ClinVar Genomic variation as it relates to human health
NM_170707.4(LMNA):c.1279C>T (p.Arg427Cys)
Germline
Classification
(10)
Uncertain significance
criteria provided, multiple submitters, no conflicts
Somatic
No data submitted for somatic clinical impact
Somatic
No data submitted for oncogenicity
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation | Variation Viewer | Related variants | ||
---|---|---|---|---|---|---|
HI score | TS score | Within gene | All | |||
LMNA | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
1810 | 2087 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (2) |
|
Jun 30, 2023 | RCV000182369.9 | |
Uncertain significance (1) |
|
Dec 6, 2023 | RCV000653931.10 | |
Uncertain significance (1) |
|
Jan 16, 2024 | RCV001181813.4 | |
Likely pathogenic (1) |
|
- | RCV002463440.1 | |
Uncertain significance (1) |
|
Sep 28, 2021 | RCV002381591.1 | |
Uncertain significance (1) |
|
Jul 20, 2021 | RCV002492808.1 | |
Uncertain significance (1) |
|
Nov 27, 2023 | RCV003479048.1 | |
Uncertain significance (1) |
|
Sep 5, 2023 | RCV003996715.1 | |
Uncertain significance (1) |
|
Jan 9, 2024 | RCV003967449.1 |
Citations for germline classification of this variant
HelpText-mined citations for rs373584456 ...
HelpThese citations are identified by LitVar using
the rs number, so they may include citations for more than one variant
at this location. Please review the LitVar results carefully for your
variant of interest.
Record last updated Apr 20, 2024