"Ambry Genetics"[submitter] AND "CHMP3-AS1"[gene] - ClinVar

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Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2612097	NM_016079.4(CHMP3):c.40G>A (p.Glu14Lys)	CHMP3, CHMP3-AS1 +2 more (E14K)	Single nucleotide variant (non-coding transcript variant +3 more)	not specified	GUncertain significance
Select item 2455594	NM_005667.4(RNF103):c.1967G>A (p.Arg656Gln)	CHMP3-AS1, RNF103 +1 more (R656Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2252550	NM_005667.4(RNF103):c.1815A>C (p.Glu605Asp)	CHMP3-AS1, RNF103 +1 more (E601D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2551548	NM_005667.4(RNF103):c.1814A>G (p.Glu605Gly)	CHMP3-AS1, RNF103 +1 more (E601G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2619263	NM_005667.4(RNF103):c.1724C>T (p.Ala575Val)	CHMP3-AS1, RNF103 +1 more (A575V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2360386	NM_005667.4(RNF103):c.1616C>G (p.Ser539Trp)	CHMP3-AS1, RNF103 +1 more (S535W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2257118	NM_005667.4(RNF103):c.1589A>C (p.Glu530Ala)	CHMP3-AS1, RNF103 +1 more (E530A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3154914	NM_005667.4(RNF103):c.1584G>A (p.Met528Ile)	CHMP3-AS1, RNF103 +1 more (M528I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2266206	NM_005667.4(RNF103):c.1547G>A (p.Arg516Gln)	CHMP3-AS1, RNF103 +1 more (R516Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2278538	NM_005667.4(RNF103):c.1480G>A (p.Ala494Thr)	CHMP3-AS1, RNF103 +1 more (A490T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2359513	NM_005667.4(RNF103):c.1343A>G (p.Asn448Ser)	CHMP3-AS1, RNF103 +1 more (N444S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2203780	NM_005667.4(RNF103):c.1319G>A (p.Arg440His)	CHMP3-AS1, RNF103 +1 more (R440H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2333712	NM_005667.4(RNF103):c.1306A>G (p.Lys436Glu)	CHMP3-AS1, RNF103 +1 more (K432E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3154918	NM_005667.4(RNF103):c.819C>G (p.Asn273Lys)	CHMP3-AS1, RNF103 +1 more (N273K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2602226	NM_005667.4(RNF103):c.810T>A (p.Asn270Lys)	CHMP3-AS1, RNF103 +1 more (N266K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2252496	NM_005667.4(RNF103):c.761G>C (p.Ser254Thr)	CHMP3-AS1, RNF103 +1 more (S254T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3154917	NM_005667.4(RNF103):c.712T>C (p.Tyr238His)	CHMP3-AS1, RNF103 +1 more (Y238H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2358585	NM_005667.4(RNF103):c.692A>G (p.Asp231Gly)	CHMP3-AS1, RNF103 +1 more (D231G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2368437	NM_005667.4(RNF103):c.684T>A (p.Asn228Lys)	CHMP3-AS1, RNF103 +1 more (N228K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2518370	NM_005667.4(RNF103):c.584G>A (p.Arg195His)	CHMP3-AS1, RNF103 +1 more (R195H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2618482	NM_005667.4(RNF103):c.578G>A (p.Ser193Asn)	CHMP3-AS1, RNF103 +1 more (S189N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2328907	NM_005667.4(RNF103):c.548C>T (p.Ser183Leu)	CHMP3-AS1, RNF103 +1 more (S179L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2234483	NM_005667.4(RNF103):c.521T>C (p.Ile174Thr)	CHMP3-AS1, RNF103 +1 more (I174T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3154916	NM_005667.4(RNF103):c.464A>G (p.Asn155Ser)	CHMP3-AS1, RNF103 +1 more (N151S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2557576	NM_005667.4(RNF103):c.416A>G (p.Lys139Arg)	CHMP3-AS1, RNF103 +1 more (K135R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2406531	NM_005667.4(RNF103):c.397G>C (p.Gly133Arg)	CHMP3-AS1, RNF103 +1 more (G129R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 26