Annotation Detail
Information
- Associated Genes
- FGFR3
- Associated Variants
-
FGFR3 p.Lys652Thr (p.K652T)
(
ENST00000340107.9,
ENST00000352904.6,
ENST00000412135.7,
ENST00000440486.8,
ENST00000481110.7 )
FGFR3 p.Lys652Thr (p.K652T) ( ENST00000340107.9, ENST00000352904.6, ENST00000412135.7, ENST00000440486.8, ENST00000481110.7 ) - Associated Disease
- FGFR3-related disorder
- Source Database
- ClinVar
- Description
- NM_000142.5(FGFR3):c.1949A>C (p.Lys650Thr) AND FGFR3-related disorder
- ClinVar Allele ID
- 76763
- ClinVar RefSeq Alternation Syntax
- NM_001354810.2:c.1952A>C
- ClinVar RefSeq Alternation Syntax
- NM_001354809.2:c.1952A>C
- ClinVar RefSeq Alternation Syntax
- NM_001163213.2:c.1955A>C
- ClinVar RefSeq Alternation Syntax
- NM_022965.4:c.1613A>C
- ClinVar RefSeq Alternation Syntax
- NR_148971.2:n.2375A>C
- ClinVar RefSeq Alternation Syntax
- NM_000142.5:c.1949A>C
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2023-08-16
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001254893
- ClinVar Disease
- FGFR3-related disorder
- Observed Origin Sample
- germline
Drugs