Annotation Detail
Information
- Associated Genes
- LAMB3
- Associated Variants
-
LAMB3 p.Ser708= (p.S708=)
(
ENST00000356082.9,
ENST00000391911.5,
ENST00000367030.7 )
LAMB3 p.Ser708= (p.S708=) ( ENST00000356082.9, ENST00000367030.7, ENST00000391911.5 ) - Associated Disease
- amelogenesis imperfecta type 1A
- Source Database
- ClinVar
- Description
- NM_000228.3(LAMB3):c.2124T>C (p.Ser708=) AND Amelogenesis imperfecta type 1A
- ClinVar Allele ID
- 279994
- ClinVar RefSeq Alternation Syntax
- NM_000228.3:c.2124T>C
- ClinVar RefSeq Alternation Syntax
- NM_001127641.1:c.2124T>C
- ClinVar RefSeq Alternation Syntax
- NM_001017402.2:c.2124T>C
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2021-07-08
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001537658
- ClinVar Disease
- Amelogenesis imperfecta type 1A
- Observed Origin Sample
- germline
Drugs