Variant
FLNC A1186V
NM_001458.5(FLNC):c.3557C>T (p.Ala1186Val)
- p.Ala1186Val
- p.A1186V
- rs1114167361
- ClinVar classification
- Pathogenic
- Review status
- 2 stars out of 4criteria provided, multiple submitters, no conflicts
- Last evaluated
- 19 December 2025
Data current to ClinVar release 2026-10-12 · Dante Labs data release 2026.10.16-c6eea6bfFacts last changed 16 October 2026
Summary
A1186V is a missense variant in FLNC: it changes a single amino acid in the protein the gene encodes. ClinVar classifies it as pathogenic for distal myopathy with posterior leg and anterior hand involvement (criteria provided, multiple submitters, no conflicts). ClinVar also lists it under 2 more conditions.
ClinVar classifications
| Condition | Classification | Review status | Submissions | Last evaluated |
|---|---|---|---|---|
| distal myopathy with posterior leg and anterior hand involvementClinVar VCV000427928 (opens in a new tab) | Pathogenic | 2 stars out of 4criteria provided, multiple submitters, no conflicts | 3 submissions | 19 December 2025 |
| hypertrophic cardiomyopathy 26ClinVar VCV000427928 (opens in a new tab) | Pathogenic/likely pathogenic | 2 stars out of 4criteria provided, multiple submitters, no conflicts | 4 submissions | 30 March 2025 |
| myofibrillar myopathy 5ClinVar VCV000427928 (opens in a new tab) | Pathogenic | 2 stars out of 4criteria provided, multiple submitters, no conflicts | 4 submissions | 30 March 2025 |
Classifications as ClinVar records them in release 2026-10-12. ClinVar updates them as evidence is reviewed.
Where it lies in FLNC
A1186V lies in exon 21 of the 48 in FLNC's MANE Select transcript, NM_001458.5.
Molecular details
| Gene | FLNC |
|---|---|
| Transcript | NM_001458.5MANE Select |
| Coding DNA change (HGVS c.) | c.3557C>T |
| Protein change (HGVS p.) | p.Ala1186Valp.A1186V |
| Predicted consequence | Missensemissense_variant (opens in a new tab) |
| Predicted impact | Moderate |
| Position (GRCh38) | chr7:128845022 C>T |
| Position (GRCh37) | chr7:128485076 C>T |
| dbSNP ID | rs1114167361 (opens in a new tab) |
| ClinVar Variation ID | VCV000427928 (opens in a new tab) |
| ClinVar Allele ID | 419002 |
| ClinGen Allele Registry ID | CA369197234 (opens in a new tab) |
| ClinVar name | NM_001458.5(FLNC):c.3557C>T (p.Ala1186Val) |
FLNC A1186V in other databases
Reports that look at this variant (3)
These Genome Test condition reports include A1186V among the variants they look at.
| Report | Conditions | Inheritance |
|---|---|---|
| Distal Myopathies | Distal myopathy | |
| Hypertrophic Cardiomyopathy | Hypertrophic Cardiomyopathy | Autosomal dominant |
| Myofibrillar Myopathies | Myofibrillar myopathy |
Other variants in FLNC
- A193TPathogenic2 stars out of 4
- c.970-4A>GPathogenic2 stars out of 4
- c.2550+2T>CPathogenic/likely pathogenic2 stars out of 4
- c.3193-2A>GLikely pathogenic2 stars out of 4
- c.3791-1G>CPathogenic/likely pathogenic2 stars out of 4
- c.5199+1G>TPathogenic/likely pathogenic2 stars out of 4
- c.6727+1G>ALikely pathogenic2 stars out of 4
- D1061Ifs*17Pathogenic2 stars out of 4
- F298Wfs*48Pathogenic/likely pathogenic2 stars out of 4
- F2165Sfs*10Pathogenic/likely pathogenic2 stars out of 4
Limitations
This page describes publicly available information about a genetic variant. It is not a diagnosis, and it says nothing about whether you or anyone else carries this variant.
Classifications come from ClinVar and change as new evidence is reviewed. A classification here may differ from the one in ClinVar today, or from the one a laboratory reports.
Whole genome sequencing with short reads can miss or miscall some variants, particularly in repeated or highly similar stretches of DNA and in large insertions, deletions or rearrangements.
If you have questions about a variant in your own results or in your family, talk to a genetic counsellor or your doctor.
Sources & credits
- Classifications from ClinVar (release 2026-10-12), National Center for Biotechnology Information.
- Condition terms from the Mondo Disease Ontology (release 2026-10-06), used under CC BY 4.0.
- Gene symbols and names from the HUGO Gene Nomenclature Committee (release 2026-10-16).
- Allele identifiers from the ClinGen Allele Registry (release 2026-10-16-c4908f54).
- Reference SNP identifiers from dbSNP (release b157), National Center for Biotechnology Information.
- Gene–disease links from the Gene Curation Coalition, GenCC (release 2026-10-16).
- Difficult regions from the Genome in a Bottle Consortium (release v3.6).
- Transcripts from MANE (release v1.5), NCBI and EMBL-EBI.
- Predicted consequences from mehari (release 0.11.0), with transcript models from cdot.
- Built from Dante Labs data release 2026.10.16-c6eea6bf of 16 October 2026.
Cite this page
Dante Labs. (16 October 2026). FLNC A1186V (c.3557C>T, rs1114167361) (Version 2026.10.16-c6eea6bf). Retrieved 17 October 2026, from https://dantelabs.com/genes/flnc/variants/a1186v
Dante Labs. FLNC A1186V (c.3557C>T, rs1114167361) [Internet]. Version 2026.10.16-c6eea6bf. 16 October 2026 [cited 17 October 2026]. Available from: https://dantelabs.com/genes/flnc/variants/a1186v
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