Annotation Detail
Information
- Associated Genes
- LITAF
- Associated Variants
-
LITAF p.Ala129Thr (p.A129T)
(
ENST00000571688.5,
ENST00000574763.5,
ENST00000576036.5,
ENST00000571459.5,
ENST00000413364.6,
ENST00000572255.5,
ENST00000570904.5,
ENST00000339430.9,
ENST00000622633.5 )
LITAF p.Ala129Thr (p.A129T) ( ENST00000339430.9, ENST00000413364.6, ENST00000570904.5, ENST00000571459.5, ENST00000571688.5, ENST00000572255.5, ENST00000574763.5, ENST00000576036.5, ENST00000622633.5 ) - Associated Disease
- Charcot-Marie-Tooth disease type 1C
- Source Database
- ClinVar
- Description
- NM_001136472.2(LITAF):c.385G>A (p.Ala129Thr) AND Charcot-Marie-Tooth disease type 1C
- ClinVar Allele ID
- 204477
- ClinVar RefSeq Alternation Syntax
- NM_001136473.1:c.*24G>A
- ClinVar RefSeq Alternation Syntax
- NM_001136472.2:c.385G>A
- ClinVar RefSeq Alternation Syntax
- NM_004862.4:c.385G>A
- ClinVar RefSeq Alternation Syntax
- NR_024320.2:n.519G>A
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2021-04-16
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000192669
- ClinVar Disease
- Charcot-Marie-Tooth disease type 1C
- Observed Origin Sample
- germline
Drugs