"Ambry Genetics"[submitter] AND "HSF5"[gene] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3284893	NM_001080439.3(HSF5):c.1688A>G (p.His563Arg)	HSF5 (H563R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3107225	NM_001080439.3(HSF5):c.1676G>C (p.Arg559Thr)	HSF5 (R559T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107224	NM_001080439.3(HSF5):c.1576C>T (p.Arg526Cys)	HSF5 (R526C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455813	NM_001080439.3(HSF5):c.1539C>A (p.His513Gln)	HSF5 (H513Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621493	NM_001080439.3(HSF5):c.1252A>C (p.Ser418Arg)	HSF5 (S418R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273852	NM_001080439.3(HSF5):c.985A>G (p.Thr329Ala)	HSF5 (T329A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3284892	NM_001080439.3(HSF5):c.926C>G (p.Ala309Gly)	HSF5 (A309G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268197	NM_001080439.3(HSF5):c.778A>G (p.Arg260Gly)	HSF5 (R260G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468945	NM_001080439.3(HSF5):c.667C>T (p.Arg223Trp)	HSF5 (R223W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107227	NM_001080439.3(HSF5):c.602C>T (p.Ser201Phe)	HSF5 (S201F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353717	NM_001080439.3(HSF5):c.562G>A (p.Val188Ile)	HSF5 (V188I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107226	NM_001080439.3(HSF5):c.541G>A (p.Glu181Lys)	HSF5, LOC130061297 (E181K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544605	NM_001080439.3(HSF5):c.466C>G (p.Leu156Val)	HSF5, LOC130061297 (L156V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495437	NM_001080439.3(HSF5):c.316G>A (p.Gly106Arg)	HSF5 (G106R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212337	NM_001080439.3(HSF5):c.199G>A (p.Ala67Thr)	HSF5, LOC130061298 (A67T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3284894	NM_001080439.3(HSF5):c.158C>A (p.Pro53Gln)	HSF5, LOC130061298 (P53Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510917	NM_001080439.3(HSF5):c.77G>A (p.Arg26His)	HSF5 (R26H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance