Annotation Detail
Information
- Associated Genes
- RET
- Associated Variants
-
RET p.Arg959Trp (p.R959W)
(
ENST00000340058.6,
ENST00000355710.8,
ENST00000615310.5,
ENST00000713926.1 )
RET p.Arg959Trp (p.R959W) ( ENST00000340058.6, ENST00000355710.8, ENST00000615310.5, ENST00000713926.1 ) - Associated Disease
- Hereditary cancer-predisposing syndrome
- Source Database
- ClinVar
- Description
- NM_020975.6(RET):c.2875C>T (p.Arg959Trp) AND Hereditary cancer-predisposing syndrome
- ClinVar Allele ID
- 138919
- ClinVar RefSeq Alternation Syntax
- NM_001406770.1:c.2587C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406768.1:c.2611C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406776.1:c.2149C>T
- ClinVar RefSeq Alternation Syntax
- NM_020975.6:c.2875C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406781.1:c.1978C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406759.1:c.2875C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406777.1:c.2149C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406778.1:c.2149C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406780.1:c.1978C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406773.1:c.2437C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406787.1:c.1843C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406766.1:c.2587C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406767.1:c.2587C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406783.1:c.1849C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406790.1:c.1690C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406760.1:c.2875C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406774.1:c.2350C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406763.1:c.2740C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406786.1:c.1849C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406771.1:c.2437C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406772.1:c.2479C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406765.1:c.2740C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406764.1:c.2746C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406785.1:c.1858C>T
- ClinVar RefSeq Alternation Syntax
- NM_001355216.2:c.2113C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406784.1:c.1885C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406788.1:c.1690C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406791.1:c.1570C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406779.1:c.1978C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406761.1:c.2746C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406793.1:c.1426C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406762.1:c.2746C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406794.1:c.1426C>T
- ClinVar RefSeq Alternation Syntax
- NM_020630.7:c.2875C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406782.1:c.1978C>T
- ClinVar RefSeq Alternation Syntax
- NM_000323.2:c.2875C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406792.1:c.1426C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406789.1:c.1690C>T
- ClinVar RefSeq Alternation Syntax
- NM_020629.2:c.2875C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406743.1:c.2875C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406769.1:c.2479C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406744.1:c.2875C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406775.1:c.2149C>T
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2023-08-30
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002433615
- ClinVar Disease
- Hereditary cancer-predisposing syndrome
- Observed Origin Sample
- germline
Drugs