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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 25

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HGVS	dbSNP	gnomAD frequency
NM_004448.4(ERBB2):c.2570A>G (p.Asn857Ser)	rs28933370	0.00001
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.2313_2324dup (p.Tyr772_Ala775dup)	rs397516975
NM_004448.4(ERBB2):c.2314_2325dup (p.Tyr772_Ala775dup)	rs397516977
NM_004448.4(ERBB2):c.2320del (p.Met774fs)	rs397516978
NM_004448.4(ERBB2):c.2324_2325insCTCCGTGATGGC (p.Ala775_Gly776insSerValMetAla)	rs397516976
NM_004448.4(ERBB2):c.2325_2326insTCCGTGATGGCT (p.Ala775_Gly776insSerValMetAla)	rs1555618025
NM_004448.4(ERBB2):c.2326G>A (p.Gly776Ser)	rs28933369
NM_004448.4(ERBB2):c.2326_2327insTGT (p.Gly776delinsValCys)	rs397516979
NM_004448.4(ERBB2):c.2326_2327insTTT (p.Gly776delinsValCys)	rs397516979
NM_004448.4(ERBB2):c.2326delinsTTAT (p.Gly776delinsLeuCys)	rs397516980
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.2332_2340dup (p.Gly778_Pro780dup)	rs397516982
NM_004448.4(ERBB2):c.2524G>A (p.Val842Ile)	rs1057519738
NM_004448.4(ERBB2):c.926G>A (p.Gly309Glu)	rs1057519787
NM_004448.4(ERBB2):c.929C>A (p.Ser310Tyr)	rs1057519816
NM_004448.4(ERBB2):c.929C>T (p.Ser310Phe)	rs1057519816

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