Tmem184a Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

62 records found for search term Tmem184a

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597753529	CV3613577	single nucleotide variant	NM_001097620.2(TMEM184A):c.13T>A (p.Ser5Thr)	not specified [RCV004867389]	uncertain significance	7	1555472	1555472	Human		name
597753552	CV3613582	single nucleotide variant	NM_001097620.2(TMEM184A):c.22C>A (p.Leu8Met)	not specified [RCV004867394]	uncertain significance	7	1555463	1555463	Human		name
156277953	CV2330881	single nucleotide variant	NM_001097620.2(TMEM184A):c.80C>T (p.Pro27Leu)	not specified [RCV004185935]	uncertain significance	7	1555405	1555405	Human		name
329365679	CV2440975	single nucleotide variant	NM_001097620.2(TMEM184A):c.28A>G (p.Thr10Ala)	not specified [RCV004261356]	uncertain significance	7	1555457	1555457	Human		name
401878611	CV2770710	single nucleotide variant	NM_001097620.2(TMEM184A):c.29C>T (p.Thr10Ile)	not specified [RCV004349754]	uncertain significance	7	1555456	1555456	Human		name
401863767	CV2770711	single nucleotide variant	NM_001097620.2(TMEM184A):c.32C>T (p.Ala11Val)	not specified [RCV004349755]	uncertain significance	7	1555453	1555453	Human		name
15155970	CV710885	single nucleotide variant	NM_001097620.2(TMEM184A):c.804G>A (p.Ser268=)	not provided [RCV000969023]	benign	7	1548529	1548529	Human		name
15117371	CV710886	single nucleotide variant	NM_001097620.2(TMEM184A):c.582C>T (p.Pro194=)	not provided [RCV000962193]	benign	7	1549916	1549916	Human		name
15192403	CV722407	single nucleotide variant	NM_001097620.2(TMEM184A):c.528C>T (p.Ile176=)	not provided [RCV000888653]	benign	7	1550147	1550147	Human		name
155948038	CV2271954	single nucleotide variant	NM_001097620.2(TMEM184A):c.235C>T (p.Arg79Cys)	not specified [RCV004124772]	uncertain significance	7	1550967	1550967	Human		name
329382493	CV2449024	single nucleotide variant	NM_001097620.2(TMEM184A):c.274C>T (p.Arg92Cys)	not specified [RCV004264099]	uncertain significance	7	1550928	1550928	Human		name
329369714	CV2461194	single nucleotide variant	NM_001097620.2(TMEM184A):c.263G>A (p.Arg88His)	not specified [RCV004267391]	uncertain significance	7	1550939	1550939	Human		name
329363258	CV2464996	single nucleotide variant	NM_001097620.2(TMEM184A):c.155C>T (p.Ser52Phe)	not specified [RCV004284908]	uncertain significance	7	1555330	1555330	Human		name
401895058	CV2792749	single nucleotide variant	NM_001097620.2(TMEM184A):c.202G>C (p.Val68Leu)	not specified [RCV004365510]	likely benign	7	1555283	1555283	Human		name
405752988	CV3336162	single nucleotide variant	NM_001097620.2(TMEM184A):c.104T>C (p.Met35Thr)	not specified [RCV004467389]	uncertain significance	7	1555381	1555381	Human		name
407453506	CV3486477	single nucleotide variant	NM_001097620.2(TMEM184A):c.256G>A (p.Glu86Lys)	not specified [RCV004684567]	uncertain significance	7	1550946	1550946	Human		name
597753543	CV3613580	single nucleotide variant	NM_001097620.2(TMEM184A):c.187G>A (p.Val63Met)	not specified [RCV004867392]	uncertain significance	7	1555298	1555298	Human		name
597753556	CV3613583	single nucleotide variant	NM_001097620.2(TMEM184A):c.143T>A (p.Leu48His)	not specified [RCV004867395]	uncertain significance	7	1555342	1555342	Human		name
597753570	CV3613586	single nucleotide variant	NM_001097620.2(TMEM184A):c.182T>C (p.Ile61Thr)	not specified [RCV004867398]	uncertain significance	7	1555303	1555303	Human		name
598213549	CV3917529	single nucleotide variant	NM_001097620.2(TMEM184A):c.217C>G (p.Gln73Glu)	not specified [RCV005292336]	uncertain significance	7	1555268	1555268	Human		name
15149251	CV722410	single nucleotide variant	NM_001097620.2(TMEM184A):c.116G>A (p.Gly39Glu)	not provided [RCV000879126]	benign	7	1555369	1555369	Human		name
156379789	CV2211581	single nucleotide variant	NM_001097620.2(TMEM184A):c.416G>A (p.Cys139Tyr)	not specified [RCV004084481]	uncertain significance	7	1550365	1550365	Human		name
156036452	CV2218341	single nucleotide variant	NM_001097620.2(TMEM184A):c.748C>T (p.Arg250Trp)	not specified [RCV004088854]	uncertain significance	7	1548585	1548585	Human		name
156177397	CV2220400	single nucleotide variant	NM_001097620.2(TMEM184A):c.319A>G (p.Ser107Gly)	not specified [RCV004095807]	uncertain significance	7	1550883	1550883	Human		name
156121274	CV2275998	single nucleotide variant	NM_001097620.2(TMEM184A):c.988G>A (p.Ala330Thr)	not specified [RCV004141677]	uncertain significance	7	1547766	1547766	Human		name
156039521	CV2279036	single nucleotide variant	NM_001097620.2(TMEM184A):c.630C>A (p.His210Gln)	not specified [RCV004145718]	uncertain significance	7	1549868	1549868	Human		name
156047831	CV2315722	single nucleotide variant	NM_001097620.2(TMEM184A):c.353T>A (p.Val118Asp)	not specified [RCV004169736]	uncertain significance	7	1550849	1550849	Human		name
156267318	CV2371773	single nucleotide variant	NM_001097620.2(TMEM184A):c.931G>A (p.Val311Met)	not specified [RCV004219435]	uncertain significance	7	1547823	1547823	Human		name
156149763	CV2394601	single nucleotide variant	NM_001097620.2(TMEM184A):c.361G>A (p.Asp121Asn)	not specified [RCV004240949]	uncertain significance	7	1550841	1550841	Human		name
329355801	CV2430492	single nucleotide variant	NM_001097620.2(TMEM184A):c.854C>T (p.Pro285Leu)	not specified [RCV004252078]	uncertain significance	7	1547900	1547900	Human		name
329354662	CV2444645	single nucleotide variant	NM_001097620.2(TMEM184A):c.727T>C (p.Phe243Leu)	not specified [RCV004258910]	uncertain significance	7	1548606	1548606	Human		name
401769907	CV2693137	single nucleotide variant	NM_001097620.2(TMEM184A):c.479C>A (p.Ser160Tyr)	not specified [RCV004308667]	uncertain significance	7	1550196	1550196	Human		name
401872775	CV2764333	single nucleotide variant	NM_001097620.2(TMEM184A):c.655G>A (p.Gly219Ser)	not specified [RCV004338906]	uncertain significance	7	1548678	1548678	Human		name
405753008	CV3336165	single nucleotide variant	NM_001097620.2(TMEM184A):c.539G>A (p.Arg180His)	not specified [RCV004467392]	uncertain significance	7	1550136	1550136	Human		name
405753016	CV3336166	single nucleotide variant	NM_001097620.2(TMEM184A):c.547A>G (p.Lys183Glu)	not specified [RCV004467393]	uncertain significance	7	1550128	1550128	Human		name
405753023	CV3336167	single nucleotide variant	NM_001097620.2(TMEM184A):c.779C>T (p.Thr260Ile)	not specified [RCV004467394]	uncertain significance	7	1548554	1548554	Human		name
405753030	CV3336168	single nucleotide variant	NM_001097620.2(TMEM184A):c.907G>A (p.Gly303Ser)	not specified [RCV004467395]	uncertain significance	7	1547847	1547847	Human		name
405753036	CV3336169	single nucleotide variant	NM_001097620.2(TMEM184A):c.922A>G (p.Ile308Val)	not specified [RCV004467396]	uncertain significance	7	1547832	1547832	Human		name
405753042	CV3336170	single nucleotide variant	NM_001097620.2(TMEM184A):c.996G>C (p.Lys332Asn)	not specified [RCV004467397]	uncertain significance	7	1547758	1547758	Human		name
407458700	CV3486476	single nucleotide variant	NM_001097620.2(TMEM184A):c.685G>T (p.Ala229Ser)	not specified [RCV004686908]	uncertain significance	7	1548648	1548648	Human		name
597753525	CV3613576	single nucleotide variant	NM_001097620.2(TMEM184A):c.338A>G (p.Asp113Gly)	not specified [RCV004867388]	likely benign	7	1550864	1550864	Human		name
597753533	CV3613578	single nucleotide variant	NM_001097620.2(TMEM184A):c.509G>A (p.Arg170Gln)	not specified [RCV004867390]	uncertain significance	7	1550166	1550166	Human		name
597753547	CV3613581	single nucleotide variant	NM_001097620.2(TMEM184A):c.301G>A (p.Ala101Thr)	not specified [RCV004867393]	uncertain significance	7	1550901	1550901	Human		name
597753561	CV3613584	single nucleotide variant	NM_001097620.2(TMEM184A):c.718C>G (p.Leu240Val)	not specified [RCV004867396]	uncertain significance	7	1548615	1548615	Human		name
598213527	CV3917525	single nucleotide variant	NM_001097620.2(TMEM184A):c.754T>C (p.Phe252Leu)	not specified [RCV005292332]	uncertain significance	7	1548579	1548579	Human		name
598213532	CV3917526	single nucleotide variant	NM_001097620.2(TMEM184A):c.988G>T (p.Ala330Ser)	not specified [RCV005292333]	likely benign	7	1547766	1547766	Human		name
598213544	CV3917528	single nucleotide variant	NM_001097620.2(TMEM184A):c.588G>A (p.Met196Ile)	not specified [RCV005292335]	uncertain significance	7	1549910	1549910	Human		name
598213555	CV3917531	single nucleotide variant	NM_001097620.2(TMEM184A):c.998A>G (p.Lys333Arg)	not specified [RCV005292337]	uncertain significance	7	1547756	1547756	Human		name
156270171	CV2290022	single nucleotide variant	NM_001097620.2(TMEM184A):c.1225C>G (p.Pro409Ala)	not specified [RCV004152721]	uncertain significance	7	1546969	1546969	Human		name
156260114	CV2305043	single nucleotide variant	NM_001097620.2(TMEM184A):c.1178C>T (p.Ser393Phe)	not specified [RCV004168930]	uncertain significance	7	1547016	1547016	Human		name
156087884	CV2337055	single nucleotide variant	NM_001097620.2(TMEM184A):c.1225C>T (p.Pro409Ser)	not specified [RCV004192820]	uncertain significance	7	1546969	1546969	Human		name
329402691	CV2451239	single nucleotide variant	NM_001097620.2(TMEM184A):c.1021G>A (p.Ala341Thr)	not specified [RCV004270152]	uncertain significance	7	1547173	1547173	Human		name
401751163	CV2715885	single nucleotide variant	NM_001097620.2(TMEM184A):c.1235A>G (p.Asp412Gly)	not specified [RCV004328998]	uncertain significance	7	1546959	1546959	Human		name
401885578	CV2768271	single nucleotide variant	NM_001097620.2(TMEM184A):c.1187G>A (p.Ser396Asn)	not specified [RCV004350261]	uncertain significance	7	1547007	1547007	Human		name
401860164	CV2768505	single nucleotide variant	NM_001097620.2(TMEM184A):c.1108G>A (p.Ala370Thr)	not specified [RCV004344387]	uncertain significance	7	1547086	1547086	Human		name
401892152	CV2775968	single nucleotide variant	NM_001097620.2(TMEM184A):c.1044C>A (p.Ser348Arg)	not specified [RCV004344984]	uncertain significance	7	1547150	1547150	Human		name
405752994	CV3336163	single nucleotide variant	NM_001097620.2(TMEM184A):c.1105C>T (p.Pro369Ser)	not specified [RCV004467390]	uncertain significance	7	1547089	1547089	Human		name
405753001	CV3336164	single nucleotide variant	NM_001097620.2(TMEM184A):c.1120T>C (p.Tyr374His)	not specified [RCV004467391]	uncertain significance	7	1547074	1547074	Human		name
597753538	CV3613579	single nucleotide variant	NM_001097620.2(TMEM184A):c.1052G>T (p.Arg351Met)	not specified [RCV004867391]	uncertain significance	7	1547142	1547142	Human		name
598213539	CV3917527	single nucleotide variant	NM_001097620.2(TMEM184A):c.1136C>T (p.Thr379Met)	not specified [RCV005292334]	uncertain significance	7	1547058	1547058	Human		name
598178546	CV3917530	single nucleotide variant	NM_001097620.2(TMEM184A):c.1201A>G (p.Ser401Gly)	not specified [RCV005285992]	uncertain significance	7	1546993	1546993	Human		name
15157980	CV699957	microsatellite	NM_001097620.2(TMEM184A):c.1171GGC[3] (p.Gly392dup)	not provided [RCV000946987]	benign	7	1547017	1547018	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