Krt25 Variant Search Result - Rat Genome Database

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94 records found for search term Krt25

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401904155	CV2811323	single nucleotide variant	NM_181534.4(KRT25):c.-2C>A	KRT25-related disorder [RCV004757587]\|not provided [RCV003419727]	benign	17	40755273	40755273	Human	1	name , trait , alternate_id
597856404	CV3816569	single nucleotide variant	NM_181534.4(KRT25):c.670-5T>C	not provided [RCV005146141]	likely benign	17	40751331	40751331	Human		name
150503793	CV1257867	single nucleotide variant	NM_181534.4(KRT25):c.430-91C>A	not provided [RCV001677555]	benign	17	40754559	40754559	Human		name
156230445	CV1959148	single nucleotide variant	NM_181534.4(KRT25):c.670-17C>T	not provided [RCV002596789]	likely benign	17	40751343	40751343	Human		name
156397883	CV2009225	single nucleotide variant	NM_181534.4(KRT25):c.832-11T>C	not provided [RCV002725745]	likely benign	17	40751090	40751090	Human		name
150461773	CV1214554	single nucleotide variant	NM_181534.4(KRT25):c.1243+33A>C	not provided [RCV001613547]	benign	17	40749225	40749225	Human		name
150501732	CV1241015	single nucleotide variant	NM_181534.4(KRT25):c.669+212G>A	not provided [RCV001656910]	benign	17	40753648	40753648	Human		name
150472517	CV1252257	single nucleotide variant	NM_181534.4(KRT25):c.429+166C>G	not provided [RCV001671458]	benign	17	40754677	40754677	Human		name
150499015	CV1270750	single nucleotide variant	NM_181534.4(KRT25):c.669+208A>G	not provided [RCV001689299]	benign	17	40753652	40753652	Human		name
405255492	CV3172473	single nucleotide variant	NM_181534.4(KRT25):c.1176-14C>T	not provided [RCV003872411]	likely benign	17	40749339	40749339	Human		name
597870646	CV3749942	single nucleotide variant	NM_181534.4(KRT25):c.1176-13G>A	not provided [RCV005068623]	likely benign	17	40749338	40749338	Human		name
401895525	CV2774415	single nucleotide variant	NM_181534.4(KRT25):c.16T>C (p.Ser6Pro)	not specified [RCV004347754]	uncertain significance	17	40755256	40755256	Human		name
405183183	CV3024486	single nucleotide variant	NM_181534.4(KRT25):c.189C>T (p.Pro63=)	not provided [RCV003705678]	likely benign	17	40755083	40755083	Human		name
15115731	CV740720	single nucleotide variant	NM_181534.4(KRT25):c.268C>T (p.Leu90=)	not provided [RCV000895080]	likely benign	17	40755004	40755004	Human		name
15203459	CV755822	single nucleotide variant	NM_181534.4(KRT25):c.243G>A (p.Val81=)	KRT25-related disorder [RCV003895557]\|not provided [RCV000914016]	benign\|likely benign	17	40755029	40755029	Human	1	name , trait , alternate_id
150492380	CV1266642	single nucleotide variant	NM_181534.4(KRT25):c.312C>T (p.Asn104=)	not provided [RCV001687964]	benign	17	40754960	40754960	Human		name
156373750	CV1901947	single nucleotide variant	NM_181534.4(KRT25):c.648C>T (p.Tyr216=)	KRT25-related disorder [RCV003943778]\|not provided [RCV003092683]	benign\|likely benign	17	40753881	40753881	Human	1	name , trait , alternate_id
155910197	CV2041153	single nucleotide variant	NM_181534.4(KRT25):c.990C>T (p.Thr330=)	not provided [RCV002771525]	likely benign	17	40750565	40750565	Human		name
156020450	CV2141231	single nucleotide variant	NM_181534.4(KRT25):c.339C>T (p.Gly113=)	not provided [RCV002976128]	likely benign	17	40754933	40754933	Human		name
156220205	CV2345005	single nucleotide variant	NM_181534.4(KRT25):c.55G>A (p.Gly19Arg)	not specified [RCV004193293]	uncertain significance	17	40755217	40755217	Human		name
401723421	CV2737826	single nucleotide variant	NM_181534.4(KRT25):c.44G>A (p.Arg15His)	not provided [RCV003314998]	uncertain significance	17	40755228	40755228	Human		name
405223265	CV3061091	single nucleotide variant	NM_181534.4(KRT25):c.543T>C (p.Ser181=)	not provided [RCV003733565]	likely benign	17	40753986	40753986	Human		name
405214991	CV3169958	single nucleotide variant	NM_181534.4(KRT25):c.591C>T (p.Thr197=)	not provided [RCV003862563]	likely benign	17	40753938	40753938	Human		name
407499815	CV3445483	single nucleotide variant	NM_181534.4(KRT25):c.49A>G (p.Thr17Ala)	not specified [RCV004644457]	uncertain significance	17	40755223	40755223	Human		name
407499828	CV3445487	single nucleotide variant	NM_181534.4(KRT25):c.29G>A (p.Arg10Lys)	not specified [RCV004644460]	uncertain significance	17	40755243	40755243	Human		name
597970173	CV3801880	single nucleotide variant	NM_181534.4(KRT25):c.678A>G (p.Gln226=)	not provided [RCV005141672]	likely benign	17	40751318	40751318	Human		name
15167177	CV704124	single nucleotide variant	NM_181534.4(KRT25):c.438A>C (p.Ala146=)	not provided [RCV000949000]	benign	17	40754460	40754460	Human		name
150512175	CV1242897	single nucleotide variant	NM_181534.4(KRT25):c.197G>C (p.Gly66Ala)	not provided [RCV001661251]	benign	17	40755075	40755075	Human		name
150451000	CV1272449	single nucleotide variant	NM_181534.4(KRT25):c.161C>T (p.Ser54Leu)	not provided [RCV001691930]	benign	17	40755111	40755111	Human		name
156033422	CV2236243	single nucleotide variant	NM_181534.4(KRT25):c.141T>A (p.Ser47Arg)	not specified [RCV004107944]	uncertain significance	17	40755131	40755131	Human		name
329367658	CV2456976	single nucleotide variant	NM_181534.4(KRT25):c.248T>C (p.Met83Thr)	not specified [RCV004270913]	uncertain significance	17	40755024	40755024	Human		name
405221849	CV2908124	single nucleotide variant	NM_181534.4(KRT25):c.214C>T (p.Arg72Trp)	KRT25-related disorder [RCV003929269]\|not provided [RCV003568471]	likely benign	17	40755058	40755058	Human	1	name , trait , alternate_id
405254319	CV3045267	single nucleotide variant	NM_181534.4(KRT25):c.1017G>A (p.Ala339=)	not provided [RCV003722840]	likely benign	17	40750538	40750538	Human		name
405138425	CV3130795	single nucleotide variant	NM_181534.4(KRT25):c.215G>C (p.Arg72Pro)	not provided [RCV003839029]	uncertain significance	17	40755057	40755057	Human		name
405817281	CV3273021	single nucleotide variant	NM_181534.4(KRT25):c.110G>A (p.Gly37Asp)	not specified [RCV004412266]	uncertain significance	17	40755162	40755162	Human		name
405817283	CV3273023	single nucleotide variant	NM_181534.4(KRT25):c.245C>T (p.Thr82Ile)	not specified [RCV004412268]	uncertain significance	17	40755027	40755027	Human		name
407459923	CV3445484	single nucleotide variant	NM_181534.4(KRT25):c.176G>A (p.Gly59Glu)	not specified [RCV004633710]	uncertain significance	17	40755096	40755096	Human		name
407499819	CV3445485	single nucleotide variant	NM_181534.4(KRT25):c.191G>A (p.Cys64Tyr)	not specified [RCV004644458]	uncertain significance	17	40755081	40755081	Human		name
597798048	CV3698459	single nucleotide variant	NM_181534.4(KRT25):c.215G>A (p.Arg72Gln)	not specified [RCV004936005]	uncertain significance	17	40755057	40755057	Human		name
597798065	CV3698465	single nucleotide variant	NM_181534.4(KRT25):c.265C>T (p.Arg89Cys)	not specified [RCV004936011]	uncertain significance	17	40755007	40755007	Human		name
598162860	CV3980326	single nucleotide variant	NM_181534.4(KRT25):c.176G>C (p.Gly59Ala)	not specified [RCV005368725]	likely benign	17	40755096	40755096	Human		name
15150824	CV727158	single nucleotide variant	NM_181534.4(KRT25):c.1089G>A (p.Lys363=)	not provided [RCV000879465]	benign	17	40750466	40750466	Human		name
127282730	CV1082998	single nucleotide variant	NM_181534.4(KRT25):c.891T>G (p.Asn297Lys)	not provided [RCV001411318]\|not specified [RCV004038074]	likely benign\|uncertain significance	17	40751020	40751020	Human		name
156372304	CV1920917	single nucleotide variant	NM_181534.4(KRT25):c.539A>T (p.Gln180Leu)	not provided [RCV002603281]\|not specified [RCV004069022]	uncertain significance	17	40753990	40753990	Human		name
156083470	CV2012098	single nucleotide variant	NM_181534.4(KRT25):c.799C>T (p.Arg267Cys)	not provided [RCV002706065]	uncertain significance	17	40751197	40751197	Human		name
156248693	CV2097939	single nucleotide variant	NM_181534.4(KRT25):c.800G>A (p.Arg267His)	not provided [RCV002895184]	benign	17	40751196	40751196	Human		name
10407759	CV213953	single nucleotide variant	NM_181534.4(KRT25):c.950T>C (p.Leu317Pro)	Hypotrichosis 8 [RCV000201248]\|Wooly hair, autosomal recessive 3 [RCV000203575]	pathogenic\|likely pathogenic	17	40750961	40750961	Human	2	name
155964728	CV2210069	single nucleotide variant	NM_181534.4(KRT25):c.517G>A (p.Glu173Lys)	not specified [RCV004076498]	uncertain significance	17	40754012	40754012	Human		name
156329271	CV2213805	single nucleotide variant	NM_181534.4(KRT25):c.470A>C (p.Gln157Pro)	not specified [RCV004089865]	uncertain significance	17	40754428	40754428	Human		name
156369360	CV2263323	single nucleotide variant	NM_181534.4(KRT25):c.523G>C (p.Glu175Gln)	not specified [RCV004133597]	uncertain significance	17	40754006	40754006	Human		name
156335854	CV2273045	single nucleotide variant	NM_181534.4(KRT25):c.474C>G (p.Ile158Met)	not specified [RCV004137697]	uncertain significance	17	40754424	40754424	Human		name
156061482	CV2323174	single nucleotide variant	NM_181534.4(KRT25):c.962A>C (p.His321Pro)	not specified [RCV004187575]	uncertain significance	17	40750593	40750593	Human		name
155980203	CV2336886	single nucleotide variant	NM_181534.4(KRT25):c.932T>C (p.Ile311Thr)	not specified [RCV004190504]	uncertain significance	17	40750979	40750979	Human		name
156180795	CV2356114	single nucleotide variant	NM_181534.4(KRT25):c.736G>A (p.Val246Met)	Wooly hair, autosomal recessive 3 [RCV005021746]\|not specified [RCV004203524]	uncertain significance	17	40751260	40751260	Human	1	name
156105589	CV2387026	single nucleotide variant	NM_181534.4(KRT25):c.731C>T (p.Pro244Leu)	not specified [RCV004226776]	uncertain significance	17	40751265	40751265	Human		name
11522866	CV244036	single nucleotide variant	NM_181534.4(KRT25):c.712G>T (p.Val238Leu)	Autosomal Recessive Hypotrichosis with Woolly Hair [RCV000234939]\|Wooly hair, autosomal recessive 3 [RCV000490551]	pathogenic	17	40751284	40751284	Human	1	name
329358898	CV2450741	single nucleotide variant	NM_181534.4(KRT25):c.440C>T (p.Ser147Phe)	not specified [RCV004267677]	uncertain significance	17	40754458	40754458	Human		name
329396827	CV2468245	single nucleotide variant	NM_181534.4(KRT25):c.486G>C (p.Arg162Ser)	not specified [RCV004275812]	uncertain significance	17	40754412	40754412	Human		name
329392172	CV2470440	single nucleotide variant	NM_181534.4(KRT25):c.604G>A (p.Asp202Asn)	not specified [RCV004273467]	uncertain significance	17	40753925	40753925	Human		name
401772196	CV2719565	single nucleotide variant	NM_181534.4(KRT25):c.313G>A (p.Ala105Thr)	not specified [RCV004327243]	uncertain significance	17	40754959	40754959	Human		name
401896548	CV2780929	single nucleotide variant	NM_181534.4(KRT25):c.556G>A (p.Val186Ile)	not specified [RCV004354469]	uncertain significance	17	40753973	40753973	Human		name
401883050	CV2788641	single nucleotide variant	NM_181534.4(KRT25):c.428A>C (p.Gln143Pro)	not specified [RCV004361128]	uncertain significance	17	40754844	40754844	Human		name
405119872	CV2891620	single nucleotide variant	NM_181534.4(KRT25):c.496G>A (p.Asp166Asn)	not provided [RCV003558941]	likely benign	17	40754402	40754402	Human		name
405141477	CV2903791	single nucleotide variant	NM_181534.4(KRT25):c.666A>T (p.Lys222Asn)	not provided [RCV003560790]	likely benign	17	40753863	40753863	Human		name
405817284	CV3273024	single nucleotide variant	NM_181534.4(KRT25):c.370C>T (p.Arg124Cys)	not specified [RCV004412269]	uncertain significance	17	40754902	40754902	Human		name
405817285	CV3273025	single nucleotide variant	NM_181534.4(KRT25):c.409A>C (p.Ile137Leu)	not specified [RCV004412270]	uncertain significance	17	40754863	40754863	Human		name
405817286	CV3273026	single nucleotide variant	NM_181534.4(KRT25):c.574G>A (p.Val192Ile)	not specified [RCV004412271]	uncertain significance	17	40753955	40753955	Human		name
407499811	CV3445482	single nucleotide variant	NM_181534.4(KRT25):c.828G>C (p.Glu276Asp)	not specified [RCV004644456]	uncertain significance	17	40751168	40751168	Human		name
407499832	CV3445488	single nucleotide variant	NM_181534.4(KRT25):c.670G>C (p.Glu224Gln)	not specified [RCV004644461]	uncertain significance	17	40751326	40751326	Human		name
407459928	CV3445489	single nucleotide variant	NM_181534.4(KRT25):c.994A>G (p.Ser332Gly)	not specified [RCV004633711]	likely benign	17	40750561	40750561	Human		name
597798043	CV3698457	single nucleotide variant	NM_181534.4(KRT25):c.761A>G (p.Asn254Ser)	not specified [RCV004936003]	uncertain significance	17	40751235	40751235	Human		name
597798045	CV3698458	single nucleotide variant	NM_181534.4(KRT25):c.632G>A (p.Ser211Asn)	not specified [RCV004936004]	uncertain significance	17	40753897	40753897	Human		name
597798054	CV3698461	single nucleotide variant	NM_181534.4(KRT25):c.562G>C (p.Gly188Arg)	not specified [RCV004936007]	uncertain significance	17	40753967	40753967	Human		name
597798060	CV3698463	single nucleotide variant	NM_181534.4(KRT25):c.434T>A (p.Ile145Asn)	not specified [RCV004936009]	uncertain significance	17	40754464	40754464	Human		name
597798068	CV3698466	single nucleotide variant	NM_181534.4(KRT25):c.525G>T (p.Glu175Asp)	not specified [RCV004936012]	uncertain significance	17	40754004	40754004	Human		name
597798071	CV3698467	single nucleotide variant	NM_181534.4(KRT25):c.403C>T (p.Pro135Ser)	not specified [RCV004936013]	uncertain significance	17	40754869	40754869	Human		name
597911340	CV3770469	single nucleotide variant	NM_181534.4(KRT25):c.956C>A (p.Thr319Lys)	not provided [RCV005113770]	benign	17	40750955	40750955	Human		name
598162866	CV3980327	single nucleotide variant	NM_181534.4(KRT25):c.439T>C (p.Ser147Pro)	not specified [RCV005368726]	uncertain significance	17	40754459	40754459	Human		name
598162871	CV3980328	single nucleotide variant	NM_181534.4(KRT25):c.977C>G (p.Ser326Cys)	not specified [RCV005368727]	uncertain significance	17	40750578	40750578	Human		name
598184129	CV3980329	single nucleotide variant	NM_181534.4(KRT25):c.503T>C (p.Phe168Ser)	not specified [RCV005353021]	uncertain significance	17	40754395	40754395	Human		name
15130022	CV715432	single nucleotide variant	NM_181534.4(KRT25):c.436G>A (p.Ala146Thr)	not provided [RCV000964361]	likely benign	17	40754462	40754462	Human		name
15188155	CV727159	single nucleotide variant	NM_181534.4(KRT25):c.716A>C (p.Glu239Ala)	not provided [RCV000887452]	benign	17	40751280	40751280	Human		name
8636138	CV91362	single nucleotide variant	NM_181534.3(KRT25):c.661C>T (p.His221Tyr)	Malignant melanoma [RCV000071460]	not provided	17	40753868	40753868	Human		name
156146010	CV1932095	single nucleotide variant	NM_181534.4(KRT25):c.1317G>C (p.Arg439Ser)	not provided [RCV002623834]	uncertain significance	17	40748313	40748313	Human		name
156130033	CV2279757	single nucleotide variant	NM_181534.4(KRT25):c.1246C>G (p.Pro416Ala)	not specified [RCV004144371]	uncertain significance	17	40748384	40748384	Human		name
156255088	CV2325713	single nucleotide variant	NM_181534.4(KRT25):c.1004G>T (p.Cys335Phe)	not specified [RCV004180114]	uncertain significance	17	40750551	40750551	Human		name
401890410	CV2778681	single nucleotide variant	NM_181534.4(KRT25):c.1036G>A (p.Gly346Arg)	not specified [RCV004346599]	uncertain significance	17	40750519	40750519	Human		name
405195006	CV2925672	single nucleotide variant	NM_181534.4(KRT25):c.1007C>G (p.Ala336Gly)	not provided [RCV003565194]	benign	17	40750548	40750548	Human		name
405817282	CV3273022	single nucleotide variant	NM_181534.4(KRT25):c.1231A>G (p.Ser411Gly)	not specified [RCV004412267]	uncertain significance	17	40749270	40749270	Human		name
407499807	CV3445481	single nucleotide variant	NM_181534.4(KRT25):c.1186T>G (p.Ser396Ala)	not specified [RCV004644455]	uncertain significance	17	40749315	40749315	Human		name
597798057	CV3698462	single nucleotide variant	NM_181534.4(KRT25):c.1189G>A (p.Gly397Arg)	not specified [RCV004936008]	uncertain significance	17	40749312	40749312	Human		name
597798063	CV3698464	single nucleotide variant	NM_181534.4(KRT25):c.1010A>T (p.Gln337Leu)	not specified [RCV004936010]	uncertain significance	17	40750545	40750545	Human		name
126738705	CV1021637	insertion	NM_181534.4(KRT25):c.773_774insACAACATGTT (p.Tyr259fs)	Autosomal recessive woolly hair 3 [RCV001335584]	pathogenic	17	40751222	40751223	Human		name
126738708	CV1021636	insertion	NM_181534.4(KRT25):c.775_776insTCTGCTGAACAAC (p.Tyr259delinsPheCysTer)	Autosomal recessive woolly hair 3 [RCV001335585]	pathogenic	17	40751220	40751221	Human		name

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