ClinVar Miner

List of variants in gene ERBB2 reported as likely pathogenic for bladder transitional cell carcinoma

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_004448.4(ERBB2):c.2033G>A (p.Arg678Gln) rs1057519862
NM_004448.4(ERBB2):c.2263T>A (p.Leu755Met) rs1057519890
NM_004448.4(ERBB2):c.2263_2264delinsCC (p.Leu755Pro) rs121913469
NM_004448.4(ERBB2):c.2264T>C (p.Leu755Ser) rs121913470
NM_004448.4(ERBB2):c.2264T>G (p.Leu755Trp) rs121913470
NM_004448.4(ERBB2):c.2305G>A (p.Asp769Asn) rs121913468
NM_004448.4(ERBB2):c.2305G>C (p.Asp769His) rs121913468
NM_004448.4(ERBB2):c.2305G>T (p.Asp769Tyr) rs121913468
NM_004448.4(ERBB2):c.929C>A (p.Ser310Tyr) rs1057519816
NM_004448.4(ERBB2):c.929C>T (p.Ser310Phe) rs1057519816

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.