Fam135a Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)

108 records found for search term Fam135a

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8582163	CV116632	single nucleotide variant	NM_001105531.2(FAM135A):c.157+2448G>C	Lung cancer [RCV000097155]	uncertain significance	6	70455019	70455019	Human		name
8582164	CV116633	single nucleotide variant	NM_001105531.2(FAM135A):c.158-7398A>G	Lung cancer [RCV000097156]	uncertain significance	6	70468012	70468012	Human		name
155989213	CV2259670	single nucleotide variant	NM_001162529.3(FAM135A):c.233A>G (p.Asn78Ser)	not specified [RCV004116702]	uncertain significance	6	70475485	70475485	Human		name
156346686	CV2353688	single nucleotide variant	NM_001162529.3(FAM135A):c.288T>A (p.Asp96Glu)	not specified [RCV004201705]	uncertain significance	6	70475540	70475540	Human		name
156220296	CV2393706	single nucleotide variant	NM_001162529.3(FAM135A):c.260T>C (p.Met87Thr)	not specified [RCV004231508]	uncertain significance	6	70475512	70475512	Human		name
329386847	CV2439441	single nucleotide variant	NM_001162529.3(FAM135A):c.109C>T (p.Pro37Ser)	not specified [RCV004249730]	uncertain significance	6	70452523	70452523	Human		name
329401398	CV2460864	single nucleotide variant	NM_001162529.3(FAM135A):c.197T>A (p.Leu66Gln)	not specified [RCV004271170]	uncertain significance	6	70475449	70475449	Human		name
8632148	CV87354	single nucleotide variant	NM_001105531.2(FAM135A):c.1776C>T (p.Val592=)	Malignant melanoma [RCV000067445]	not provided	6	70525448	70525448	Human		name
156114347	CV2225074	single nucleotide variant	NM_001162529.3(FAM135A):c.575A>G (p.Asn192Ser)	not specified [RCV004094895]	uncertain significance	6	70480933	70480933	Human		name
156272126	CV2247303	single nucleotide variant	NM_001162529.3(FAM135A):c.793G>A (p.Glu265Lys)	not specified [RCV004108653]	uncertain significance	6	70482124	70482124	Human		name
155909865	CV2303474	single nucleotide variant	NM_001162529.3(FAM135A):c.317A>G (p.Glu106Gly)	not specified [RCV004161586]	uncertain significance	6	70475682	70475682	Human		name
156336388	CV2360727	single nucleotide variant	NM_001162529.3(FAM135A):c.551G>A (p.Arg184His)	not specified [RCV004213513]	uncertain significance	6	70480909	70480909	Human		name
11542099	CV248609	single nucleotide variant	NM_001162529.3(FAM135A):c.474C>G (p.Tyr158Ter)	Histiocytoid cardiomyopathy [RCV000240611]	likely benign	6	70477264	70477264	Human	2	name
401735921	CV2689211	single nucleotide variant	NM_001162529.3(FAM135A):c.540A>G (p.Ile180Met)	not specified [RCV004306057]	uncertain significance	6	70477330	70477330	Human		name
401897478	CV2787083	single nucleotide variant	NM_001162529.3(FAM135A):c.854A>G (p.Glu285Gly)	not specified [RCV004366189]	uncertain significance	6	70491064	70491064	Human		name
401915806	CV2820477	single nucleotide variant	NM_001162529.3(FAM135A):c.3003T>C (p.Asp1001=)	not provided [RCV003428870]	likely benign	6	70526087	70526087	Human		name
405726588	CV3259787	single nucleotide variant	NM_001162529.3(FAM135A):c.3615C>T (p.Ala1205=)	not specified [RCV004378667]	likely benign	6	70528292	70528292	Human		name
405726629	CV3259792	single nucleotide variant	NM_001162529.3(FAM135A):c.487G>A (p.Val163Ile)	not specified [RCV004378672]	uncertain significance	6	70477277	70477277	Human		name
405726645	CV3259793	single nucleotide variant	NM_001162529.3(FAM135A):c.544T>C (p.Phe182Leu)	not specified [RCV004378673]	uncertain significance	6	70480902	70480902	Human		name
405726653	CV3259794	single nucleotide variant	NM_001162529.3(FAM135A):c.943A>T (p.Met315Leu)	not specified [RCV004378674]	uncertain significance	6	70502705	70502705	Human		name
405726661	CV3259795	single nucleotide variant	NM_001162529.3(FAM135A):c.986A>C (p.Glu329Ala)	not specified [RCV004378675]	uncertain significance	6	70502748	70502748	Human		name
407507903	CV3435463	single nucleotide variant	NM_001162529.3(FAM135A):c.886C>T (p.Pro296Ser)	not specified [RCV004625268]	uncertain significance	6	70502648	70502648	Human		name
407507913	CV3435466	single nucleotide variant	NM_001162529.3(FAM135A):c.499A>G (p.Thr167Ala)	not specified [RCV004625271]	uncertain significance	6	70477289	70477289	Human		name
597737130	CV3668491	single nucleotide variant	NM_001162529.3(FAM135A):c.376G>T (p.Asp126Tyr)	not specified [RCV004920775]	uncertain significance	6	70477166	70477166	Human		name
597737189	CV3668503	single nucleotide variant	NM_001162529.3(FAM135A):c.703C>T (p.His235Tyr)	not specified [RCV004920787]	uncertain significance	6	70482034	70482034	Human		name
597737233	CV3668512	single nucleotide variant	NM_001162529.3(FAM135A):c.334T>C (p.Ser112Pro)	not specified [RCV004920796]	uncertain significance	6	70475699	70475699	Human		name
597737263	CV3668518	single nucleotide variant	NM_001162529.3(FAM135A):c.497T>C (p.Val166Ala)	not specified [RCV004920802]	uncertain significance	6	70477287	70477287	Human		name
598224570	CV3965849	single nucleotide variant	NM_001162529.3(FAM135A):c.835G>A (p.Val279Ile)	not specified [RCV005341317]	uncertain significance	6	70491045	70491045	Human		name
155924083	CV2212576	single nucleotide variant	NM_001162529.3(FAM135A):c.2708T>C (p.Leu903Ser)	not specified [RCV004091441]	uncertain significance	6	70525792	70525792	Human		name
156032277	CV2218265	single nucleotide variant	NM_001162529.3(FAM135A):c.1490T>C (p.Leu497Pro)	not specified [RCV004088458]	uncertain significance	6	70524574	70524574	Human		name
155957766	CV2282110	single nucleotide variant	NM_001162529.3(FAM135A):c.2032C>G (p.Pro678Ala)	not specified [RCV004138850]	uncertain significance	6	70525116	70525116	Human		name
156008793	CV2294271	single nucleotide variant	NM_001162529.3(FAM135A):c.2077C>G (p.Leu693Val)	not specified [RCV004151406]	uncertain significance	6	70525161	70525161	Human		name
155967739	CV2312757	single nucleotide variant	NM_001162529.3(FAM135A):c.2101T>G (p.Ser701Ala)	not specified [RCV004169476]	uncertain significance	6	70525185	70525185	Human		name
329357932	CV2427886	single nucleotide variant	NM_001162529.3(FAM135A):c.1261T>G (p.Leu421Val)	not specified [RCV004252657]	uncertain significance	6	70524345	70524345	Human		name
329356270	CV2430665	single nucleotide variant	NM_001162529.3(FAM135A):c.1918T>C (p.Ser640Pro)	not specified [RCV004253854]	uncertain significance	6	70525002	70525002	Human		name
329384714	CV2435181	single nucleotide variant	NM_001162529.3(FAM135A):c.1762C>T (p.Pro588Ser)	not specified [RCV004252818]	uncertain significance	6	70524846	70524846	Human		name
401759683	CV2698590	single nucleotide variant	NM_001162529.3(FAM135A):c.1588G>A (p.Ala530Thr)	not specified [RCV004299074]	uncertain significance	6	70524672	70524672	Human		name
401763675	CV2717085	single nucleotide variant	NM_001162529.3(FAM135A):c.1341C>G (p.Ser447Arg)	not specified [RCV004330109]	uncertain significance	6	70524425	70524425	Human		name
401729527	CV2733133	single nucleotide variant	NM_001162529.3(FAM135A):c.1775A>G (p.Asn592Ser)	not specified [RCV004332063]	uncertain significance	6	70524859	70524859	Human		name
405726438	CV3259771	single nucleotide variant	NM_001162529.3(FAM135A):c.1057T>C (p.Cys353Arg)	not specified [RCV004378651]	uncertain significance	6	70522540	70522540	Human		name
405726447	CV3259772	single nucleotide variant	NM_001162529.3(FAM135A):c.1250T>C (p.Val417Ala)	not specified [RCV004378652]	uncertain significance	6	70524113	70524113	Human		name
405726459	CV3259773	single nucleotide variant	NM_001162529.3(FAM135A):c.1253C>A (p.Thr418Asn)	not specified [RCV004378653]	uncertain significance	6	70524116	70524116	Human		name
405726466	CV3259774	single nucleotide variant	NM_001162529.3(FAM135A):c.1408A>C (p.Thr470Pro)	not specified [RCV004378654]	uncertain significance	6	70524492	70524492	Human		name
405726482	CV3259776	single nucleotide variant	NM_001162529.3(FAM135A):c.1688C>T (p.Thr563Ile)	not specified [RCV004378656]	uncertain significance	6	70524772	70524772	Human		name
405726491	CV3259777	single nucleotide variant	NM_001162529.3(FAM135A):c.1769T>C (p.Ile590Thr)	not specified [RCV004378657]	uncertain significance	6	70524853	70524853	Human		name
405726500	CV3259778	single nucleotide variant	NM_001162529.3(FAM135A):c.1894C>T (p.His632Tyr)	not specified [RCV004378658]	uncertain significance	6	70524978	70524978	Human		name
405726508	CV3259779	single nucleotide variant	NM_001162529.3(FAM135A):c.2122A>G (p.Ile708Val)	not specified [RCV004378659]	uncertain significance	6	70525206	70525206	Human		name
405726516	CV3259780	single nucleotide variant	NM_001162529.3(FAM135A):c.2441A>G (p.Asn814Ser)	not specified [RCV004378660]	uncertain significance	6	70525525	70525525	Human		name
405726529	CV3259781	single nucleotide variant	NM_001162529.3(FAM135A):c.2648A>G (p.Asp883Gly)	not specified [RCV004378661]	uncertain significance	6	70525732	70525732	Human		name
405726538	CV3259782	single nucleotide variant	NM_001162529.3(FAM135A):c.2660A>G (p.Lys887Arg)	not specified [RCV004378662]	uncertain significance	6	70525744	70525744	Human		name
407507899	CV3435462	single nucleotide variant	NM_001162529.3(FAM135A):c.2209C>A (p.Pro737Thr)	not specified [RCV004625267]	uncertain significance	6	70525293	70525293	Human		name
407507906	CV3435464	single nucleotide variant	NM_001162529.3(FAM135A):c.1721G>A (p.Ser574Asn)	not specified [RCV004625269]	uncertain significance	6	70524805	70524805	Human		name
407507916	CV3435467	single nucleotide variant	NM_001162529.3(FAM135A):c.1169C>G (p.Pro390Arg)	not specified [RCV004625272]	uncertain significance	6	70524032	70524032	Human		name
597737135	CV3668492	single nucleotide variant	NM_001162529.3(FAM135A):c.1539C>G (p.Asn513Lys)	not specified [RCV004920776]	uncertain significance	6	70524623	70524623	Human		name
597737149	CV3668495	single nucleotide variant	NM_001162529.3(FAM135A):c.1787A>T (p.Asp596Val)	not specified [RCV004920779]	uncertain significance	6	70524871	70524871	Human		name
597737154	CV3668496	single nucleotide variant	NM_001162529.3(FAM135A):c.1783C>T (p.Pro595Ser)	not specified [RCV004920780]	uncertain significance	6	70524867	70524867	Human		name
597737159	CV3668497	single nucleotide variant	NM_001162529.3(FAM135A):c.1317G>T (p.Met439Ile)	not specified [RCV004920781]	uncertain significance	6	70524401	70524401	Human		name
597737184	CV3668502	single nucleotide variant	NM_001162529.3(FAM135A):c.2537A>T (p.Asp846Val)	not specified [RCV004920786]	uncertain significance	6	70525621	70525621	Human		name
597737193	CV3668504	single nucleotide variant	NM_001162529.3(FAM135A):c.1691A>G (p.Tyr564Cys)	not specified [RCV004920788]	uncertain significance	6	70524775	70524775	Human		name
597737201	CV3668506	single nucleotide variant	NM_001162529.3(FAM135A):c.2054A>C (p.Glu685Ala)	not specified [RCV004920790]	uncertain significance	6	70525138	70525138	Human		name
597737214	CV3668508	single nucleotide variant	NM_001162529.3(FAM135A):c.1825T>C (p.Cys609Arg)	not specified [RCV004920792]	uncertain significance	6	70524909	70524909	Human		name
597737223	CV3668510	single nucleotide variant	NM_001162529.3(FAM135A):c.2381G>A (p.Gly794Glu)	not specified [RCV004920794]	uncertain significance	6	70525465	70525465	Human		name
597737243	CV3668514	single nucleotide variant	NM_001162529.3(FAM135A):c.1436C>T (p.Ser479Phe)	not specified [RCV004920798]	uncertain significance	6	70524520	70524520	Human		name
597737258	CV3668517	single nucleotide variant	NM_001162529.3(FAM135A):c.2110A>G (p.Lys704Glu)	not specified [RCV004920801]	uncertain significance	6	70525194	70525194	Human		name
598224565	CV3965848	single nucleotide variant	NM_001162529.3(FAM135A):c.1319A>C (p.Asp440Ala)	not specified [RCV005341316]	uncertain significance	6	70524403	70524403	Human		name
598224576	CV3965850	single nucleotide variant	NM_001162529.3(FAM135A):c.2963C>T (p.Thr988Ile)	not specified [RCV005341318]	uncertain significance	6	70526047	70526047	Human		name
598224583	CV3965852	single nucleotide variant	NM_001162529.3(FAM135A):c.2224A>G (p.Lys742Glu)	not specified [RCV005341319]	uncertain significance	6	70525308	70525308	Human		name
598224614	CV3965856	single nucleotide variant	NM_001162529.3(FAM135A):c.1578G>C (p.Leu526Phe)	not specified [RCV005341323]	uncertain significance	6	70524662	70524662	Human		name
598224640	CV3965859	single nucleotide variant	NM_001162529.3(FAM135A):c.1577T>G (p.Leu526Trp)	not specified [RCV005341326]	uncertain significance	6	70524661	70524661	Human		name
598224647	CV3965860	single nucleotide variant	NM_001162529.3(FAM135A):c.2010G>C (p.Glu670Asp)	not specified [RCV005341327]	uncertain significance	6	70525094	70525094	Human		name
598224655	CV3965861	single nucleotide variant	NM_001162529.3(FAM135A):c.2236G>C (p.Val746Leu)	not specified [RCV005341328]	uncertain significance	6	70525320	70525320	Human		name
156329693	CV2213887	single nucleotide variant	NM_001162529.3(FAM135A):c.3344A>G (p.His1115Arg)	not specified [RCV004083620]	uncertain significance	6	70526428	70526428	Human		name
156073449	CV2251563	single nucleotide variant	NM_001162529.3(FAM135A):c.3314A>G (p.Tyr1105Cys)	not specified [RCV004117518]	uncertain significance	6	70526398	70526398	Human		name
155955763	CV2281846	single nucleotide variant	NM_001162529.3(FAM135A):c.4102G>A (p.Ala1368Thr)	not specified [RCV004136850]	uncertain significance	6	70536396	70536396	Human		name
155923593	CV2351775	single nucleotide variant	NM_001162529.3(FAM135A):c.3244G>T (p.Asp1082Tyr)	not specified [RCV004197932]	uncertain significance	6	70526328	70526328	Human		name
156073767	CV2376926	single nucleotide variant	NM_001162529.3(FAM135A):c.3892A>G (p.Ser1298Gly)	not specified [RCV004229615]	uncertain significance	6	70533781	70533781	Human		name
156079636	CV2384544	single nucleotide variant	NM_001162529.3(FAM135A):c.4231C>T (p.Leu1411Phe)	not specified [RCV004232340]	uncertain significance	6	70556752	70556752	Human		name
329358784	CV2425376	single nucleotide variant	NM_001162529.3(FAM135A):c.3361G>C (p.Glu1121Gln)	not specified [RCV004251037]	uncertain significance	6	70526445	70526445	Human		name
329371117	CV2461953	single nucleotide variant	NM_001162529.3(FAM135A):c.4153T>C (p.Ser1385Pro)	not specified [RCV004271853]	uncertain significance	6	70538326	70538326	Human		name
401893436	CV2765265	single nucleotide variant	NM_001162529.3(FAM135A):c.3100G>A (p.Val1034Ile)	not specified [RCV004339788]	uncertain significance	6	70526184	70526184	Human		name
401862446	CV2775305	single nucleotide variant	NM_001162529.3(FAM135A):c.3436A>G (p.Thr1146Ala)	not specified [RCV004348421]	likely benign	6	70526520	70526520	Human		name
405726549	CV3259783	single nucleotide variant	NM_001162529.3(FAM135A):c.3050G>T (p.Ser1017Ile)	not specified [RCV004378663]	uncertain significance	6	70526134	70526134	Human		name
405726560	CV3259784	single nucleotide variant	NM_001162529.3(FAM135A):c.3202G>A (p.Glu1068Lys)	not specified [RCV004378664]	uncertain significance	6	70526286	70526286	Human		name
405726566	CV3259785	single nucleotide variant	NM_001162529.3(FAM135A):c.3343C>T (p.His1115Tyr)	not specified [RCV004378665]	uncertain significance	6	70526427	70526427	Human		name
405726576	CV3259786	single nucleotide variant	NM_001162529.3(FAM135A):c.3467C>T (p.Pro1156Leu)	not specified [RCV004378666]	uncertain significance	6	70526551	70526551	Human		name
405726593	CV3259788	single nucleotide variant	NM_001162529.3(FAM135A):c.4036C>T (p.Leu1346Phe)	not specified [RCV004378668]	uncertain significance	6	70536330	70536330	Human		name
405726603	CV3259789	single nucleotide variant	NM_001162529.3(FAM135A):c.4234C>G (p.His1412Asp)	not specified [RCV004378669]	uncertain significance	6	70556755	70556755	Human		name
405726613	CV3259790	single nucleotide variant	NM_001162529.3(FAM135A):c.4352A>G (p.Tyr1451Cys)	not specified [RCV004378670]	uncertain significance	6	70559725	70559725	Human		name
405726622	CV3259791	single nucleotide variant	NM_001162529.3(FAM135A):c.4364T>C (p.Ile1455Thr)	not specified [RCV004378671]	uncertain significance	6	70559737	70559737	Human		name
407507887	CV3435459	single nucleotide variant	NM_001162529.3(FAM135A):c.3098T>C (p.Ile1033Thr)	not specified [RCV004625264]	uncertain significance	6	70526182	70526182	Human		name
407507893	CV3435460	single nucleotide variant	NM_001162529.3(FAM135A):c.3832G>A (p.Gly1278Arg)	not specified [RCV004625265]	uncertain significance	6	70533216	70533216	Human		name
407507896	CV3435461	single nucleotide variant	NM_001162529.3(FAM135A):c.3937A>T (p.Ile1313Leu)	not specified [RCV004625266]	uncertain significance	6	70533826	70533826	Human		name
407507910	CV3435465	single nucleotide variant	NM_001162529.3(FAM135A):c.4442A>G (p.Asn1481Ser)	not specified [RCV004625270]	uncertain significance	6	70559815	70559815	Human		name
597737139	CV3668493	single nucleotide variant	NM_001162529.3(FAM135A):c.3572C>T (p.Ser1191Leu)	not specified [RCV004920777]	uncertain significance	6	70526656	70526656	Human		name
597737164	CV3668498	single nucleotide variant	NM_001162529.3(FAM135A):c.4315A>G (p.Lys1439Glu)	not specified [RCV004920782]	uncertain significance	6	70556836	70556836	Human		name
597737169	CV3668499	single nucleotide variant	NM_001162529.3(FAM135A):c.4150G>T (p.Gly1384Cys)	not specified [RCV004920783]	uncertain significance	6	70538323	70538323	Human		name
597737174	CV3668500	single nucleotide variant	NM_001162529.3(FAM135A):c.4384G>C (p.Val1462Leu)	not specified [RCV004920784]	uncertain significance	6	70559757	70559757	Human		name
597737179	CV3668501	single nucleotide variant	NM_001162529.3(FAM135A):c.3109G>A (p.Gly1037Arg)	not specified [RCV004920785]	uncertain significance	6	70526193	70526193	Human		name
597737209	CV3668507	single nucleotide variant	NM_001162529.3(FAM135A):c.3282G>T (p.Met1094Ile)	not specified [RCV004920791]	uncertain significance	6	70526366	70526366	Human		name
597737218	CV3668509	single nucleotide variant	NM_001162529.3(FAM135A):c.3431T>C (p.Met1144Thr)	not specified [RCV004920793]	uncertain significance	6	70526515	70526515	Human		name
597737228	CV3668511	single nucleotide variant	NM_001162529.3(FAM135A):c.3505T>G (p.Ser1169Ala)	not specified [RCV004920795]	uncertain significance	6	70526589	70526589	Human		name
597737238	CV3668513	single nucleotide variant	NM_001162529.3(FAM135A):c.3290A>G (p.Asn1097Ser)	not specified [RCV004920797]	uncertain significance	6	70526374	70526374	Human		name
597737248	CV3668515	single nucleotide variant	NM_001162529.3(FAM135A):c.3282G>A (p.Met1094Ile)	not specified [RCV004920799]	uncertain significance	6	70526366	70526366	Human		name
598194950	CV3965851	single nucleotide variant	NM_001162529.3(FAM135A):c.3253G>A (p.Asp1085Asn)	not specified [RCV005335491]	uncertain significance	6	70526337	70526337	Human		name
598224590	CV3965853	single nucleotide variant	NM_001162529.3(FAM135A):c.3049A>G (p.Ser1017Gly)	not specified [RCV005341320]	uncertain significance	6	70526133	70526133	Human		name
598224597	CV3965854	single nucleotide variant	NM_001162529.3(FAM135A):c.3512A>G (p.Lys1171Arg)	not specified [RCV005341321]	uncertain significance	6	70526596	70526596	Human		name
598224622	CV3965857	single nucleotide variant	NM_001162529.3(FAM135A):c.3058C>G (p.His1020Asp)	not specified [RCV005341324]	uncertain significance	6	70526142	70526142	Human		name
598224630	CV3965858	single nucleotide variant	NM_001162529.3(FAM135A):c.3299A>G (p.Tyr1100Cys)	not specified [RCV005341325]	uncertain significance	6	70526383	70526383	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Create Name:

Description:

Send us a Message