Cldn10 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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41 records found for search term Cldn10

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150456478	CV1260017	single nucleotide variant	NM_006984.5(CLDN10):c.*11T>G	not provided [RCV001681496]	benign	13	95578025	95578025	Human		name
150478746	CV1273348	single nucleotide variant	NM_182848.4(CLDN10):c.-78A>G	not provided [RCV001696551]	benign	13	95433756	95433756	Human		name
150336878	CV1172551	single nucleotide variant	NM_182848.4(CLDN10):c.214+179C>T	not provided [RCV001541250]	benign	13	95434226	95434226	Human		name
150433214	CV1230449	single nucleotide variant	NM_006984.5(CLDN10):c.220+132A>C	not provided [RCV001643394]	benign	13	95553105	95553105	Human		name
150494300	CV1267326	single nucleotide variant	NM_006984.5(CLDN10):c.220+106C>T	not provided [RCV001688354]	benign	13	95553079	95553079	Human		name
150513167	CV1211839	single nucleotide variant	NM_182848.4(CLDN10):c.215-7578G>A	not provided [RCV001598360]	benign	13	95552554	95552554	Human		name
150515576	CV1227602	deletion	NM_182848.4(CLDN10):c.215-7613del	not provided [RCV001638876]	benign	13	95552517	95552517	Human		name
8583402	CV117963	single nucleotide variant	NM_001160100.1(CLDN10):c.157+55141T>C	Lung cancer [RCV000098484]	uncertain significance	13	95489131	95489131	Human		name
13435677	CV432259	single nucleotide variant	NM_006984.5(CLDN10):c.2T>C (p.Met1Thr)	HELIX syndrome [RCV000505532]	pathogenic	13	95552755	95552755	Human	1	name
405290899	CV3208657	single nucleotide variant	NM_006984.5(CLDN10):c.228A>C (p.Ile76=)	CLDN10-related disorder [RCV003927293]	benign	13	95560139	95560139	Human		name , trait , alternate_id
156060159	CV2391847	single nucleotide variant	NM_006984.5(CLDN10):c.62T>C (p.Val21Ala)	Inborn genetic diseases [RCV002759868]	uncertain significance	13	95552815	95552815	Human	1	name
405295189	CV3211093	single nucleotide variant	NM_006984.5(CLDN10):c.402A>C (p.Gly134=)	CLDN10-related disorder [RCV003937089]	benign	13	95560401	95560401	Human		name , trait , alternate_id
405685580	CV3306582	single nucleotide variant	NM_006984.5(CLDN10):c.35T>C (p.Met12Thr)	Inborn genetic diseases [RCV004444299]	uncertain significance	13	95552788	95552788	Human	1	name
8621481	CV75455	single nucleotide variant	NM_006984.5(CLDN10):c.318C>T (p.Val106=)	not provided [RCV000054677]	uncertain significance	13	95560229	95560229	Human		name
156272818	CV2195344	single nucleotide variant	NM_006984.5(CLDN10):c.271T>C (p.Phe91Leu)	Inborn genetic diseases [RCV002669653]	uncertain significance	13	95560182	95560182	Human	1	name
156298695	CV2310650	single nucleotide variant	NM_006984.5(CLDN10):c.242G>A (p.Gly81Glu)	Inborn genetic diseases [RCV002897749]	uncertain significance	13	95560153	95560153	Human	1	name
156190254	CV2356720	single nucleotide variant	NM_182848.4(CLDN10):c.101C>T (p.Ala34Val)	Inborn genetic diseases [RCV002984568]	uncertain significance	13	95433934	95433934	Human	1	name
329373513	CV2447282	single nucleotide variant	NM_006984.5(CLDN10):c.256G>T (p.Ala86Ser)	Inborn genetic diseases [RCV003185177]	uncertain significance	13	95560167	95560167	Human	1	name
401757646	CV2707893	single nucleotide variant	NM_006984.5(CLDN10):c.198C>A (p.Phe66Leu)	Inborn genetic diseases [RCV003256117]	uncertain significance	13	95552951	95552951	Human	1	name
401796637	CV2739601	single nucleotide variant	NM_006984.5(CLDN10):c.138G>A (p.Trp46Ter)	HELIX syndrome [RCV003319566]	pathogenic	13	95552891	95552891	Human	1	name
405685574	CV3306581	single nucleotide variant	NM_006984.5(CLDN10):c.127G>T (p.Ala43Ser)	Inborn genetic diseases [RCV004444298]	uncertain significance	13	95552880	95552880	Human	1	name
405853736	CV3395166	single nucleotide variant	NM_006984.5(CLDN10):c.142A>C (p.Asn48His)	HELIX syndrome [RCV004555308]	likely pathogenic	13	95552895	95552895	Human	1	name
597647165	CV3660249	single nucleotide variant	NM_006984.5(CLDN10):c.247A>G (p.Met83Val)	Inborn genetic diseases [RCV004973951]	uncertain significance	13	95560158	95560158	Human	1	name
597647174	CV3660251	single nucleotide variant	NM_006984.5(CLDN10):c.143A>G (p.Asn48Ser)	Inborn genetic diseases [RCV004973953]	uncertain significance	13	95552896	95552896	Human	1	name
13435675	CV432257	single nucleotide variant	NM_006984.5(CLDN10):c.144C>G (p.Asn48Lys)	HELIX syndrome [RCV000505520]	pathogenic	13	95552897	95552897	Human	1	name
38598073	CV963165	deletion	NM_006984.5(CLDN10):c.653del (p.Pro218fs)	HELIX syndrome [RCV001251100]	pathogenic\|likely pathogenic	13	95577978	95577978	Human	1	name
156330176	CV2210566	single nucleotide variant	NM_006984.5(CLDN10):c.358G>T (p.Ala120Ser)	Inborn genetic diseases [RCV002673215]	uncertain significance	13	95560269	95560269	Human	1	name
156071048	CV2267209	single nucleotide variant	NM_006984.5(CLDN10):c.554A>G (p.Asp185Gly)	Inborn genetic diseases [RCV002823451]	uncertain significance	13	95577320	95577320	Human	1	name
401719018	CV2679387	single nucleotide variant	NM_006984.5(CLDN10):c.620A>G (p.Tyr207Cys)	Inborn genetic diseases [RCV003243565]	uncertain significance	13	95577947	95577947	Human	1	name
401910104	CV2813962	single nucleotide variant	NM_006984.5(CLDN10):c.610C>T (p.Arg204Trp)	not provided [RCV003398344]	uncertain significance	13	95577937	95577937	Human		name
405685583	CV3306583	single nucleotide variant	NM_006984.5(CLDN10):c.371T>C (p.Phe124Ser)	Inborn genetic diseases [RCV004444300]	uncertain significance	13	95560282	95560282	Human	1	name
405685588	CV3306584	single nucleotide variant	NM_006984.5(CLDN10):c.649A>C (p.Asn217His)	Inborn genetic diseases [RCV004444301]	uncertain significance	13	95577976	95577976	Human	1	name
407462338	CV3419344	single nucleotide variant	NM_006984.5(CLDN10):c.442G>A (p.Asp148Asn)	Inborn genetic diseases [RCV004612879]	uncertain significance	13	95560441	95560441	Human	1	name
407462341	CV3419345	single nucleotide variant	NM_006984.5(CLDN10):c.647C>T (p.Thr216Ile)	Inborn genetic diseases [RCV004612880]	uncertain significance	13	95577974	95577974	Human	1	name
407572834	CV3497044	single nucleotide variant	NM_006984.5(CLDN10):c.497G>A (p.Trp166Ter)	HELIX syndrome [RCV004698912]	pathogenic	13	95577263	95577263	Human	1	name
597647169	CV3660250	single nucleotide variant	NM_006984.5(CLDN10):c.634G>A (p.Asp212Asn)	Inborn genetic diseases [RCV004973952]	uncertain significance	13	95577961	95577961	Human	1	name
13435676	CV432258	single nucleotide variant	NM_006984.5(CLDN10):c.392C>T (p.Ser131Leu)	HELIX syndrome [RCV000505524]	pathogenic	13	95560391	95560391	Human	1	name
15040301	CV682738	single nucleotide variant	NM_006984.5(CLDN10):c.431C>T (p.Thr144Met)	Hypokalemia [RCV000856682]\|Inborn genetic diseases [RCV003169089]	uncertain significance	13	95560430	95560430	Human	5	name
8621482	CV75456	single nucleotide variant	NM_006984.5(CLDN10):c.420C>A (p.Asn140Lys)	not provided [RCV000054678]	uncertain significance	13	95560419	95560419	Human		name
8621483	CV75457	single nucleotide variant	NM_006984.5(CLDN10):c.505G>T (p.Ala169Ser)	not provided [RCV000054679]	uncertain significance	13	95577271	95577271	Human		name
598201969	CV3891255	microsatellite	NM_006984.5(CLDN10):c.644CAA[1] (p.Thr216del)	HELIX syndrome [RCV005255073]	uncertain significance	13	95577969	95577971	Human		name

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