"Ambry Genetics"[submitter] AND "MUC22"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2293052	NM_001395414.1(MUC22):c.98A>C (p.Lys33Thr)	MUC22 (K36T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2282084	NM_001395414.1(MUC22):c.147G>A (p.Met49Ile)	MUC22 (M49I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395521	NM_001395414.1(MUC22):c.239C>T (p.Thr80Ile)	MUC22 (T80I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349311	NM_001395414.1(MUC22):c.241A>G (p.Met81Val)	MUC22 (M84V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296904	NM_001395414.1(MUC22):c.257C>G (p.Ala86Gly)	MUC22 (A86G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2603574	NM_001395414.1(MUC22):c.284C>A (p.Thr95Lys)	MUC22 (T95K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242929	NM_001395414.1(MUC22):c.352A>G (p.Thr118Ala)	MUC22 (T118A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462964	NM_001395414.1(MUC22):c.385G>A (p.Val129Met)	MUC22 (V129M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2324571	NM_001395414.1(MUC22):c.481G>T (p.Ala161Ser)	MUC22 (A164S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296913	NM_001395414.1(MUC22):c.497C>T (p.Thr166Met)	MUC22 (T166M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3220510	NM_001395414.1(MUC22):c.524C>A (p.Thr175Asn)	MUC22 (T175N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222593	NM_001395414.1(MUC22):c.587C>G (p.Thr196Ser)	MUC22 (T196S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514008	NM_001395414.1(MUC22):c.611A>G (p.Glu204Gly)	MUC22 (E204G +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2554089	NM_001395414.1(MUC22):c.641A>G (p.Glu214Gly)	MUC22 (E214G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296914	NM_001395414.1(MUC22):c.701G>T (p.Gly234Val)	MUC22 (G234V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495898	NM_001395414.1(MUC22):c.743T>C (p.Ile248Thr)	MUC22 (I248T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375572	NM_001395414.1(MUC22):c.749C>T (p.Ala250Val)	MUC22 (A250V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353502	NM_001395414.1(MUC22):c.787G>T (p.Ala263Ser)	MUC22 (A266S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3220527	NM_001395414.1(MUC22):c.829A>G (p.Thr277Ala)	MUC22 (T277A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398454	NM_001395414.1(MUC22):c.838A>T (p.Ile280Phe)	MUC22 (I280F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391551	NM_001395414.1(MUC22):c.858G>C (p.Glu286Asp)	MUC22 (E289D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465186	NM_001395414.1(MUC22):c.865A>G (p.Thr289Ala)	MUC22 (T289A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398455	NM_001395414.1(MUC22):c.871T>A (p.Ser291Thr)	MUC22 (S291T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465187	NM_001395414.1(MUC22):c.877G>A (p.Ala293Thr)	MUC22 (A293T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3220543	NM_001395414.1(MUC22):c.895A>C (p.Thr299Pro)	MUC22 (T299P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2493627	NM_001395414.1(MUC22):c.896C>T (p.Thr299Ile)	MUC22 (T302I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274846	NM_001395414.1(MUC22):c.896C>A (p.Thr299Asn)	MUC22 (T299N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343518	NM_001395414.1(MUC22):c.916C>G (p.Gln306Glu)	MUC22 (Q306E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296906	NM_001395414.1(MUC22):c.926T>C (p.Ile309Thr)	MUC22 (I309T +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2349369	NM_001395414.1(MUC22):c.935T>C (p.Ile312Thr)	MUC22 (I312T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398456	NM_001395414.1(MUC22):c.937T>A (p.Ser313Thr)	MUC22 (S313T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350436	NM_001395414.1(MUC22):c.955A>G (p.Thr319Ala)	MUC22 (T322A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274040	NM_001395414.1(MUC22):c.956C>T (p.Thr319Ile)	MUC22 (T319I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3220564	NM_001395414.1(MUC22):c.976G>A (p.Glu326Lys)	MUC22 (E326K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3220569	NM_001395414.1(MUC22):c.977A>G (p.Glu326Gly)	MUC22 (E326G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3220214	NM_001395414.1(MUC22):c.1009A>T (p.Thr337Ser)	MUC22 (T340S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546695	NM_001395414.1(MUC22):c.1015A>G (p.Thr339Ala)	MUC22 (T339A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310242	NM_001395414.1(MUC22):c.1018G>T (p.Ala340Ser)	MUC22 (A343S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590516	NM_001395414.1(MUC22):c.1072A>G (p.Thr358Ala)	MUC22 (T361A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3220229	NM_001395414.1(MUC22):c.1117G>A (p.Gly373Ser)	MUC22 (G373S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274696	NM_001395414.1(MUC22):c.1133C>A (p.Thr378Lys)	MUC22 (T378K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3220235	NM_001395414.1(MUC22):c.1151C>G (p.Ser384Cys)	MUC22 (S384C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343813	NM_001395414.1(MUC22):c.1162G>A (p.Val388Ile)	MUC22 (V391I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541650	NM_001395414.1(MUC22):c.1186A>T (p.Thr396Ser)	MUC22 (T396S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2298495	NM_001395414.1(MUC22):c.1222A>G (p.Thr408Ala)	MUC22 (T408A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273936	NM_001395414.1(MUC22):c.1322C>A (p.Thr441Asn)	MUC22 (T441N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358636	NM_001395414.1(MUC22):c.1384A>G (p.Thr462Ala)	MUC22 (T465A +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2358637	NM_001395414.1(MUC22):c.1385C>A (p.Thr462Lys)	MUC22 (T462K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258491	NM_001395414.1(MUC22):c.1418A>C (p.His473Pro)	MUC22 (H473P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518556	NM_001395414.1(MUC22):c.1463A>G (p.Lys488Arg)	MUC22 (K488R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2477524	NM_001395414.1(MUC22):c.1474G>T (p.Ala492Ser)	MUC22 (A495S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219408	NM_001395414.1(MUC22):c.1504G>A (p.Gly502Ser)	MUC22 (G502S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338931	NM_001395414.1(MUC22):c.1561G>A (p.Glu521Lys)	MUC22 (E521K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3220268	NM_001395414.1(MUC22):c.1601A>G (p.Glu534Gly)	MUC22 (E534G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598775	NM_001395414.1(MUC22):c.1633C>A (p.Pro545Thr)	MUC22 (P545T +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2378516	NM_001395414.1(MUC22):c.1702G>T (p.Val568Phe)	MUC22 (V568F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296911	NM_001395414.1(MUC22):c.1705T>C (p.Ser569Pro)	MUC22 (S569P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295029	NM_001395414.1(MUC22):c.1715G>A (p.Ser572Asn)	MUC22 (S572N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296910	NM_001395414.1(MUC22):c.1747T>C (p.Ser583Pro)	MUC22 (S583P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2264560	NM_001395414.1(MUC22):c.1949C>T (p.Thr650Ile)	MUC22 (T653I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2209491	NM_001395414.1(MUC22):c.1966A>C (p.Thr656Pro)	MUC22 (T659P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365995	NM_001395414.1(MUC22):c.1985A>G (p.Asp662Gly)	MUC22 (D665G +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2394521	NM_001395414.1(MUC22):c.2000C>T (p.Thr667Ile)	MUC22 (T667I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355649	NM_001395414.1(MUC22):c.2005T>C (p.Cys669Arg)	MUC22 (C672R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3220288	NM_001395414.1(MUC22):c.2069C>T (p.Thr690Ile)	MUC22 (T690I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535205	NM_001395414.1(MUC22):c.2074G>A (p.Gly692Ser)	MUC22 (G692S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318445	NM_001395414.1(MUC22):c.2224G>T (p.Gly742Cys)	MUC22 (G742C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378872	NM_001395414.1(MUC22):c.2242G>T (p.Val748Phe)	MUC22 (V748F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296917	NM_001395414.1(MUC22):c.2264C>A (p.Thr755Asn)	MUC22 (T755N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488592	NM_001395414.1(MUC22):c.2320G>A (p.Glu774Lys)	MUC22 (E774K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390196	NM_001395414.1(MUC22):c.2428A>G (p.Thr810Ala)	MUC22 (T813A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3220315	NM_001395414.1(MUC22):c.2524G>A (p.Gly842Ser)	MUC22 (G842S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393960	NM_001395414.1(MUC22):c.2540C>T (p.Thr847Ile)	MUC22 (T847I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287738	NM_001395414.1(MUC22):c.2573C>T (p.Ala858Val)	MUC22 (A858V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296909	NM_001395414.1(MUC22):c.2582C>A (p.Ala861Glu)	MUC22 (A864E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2307158	NM_001395414.1(MUC22):c.2648C>T (p.Ser883Phe)	MUC22 (S883F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2224234	NM_001395414.1(MUC22):c.2669C>T (p.Thr890Ile)	MUC22 (T890I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206740	NM_001395414.1(MUC22):c.2728A>C (p.Thr910Pro)	MUC22 (T910P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296903	NM_001395414.1(MUC22):c.2774C>T (p.Thr925Ile)	MUC22 (T925I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398954	NM_001395414.1(MUC22):c.2782G>A (p.Val928Ile)	MUC22 (V928I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320013	NM_001395414.1(MUC22):c.2783T>C (p.Val928Ala)	MUC22 (V928A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514353	NM_001395414.1(MUC22):c.2800G>A (p.Glu934Lys)	MUC22 (E937K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461602	NM_001395414.1(MUC22):c.2900C>T (p.Thr967Ile)	MUC22 (T970I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3220345	NM_001395414.1(MUC22):c.2935A>T (p.Ile979Phe)	MUC22 (I979F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407719	NM_001395414.1(MUC22):c.2957C>G (p.Thr986Arg)	MUC22 (T989R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296920	NM_001395414.1(MUC22):c.2959G>A (p.Ala987Thr)	MUC22 (A990T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273526	NM_001395414.1(MUC22):c.3020C>T (p.Ala1007Val)	MUC22 (A1007V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532111	NM_001395414.1(MUC22):c.3056C>A (p.Thr1019Asn)	MUC22 (T1022N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275749	NM_001395414.1(MUC22):c.3104C>G (p.Thr1035Ser)	MUC22 (T1038S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3220354	NM_001395414.1(MUC22):c.3239C>A (p.Ala1080Glu)	MUC22 (A1080E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319734	NM_001395414.1(MUC22):c.3254T>A (p.Ile1085Asn)	MUC22 (I1088N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296915	NM_001395414.1(MUC22):c.3269C>T (p.Ala1090Val)	MUC22 (A1093V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3220361	NM_001395414.1(MUC22):c.3293C>A (p.Thr1098Asn)	MUC22 (T1101N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229251	NM_001395414.1(MUC22):c.3364A>G (p.Ser1122Gly)	MUC22 (S1122G +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3220366	NM_001395414.1(MUC22):c.3389C>T (p.Thr1130Ile)	MUC22 (T1130I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360484	NM_001395414.1(MUC22):c.3412G>C (p.Ala1138Pro)	MUC22 (A1141P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3220375	NM_001395414.1(MUC22):c.3470C>T (p.Thr1157Ile)	MUC22 (T1157I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3220382	NM_001395414.1(MUC22):c.3619A>G (p.Thr1207Ala)	MUC22 (T1210A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343333	NM_001395414.1(MUC22):c.3623T>C (p.Val1208Ala)	MUC22 (V1211A +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2343334	NM_001395414.1(MUC22):c.3628G>A (p.Ala1210Thr)	MUC22 (A1210T +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign

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