Annotation Detail
Information
- Associated Genes
- RET
- Associated Variants
-
RET p.Thr170Ile (p.T170I)
(
ENST00000638465.2,
ENST00000683278.2,
ENST00000640619.2,
ENST00000340058.6,
ENST00000713926.1,
ENST00000355710.8,
ENST00000684216.2,
ENST00000615310.5 )
RET p.Thr170Ile (p.T170I) ( ENST00000340058.6, ENST00000355710.8, ENST00000615310.5, ENST00000638465.2, ENST00000640619.2, ENST00000683278.2, ENST00000684216.2, ENST00000713926.1 ) - Associated Disease
- Hereditary cancer-predisposing syndrome
- Source Database
- ClinVar
- Description
- NM_020975.6(RET):c.509C>T (p.Thr170Ile) AND Hereditary cancer-predisposing syndrome
- ClinVar Allele ID
- 50283
- ClinVar RefSeq Alternation Syntax
- NM_001406764.1:c.380C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406768.1:c.380C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406774.1:c.380C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406785.1:c.509C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406772.1:c.509C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406782.1:c.509C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406761.1:c.380C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406779.1:c.509C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406781.1:c.509C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406759.1:c.509C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406769.1:c.509C>T
- ClinVar RefSeq Alternation Syntax
- NM_020975.6:c.509C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406762.1:c.380C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406765.1:c.509C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406771.1:c.509C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406760.1:c.509C>T
- ClinVar RefSeq Alternation Syntax
- NM_020629.2:c.509C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406787.1:c.509C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406780.1:c.509C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406786.1:c.380C>T
- ClinVar RefSeq Alternation Syntax
- NM_020630.7:c.509C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406783.1:c.380C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406743.1:c.509C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406744.1:c.509C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406763.1:c.509C>T
- ClinVar RefSeq Alternation Syntax
- NM_001406773.1:c.509C>T
- ClinVar RefSeq Alternation Syntax
- NM_000323.2:c.509C>T
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2024-02-28
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001023532
- ClinVar Disease
- Hereditary cancer-predisposing syndrome
- Observed Origin Sample
- germline
Drugs