"ITMI"[submitter] AND "ERBB2"[gene] - ClinVar

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Items: 32

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 135519	NM_001289936.2(ERBB2):c.22C>A (p.Pro8Thr)	ERBB2 (P8T)	Single nucleotide variant (missense variant +1 more)	not specified	Gnot provided
Select item 134067	NM_004448.4(ERBB2):c.43C>T (p.Leu15Phe)	ERBB2 (L15F)	Single nucleotide variant (missense variant +3 more)	not provided	GLikely benign
Select item 134076	NM_004448.4(ERBB2):c.93G>T (p.Met31Ile)	ERBB2 (M1I +2 more)	Single nucleotide variant (missense variant +3 more)	not provided	GLikely benign
Select item 134074	NM_004448.4(ERBB2):c.133A>G (p.Met45Val)	ERBB2 (M15V +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	Gnot provided
Select item 134075	NM_004448.4(ERBB2):c.140G>A (p.Arg47His)	ERBB2 (R17H +2 more)	Single nucleotide variant (missense variant +2 more)	not provided	GBenign
Select item 134087	NM_004448.4(ERBB2):c.236A>C (p.Glu79Ala)	ERBB2 (E49A +3 more)	Single nucleotide variant (missense variant +2 more)	not provided	GLikely benign
Select item 134088	NM_004448.4(ERBB2):c.383C>G (p.Pro128Arg)	ERBB2 (P128R +3 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 134090	NM_004448.4(ERBB2):c.428G>A (p.Arg143Gln)	ERBB2 (R113Q +3 more)	Single nucleotide variant (missense variant +2 more)	not provided	GBenign/Likely benign
Select item 134089	NM_004448.4(ERBB2):c.433C>T (p.Leu145Phe)	ERBB2 (L115F +3 more)	Single nucleotide variant (missense variant +2 more)	not provided	GLikely benign
Select item 134091	NM_004448.4(ERBB2):c.734C>T (p.Thr245Met)	ERBB2 (T215M +5 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 135520	NM_004448.4(ERBB2):c.1021+19C>T	ERBB2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 135521	NM_004448.4(ERBB2):c.1021+31C>T	ERBB2	Single nucleotide variant (intron variant)	not specified	Gnot provided
Select item 135522	NM_004448.4(ERBB2):c.1021+48C>T	ERBB2	Single nucleotide variant (intron variant)	not specified	Gnot provided
Select item 134068	NM_004448.4(ERBB2):c.1157C>A (p.Ala386Asp)	ERBB2 (A356D +8 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign/Likely benign
Select item 134069	NM_004448.4(ERBB2):c.1169C>T (p.Ala390Val)	ERBB2 (A360V +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	Gnot provided
Select item 134070	NM_004448.4(ERBB2):c.1231T>G (p.Tyr411Asp)	ERBB2 (Y381D +8 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 134072	NM_004448.4(ERBB2):c.1356G>T (p.Trp452Cys)	ERBB2 (W422C +9 more)	Single nucleotide variant (missense variant +2 more)	not provided	GBenign
Select item 134071	NM_004448.4(ERBB2):c.1466C>T (p.Pro489Leu)	ERBB2 (P459L +9 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 134073	NM_004448.4(ERBB2):c.1793C>A (p.Ala598Asp)	ERBB2 (A568D +12 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 13874	NM_004448.4(ERBB2):c.1960A>G (p.Ile654Val)	ERBB2 (I654V +13 more)	Single nucleotide variant (missense variant +2 more)	not provided	GBenign
Select item 13873	NM_004448.4(ERBB2):c.1963A>G (p.Ile655Val)	ERBB2 (I655V +13 more)	Single nucleotide variant (missense variant +2 more)	not provided	GBenign
Select item 134077	NM_004448.4(ERBB2):c.2440C>T (p.Arg814Cys)	ERBB2 (R784C +18 more)	Single nucleotide variant (missense variant +2 more)	not specified	Gnot provided
Select item 44994	NM_004448.4(ERBB2):c.2443G>A (p.Gly815Arg)	ERBB2 (G815R +18 more)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GBenign/Likely benign
Select item 134078	NM_004448.4(ERBB2):c.2790G>T (p.Glu930Asp)	ERBB2 (E900D +21 more)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GBenign/Likely benign
Select item 134079	NM_004448.4(ERBB2):c.3182T>C (p.Leu1061Pro)	ERBB2 (L1031P +23 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 134080	NM_004448.4(ERBB2):c.3427C>A (p.Pro1143Thr)	ERBB2 (P1113T +23 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 134081	NM_004448.4(ERBB2):c.3428C>T (p.Pro1143Leu)	ERBB2 (P1113L +23 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 134085	NM_004448.4(ERBB2):c.3482G>A (p.Arg1161Gln)	ERBB2 (R1131Q +23 more)	Single nucleotide variant (missense variant +2 more)	not provided	GBenign
Select item 134082	NM_004448.4(ERBB2):c.3508C>G (p.Pro1170Ala)	ERBB2 (P1140A +23 more)	Single nucleotide variant (missense variant +2 more)	not provided	GBenign
Select item 134083	NM_004448.4(ERBB2):c.3620C>T (p.Pro1207Leu)	ERBB2 (P1177L +23 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 134084	NM_004448.4(ERBB2):c.3647C>A (p.Ala1216Asp)	ERBB2 (A1186D +23 more)	Single nucleotide variant (missense variant +2 more)	not provided	GBenign/Likely benign
Select item 134086	NM_004448.4(ERBB2):c.3689G>T (p.Arg1230Leu)	ERBB2 (R1200L +23 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance

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Items: 32