Annotation Detail

Information
Associated Genes
KIT
Associated Variants
KIT p.Asp817Val (p.D817V) ( ENST00000288135.6, ENST00000412167.7, ENST00000686011.1, ENST00000687109.1, ENST00000687246.1, ENST00000687295.1, ENST00000689832.1, ENST00000689994.1, ENST00000690543.1, ENST00000692783.1 )
KIT p.Asp817Val (p.D817V) ( ENST00000686011.1, ENST00000687109.1, ENST00000288135.6, ENST00000412167.7, ENST00000687246.1, ENST00000687295.1, ENST00000689832.1, ENST00000689994.1, ENST00000690543.1, ENST00000692783.1 )
Associated Disease
MAST CELL LEUKEMIA, SOMATIC
Source Database
ClinVar
Description
NM_000222.3(KIT):c.2447A>T (p.Asp816Val) AND MAST CELL LEUKEMIA, SOMATIC
ClinVar Allele ID
28891
ClinVar RefSeq Alternation Syntax
NM_001385284.1:c.2450A>T
ClinVar RefSeq Alternation Syntax
NM_001385290.1:c.2447A>T
ClinVar RefSeq Alternation Syntax
NM_001385286.1:c.2432A>T
ClinVar RefSeq Alternation Syntax
NM_001385292.1:c.2435A>T
ClinVar RefSeq Alternation Syntax
NM_001385288.1:c.2438A>T
ClinVar RefSeq Alternation Syntax
NM_001093772.2:c.2435A>T
ClinVar RefSeq Alternation Syntax
NM_000222.3:c.2447A>T
ClinVar RefSeq Alternation Syntax
NM_001385285.1:c.2444A>T
Clinical Significance Description
Pathogenic
Clinical Significance Last Update
2001-08-15
Clinical Significance Review Status
no assertion criteria provided
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000656673
ClinVar Disease
MAST CELL LEUKEMIA, SOMATIC
Observed Origin Sample
somatic
Pubmed
19262599
Pubmed
7479840
Pubmed
11380399
Pubmed
9990072
Pubmed
9827716
Pubmed
8589724
Pubmed
7691885
Pubmed
11493470
Pubmed
19865100
Drugs