MUC5B[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 30126	NM_002458.2(MUC5B):c.-3133G>T	MUC5B	Single nucleotide variant	not provided +1 more	GBenign; risk factor
Select item 1225333	NC_000011.10:g.1222830G>A	MUC5B	Single nucleotide variant	not provided	GBenign
Select item 1226529	NC_000011.10:g.1222850C>G	MUC5B	Single nucleotide variant	not provided	GBenign
Select item 1274465	NC_000011.10:g.1222967G>A	MUC5B	Single nucleotide variant	not provided	GBenign
Select item 1296791	NC_000011.10:g.1222989T>C	MUC5B	Single nucleotide variant	not provided	GBenign
Select item 2641179	NM_002458.3(MUC5B):c.70+8C>T	MUC5B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 163990	NM_002458.3(MUC5B):c.101A>G (p.Glu34Gly)	MUC5B (E34G)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 778507	NM_002458.3(MUC5B):c.127+9C>T	MUC5B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 759460	NM_002458.3(MUC5B):c.144G>A (p.Ser48=)	MUC5B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 163991	NM_002458.3(MUC5B):c.151C>T (p.Arg51Trp)	MUC5B (R51W)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign
Select item 3149556	NM_002458.3(MUC5B):c.178A>G (p.Thr60Ala)	MUC5B (T60A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618980	NM_002458.3(MUC5B):c.196A>G (p.Ser66Gly)	MUC5B (S66G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 505060	NM_002458.3(MUC5B):c.200-12C>T	MUC5B	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 2320835	NM_002458.3(MUC5B):c.211G>A (p.Ala71Thr)	MUC5B (A71T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238003	NM_002458.3(MUC5B):c.226G>T (p.Val76Leu)	MUC5B (V76L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2614565	NM_002458.3(MUC5B):c.304G>A (p.Val102Met)	MUC5B (V102M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 163992	NM_002458.3(MUC5B):c.324C>T (p.Arg108=)	MUC5B	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 2521845	NM_002458.3(MUC5B):c.328G>A (p.Ala110Thr)	MUC5B (A110T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2641180	NM_002458.3(MUC5B):c.356G>A (p.Arg119His)	MUC5B (R119H)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2213558	NM_002458.3(MUC5B):c.391C>T (p.Arg131Cys)	MUC5B (R131C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249756	NM_002458.3(MUC5B):c.428C>G (p.Ala143Gly)	MUC5B (A143G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274398	NM_002458.3(MUC5B):c.436G>A (p.Gly146Ser)	MUC5B (G146S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 163993	NM_002458.3(MUC5B):c.442G>A (p.Val148Ile)	MUC5B (V148I)	Single nucleotide variant (missense variant)	not specified	GBenign
Select item 756307	NM_002458.3(MUC5B):c.450C>T (p.Ile150=)	MUC5B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1282609	NM_002458.3(MUC5B):c.462-64G>T	MUC5B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 720434	NM_002458.3(MUC5B):c.492C>T (p.Leu164=)	MUC5B	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2495256	NM_002458.3(MUC5B):c.547T>C (p.Phe183Leu)	MUC5B (F183L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 163994	NM_002458.3(MUC5B):c.576+9G>T	MUC5B	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 1290452	NM_002458.3(MUC5B):c.577-47T>G	MUC5B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2641181	NM_002458.3(MUC5B):c.642G>A (p.Pro214=)	MUC5B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3150107	NM_002458.3(MUC5B):c.659A>G (p.Tyr220Cys)	MUC5B (Y220C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1283161	NM_002458.3(MUC5B):c.667+95C>T	MUC5B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1248788	NM_002458.3(MUC5B):c.667+103A>G	MUC5B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2286836	NM_002458.3(MUC5B):c.703C>A (p.Gln235Lys)	MUC5B (Q235K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 178783	NM_002458.3(MUC5B):c.723G>A (p.Thr241=)	MUC5B	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 178784	NM_002458.3(MUC5B):c.757G>A (p.Gly253Ser)	MUC5B (G253S)	Single nucleotide variant (missense variant)	not specified	GBenign
Select item 1243572	NM_002458.3(MUC5B):c.775-258G>T	MUC5B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1289353	NM_002458.3(MUC5B):c.775-193C>G	MUC5B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2224799	NM_002458.3(MUC5B):c.826G>A (p.Ala276Thr)	MUC5B (A276T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220664	NM_002458.3(MUC5B):c.845C>T (p.Ala282Val)	MUC5B (A282V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 504730	NM_002458.3(MUC5B):c.845C>A (p.Ala282Glu)	MUC5B (A282E)	Single nucleotide variant (missense variant)	not specified	GConflicting classifications of pathogenicity
Select item 1049165	NM_002458.3(MUC5B):c.854C>T (p.Ala285Val)	MUC5B (A285V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2331824	NM_002458.3(MUC5B):c.870C>A (p.Asp290Glu)	MUC5B (D290E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333847	NM_002458.3(MUC5B):c.928G>A (p.Ala310Thr)	MUC5B (A310T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150491	NM_002458.3(MUC5B):c.933C>A (p.His311Gln)	MUC5B (H311Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 178785	NM_002458.3(MUC5B):c.933C>T (p.His311=)	MUC5B	Single nucleotide variant (synonymous variant)	not specified	GBenign
Select item 2220507	NM_002458.3(MUC5B):c.934G>A (p.Ala312Thr)	MUC5B (A312T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530132	NM_002458.3(MUC5B):c.941G>T (p.Gly314Val)	MUC5B (G314V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2641182	NM_002458.3(MUC5B):c.976C>T (p.Pro326Ser)	MUC5B (P326S)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1296797	NM_002458.3(MUC5B):c.976+180G>A	MUC5B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1274852	NM_002458.3(MUC5B):c.976+188A>G	MUC5B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1222484	NM_002458.3(MUC5B):c.977-179G>A	MUC5B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1253055	NM_002458.3(MUC5B):c.977-158G>T	MUC5B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1271784	NM_002458.3(MUC5B):c.977-16A>G	MUC5B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 718453	NM_002458.3(MUC5B):c.977-5C>T	MUC5B	Single nucleotide variant (intron variant)	not provided	GBenign/Likely benign
Select item 2483649	NM_002458.3(MUC5B):c.1025G>A (p.Cys342Tyr)	MUC5B (C342Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3220606	NM_002458.3(MUC5B):c.1028C>T (p.Thr343Met)	MUC5B (T343M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 178786	NM_002458.3(MUC5B):c.1065C>T (p.Cys355=)	MUC5B	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1277723	NM_002458.3(MUC5B):c.1102+58C>T	MUC5B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1225060	NM_002458.3(MUC5B):c.1102+78G>C	MUC5B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1265189	NM_002458.3(MUC5B):c.1102+154C>T	MUC5B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1222298	NM_002458.3(MUC5B):c.1102+171C>T	MUC5B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1243713	NM_002458.3(MUC5B):c.1103-117G>A	MUC5B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 178787	NM_002458.3(MUC5B):c.1103-11G>C	MUC5B	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2297597	NM_002458.3(MUC5B):c.1171G>A (p.Gly391Ser)	MUC5B (G391S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486051	NM_002458.3(MUC5B):c.1213A>C (p.Ser405Arg)	MUC5B (S405R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540376	NM_002458.3(MUC5B):c.1223C>T (p.Thr408Ile)	MUC5B (T408I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526732	NM_002458.3(MUC5B):c.1228T>G (p.Ser410Ala)	MUC5B (S410A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 178788	NM_002458.3(MUC5B):c.1287C>T (p.Gly429=)	MUC5B	Single nucleotide variant (synonymous variant)	not specified	GBenign
Select item 3149115	NM_002458.3(MUC5B):c.1289G>A (p.Gly430Glu)	MUC5B (G430E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274130	NM_002458.3(MUC5B):c.1384G>A (p.Val462Met)	MUC5B (V462M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2641183	NM_002458.3(MUC5B):c.1422C>T (p.Asn474=)	MUC5B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2513356	NM_002458.3(MUC5B):c.1439C>T (p.Ala480Val)	MUC5B (A480V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 226731	NM_002458.3(MUC5B):c.1440G>A (p.Ala480=)	MUC5B	Single nucleotide variant (synonymous variant)	not specified	GBenign
Select item 2374446	NM_002458.3(MUC5B):c.1456G>A (p.Asp486Asn)	MUC5B (D486N)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2522128	NM_002458.3(MUC5B):c.1462G>A (p.Gly488Arg)	MUC5B (G488R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1262521	NM_002458.3(MUC5B):c.1471-119T>C	MUC5B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 504731	NM_002458.3(MUC5B):c.1497C>T (p.Gly499=)	MUC5B	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign/Likely benign
Select item 3149364	NM_002458.3(MUC5B):c.1513A>G (p.Ile505Val)	MUC5B (I505V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3042760	NM_002458.3(MUC5B):c.1520C>T (p.Thr507Met)	MUC5B (T507M)	Single nucleotide variant (missense variant)	MUC5B-related disorder	GLikely benign
Select item 3149375	NM_002458.3(MUC5B):c.1535C>T (p.Ser512Leu)	MUC5B (S512L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 226733	NM_002458.3(MUC5B):c.1541-5G>A	MUC5B	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 163995	NM_002458.3(MUC5B):c.1596G>C (p.Leu532=)	MUC5B	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 2641184	NM_002458.3(MUC5B):c.1611G>A (p.Leu537=)	MUC5B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1289332	NM_002458.3(MUC5B):c.1679-90C>T	MUC5B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3149551	NM_002458.3(MUC5B):c.1739T>A (p.Val580Glu)	MUC5B (V580E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287930	NM_002458.3(MUC5B):c.1748C>T (p.Thr583Met)	MUC5B (T583M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 163996	NM_002458.3(MUC5B):c.1843+11C>G	MUC5B	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 3149559	NM_002458.3(MUC5B):c.1883C>T (p.Pro628Leu)	MUC5B (P628L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 795873	NM_002458.3(MUC5B):c.1887C>A (p.Asn629Lys)	MUC5B (N629K)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3149564	NM_002458.3(MUC5B):c.1900C>T (p.Arg634Cys)	MUC5B (R634C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2641185	NM_002458.3(MUC5B):c.1923C>G (p.Pro641=)	MUC5B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3149565	NM_002458.3(MUC5B):c.1933C>T (p.His645Tyr)	MUC5B (H645Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1266859	NM_002458.3(MUC5B):c.1939-18T>C	MUC5B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2619250	NM_002458.3(MUC5B):c.1970G>A (p.Arg657Gln)	MUC5B (R657Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3149576	NM_002458.3(MUC5B):c.1993G>T (p.Ala665Ser)	MUC5B (A665S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1048928	NM_002458.3(MUC5B):c.1994C>T (p.Ala665Val)	MUC5B (A665V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3149578	NM_002458.3(MUC5B):c.2000C>A (p.Ser667Tyr)	MUC5B (S667Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 163997	NM_002458.3(MUC5B):c.2007T>C (p.Tyr669=)	MUC5B	Single nucleotide variant (synonymous variant)	not specified	GBenign
Select item 1677809	NM_002458.3(MUC5B):c.2029G>A (p.Gly677Ser)	MUC5B (G677S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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