"Ambry Genetics"[submitter] AND "DCAF6"[gene] - ClinVar

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

Search results

Items: 67

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2259165	NM_018417.6(ADCY10):c.1604G>T (p.Gly535Val)	ADCY10, DCAF6 (G535V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1063254	NM_018417.6(ADCY10):c.1595T>C (p.Leu532Pro)	ADCY10, DCAF6 (L379P +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2516393	NM_018417.6(ADCY10):c.1580T>C (p.Met527Thr)	ADCY10, DCAF6 (M435T +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 3081135	NM_018417.6(ADCY10):c.1489A>T (p.Met497Leu)	ADCY10, DCAF6 (M344L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1714660	NM_018417.6(ADCY10):c.1451A>G (p.Tyr484Cys)	ADCY10, DCAF6 (Y331C +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2523191	NM_018417.6(ADCY10):c.1421C>T (p.Ala474Val)	ADCY10, DCAF6 (A321V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592146	NM_018417.6(ADCY10):c.1385A>G (p.Tyr462Cys)	ADCY10, DCAF6 (Y370C +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2343775	NM_018417.6(ADCY10):c.1372C>T (p.Pro458Ser)	ADCY10, DCAF6 (P305S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2531151	NM_018417.6(ADCY10):c.1336C>T (p.Pro446Ser)	ADCY10, DCAF6 (P354S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206571	NM_018417.6(ADCY10):c.1283A>G (p.Asp428Gly)	ADCY10, DCAF6 (D428G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367996	NM_018417.6(ADCY10):c.1207G>A (p.Glu403Lys)	ADCY10, DCAF6 (E250K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367890	NM_018417.6(ADCY10):c.1199T>C (p.Val400Ala)	ADCY10, DCAF6 (V247A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2256365	NM_018417.6(ADCY10):c.1052C>G (p.Pro351Arg)	ADCY10, DCAF6 (P351R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242706	NM_018417.6(ADCY10):c.959A>C (p.His320Pro)	ADCY10, DCAF6 (H167P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081347	NM_018417.6(ADCY10):c.878C>T (p.Thr293Met)	ADCY10, DCAF6 (T201M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296104	NM_018417.6(ADCY10):c.801G>T (p.Lys267Asn)	ADCY10, DCAF6 (K175N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081342	NM_018417.6(ADCY10):c.767A>G (p.Lys256Arg)	ADCY10, DCAF6 (K256R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081340	NM_018417.6(ADCY10):c.761C>T (p.Thr254Met)	ADCY10, DCAF6 (T101M +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2553976	NM_018417.6(ADCY10):c.709A>T (p.Met237Leu)	ADCY10, DCAF6 (M84L +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2377830	NM_018417.6(ADCY10):c.586C>T (p.Leu196Phe)	ADCY10, DCAF6 (L104F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2561081	NM_018417.6(ADCY10):c.512C>G (p.Ala171Gly)	ADCY10, DCAF6 (A79G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314945	NM_018417.6(ADCY10):c.448G>A (p.Gly150Ser)	ADCY10, DCAF6 (G58S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2540528	NM_018417.6(ADCY10):c.315G>C (p.Trp105Cys)	ADCY10, DCAF6 (W105C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2227969	NM_018417.6(ADCY10):c.230A>G (p.Tyr77Cys)	ADCY10, DCAF6 (Y77C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3081150	NM_018417.6(ADCY10):c.163A>T (p.Thr55Ser)	ADCY10, DCAF6 (T55S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2270029	NM_001143674.4(MPC2):c.257C>T (p.Ser86Leu)	DCAF6, MPC2 (S86L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2290824	NM_001143674.4(MPC2):c.31G>C (p.Ala11Pro)	DCAF6, MPC2 (A11P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2604354	NM_001198956.2(DCAF6):c.71C>T (p.Pro24Leu)	DCAF6, LOC129931878 +1 more (P24L)	Single nucleotide variant (5 prime UTR variant +3 more)	not specified	GUncertain significance
Select item 2288209	NM_001198956.2(DCAF6):c.155G>A (p.Gly52Asp)	DCAF6 (G52D)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3080326	NM_001198956.2(DCAF6):c.173G>A (p.Cys58Tyr)	DCAF6 (C58Y)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2624263	NM_001198956.2(DCAF6):c.218C>T (p.Thr73Ile)	DCAF6 (T73I)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2531013	NM_001198956.2(DCAF6):c.310C>T (p.Pro104Ser)	DCAF6 (P73S +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2544034	NM_001198956.2(DCAF6):c.391A>G (p.Thr131Ala)	DCAF6 (T100A +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2271539	NM_001198956.2(DCAF6):c.413C>T (p.Thr138Met)	DCAF6 (T138M +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2293694	NM_001198956.2(DCAF6):c.472C>G (p.Leu158Val)	DCAF6, LOC126805909 (L127V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2623586	NM_001198956.2(DCAF6):c.514C>T (p.Arg172Cys)	DCAF6, LOC126805909 (R141C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2495761	NM_001198956.2(DCAF6):c.727C>T (p.Arg243Cys)	DCAF6 (R212C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2209353	NM_001198956.2(DCAF6):c.728G>A (p.Arg243His)	DCAF6 (R243H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2454763	NM_001198956.2(DCAF6):c.751A>G (p.Asn251Asp)	DCAF6 (N104D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2213667	NM_001198956.2(DCAF6):c.867A>C (p.Glu289Asp)	DCAF6 (E258D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2526214	NM_001198956.2(DCAF6):c.877C>T (p.Pro293Ser)	DCAF6 (P146S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3080331	NM_001198956.2(DCAF6):c.926G>A (p.Arg309His)	DCAF6 (R309H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2271424	NM_001198956.2(DCAF6):c.1097G>A (p.Arg366Gln)	DCAF6 (R366Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2370657	NM_001198956.2(DCAF6):c.1195A>G (p.Met399Val)	DCAF6 (M252V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2317666	NM_001198956.2(DCAF6):c.1270A>C (p.Thr424Pro)	DCAF6 (T277P +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2277565	NM_001198956.2(DCAF6):c.1283C>T (p.Thr428Ile)	DCAF6 (T428I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2272287	NM_001198956.2(DCAF6):c.1309C>G (p.Leu437Val)	DCAF6 (L290V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2605527	NM_001198956.2(DCAF6):c.1312T>C (p.Ser438Pro)	DCAF6 (S291P +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2312883	NM_001198956.2(DCAF6):c.1315T>C (p.Ser439Pro)	DCAF6 (S408P +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3080322	NM_001198956.2(DCAF6):c.1382T>G (p.Phe461Cys)	DCAF6 (F461C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2407077	NM_001198956.2(DCAF6):c.1412G>A (p.Arg471His)	DCAF6 (R440H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3080323	NM_001198956.2(DCAF6):c.1444G>A (p.Ala482Thr)	DCAF6 (A451T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2608817	NM_001198956.2(DCAF6):c.1481C>A (p.Thr494Asn)	DCAF6 (T494N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2343913	NM_001198956.2(DCAF6):c.1517A>G (p.His506Arg)	DCAF6 (H475R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3080324	NM_001198956.2(DCAF6):c.1582G>A (p.Gly528Arg)	DCAF6 (G497R +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2461173	NM_001198956.2(DCAF6):c.1589T>C (p.Met530Thr)	DCAF6 (M499T +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3080325	NM_001198956.2(DCAF6):c.1594C>T (p.Leu532Phe)	DCAF6 (L532F +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2279972	NM_001198956.2(DCAF6):c.1600G>A (p.Glu534Lys)	DCAF6 (E503K +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3080327	NM_001198956.2(DCAF6):c.1757T>C (p.Ile586Thr)	DCAF6 (I362T +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3080328	NM_001198956.2(DCAF6):c.1791A>C (p.Glu597Asp)	DCAF6 (E373D +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2358757	NM_001198956.2(DCAF6):c.1798G>A (p.Val600Ile)	DCAF6 (V396I +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2399474	NM_001198956.2(DCAF6):c.1802C>T (p.Pro601Leu)	DCAF6 (P524L +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2293772	NM_001198956.2(DCAF6):c.1891G>C (p.Val631Leu)	DCAF6 (V407L +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2391414	NM_001198956.2(DCAF6):c.2137A>C (p.Thr713Pro)	DCAF6 (T489P +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2483430	NM_001198956.2(DCAF6):c.2138C>T (p.Thr713Ile)	DCAF6 (T509I +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2294780	NM_001198956.2(DCAF6):c.2233A>G (p.Arg745Gly)	DCAF6 (R521G +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3080330	NM_001198956.2(DCAF6):c.2842G>A (p.Glu948Lys)	DCAF6 (E891K +8 more)	Single nucleotide variant (missense variant +1 more)	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: 67