Annotation Detail

Information
Associated Genes
TYK2
Associated Variants
TYK2 p.Pro1104Ala (p.P1104A) ( ENST00000524462.5, ENST00000525621.6, ENST00000525976.6, ENST00000531836.6, ENST00000699360.1, ENST00000699365.1 )
TYK2 p.Pro1104Ala (p.P1104A) ( ENST00000524462.5, ENST00000525621.6, ENST00000525976.6, ENST00000531836.6, ENST00000699360.1, ENST00000699365.1 )
Associated Disease
not provided
Source Database
ClinVar
Description
NM_003331.5(TYK2):c.3310C>G (p.Pro1104Ala) AND not provided
ClinVar Allele ID
141572
ClinVar RefSeq Alternation Syntax
NM_003331.5:c.3310C>G
Clinical Significance Description
Likely benign
Clinical Significance Review Status
no assertion criteria provided
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV001701518
ClinVar Disease
not provided
Observed Origin Sample
germline
Drugs