Galnt14 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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75 records found for search term Galnt14

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15128901	CV778935	single nucleotide variant	NM_024572.4(GALNT14):c.533-10C>T	not provided [RCV000964165]	benign	2	30955749	30955749	Human		name
8630317	CV85472	single nucleotide variant	NM_024572.3(GALNT14):c.129+23156C>T	Malignant melanoma [RCV000065555]	not provided	2	31114802	31114802	Human		name
8577111	CV111481	single nucleotide variant	NM_001253826.1(GALNT14):c.843-1115A>T	Lung cancer [RCV000092004]	uncertain significance	2	30943419	30943419	Human		name
156220565	CV2254164	single nucleotide variant	NM_024572.4(GALNT14):c.5G>C (p.Arg2Pro)	not specified [RCV004129594]	uncertain significance	2	31138082	31138082	Human		name
405749145	CV3254391	single nucleotide variant	NM_024572.4(GALNT14):c.8G>T (p.Arg3Leu)	not specified [RCV004392470]	uncertain significance	2	31138079	31138079	Human		name
598202986	CV3973879	single nucleotide variant	NM_024572.4(GALNT14):c.5G>A (p.Arg2Gln)	not specified [RCV005337187]	uncertain significance	2	31138082	31138082	Human		name
329371625	CV2454817	single nucleotide variant	NM_024572.4(GALNT14):c.14C>G (p.Thr5Ser)	not specified [RCV004270329]	uncertain significance	2	31138073	31138073	Human		name
405749104	CV3254385	single nucleotide variant	NM_024572.4(GALNT14):c.399T>C (p.Ser133=)	not specified [RCV004392464]	likely benign	2	30958464	30958464	Human		name
15098440	CV697550	single nucleotide variant	NM_024572.4(GALNT14):c.594C>T (p.Leu198=)	not provided [RCV000958559]	benign	2	30955678	30955678	Human		name
8630316	CV85471	single nucleotide variant	NM_024572.3(GALNT14):c.456C>T (p.Phe152=)	Malignant melanoma [RCV000065554]	not provided	2	30958407	30958407	Human		name
156366569	CV2203353	single nucleotide variant	NM_024572.4(GALNT14):c.239A>G (p.Asn80Ser)	not specified [RCV004072583]	uncertain significance	2	30992898	30992898	Human		name
156132669	CV2206662	single nucleotide variant	NM_024572.4(GALNT14):c.139G>A (p.Ala47Thr)	not specified [RCV004081000]	uncertain significance	2	30992998	30992998	Human		name
156182460	CV2338202	single nucleotide variant	NM_024572.4(GALNT14):c.202C>T (p.Arg68Cys)	not specified [RCV004186271]	uncertain significance	2	30992935	30992935	Human		name
329373573	CV2434537	single nucleotide variant	NM_024572.4(GALNT14):c.179G>A (p.Arg60Gln)	not specified [RCV004254239]	uncertain significance	2	30992958	30992958	Human		name
401896766	CV2788760	single nucleotide variant	NM_024572.4(GALNT14):c.209G>A (p.Gly70Asp)	not specified [RCV004361228]	uncertain significance	2	30992928	30992928	Human		name
405749087	CV3254382	single nucleotide variant	NM_024572.4(GALNT14):c.292C>T (p.His98Tyr)	not specified [RCV004392461]	uncertain significance	2	30992845	30992845	Human		name
407503427	CV3436282	single nucleotide variant	NM_024572.4(GALNT14):c.125C>T (p.Pro42Leu)	not specified [RCV004623755]	uncertain significance	2	31137962	31137962	Human		name
598202998	CV3973881	single nucleotide variant	NM_024572.4(GALNT14):c.223A>G (p.Lys75Glu)	not specified [RCV005337189]	uncertain significance	2	30992914	30992914	Human		name
15164846	CV708230	single nucleotide variant	NM_024572.4(GALNT14):c.1494C>T (p.Asp498=)	not provided [RCV000970819]	benign	2	30912229	30912229	Human		name
15164849	CV708231	single nucleotide variant	NM_024572.4(GALNT14):c.205G>A (p.Val69Ile)	not provided [RCV000970820]	benign	2	30992932	30992932	Human		name
8625352	CV80475	single nucleotide variant	NM_024572.3(GALNT14):c.1338G>A (p.Leu446=)	Malignant melanoma [RCV000060552]	not provided	2	30924161	30924161	Human		name
8630315	CV85470	single nucleotide variant	NM_024572.3(GALNT14):c.1449C>T (p.Phe483=)	Malignant melanoma [RCV000065553]	not provided	2	30912274	30912274	Human		name
156163951	CV2246720	single nucleotide variant	NM_024572.4(GALNT14):c.472G>A (p.Asp158Asn)	not specified [RCV004110440]	uncertain significance	2	30955972	30955972	Human		name
156068623	CV2280699	single nucleotide variant	NM_024572.4(GALNT14):c.632C>T (p.Pro211Leu)	not specified [RCV004143160]	uncertain significance	2	30955640	30955640	Human		name
156248619	CV2307257	single nucleotide variant	NM_024572.4(GALNT14):c.300A>T (p.Arg100Ser)	not specified [RCV004159714]	uncertain significance	2	30966302	30966302	Human		name
156178548	CV2331323	single nucleotide variant	NM_024572.4(GALNT14):c.377C>T (p.Thr126Met)	not specified [RCV004183967]	uncertain significance	2	30966225	30966225	Human		name
156195434	CV2347493	single nucleotide variant	NM_024572.4(GALNT14):c.317A>C (p.Tyr106Ser)	not specified [RCV004200442]	uncertain significance	2	30966285	30966285	Human		name
156305430	CV2369474	single nucleotide variant	NM_024572.4(GALNT14):c.796G>A (p.Ala266Thr)	not specified [RCV004210411]	uncertain significance	2	30944889	30944889	Human		name
329356294	CV2430677	single nucleotide variant	NM_024572.4(GALNT14):c.547C>T (p.Arg183Trp)	not specified [RCV004253866]	uncertain significance	2	30955725	30955725	Human		name
401769097	CV2696680	single nucleotide variant	NM_024572.4(GALNT14):c.580A>T (p.Thr194Ser)	not specified [RCV004290661]	uncertain significance	2	30955692	30955692	Human		name
401893720	CV2759892	single nucleotide variant	NM_024572.4(GALNT14):c.431G>A (p.Arg144Gln)	not specified [RCV004345319]	likely benign	2	30958432	30958432	Human		name
401866481	CV2775563	single nucleotide variant	NM_024572.4(GALNT14):c.436A>G (p.Ile146Val)	not specified [RCV004350731]	uncertain significance	2	30958427	30958427	Human		name
405258825	CV3215161	single nucleotide variant	NM_024572.4(GALNT14):c.976G>A (p.Val326Ile)	GALNT14-related disorder [RCV003942208]	likely benign	2	30932150	30932150	Human		name , trait , alternate_id
405749092	CV3254383	single nucleotide variant	NM_024572.4(GALNT14):c.350T>C (p.Ile117Thr)	not specified [RCV004392462]	uncertain significance	2	30966252	30966252	Human		name
405749097	CV3254384	single nucleotide variant	NM_024572.4(GALNT14):c.362A>G (p.Asn121Ser)	not specified [RCV004392463]	uncertain significance	2	30966240	30966240	Human		name
405749112	CV3254386	single nucleotide variant	NM_024572.4(GALNT14):c.553C>T (p.Arg185Trp)	not specified [RCV004392465]	uncertain significance	2	30955719	30955719	Human		name
405749119	CV3254387	single nucleotide variant	NM_024572.4(GALNT14):c.623G>T (p.Trp208Leu)	not specified [RCV004392466]	uncertain significance	2	30955649	30955649	Human		name
405749124	CV3254388	single nucleotide variant	NM_024572.4(GALNT14):c.631C>G (p.Pro211Ala)	not specified [RCV004392467]	uncertain significance	2	30955641	30955641	Human		name
405749128	CV3254389	single nucleotide variant	NM_024572.4(GALNT14):c.832C>T (p.Pro278Ser)	not specified [RCV004392468]	uncertain significance	2	30942300	30942300	Human		name
405749139	CV3254390	single nucleotide variant	NM_024572.4(GALNT14):c.862G>A (p.Asp288Asn)	not specified [RCV004392469]	uncertain significance	2	30942270	30942270	Human		name
405749151	CV3254392	single nucleotide variant	NM_024572.4(GALNT14):c.989G>A (p.Arg330Gln)	not specified [RCV004392471]	uncertain significance	2	30932137	30932137	Human		name
407503413	CV3436278	single nucleotide variant	NM_024572.4(GALNT14):c.856G>A (p.Val286Met)	not specified [RCV004623751]	uncertain significance	2	30942276	30942276	Human		name
407503416	CV3436279	single nucleotide variant	NM_024572.4(GALNT14):c.371G>A (p.Arg124His)	not specified [RCV004623752]	uncertain significance	2	30966231	30966231	Human		name
407503419	CV3436280	single nucleotide variant	NM_024572.4(GALNT14):c.503T>G (p.Val168Gly)	not specified [RCV004623753]	uncertain significance	2	30955941	30955941	Human		name
407503424	CV3436281	single nucleotide variant	NM_024572.4(GALNT14):c.568G>T (p.Ala190Ser)	not specified [RCV004623754]	uncertain significance	2	30955704	30955704	Human		name
597779869	CV3673640	single nucleotide variant	NM_024572.4(GALNT14):c.815C>T (p.Thr272Met)	not specified [RCV004930487]	uncertain significance	2	30944870	30944870	Human		name
597753917	CV3673642	single nucleotide variant	NM_024572.4(GALNT14):c.490A>G (p.Lys164Glu)	not specified [RCV004924250]	uncertain significance	2	30955954	30955954	Human		name
597753923	CV3673643	single nucleotide variant	NM_024572.4(GALNT14):c.332C>T (p.Pro111Leu)	not specified [RCV004924251]	uncertain significance	2	30966270	30966270	Human		name
598203005	CV3973882	single nucleotide variant	NM_024572.4(GALNT14):c.689T>C (p.Ile230Thr)	not specified [RCV005337190]	uncertain significance	2	30945836	30945836	Human		name
10044429	CV188275	single nucleotide variant	NM_024572.4(GALNT14):c.1273C>T (p.Arg425Ter)	Non-immune hydrops fetalis [RCV000170583]\|not provided [RCV003989475]	pathogenic\|likely pathogenic\|no classifications from unflagged records	2	30924226	30924226	Human	2	name
156274525	CV2202632	single nucleotide variant	NM_024572.4(GALNT14):c.1603G>T (p.Val535Phe)	not specified [RCV004082888]	uncertain significance	2	30910957	30910957	Human		name
156364081	CV2262768	single nucleotide variant	NM_024572.4(GALNT14):c.1147G>A (p.Gly383Arg)	not specified [RCV004130942]	uncertain significance	2	30929399	30929399	Human		name
156347015	CV2297792	single nucleotide variant	NM_024572.4(GALNT14):c.1616A>G (p.Glu539Gly)	not specified [RCV004157746]	uncertain significance	2	30910944	30910944	Human		name
155906829	CV2303389	single nucleotide variant	NM_024572.4(GALNT14):c.1367A>G (p.Asp456Gly)	not specified [RCV004159120]	uncertain significance	2	30924132	30924132	Human		name
156059535	CV2305334	single nucleotide variant	NM_024572.4(GALNT14):c.1063A>G (p.Thr355Ala)	not specified [RCV004171246]	uncertain significance	2	30929483	30929483	Human		name
156043073	CV2311021	single nucleotide variant	NM_024572.4(GALNT14):c.1570G>A (p.Gly524Ser)	not specified [RCV004164040]	uncertain significance	2	30910990	30910990	Human		name
156055101	CV2326555	single nucleotide variant	NM_024572.4(GALNT14):c.1465G>A (p.Val489Ile)	not specified [RCV004183103]	uncertain significance	2	30912258	30912258	Human		name
156184018	CV2328009	single nucleotide variant	NM_024572.4(GALNT14):c.1049C>T (p.Thr350Met)	not specified [RCV004179317]	uncertain significance	2	30932077	30932077	Human		name
156145022	CV2383972	single nucleotide variant	NM_024572.4(GALNT14):c.1456G>A (p.Ala486Thr)	not specified [RCV004224949]	uncertain significance	2	30912267	30912267	Human		name
156080339	CV2384628	single nucleotide variant	NM_024572.4(GALNT14):c.1555G>C (p.Asp519His)	not specified [RCV004232410]	uncertain significance	2	30911005	30911005	Human		name
329373755	CV2452645	single nucleotide variant	NM_024572.4(GALNT14):c.1114G>T (p.Ala372Ser)	not specified [RCV004275214]	uncertain significance	2	30929432	30929432	Human		name
329357203	CV2457581	single nucleotide variant	NM_024572.4(GALNT14):c.1600G>A (p.Val534Ile)	not specified [RCV004269167]	uncertain significance	2	30910960	30910960	Human		name
401728958	CV2673104	single nucleotide variant	NM_024572.4(GALNT14):c.1280G>A (p.Arg427Lys)	not specified [RCV004284089]	uncertain significance	2	30924219	30924219	Human		name
401738018	CV2676101	single nucleotide variant	NM_024572.4(GALNT14):c.1007G>A (p.Arg336Gln)	not specified [RCV004284326]	uncertain significance	2	30932119	30932119	Human		name
401728607	CV2729687	single nucleotide variant	NM_024572.4(GALNT14):c.1276C>G (p.Gln426Glu)	not specified [RCV004331945]	uncertain significance	2	30924223	30924223	Human		name
401865221	CV2768712	single nucleotide variant	NM_024572.4(GALNT14):c.1186C>T (p.Arg396Cys)	not specified [RCV004346557]	uncertain significance	2	30924789	30924789	Human		name
405285503	CV3212525	single nucleotide variant	NM_024572.4(GALNT14):c.1599C>G (p.Ile533Met)	GALNT14-related disorder [RCV003959107]	uncertain significance	2	30910961	30910961	Human		name , trait , alternate_id
405749059	CV3254378	single nucleotide variant	NM_024572.4(GALNT14):c.1262A>G (p.Lys421Arg)	not specified [RCV004392457]	uncertain significance	2	30924237	30924237	Human		name
405749073	CV3254380	single nucleotide variant	NM_024572.4(GALNT14):c.1591A>G (p.Lys531Glu)	not specified [RCV004392459]	uncertain significance	2	30910969	30910969	Human		name
405749083	CV3254381	single nucleotide variant	NM_024572.4(GALNT14):c.1647G>T (p.Met549Ile)	not specified [RCV004392460]	uncertain significance	2	30910913	30910913	Human		name
407503410	CV3436277	single nucleotide variant	NM_024572.4(GALNT14):c.1187G>A (p.Arg396His)	not specified [RCV004623750]	uncertain significance	2	30924788	30924788	Human		name
408384559	CV3504320	single nucleotide variant	NM_024572.4(GALNT14):c.1382T>A (p.Val461Glu)	GALNT14-related disorder [RCV004731915]	uncertain significance	2	30912341	30912341	Human		name , trait , alternate_id
597753914	CV3673641	single nucleotide variant	NM_024572.4(GALNT14):c.1202A>C (p.Lys401Thr)	not specified [RCV004924249]	uncertain significance	2	30924773	30924773	Human		name
598202980	CV3973878	single nucleotide variant	NM_024572.4(GALNT14):c.1179G>C (p.Lys393Asn)	not specified [RCV005337186]	uncertain significance	2	30924796	30924796	Human		name
598202992	CV3973880	single nucleotide variant	NM_024572.4(GALNT14):c.1024G>A (p.Val342Ile)	not specified [RCV005337188]	uncertain significance	2	30932102	30932102	Human		name

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