INTS1 p.Pro378=
c.1134C>T · rs2289035 · VCV1232182
Benign
Multiple submitters
Classification
Benign
ClinVar
Review
Multiple submitters ★★☆☆
ClinVar · 2 submitters
gnomAD v4.1
Common
common (popmax 75.7%, eas) — too common for a highly-penetrant pathogenic allele
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 -0.074 | GERP -3.1, phastCons 0.24 |
| Overall | ||
| CADD | 8.939 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
75.7%
East Asian · 29,360/38,806 alleles
Filtering AF
74.9%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 74.6%
Overall
44.2%
636,362/1,439,494 alleles · common
exomes 575,181/1,305,224 · genomes 61,181/134,270 · joint denominator
| Ancestry group | Frequency | 1 in |
|---|---|---|
| East Asiangrpmax | 75.7% | 1 |
| Amishnot grpmax-eligible | 61% | 2 |
| Finnishnot grpmax-eligible | 53.9% | 2 |
| Middle Eastern | 50.5% | 2 |
| South Asian | 47.4% | 2 |
| Remaining individualsnot grpmax-eligible | 46% | 2 |
| African / African-American | 43.1% | 2 |
| European (non-Finnish) | 42.5% | 2 |
| Admixed American | 41.3% | 2 |
| Ashkenazi Jewishnot grpmax-eligible | 41.3% | 2 |
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
- INTS1
- Protein
- p.Pro378=
- Coding
- c.1134C>T
- MANE Select
- NM_001080453
- dbSNP
- rs2289035
- Type
- single nucleotide variant
- Location
- chr7:1498978 (GRCh38)
- Gene constraint
- LOEUF 0.785 · pLI <0.01 (gnomAD)
- Structure
- AlphaFold pLDDT 75.49 · 8 PDB
- Residue 378
- an α-helix
Similar variants
- INTS1 c.3430-2A>C Likely pathogenic ★★ same type
- INTS1 p.Arg101Ter Likely pathogenic ★★ same type
- INTS1 p.Glu182Ter Likely pathogenic ★★ same type
- INTS1 c.1283+5G>A Uncertain significance ★★ same type
- INTS1 c.2977-5C>T Uncertain significance ★★ same type
- INTS1 p.Ala1112Val Uncertain significance ★★ ⚠ same type
- INTS1 p.Ala1505Val Uncertain significance ★★ ⚠ same type
- INTS1 p.Ala1854Val Uncertain significance ★★ ⚠ 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/ints1-p-pro378 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown