exon 6 of 34 |
| Splicing | ||
| SpliceAI | — | not assessed · substitutions only |
| Constraint at this position | ||
| Conservation | phyloP 11 | GERP 1.6, phastCons 1 |
Predicted loss-of-function is descriptive, not an applied PVS1 code.
Variant & gene context
- Gene
- SRCAP
- Protein
- p.Glu180fs
- Coding
- c.539_540del
- MANE Select
- NM_006662
- Type
- Microsatellite
- Location
- chr16:30707616 (GRCh38)
- Gene constraint
- LOEUF 0.223 · pLI 1.00 · ClinGen HI 3/3 (gnomAD)
- Residue 180
- the hsa domain; an α-helix
Similar variants
- SRCAP p.Gln2770del Uncertain significance ★★ same type
- SRCAP p.Glu3182del Uncertain significance ★★ same type
- SRCAP p.Pro2488del Uncertain significance ★★ same type
- SRCAP p.Ser2576del Uncertain significance ★★ same type
- SRCAP p.2992TVT[1] Benign/Likely benign ★★ same type
- SRCAP p.Glu2405fs Pathogenic ★ same type
- SRCAP p.Pro2426fs Pathogenic ★ same type
- SRCAP p.Pro2427fs Likely pathogenic ★ 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/srcap-p-glu180fs (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown