Annotation Detail
Information
- Associated Genes
- PALB2
- Associated Variants
-
PALB2 c.3202-9C>T
(
ENST00000261584.9,
ENST00000568219.5,
ENST00000566069.6,
ENST00000561514.3,
ENST00000697374.1,
ENST00000697376.1,
ENST00000697377.2,
ENST00000697379.2,
ENST00000697383.1,
ENST00000713774.1 )
PALB2 c.3202-9C>T ( ENST00000261584.9, ENST00000561514.3, ENST00000566069.6, ENST00000568219.5, ENST00000697374.1, ENST00000697376.1, ENST00000697377.2, ENST00000697379.2, ENST00000697383.1, ENST00000713774.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_024675.4(PALB2):c.3202-9C>T AND not provided
- ClinVar Allele ID
- 213155
- ClinVar RefSeq Alternation Syntax
- NM_024675.4:c.3202-9C>T
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2018-05-23
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001711353
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs