ClinVar Pathogenicity of Variations help
93%5%2%10010090908080707060605050404030302020101000
Benign
Pathogenic
VUS
Download SVG
Download PNG
Download CSV

∙ Please click the name of species for the protein accession number used in the alignment.
∙ A p letter used as a pointer to positions of post translational modifications in human.
∙ Protein domains illustrated above belong to Homo sapiens (Human).
∙ ClinVar stacked bar chart represents whole protein isoforms of the gene. Please, check the other protein isoforms of the gene below.
∙ If more than one transcripts below are active (with blue background color), it means all the active transcripts have the same sequence.
ENST00000355867 ENST00000375398 ENST00000375400 ENST00000535393 ENST00000538146 NP_001310528 NP_001310529 You are here now! NP_003165 NP_068506


import_contactsClinVar Data

healinggnomAD
10010090908080707060605050404030302020101000

format_align_centerProtein Domains (PFAM)
Pfam Domain filter_list Domain Name filter_list Description filter_list Positions filter_list Clan filter_list Clan Name filter_list Organism filter_list
NO RESULT FOUND
NO DOMAINS EXIST

view_listList of the diseases from DisGeNET
Disease Name filter_list Disease Category filter_list DSI* filter_list DPI** filter_list
Leukemia, Myelocytic, Acute Neoplasms ; 0.857 0.103
Acute Myeloid Leukemia, M1 Neoplasms ; 0.857 0.103
Acute Myeloid Leukemia (AML-M2) Neoplasms ; 0.857 0.103
NO RESULT FOUND
feedback

Classification of Clinicial Significance of ClinVar Data
Send a feedback about the results.