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

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3262995	NM_004343.4(CALR):c.17C>T (p.Pro6Leu)	CALR, LOC117125596 (P6L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549201	NM_004343.4(CALR):c.50C>G (p.Ala17Gly)	CALR, LOC117125596 (A17G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525549	NM_004343.4(CALR):c.50C>T (p.Ala17Val)	CALR, LOC117125596 (A17V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302004	NM_004343.4(CALR):c.88G>C (p.Gly30Arg)	CALR, LOC117125596 (G30R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309782	NM_004343.4(CALR):c.101C>T (p.Thr34Ile)	CALR (T34I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3136755	NM_004343.4(CALR):c.114C>G (p.Ile38Met)	CALR (I38M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359346	NM_004343.4(CALR):c.148G>C (p.Val50Leu)	CALR (V50L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399432	NM_004343.4(CALR):c.277G>A (p.Val93Met)	CALR (V93M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248994	NM_004343.4(CALR):c.536A>G (p.Asp179Gly)	CALR, LOC126862861 (D179G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311966	NM_004343.4(CALR):c.586T>G (p.Leu196Val)	CALR, LOC126862861 (L196V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381152	NM_004343.4(CALR):c.647C>T (p.Pro216Leu)	CALR, LOC126862861 (P216L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233331	NM_004343.4(CALR):c.817G>C (p.Gly273Arg)	CALR, LOC126862861 (G273R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401105	NM_004343.4(CALR):c.836A>G (p.Gln279Arg)	CALR, LOC126862861 (Q279R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3136756	NM_004343.4(CALR):c.890C>A (p.Pro297His)	CALR, LOC126862861 (P297H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281371	NM_004343.4(CALR):c.1031A>G (p.Asn344Ser)	CALR (N344S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305786	NM_004343.4(CALR):c.1186G>A (p.Glu396Lys)	CALR (E396K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance