ClinVar Miner

List of variants in gene ERBB2 reported as likely pathogenic for digestive system cancer

Included ClinVar conditions (140):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 14
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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.2326G>A (p.Gly776Ser) rs28933369
NM_004448.4(ERBB2):c.2329G>A (p.Val777Met) rs121913471
NM_004448.4(ERBB2):c.2329G>T (p.Val777Leu) rs121913471
NM_004448.4(ERBB2):c.2524G>A (p.Val842Ile) rs1057519738
NM_004448.4(ERBB2):c.929C>A (p.Ser310Tyr) rs1057519816
NM_004448.4(ERBB2):c.929C>T (p.Ser310Phe) rs1057519816

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