Annotation Detail
Information
- Associated Genes
- KIT
- Associated Variants
-
KIT p.Ala503_Tyr504dup (p.A503_Y504dup)
(
ENST00000288135.6,
ENST00000412167.7,
ENST00000686011.1,
ENST00000687109.1,
ENST00000687246.1,
ENST00000687295.1,
ENST00000689832.1,
ENST00000689994.1,
ENST00000690543.1,
ENST00000692783.1 )
KIT p.Ala503_Tyr504dup (p.A503_Y504dup) ( ENST00000690543.1, ENST00000692783.1, ENST00000412167.7, ENST00000686011.1, ENST00000687109.1, ENST00000687246.1, ENST00000687295.1, ENST00000689832.1, ENST00000689994.1, ENST00000288135.6 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000222.3(KIT):c.1504_1509dup (p.Tyr503_Phe504insAlaTyr) AND not provided
- ClinVar Allele ID
- 2741746
- ClinVar RefSeq Alternation Syntax
- NM_001385288.1:c.1507_1512dup
- ClinVar RefSeq Alternation Syntax
- NM_001093772.2:c.1504_1509dup
- ClinVar RefSeq Alternation Syntax
- NM_001385284.1:c.1507_1512dup
- ClinVar RefSeq Alternation Syntax
- NM_001385286.1:c.1504_1509dup
- ClinVar RefSeq Alternation Syntax
- NM_001385292.1:c.1507_1512dup
- ClinVar RefSeq Alternation Syntax
- NM_000222.3:c.1504_1509dup
- ClinVar RefSeq Alternation Syntax
- NM_001385285.1:c.1504_1509dup
- ClinVar RefSeq Alternation Syntax
- NM_001385290.1:c.1507_1512dup
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2023-02-15
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003323154
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs