Annotation Detail

Information
Associated Genes
LITAF
Associated Variants
LITAF p.Gly112Ser (p.G112S) ( ENST00000413364.6, ENST00000572255.5, ENST00000570904.5, ENST00000339430.9, ENST00000622633.5, ENST00000571459.5, ENST00000571976.1, ENST00000576036.5, ENST00000571688.5, ENST00000574763.5 )
LITAF p.Gly112Ser (p.G112S) ( ENST00000339430.9, ENST00000413364.6, ENST00000570904.5, ENST00000571459.5, ENST00000571688.5, ENST00000571976.1, 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.334G>A (p.Gly112Ser) AND Charcot-Marie-Tooth disease type 1C
ClinVar Allele ID
21096
ClinVar RefSeq Alternation Syntax
NM_001136473.1:c.334G>A
ClinVar RefSeq Alternation Syntax
NM_004862.4:c.334G>A
ClinVar RefSeq Alternation Syntax
NR_024320.2:n.468G>A
ClinVar RefSeq Alternation Syntax
NM_001136472.2:c.334G>A
Clinical Significance Description
Pathogenic
Clinical Significance Last Update
2024-01-31
Clinical Significance Review Status
criteria provided, multiple submitters, no conflicts
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000006429
ClinVar Disease
Charcot-Marie-Tooth disease type 1C
Observed Origin Sample
germline
Observed Origin Sample
unknown
Pubmed
1407588
Pubmed
15786462
Pubmed
2239969
Pubmed
15776429
Pubmed
12525712
Drugs