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

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 44

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2494317	NM_139072.4(DNER):c.2125G>A (p.Ala709Thr)	DNER (A709T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378643	NM_139072.4(DNER):c.2093G>A (p.Arg698Gln)	DNER (R698Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481370	NM_139072.4(DNER):c.1945G>A (p.Ala649Thr)	DNER (A649T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084655	NM_139072.4(DNER):c.1891C>T (p.Leu631Phe)	DNER (L631F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3273158	NM_139072.4(DNER):c.1826A>G (p.His609Arg)	DNER (H609R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347186	NM_139072.4(DNER):c.1699T>C (p.Cys567Arg)	DNER, LOC108353815 (C567R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508887	NM_139072.4(DNER):c.1574A>G (p.Asn525Ser)	DNER (N525S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389489	NM_139072.4(DNER):c.1474C>T (p.Leu492Phe)	DNER (L492F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407613	NM_139072.4(DNER):c.1448G>A (p.Arg483His)	DNER (R483H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2619802	NM_139072.4(DNER):c.1432G>T (p.Ala478Ser)	DNER (A478S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223584	NM_139072.4(DNER):c.1345G>A (p.Gly449Arg)	DNER (G449R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084653	NM_139072.4(DNER):c.1294G>A (p.Asp432Asn)	DNER (D432N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510644	NM_139072.4(DNER):c.1231C>G (p.Leu411Val)	DNER (L411V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084652	NM_139072.4(DNER):c.1180G>A (p.Asp394Asn)	DNER (D394N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516246	NM_139072.4(DNER):c.1175A>G (p.Lys392Arg)	DNER (K392R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3273156	NM_139072.4(DNER):c.1111C>A (p.Gln371Lys)	DNER (Q371K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084651	NM_139072.4(DNER):c.1088G>A (p.Ser363Asn)	DNER (S363N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084650	NM_139072.4(DNER):c.1085C>T (p.Ala362Val)	DNER (A362V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468020	NM_139072.4(DNER):c.1084G>A (p.Ala362Thr)	DNER (A362T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084649	NM_139072.4(DNER):c.1061A>C (p.Gln354Pro)	DNER (Q354P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542143	NM_139072.4(DNER):c.1046A>C (p.Glu349Ala)	DNER (E349A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272050	NM_139072.4(DNER):c.1007G>T (p.Cys336Phe)	DNER (C336F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2264044	NM_139072.4(DNER):c.998C>T (p.Thr333Ile)	DNER (T333I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461080	NM_139072.4(DNER):c.986C>T (p.Pro329Leu)	DNER (P329L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454487	NM_139072.4(DNER):c.944A>C (p.Asn315Thr)	DNER (N315T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299742	NM_139072.4(DNER):c.890G>A (p.Arg297His)	DNER (R297H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367715	NM_139072.4(DNER):c.668A>G (p.Asn223Ser)	DNER (N223S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208503	NM_139072.4(DNER):c.650C>T (p.Ser217Phe)	DNER (S217F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599972	NM_139072.4(DNER):c.640C>T (p.Arg214Cys)	DNER (R214C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265062	NM_139072.4(DNER):c.637G>A (p.Gly213Ser)	DNER (G213S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3273160	NM_139072.4(DNER):c.635G>A (p.Gly212Asp)	DNER (G212D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369389	NM_139072.4(DNER):c.613G>A (p.Ala205Thr)	DNER (A205T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515126	NM_139072.4(DNER):c.511G>A (p.Ala171Thr)	DNER (A171T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356443	NM_139072.4(DNER):c.502C>T (p.Arg168Cys)	DNER (R168C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084658	NM_139072.4(DNER):c.458T>G (p.Leu153Arg)	DNER (L153R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345730	NM_139072.4(DNER):c.452G>A (p.Arg151Gln)	DNER (R151Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3273157	NM_139072.4(DNER):c.440C>T (p.Ser147Phe)	DNER (S147F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404366	NM_139072.4(DNER):c.402G>C (p.Gln134His)	DNER (Q134H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084657	NM_139072.4(DNER):c.372T>G (p.Asn124Lys)	DNER (N124K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259519	NM_139072.4(DNER):c.355T>G (p.Tyr119Asp)	DNER (Y119D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330661	NM_139072.4(DNER):c.166G>C (p.Gly56Arg)	DNER (G56R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084659	NM_139072.4(DNER):c.88G>C (p.Gly30Arg)	DNER (G30R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084656	NM_139072.4(DNER):c.23C>T (p.Ala8Val)	DNER (A8V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084661	NM_139072.4(DNER):c.8C>T (p.Pro3Leu)	DNER (P3L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 44