"Invitae"[submitter] AND "HSPA4"[gene] - ClinVar

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Search results

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 725437	NM_002154.4(HSPA4):c.96C>T (p.Asp32=)	HSPA4	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 709819	NM_002154.4(HSPA4):c.453A>G (p.Ala151=)	HSPA4	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 747592	NM_002154.4(HSPA4):c.528A>G (p.Ala176=)	HSPA4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 769307	NM_002154.4(HSPA4):c.594A>C (p.Val198=)	HSPA4	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 783445	NM_002154.4(HSPA4):c.664-4T>A	HSPA4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 714996	NM_002154.4(HSPA4):c.826T>C (p.Leu276=)	HSPA4	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 770722	NM_002154.4(HSPA4):c.1651-10A>G	HSPA4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 770356	NM_002154.4(HSPA4):c.1946C>G (p.Thr649Ser)	HSPA4 (T649S)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 784628	NM_002154.4(HSPA4):c.2086C>T (p.Pro696Ser)	HSPA4 (P696S)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 457359	NC_000005.9:g.(?_86400000)_(154000000_?)del	ARAP3, CCDC69 +385 more	Deletion	Hereditary cancer-predisposing syndrome +1 more	GPathogenic