"Ambry Genetics"[submitter] AND "DAXX"[gene] - ClinVar

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Search results

Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2550096	NM_001141969.2(DAXX):c.2114G>A (p.Arg705Gln)	DAXX (R705Q +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3080129	NM_001141969.2(DAXX):c.2113C>T (p.Arg705Trp)	DAXX (R630W +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3080128	NM_001141969.2(DAXX):c.2014C>T (p.Pro672Ser)	DAXX (P672S +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3080127	NM_001141969.2(DAXX):c.1958G>A (p.Arg653Lys)	DAXX (R653K +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2511263	NM_001141969.2(DAXX):c.1901A>C (p.Lys634Thr)	DAXX (K646T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517285	NM_001141969.2(DAXX):c.1817G>T (p.Gly606Val)	DAXX (G618V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080126	NM_001141969.2(DAXX):c.1610C>T (p.Pro537Leu)	DAXX (P462L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080125	NM_001141969.2(DAXX):c.1511A>G (p.Asn504Ser)	DAXX (N504S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080124	NM_001141969.2(DAXX):c.1417G>A (p.Gly473Ser)	DAXX (G485S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080123	NM_001141969.2(DAXX):c.1318G>A (p.Asp440Asn)	DAXX (D440N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080121	NM_001141969.2(DAXX):c.1247G>A (p.Gly416Asp)	DAXX (G416D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245384	NM_001141969.2(DAXX):c.1198G>C (p.Gly400Arg)	DAXX (G325R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469750	NM_001141969.2(DAXX):c.1066G>A (p.Val356Met)	DAXX (V281M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554046	NM_001141969.2(DAXX):c.1042G>A (p.Val348Ile)	DAXX (V360I +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2552265	NM_001141969.2(DAXX):c.860G>A (p.Gly287Glu)	DAXX (G287E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080132	NM_001141969.2(DAXX):c.827A>G (p.Asn276Ser)	DAXX (N276S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2236579	NM_001141969.2(DAXX):c.766C>T (p.Arg256Cys)	DAXX (R256C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276566	NM_001141969.2(DAXX):c.640G>C (p.Glu214Gln)	DAXX (E226Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080131	NM_001141969.2(DAXX):c.607C>T (p.Arg203Trp)	DAXX (R203W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338683	NM_001141969.2(DAXX):c.488A>C (p.His163Pro)	DAXX (H163P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080130	NM_001141969.2(DAXX):c.485C>T (p.Thr162Ile)	DAXX (T162I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588973	NM_001141969.2(DAXX):c.350G>A (p.Arg117Gln)	DAXX (R117Q +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2219124	NM_001141969.2(DAXX):c.344G>A (p.Arg115Gln)	DAXX (R127Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401830	NM_001141969.2(DAXX):c.308C>T (p.Ala103Val)	DAXX (A115V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590132	NM_001141969.2(DAXX):c.290C>T (p.Ser97Phe)	DAXX (S109F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258998	NM_001141969.2(DAXX):c.238G>C (p.Asp80His)	DAXX (D5H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544976	NM_001141969.2(DAXX):c.236C>T (p.Ala79Val)	DAXX (A79V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302731	NM_001141969.2(DAXX):c.130C>A (p.Pro44Thr)	DAXX (P56T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2367624	NM_001141969.2(DAXX):c.77A>C (p.His26Pro)	DAXX (H26P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2605659	NM_001141969.2(DAXX):c.-63C>T	DAXX (R15W)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2405260	NM_001141969.2(DAXX):c.-84G>A	DAXX (G8S)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GLikely benign

ClinVar

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Items: 31