Muc5ac Variant Search Result - Rat Genome Database

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36 records found for search term Muc5ac

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
243053455	CV2404604	single nucleotide variant	NM_001304359.2(MUC5AC):c.211+43T>C	Lung adenocarcinoma [RCV003129631]	uncertain significance	11	1161629	1161629	Human	2	name
243053556	CV2404648	single nucleotide variant	NM_001304359.2(MUC5AC):c.1386+63G>T	Lung adenocarcinoma [RCV003129675]	uncertain significance	11	1165823	1165823	Human	2	name
243053609	CV2404598	single nucleotide variant	NM_001304359.2(MUC5AC):c.2093-112C>T	Lung adenocarcinoma [RCV003129625]	uncertain significance	11	1174770	1174770	Human	2	name
243053705	CV2404633	single nucleotide variant	NM_001304359.2(MUC5AC):c.3777-148T>A	Lung adenocarcinoma [RCV003129660]	uncertain significance	11	1180991	1180991	Human	2	name
243053553	CV2404647	single nucleotide variant	NM_001304359.2(MUC5AC):c.15862-71G>T	Lung adenocarcinoma [RCV003129674]	uncertain significance	11	1197397	1197397	Human	2	name
401909651	CV2806476	single nucleotide variant	NM_001304359.2(MUC5AC):c.285C>T (p.Asp95=)	not provided [RCV003424573]	likely benign	11	1161980	1161980	Human		name
243053379	CV2404576	single nucleotide variant	NM_001304359.2(MUC5AC):c.7242A>T (p.Ser2414=)	Lung adenocarcinoma [RCV003129603]	likely benign	11	1185387	1185387	Human	2	name
401909653	CV2806477	single nucleotide variant	NM_001304359.2(MUC5AC):c.13476T>C (p.Ala4492=)	not provided [RCV003424574]	likely benign	11	1191621	1191621	Human		name
401909654	CV2806478	single nucleotide variant	NM_001304359.2(MUC5AC):c.13539C>A (p.Pro4513=)	not provided [RCV003424575]	likely benign	11	1191684	1191684	Human		name
401909656	CV2806479	single nucleotide variant	NM_001304359.2(MUC5AC):c.13572T>C (p.Ala4524=)	not provided [RCV003424576]	likely benign	11	1191717	1191717	Human		name
401909658	CV2806480	single nucleotide variant	NM_001304359.2(MUC5AC):c.13596C>T (p.Ala4532=)	not provided [RCV003424577]	likely benign	11	1191741	1191741	Human		name
401909660	CV2806481	single nucleotide variant	NM_001304359.2(MUC5AC):c.13668T>C (p.Ala4556=)	not provided [RCV003424578]	likely benign	11	1191813	1191813	Human		name
401909662	CV2806482	single nucleotide variant	NM_001304359.2(MUC5AC):c.13719C>T (p.Pro4573=)	not provided [RCV003424579]	likely benign	11	1191864	1191864	Human		name
401909665	CV2806483	single nucleotide variant	NM_001304359.2(MUC5AC):c.13725C>G (p.Thr4575=)	not provided [RCV003424580]	likely benign	11	1191870	1191870	Human		name
401909667	CV2806484	single nucleotide variant	NM_001304359.2(MUC5AC):c.13785C>T (p.Pro4595=)	not provided [RCV003424581]	likely benign	11	1191930	1191930	Human		name
401909668	CV2806485	single nucleotide variant	NM_001304359.2(MUC5AC):c.13926A>G (p.Pro4642=)	not provided [RCV003424582]	likely benign	11	1192071	1192071	Human		name
401909670	CV2806486	single nucleotide variant	NM_001304359.2(MUC5AC):c.14034C>G (p.Ala4678=)	not provided [RCV003424583]	likely benign	11	1192179	1192179	Human		name
401909672	CV2806487	single nucleotide variant	NM_001304359.2(MUC5AC):c.14091T>C (p.Arg4697=)	not provided [RCV003424584]	likely benign	11	1192236	1192236	Human		name
401909674	CV2806488	single nucleotide variant	NM_001304359.2(MUC5AC):c.14190C>T (p.Gly4730=)	not provided [RCV003424585]	likely benign	11	1192335	1192335	Human		name
401909676	CV2806489	single nucleotide variant	NM_001304359.2(MUC5AC):c.14274C>A (p.Ala4758=)	not provided [RCV003424586]	likely benign	11	1192419	1192419	Human		name
401909677	CV2806490	single nucleotide variant	NM_001304359.2(MUC5AC):c.14295G>A (p.Val4765=)	not provided [RCV003424587]	likely benign	11	1192440	1192440	Human		name
401909682	CV2806492	single nucleotide variant	NM_001304359.2(MUC5AC):c.15225C>T (p.Arg5075=)	not provided [RCV003424589]	likely benign	11	1195046	1195046	Human		name
405853219	CV3393652	single nucleotide variant	NM_001304359.2(MUC5AC):c.14901C>T (p.Cys4967=)	not provided [RCV004546382]	likely benign	11	1194255	1194255	Human		name
596945256	CV3547769	single nucleotide variant	NM_001304359.2(MUC5AC):c.14175C>T (p.Cys4725=)	not provided [RCV004809100]	likely benign	11	1192320	1192320	Human		name
598224067	CV3894081	single nucleotide variant	NM_001304359.2(MUC5AC):c.13743T>C (p.Pro4581=)	not provided [RCV005257324]	likely benign	11	1191888	1191888	Human		name
598224078	CV3894082	single nucleotide variant	NM_001304359.2(MUC5AC):c.13749C>A (p.Thr4583=)	not provided [RCV005257325]	likely benign	11	1191894	1191894	Human		name
243053737	CV2404663	single nucleotide variant	NM_001304359.2(MUC5AC):c.6811G>T (p.Ala2271Ser)	Squamous cell carcinoma [RCV003129690]	uncertain significance	11	1184956	1184956	Human	2	name
243053585	CV2404666	single nucleotide variant	NM_001304359.2(MUC5AC):c.9463A>T (p.Thr3155Ser)	Lung adenocarcinoma [RCV003129693]	uncertain significance	11	1187608	1187608	Human	2	name
243053765	CV2404671	single nucleotide variant	NM_001304359.2(MUC5AC):c.7411G>C (p.Ala2471Pro)	Squamous cell carcinoma [RCV003129698]	uncertain significance	11	1185556	1185556	Human	2	name
329954605	CV2473319	single nucleotide variant	NM_001304359.2(MUC5AC):c.3601C>T (p.Arg1201Trp)	Keratoconus [RCV003235808]	uncertain significance	11	1180138	1180138	Human	2	name
329954606	CV2473320	single nucleotide variant	NM_001304359.2(MUC5AC):c.5459G>A (p.Arg1820Gln)	Keratoconus [RCV003235809]	uncertain significance	11	1183604	1183604	Human	2	name
243053727	CV2404657	single nucleotide variant	NM_001304359.2(MUC5AC):c.10898C>T (p.Ala3633Val)	Squamous cell carcinoma [RCV003129684]	uncertain significance	11	1189043	1189043	Human	2	name
243057680	CV2404673	single nucleotide variant	NM_001304359.2(MUC5AC):c.14615A>G (p.Glu4872Gly)	Lung adenocarcinoma [RCV003129700]	uncertain significance	11	1193519	1193519	Human	2	name
243053598	CV2404679	single nucleotide variant	NM_001304359.2(MUC5AC):c.14528C>A (p.Thr4843Asn)	Lung adenocarcinoma [RCV003129706]	uncertain significance	11	1192930	1192930	Human	2	name
329954607	CV2473321	single nucleotide variant	NM_001304359.2(MUC5AC):c.10301C>T (p.Pro3434Leu)	Keratoconus [RCV003235810]	uncertain significance	11	1188446	1188446	Human	2	name
401909680	CV2806491	single nucleotide variant	NM_001304359.2(MUC5AC):c.15020A>G (p.Asn5007Ser)	not provided [RCV003424588]	likely benign	11	1194500	1194500	Human		name

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